Last updated: 04/16/2009


<NEWS>

Pitt Researchers Create Atomic-sized One-stop Shop for Nanoelectronics

Tiny Viruses Net Pitt Professor Major Award from the National Academy of Sciences

Pitt Researchers Create Nontoxic Clean-up Method for Common, Potentially Toxic Nano Materials

Pitt, NETL Researchers Report Molecular Chain Reaction Thought to Be Impossible

Nanotech Breakthrough Could Speed Smaller Electronic Devices

Team's Invention Could Lead to New Data Storage, Retrieval Tools

Model for the Assembly of Advanced, Single-Molecule-Based Electronic Components Developed at Pitt

Nano-Sensor Developed Here Could Detect Asthma Symptoms
Postdoctoral Research Associate Wins an Award

Moving Raman to the UV Range: The Research of Pitt Professor Highlighted
in C&E News
Pitt Professor Scores Science Double-header
Grand Opening of the NanoScale Fabrication and Characterization
Facility on September 29, 2006
Small Science Gets a Big Boost: Petersens Give $5M for Nanotech
Pitt Nanotech Researcher Devises Versions of Building Blocks on a Molecular Scale
Pitt Professor, Student Win Nanotechnology Prize for Work on
"Molecular Lego(r) Set"
New Nanofabrication Capability Makes Pitt Unique in United States
"Wet" Electrons Provide Easiest Way to Transport Charge,
Pitt Researchers Find

Faster Method for Detecting Disease-Causing Mutations Developed by Pitt
Researcher


Toward a Quantum Computer, One Dot at a Time

Pitt Researchers See Electron Waves in Motion for First Time

University of Pittsburgh Announces Construction of New $6.1 Million Nanotechnology Facility, Increase in Nano Faculty
Pitt Researcher, Colleagues Create Self-Assembling Nanoparticle/Polymer Mixtures
Biochemical Sensing Systems the Size of a Fingernail Tip?
"Nano-Metals" Deform Differently from Ordinary Metals, Pitt-Led Research Team Confirms

Molecular Motors Drive Cellular Movements (Video) : Download video : Windows | Quicktime

Nano-optics Research Offers a Bright Future (Video) : Download video : Windows | Quicktime
Research in Quantum Computing (Video): Download video : Windows | Quicktime



<EVENTS>

The Institute Seminar: Prof. Brian Korgel’s Lecture on April 24th, 2009

The Institute Seminar: Prof. Thuc-Quyen Nguyen’s Lecture on April 6th, 2009

The Institute Seminar: Prof. Angel Rubio’s Lecture on March 17th, 2009

Workshop on Nanotechnology Opportunity Identification on December 10th-11th, 2008

The Institute Seminar: Dr. Eric Snow's Lecture on September 11th, 2008

The Institute Seminar: Prof. Paul Weiss' Lecture on September 4th, 2008

The Institute Seminar: Prof. Macosko's Lecture on July 10th, 2008

The Institute Seminar: Prof. Ginger's Lecture on May 16th, 2008

The Institute Seminar: Prof. Kelley's Lecture on April 25th, 2008

The Institute Seminar: Prof. Mallouk's Lecture on April 18th, 2008

The Institute Seminar: Prof. Naaman's Lecture on March 28th, 2008

The Institute Seminar: Prof. Chris Murray's Lecture on March 3rd, 2008

The Institute Seminar: Prof. Ray Baughman's Lecture on February 4th, 2008

The Institute Seminar: Prof. Paul Barbara's Lecture on October
26th, 2007

The Institute Seminar: Prof. Tamar Seideman's Lecture on May 3rd, 2007

The Institute Seminar: Dr. Richard Colton's Lecture on April 12th, 2007

The Institute Seminar: Prof. Reginald Penner's Lecture on March 9th, 2007

The Institute Seminar: Prof. Sharon Glotzer's Lecture on January 25th, 2007

The Institute Seminar: Prof. Naomi Halas' Lecture on December 7th, 2006

Nanoscience from Research to Industry (Tripartite Symposium): April 12, 2006, Chevron Science Center

The Institute Seminar: Dr. Steven Smith's Lecture on March 29, 2006

The Institute Seminar: Prof. Richard Haglund's Lecture on March 7, 2006

The Institute Seminar: Prof. Nongjian Tao's Lecture on January 27, 2006

The Institute Seminar: Prof. Banaszak Holl's Lecture on November 11, 2005

The Institute Seminar: Prof. Barbara Baird's Lecture on April 4, 2005

The Institute Seminar: Dr. Lowndes' lecture on March 18, 2005

The Institute Seminar: Professor Stockman's lecture on January 21, 2005

The Institute Seminar: Prof. Nie's lecture on December 10, 2004

The Institute Seminar: Prof. Philbert's lecture on November 19, 2004

The Institute Seminar: Prof. Steven Boxer's Lecture on October 1, 2004

Pennsylvania Nanotechnology Conference on May 25th and 26th, 2004

The Institute Seminar: Dr. Jim Hannon's Lecture on April 19th, 2004

The Institute Seminar: Prof. Mike Thorpe's Lecture on Feb 9th, 2004

The Institute Seminar: Prof. Mark Reed's Lecture on January 16th, 2004

The Institute Seminar: Dr. Danial Wayner's Lecture on Sept 16, 2003

The Institute Seminar: Prof. Milton Cole's Lecture on May 29, 2003

PSC/Pitt Workshop on Biological Ion Channels : May 21-23, 2003 at Benedum Hall Auditorium (pdf)
http://www.psc.edu/biomed/training/workshops/2003/ion/

The Institute Seminar Series: Dr. Michalske's Lecture on April 9th, 2003 (open to the public)

NanoScience and Engineering Conference, University of Pittsburgh, December 16, 2002

Pennsylvania Nanotechnology 2002, Harrisburg, PA, October 3-4, 2002

 

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Pitt Researchers Make Breakthrough in Nanotechnology by Uncovering Conductive Property of Carbon-based Molecules

Newfound ability of organic molecules to conduct electricity opens door to smaller, cheaper, and more powerful technologies

PITTSBURGH-University of Pittsburgh researchers have discovered that certain organic-or carbon-based-molecules exhibit the properties of atoms under certain circumstances and, in turn, conduct electricity as well as metal. Detailed in the April 18 edition of “Science,” the finding is a breakthrough in developing nanotechnology that provides a new strategy for designing electronic materials, including inexpensive and multifunctional organic conductors that have long been considered the key to smaller, cheaper, and faster technologies.

The Pitt team found that the hollow, soccer-ball-shaped carbon molecules known as fullerenes can hold and transfer an electrical charge much like the most highly conductive atoms, explained project head Hrvoje Petek, a professor of physics and chemistry in Pitt's School of Arts and Sciences and codirector of Pitt's Petersen Institute for NanoScience and Engineering. The research was performed by Pitt post-doctoral associates Min Feng and Jin Zhao.

When an electron was introduced into a fullerene molecule, the shape of the electron distribution mimicked that of a hydrogen atom or an atom from the alkali metal group, which includes lithium, sodium, and potassium. Moreover, when two fullerenes were placed next to each other on a copper surface, they showed the electron distribution of their chemical bond and appeared as H2, a hydrogen molecule. The assembly exhibited metal-like conductivity when the team extended it to a wire 1-molecule-wide.

“Our work provides a new perspective on what determines the electronic properties of materials,” Petek said. “The realization that hollow molecules can have metal-like conductivity opens the way to develop novel materials with electronic and chemical properties that can be tailored by shape and size.”

Although the team worked with fullerenes, the team's results apply to all hollow molecules, Petek added, including carbon nanotubes-rolled, 1-atom-thick sheets of graphite 100,000 times smaller than a human hair.

The team's research shows promise for the future of electronics based on molecular conductors. These molecule-based devices surpass the semiconductor and metal conductors of today in terms of lower cost, flexibility, and the ability to meld the speed and power of optics and electronics. Plus, unlike such inorganic conductors as silicon, molecule-based electronics can be miniaturized to a 1-dimensional scale (1-molecule-wide), which may enable them to conduct electricity with minimal loss and thus improve the performance of an electronic device.

Traditionally, the problem has been that organic conductors have not conducted electrical current very well, Petek said. The Pitt team's discovery could enable scientists to finally overcome that problem, he added.

“Metal-like behavior in a molecular material-as we have found-is highly surprising and desirable in the emerging field of molecular electronics,” he said.

“Our work is a unique example of how nanoscale materials can be used as atom-sized building blocks for molecular materials that could replace silicon and copper in electronic devices, luminescent displays, photovoltaic cells, and other technologies.”

To view the paper, visit the “Science” Web site at www.sciencemag.org.

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4/15/08/tmw

<Source: http://www.news.pitt.edu/m/FMPro?-db=ma&-lay=a&-format=d.html&id=3316&-Find>

 

 

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Inspired by Etch A SketchTM Toy, Pitt-Led Team Invents Technique for Switching Electrical Properties at Nanometric Scales

Metallic features can be written and erased at scales that approach atomic dimensions, with wide-ranging potential for information technologies, as reported online in “Nature Materials”

PITTSBURGH-A University of Pittsburgh-led research team developed a process wherein the ability to conduct electricity can be turned on and off at nanoscale dimensions. This capability holds promise for more powerful and compact information technologies including ultra-high density information storage, reconfigurable logic devices, single-electron devices, and quantum computers. These findings were published online March 2 in “Nature Materials” with the print version scheduled for April.

Led by Jeremy Levy, a professor of Physics and Astronomy in Pitt's School of Arts and Sciences, the researchers discovered how to switch, at will, the interface of two readily formed insulating materials from an electrical conductor to an insulator and back. The research's considerable technological applications stem from this adjustability, Levy said.

The process works like a microscopic Etch A SketchTM, Levy explained, referencing the drawing toy of his youth that inspired his idea. The interface lies between a crystal of strontium titanate and a 1.2 nanometer-thick layer of lanthanum aluminate, both of which are insulators. Using the sharp conducting probe of an atomic-force microscope, the team created wires less than 4 nanometers wide at the interface of the two materials. These conducting nanostructures can subsequently be erased with a reverse voltage or with light, rendering the interface an insulator once more.

“This work is not only potentially useful for technological applications, but also fascinating from a fundamental perspective,” Levy said. “The prospect of making both logic and memory devices with the same material is very intriguing, and at this small of a scale, it's almost unheard of.”

The physical model still needs tested in crucial ways, but provides an important framework for future research directions, Levy said. For example, the interface also acted as a transistor-an essential part of electronic devices that regulates electron flow-when the atomic-force probe served as a gate; further research will include creating devices that utilize single electrons for logic or storage.

The idea originated from a visit Levy made to the University of Augsburg in Germany where coauthors Jochen Mannhart and his student Stefan Thiel showed Levy how the entire interface could be switched between a conducting and insulating state. Levy thought of adapting the process to nanoscale dimensions and his student, Cheng Cen, the paper's first author, brought the idea to fruition. Research by C. Stephen Hellberg from the Naval Research Laboratory contributed to the theoretical understanding of the project. The work was supported by the Defense Advanced Research Projects Agency and the National Science Foundation.

Levy has worked in the field of oxide electronics for the last decade, and has been recognized by Pitt with the Chancellor's Distinguished Teaching Award in 2007 and the Chancellor's Distinguished Research Award in 2004.

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2/27/08/tmw

<Source: http://www.news.pitt.edu/m/FMPro?-db=ma&-lay=a&-format=d.html&id=3221&-Find>

 

 

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Pitt Receives $1 Million Grant to Research Ultrafast Time-Resolved Microscopy of Nanostructured Electronic Materials

Researchers will develop revolutionary method to probe molecular structures

PITTSBURGH-The University of Pittsburgh received a $1 million grant from the W.M. Keck Foundation to develop a groundbreaking method that will significantly advance nanoscale science and technology by allowing scientists to observe, probe, and control molecules. The revolutionary technique involves probing molecular structure with femtosecond-a billionth of a millionth of a second-temporal and atomic spatial resolution, leading to new knowledge on activating and harnessing matter at its most fundamental level.

The principal investigator for this research is Hrvoje Petek, a professor of physics and chemistry in Pitt's School of Arts and Sciences and codirector of the Petersen Institute of NanoScience and Engineering. Petek is an expert in the fields of surface femtochemistry and ultrafast microscopy. He invented ITR-PEEMtime-resolved photoemission electron microscopy, the enabling technique for this study.

“In pursuit of this grail, several leading physics and chemistry research groups around the world are exploring different ways to combine the spatial resolution of electron microscopy with temporal resolution of femtosecond laser spectroscopy,” Petek said. “ Our goal is to develop methods for interacting with single molecules in order to observe and control how they respond to stimulation by light or electrons to undergo chemical reactions or specific mechanical motion.”

Based in Los Angeles, the W.M. Keck Foundation is one of the nation's largest philanthropic organizations. Established in 1954 by the late William Myron Keck, founder of The Superior Oil Co., the foundation focuses primarily on medical research, science, and engineering.

Since 1988, the W.M. Keck Foundation has donated more than $4 million to support research in medicine, engineering, and science at Pitt. The latest grant is part of the University's “Building Our Future Together” campaign, the most successful fundraising campaign in the history of both the University and Southwestern Pennsylvania. To date, the campaign has raised more than $1.2 billion.

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2/6/08/tmw

<Source: http://www.news.pitt.edu/m/FMPro?-db=ma&-lay=a&-format=d.html&id=3186&-Find>

 

 

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Model for the Assembly of Advanced, Single-Molecule-Based Electronic Components Developed at Pitt

Template for creating one-molecule-wide wires for crafting molecular level organic semiconductors published in the Journal of the American Chemical Society
 

PITTSBURGH—Researchers based at the University of Pittsburgh have created the best method so far of assembling wire-like structures only a single molecule wide, a significant step in science’s increasing attempts to reduce the circuitry size of electronic devices to the single molecule scale and provide smaller, faster, and more energy efficient electronics. The findings were published online Sept. 26 in the Journal of the American Chemical Society (JACS).

The project presents a template for assembling molecules over troughs that are only as wide as a single atom of copper, but extend with faultless uniformity over distances corresponding to several hundred copper atoms. These ultra-thin wires are one-dimensional, which may enable them to conduct electricity with minimal loss and thus improve the performance of an electronic device, said project leader Hrvoje Petek, a professor of physics and chemistry in Pitt’s School of Arts and Sciences and codirector of Pitt’s Petersen Institute for NanoScience and Engineering (PINSE).

The published research pertains to organic—or carbon-based—soccer ball-shaped carbon molecules known as fullerenes, but the method can serve as a template for creating the molecule-scale wires from a broad range of organic molecules, Petek said. The merits of these wire-like structures can only be fully realized with organic molecules. Materials used in contemporary electronics—such as silicon—are inorganic and cannot be miniaturized to be truly one-dimensional, Petek said.

The project was conceived by Junseok Lee of the University of Virginia’s chemistry department and executed by Min Feng, a research associate in Pitt’s physics and astronomy department. Research associate Jin Zhao of Pitt’s physics and astronomy department served as the project’s theoretician. The template was developed with the chemistry group of Pitt emeritus professor John T. Yates Jr., now of the chemistry department at the University of Virginia and an advisor to PINSE.

The research was sponsored by grants from the Keck Foundation, the American Chemical Society Petroleum Research Fund, and the U.S. Department of Energy.

The paper is on the JACS Web site at pubs.acs.org/journals/jacsat/.

Related links:  Journal article at JACS

September 27, 2007

<Source: http://mac10.umc.pitt.edu/m/FMPro?-db=ma&-format=d.html&-lay=a&-sortfield=date&monthname=September&year=2007&-max=100&-recid=37204&-find=>

 

 

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People With Asthma Could Breathe Easier Anywhere With Hand-Held Pitt Nano-Sensor That Indicates Oncoming Attacks and Helps Monitor Symptoms

Portable, affordable nanotube sensor detects spikes in nitric oxide before an attack's onset, Pitt researchers report in journal “Nanotechnology”

PITTSBURGH-A sensor developed at the University of Pittsburgh could strip the element of surprise from some asthma attacks by detecting one before its onset. Fitted in a hand-held device, the tiny sensor provides people who have asthma with a simple and affordable means of keeping tabs on their condition by measuring their breath for high levels of a specific gas associated with asthma inflammation.

Researchers led by Alexander Star, a chemistry professor in Pitt's School of Arts and Sciences, created a sensor reactive to even minute amounts of nitric oxide, a gas prevalent in the breath of asthmatics, as they describe in the Aug. 22 online edition of the journal “Nanotechnology.” Star also will present his research at the American Chemical Society's 234th National Meeting slated for Aug. 19-23 in Boston. The sensor consists of a carbon nanotube-a rolled, one-atom thick sheet of graphite 100,000 times smaller than a human hair-coated with a polyethylene imine polymer.

Star cased the sensor in a hand-held device that people blow into to determine the nitric oxide content of their breath. The nitric oxide level in the breath of a person with asthma spikes as the airways grow more inflamed. High levels-perhaps two-thirds over normal-may precede an attack by one to three weeks, but possibly earlier depending on the asthma's severity, said Jigme Sethi, a Pitt assistant professor in the School of Medicine's Division of Pulmonary, Allergy, and Critical Care Medicine and a clinician at UPMC Montefiore, who plans to clinically test Star's sensor.

Besides detecting attacks early on, Star's device also provides an easy, portable method for patients and their doctors to regularly monitor their symptoms and tailor treatment accordingly, Sethi said. Physicians use nitric oxide readings to help diagnose and gauge the severity of asthma, but the current method of measuring it requires expensive machines available only in outpatient clinics, Sethi said. Star's invention could allow people with asthma to watch their nitric oxide levels as easily as people with diabetes check their blood sugar with hand-held glucose monitors, Sethi said.

Star specializes in using carbon nanotubes-which were widely introduced to science in the early 1990s-as chemical sensors and in hydrogen fuel cells. In the case of sensors, a nanotube's extreme thinness renders it extremely sensitive to small changes in their chemical environment, which makes for an excellent detector, Star said.

August 22, 2007

<Source: http://mac10.umc.pitt.edu/m/FMPro?-db=ma&-lay=a&-format=d.html&id=2995&-find>

 

 

 

 

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Dr. Jin Zhao, Postdoctoral Fellow of Physics, Receives M.T. Thomas Award for Outstanding Postdoctoral Achievement from the Environmental Molecular Sicences Laboratory (EMSL) of the Pacific Northwestern National Laboratory (PNNL)

 Dr. Jin Zhao
                 Dr. Jin Zhao

Jin Zhao, University of Pittsburgh, has been selected as the 2006 recipient of the M.T. Thomas Award for Outstanding Postdoctoral Achievement. This award is in recognition of her seminal contributions to the theory of the unoccupied electronic structure and dynamics of solid-adsorbate interfaces, which are of fundamental importance to geochemistry, atmospheric science, and energy related interfacial phenomena.

Dr. Zhao is a post-doctoral research associate in Professor Hrvoje Petek's group in the Physics and Astronomy Department at the University of Pittsburgh. According to Petek, "Jin, as the lone theorist, has been the cornerstone of all surface science research done in my experimental group for the last 3 years. I could only provide a stream of questions, and a PC to connect to the world, while it was up to her, and she did it brilliantly, to find the theoretical resources and support to chart several new directions in surface science theory." Zhao submitted her first EMSL user proposal in 2005 and was awarded 75,000 hours on EMSL's supercomputer.

Zhao's accomplishments include theoretical description and assignment of partially solvated electronic states at the protic solvent/metal oxide interfaces (H2O)/TiO2 and CH3OH/TiO2). Her theoretical discovery of the so-called "wet electron state" paves the way to understanding how the specific molecule-surface and molecule-molecule interactions define the properties of acceptor states in nonadiabatic electron transfer processes, such as photoinduced charge transfer excitation. Moreover, her theoretical interpretation of the deuterium isotope effect on interfacial electron transfer provides deep insight in proton-coupled electron transfer that is likely to have an important role specifically in the area of surface photocatalysis.

Another area of Zhao's theoretical analysis includes the description of the electronic structure of excess electrons at O atoms vacancy defects, which control the chemical and electronic properties of TiO2 surfaces. As TiO2 has important applications in catalysis, photocatalysis, sensors, and light switchable amphiphilic films, the understanding of how surface defects affect chemical reactivity is an important step in the understanding and expanding of these applications. Zhao has shown that when describing the electronic structure of metal oxides, ad hoc treatments of self-interaction effects can easily lead to incorrect conclusions concerning the extent of electron localization. By constraining her theory with high quality atomic resolution images of the excess electron charge on reduced TiO2 surfaces, she has been able to explore the range of validity of hybrid functional techniques for describing the electronic properties of metal oxide surfaces.

Zhao's work also includes the development of a simple, yet profound, broadly applicable phenomenological theory that explains the period-independent, interfacial electronic structure of alkali atoms. Her work has been the key to understanding the universal binding energy of Li-Cs chemisorbed on copper and silver; it is applicable to and has the potential to provide insight into the design of future molecular electronics devices.

Dr. Zhao obtained her Ph.D. in computational condensed matter physics from the University of Science and Technology of China, Hefei, Anhui, China in 2003. Dr. Zhao has been a post-doctoral research associate in Professor Hrvoje Petek's group in the Physics and Astronomy Department at the University of Pittsburgh since 2004.

The 2006 M.T. Thomas Award will be presented to Dr. Zhao at a ceremony following a presentation of her work (tentatively scheduled for May 24, 2007). A reception in her honor will follow.

Publications resulting, in part, due to the use of EMSL's supercomputer:

  1. Jin Zhao, Bin Li, Ken Onda, Min Feng and Hrvoje Petek, "Solvated Electrons on Metal Oxide Surfaces", Chem. Rev. 106, 4402 (2006).
  2. Jin Zhao, Bin Li, Kenneth D. Jordan, Jinlong Yang and Hrvoje Petek, "Interplay between Hydrogen Bonding and Electron Solvation on Hydrated TiO2(110)", Phys. Rev. B 73, 195309 (2006).
  3. Taketoshi Minato, Jin Zhao, Yasuyuki Sainoo, Yousoo Kim, Hiroyuki S. Kato, Maki Kawai, Ken-ichi Aika, Jinlong Yang, and Hrvoje Petek, "Correlation between the Lattice Distortion and the Local Electronic Structure at an Atom Vacancy Defect on Titanium Dioxide (110) Surface", Phys. Rev. Lett., submitted.
  4. Jin Zhao, Niko Pontius, Aimo Winklemann, Vahit Sametoglu, Atsushi Kubo, Andrei G. Borisov, Daniel Sanchez Portal, V. M. Silkin, Engene V. Chulkov, Pedro Echenique, and Hrvoje Petek, "The universal electronic structure of alkali atom/metal interface", Science, submitted.

<Source: http://www.emsl.pnl.gov/new/mt_thomas_award/zhao.shtml>

 

 

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The Research of Dr. Sanford Asher, Professor of Chemistry, Highlighted in the March 19, 2007 Issue of Chemical & Engineering News

Spectroscopic method offers large signal enhancements but until now was expensive and complicated

Mitch Jacoby

DO THINGS a little differently from the way they're usually done, and the results might turn out surprisingly well. By modifying familiar recipes, chefs sometimes produce masterpieces. By altering their daily routes, commuters may shave minutes off their travel times. Even spectroscopists stand to gain by trying something different.

 

 

 

 

 

 

 

 

 

 

 

Mitch Jacoby/C&EN

JUST A HANDFUL! Hug shows off a small,

low-cost deep-UV laser from Photon

Systems that may help boost the

popularity of UV-Raman spectroscopy

A case in point is Raman spectroscopy, an analytical technique in which samples are most often probed with light in the visible and near-infrared regions (about 400 to 700 nm). In the past several years, UV-Raman aficionados have pushed to capitalize on the benefits of carrying out a variant of the technique using ultraviolet light (typically 200 to 300 nm). Exciting samples deep in the UV region can enhance signal intensities by a factor of 1 million or more compared with conventional Raman spectroscopy. UV light also offers a method for probing certain functional groups selectively. In addition, moving to shorter excitation wavelengths can avoid interference from fluorescence, which sometimes obliterates standard Raman spectra.

Attendees of Pittcon earlier this month in Chicago learned about some of the most recent advances in the UV-Raman field. Practitioners and instrument makers gathered at a symposium to report on applications in biochemistry and catalysis and to discuss commercialization of UV-Raman instrumentation.

"It can be argued that the single most important issue in biology today is understanding how proteins fold into their native states." That assertion was made by University of Pittsburgh chemistry professor Sanford A. Asher, a pioneer of UV-Raman methodology. Asher explained that conformational variations (misfoldings) that cause proteins to adopt structures that differ from normal protein geometries have been fingered as key factors in Alzheimer's, Huntington's, and several other diseases.

 

  

ANGULAR DEPENDENCE  Folding and coiling geometries in peptides and proteins are specified by amide Ψ and Φ dihedral angles.

"If we understood the mechanism through which proteins fold or misfold, we would have an opportunity to intervene chemically," he said. So Asher's group has been probing protein-folding processes with UV-Raman spectroscopy, a method that, he argued, is particularly well-suited to studying dilute solutions.

The nuances of a protein's folding and coiling geometry, which collectively are known as a protein's secondary structure, are dictated in large part by hydrogen-bonding interactions along the molecule's peptide backbone. As Asher pointed out, it's known from X-ray crystallography studies and other types of analyses that proteins often adopt a combination of common secondary structural motifs, including the so-called random coil, which is reminiscent of cooked spaghetti, and the more orderly α-helix and β-sheet arrangements.

The particular conformation adopted by a peptide chain is determined by rotations about C-C and C-N amide bonds and the resulting dihedral angles, known as the Ramachandran Ψ and Φ angles, respectively. These angles are named for the Indian biophysicist G. N. Ramachandran, who began studying them in the 1960s.

To get a spectroscopic handle on the secondary structure, Asher's group analyzed UV-Raman data from a number of proteins and peptides with known secondary structures and determined how amide vibrational bands correlate with the various geometries. Then they calculated basis spectra, which represent the Raman signals that would be measured from proteins that adopt only a single structural motif-for example, pure α-helix. Next, they showed that measured spectra could be modeled by the sum of appropriately weighted basis spectra, thereby providing a way to determine secondary structures of previously uncharacterized peptides and proteins.

Mug Title

Asher

 

Mug Title

Stair

Mitch Jacoby/C&EN (both)

 

THOSE RESULTS set the stage for a number of follow-up studies and key findings. For example, the Pittsburgh group observed that as polyglutamic acid is heated, it undergoes a structural transition (melts) from the α-helix conformation to a random coil. As the conformation evolves, a large change occurs in the Ψ angle, which in turn causes a large change in the frequency of one of the amide vibrational bands known as the amide III3 band. In contrast, the researchers found that the band depends only weakly on the Φ angle.

Following other UV-Raman studies, Alexander V. Mikhonin, a graduate student in Asher's group, developed a method for determining Ψ angles from spectra measured under various experimental conditions. That development is noteworthy, Asher argued, because the Ψ angle serves as a textbook-type reaction coordinate for evolution of protein and peptide secondary structures. As such, the researchers uncovered a way to experimentally monitor secondary structures as they evolve.

The team then used that methodology to interrogate α-helix melting in a number of samples, including a 21-residue peptide known as AP, which consists mainly of alanine units. Some of the main findings of that investigation are that AP melts at a significantly higher temperature than previously reported and that other types of conformations melt before the α-helices unfold. Furthermore, in the melted state, AP's structure closely resembles that of polyproline II, which consists of left-handed helices with three residues per helical turn. (J. Am. Chem. Soc. 2006, 128, 13789).

MOVING A STEP closer to a detailed understanding of secondary structure, the Pittsburgh group recently showed that the distribution of Ψ angles can be used to calculate energy landscapes associated with peptide conformations. The plots dictate which structures are energetically favored and which are blocked by energy barriers.

 

 

 Courtesy of Sanford A. Asher
MELTDOWN  Analysis via UV-Raman spectroscopy reveals molecular details of the process by which this coiled 21-residue peptide (left) unfolds (melts).

Switching gears, Northwestern University chemistry professor Peter C. Stair lauded the ability of UV-Raman spectroscopy to probe reactions occurring at the surfaces of heterogeneous catalysts. "There is virtually no other technique that can see the catalyst and the molecules [reactants and products] in a single measurement and under reaction conditions," Stair declared. He added that before the development of UV-Raman methods, researchers' efforts were often thwarted by fluorescence signals that buried the Raman data.

Drawing on results of an investigation of butane dehydrogenation on supported vanadia catalysts, Stair demonstrated that UV-Raman analysis sheds light on several experimental parameters. For example, the results show that at a catalyst loading (concentration on the support material) of roughly one vanadium atom per square nanometer, which corresponds to an active form of the catalyst, vanadia consists of roughly equal proportions of monomeric and polymeric forms of V=O. At higher loadings, the polymeric form prevails and the catalyst is inactive. The method also indicates that while the catalyst is active, it's coated with a carbonaceous (coke) layer that resembles polystyrene. In contrast, layers composed of coronene, pyrene, and other polycyclic aromatic hydrocarbons with 2-D sheetlike structures poison the catalyst.

Despite the strengths of UV-Raman spectroscopy, the method is not practiced in many labs today. William F. Hug, president of Photon Systems, a Covina, Calif., maker of low-cost UV lasers and other equipment, remarked that widely used analytical instruments such as UV-visible spectrometers are easy to operate, are rugged, require little or no servicing, and are relatively inexpensive (in the $15,000 to $80,000 range). UV-Raman instruments, in sharp contrast, are used strictly by specialists, and systems with high-end deep-UV lasers can cost well over a half-million dollars, he said.

The good news, according to Hug, is that the past several years have seen "tremendous progress" in lowering the costs of UV lasers, detectors, lenses, mirrors, and other components of UV-Raman systems. Hug's presentation touched off an impromptu discussion of analytical-method limitations that culminated with symposium organizer Michael W. Blades of the University of British Columbia declaring that "nothing is really holding back UV-Raman anymore." He added, "We should expect more of these sessions and better attendance in the future."

<Source: Chemical & Engineering News, March 19, 2007 (Volume 85, Number 12) pp. 59-60.>

 

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Pitt Professor Scores Science Double-header

Anna Balazs and Victor Yashin
James Knox/Tribune-Review

By Allison M. Heinrichs
TRIBUNE-REVIEW
Friday, November 17, 2006

Anna Balazs is becoming a Science celebrity.

The University of Pittsburgh engineering professor published her second article of the month in the international weekly magazine Science -- a peer-reviewed journal in which scientists strive to get their work published.

"We are a selective journal. We only publish about 8 percent of the papers that are sent to us," said Katrina Kelner, a deputy editor at Science. "Although I wouldn't say we've never (had an author publish two articles in less than a month) before, it certainly isn't common."

Balazs is lead author on an article titled "Nanoparticle Polymer Composites: Where Two Small Worlds Meet" in today's issue of Science. She co-authored an article about pulsating gels in the Nov. 3 issue.

Both articles tackle subjects in the field of materials engineering.

Balazs and co-authors Todd Emrick and Thomas Russell, professors at the University of Massachusetts in Amherst, review the latest research in incorporating nanoparticles with flexible, easy-to-mold plastics. Nanoparticles are inorganic particles 1,000 times smaller than the width of a human hair that are prized for their electrical, optical and mechanical properties.

Plastics and nanoparticles "both have very desirable properties and when you integrate the two, the sum is better than the parts," said Balazs, who works in Pitt's department of chemical and petroleum engineering. "When you combine the two you get a material that is tough, but also stiff."

For example, if an automobile company wants to make a lightweight but strong car, the company could create a material that suits its needs, rather than adapting the car design to available materials, such as steel, aluminum and plastic.

In her earlier article, Balazs and postdoctoral student Victor Yashin explored "pulsating gels," polymer gels that expand and contract like a beating heart when put in a chemical solution.

Scientists have known about the gels for a half-century, but Balazs and Yashin developed a mathematical model to explain how their shapes change as they pulsate. This gives people experimenting with the gels -- which could be useful as muscles in robots -- a "recipe" to follow.

"It's like telling someone how to bake a cake," Balazs said. "If they follow your directions, the cake should come out perfectly."

In the case of pulsating gels, experimentalists confirmed that the recipe, in this case a mathematical model, is correct.

"That's such an amazing high," Balazs said. "It's just an incredibly joyous feeling -- it's validation for all your hard work."

Balazs, who has been with Pitt since 1987, spreads that "high" to her colleagues and students, said professor Bob Enick, chairman of the department.

"She has the enthusiasm of a young child opening a gift, and it's contagious," Enick said. "She sets an example for the rest of us."

Allison M. Heinrichs can be reached at aheinrichs@tribweb.com or (412) 380-5607.

 

 

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Electrons ‘In Limbo’ Seen for First Time

Two recent papers by Pitt physicist offer a deeper understanding of how electrons behave on surfaces, with applications in electronics and energy

PITTSBURGH—Hrvoje Petek, University of Pittsburgh professor of physics and codirector of Pitt’s Gertrude E. and John M. Petersen Institute of NanoScience and Engineering (PINSE), has published two papers in recent weeks that literally illuminate how electrons behave on various surfaces.

In the first paper, Petek and Miroslav Nyvlt of Charles University in Prague explored the properties of metals under intense light—a situation “where the classical physics of electron emission from metals emerges from its quantum roots,” says Petek. They found that when light of a certain energy and intensity is shone onto a metal surface, a few electrons in the metal become stuck on the surface (that is, they are neither emitted from nor reabsorbed into the metal). As Petek puts it, the electrons are “in limbo.”

These electrons undergo the process of “total internal reflection”—a process well known for light, but observed by Petek and Nyvlt for the first time in electrons.

These findings, published in the March 3 issue of Physical Review Letters (PRL), could lead to the ability to transmit electrons, without scattering, over larger distances than previously possible. For example, electrons on the surface of carbon nanotubes could be excited to make “very small and very fast” transistors, Petek says.

“We anticipate that these elusive electrons will provide exquisite probes for how photons and electrons interact with metal surfaces,” he adds.

In Petek’s second paper, published in the current issue of Science, he and Pitt Professor of Chemistry Kenneth Jordan, a PINSE researcher, make new progress toward extracting hydrogen from water using titanium dioxide as a catalyst.

In a May 2005 Science paper, Petek and Jordan presented their findings on the properties of water on the surface of titanium dioxide. In their current experiment, they used methanol instead of water, because they discovered that excited electrons last longer in methanol than in water, allowing chemical reactions to be observed.

This research shows how protons in methanol molecules move in such a way that they control the reabsorption of electrons into the titanium dioxide. Such motion, correlated between protons and electrons, is needed to convert light into chemical energy on solid surfaces, as well as by light-harvesting proteins.

PINSE is an integrated, multidisciplinary organization that brings coherence to the University’s research efforts and resources in the fields of nanoscale science and engineering. More information about PINSE can be found at www.nano.pitt.edu.

The work for the PRL paper was performed at the Max Planck Institute of Microstructure Physics in Halle, Germany, where Petek was an Alexander von Humboldt Senior Scholar and Nyvlt was the group leader. Other authors on the paper are Francesco Bisio, now at the University of Genoa; Jirka Franta, now at Charles University; and Jurgen Kirschner, director of the Max Planck Institute.

That work was supported by the Alexander von Humboldt Foundation, the U.S. National Science Foundation, the Italian National Research Council, and the Czech Ministry of Education.

In addition to Petek and Jordan, authors on the Science paper are postdoctoral fellows Jin Zhao and Ken Onda and graduate student Bin Li, all of Pitt's Department of Physics and Astronomy, and Jinlong Yang of the University of Science and Technology of China. The work was supported by the U.S. Department of Defense Multidisciplinary University Research Initiative program, the New Energy Development Organization of Japan, and the National Science Foundations of the United States and China.
 

 

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University of Pittsburgh Announces $5 Million Gift to Advance Nanoscale Science and Engineering Research

Gift from John M. and Gertrude E. Petersen for Pitt's Institute of NanoScience and Engineering gives the University a competitive edge as an international leader in a new and potentially revolutionary field

Big research push from matter as small as one eighty-thousandth of the width of a human hair

PITTSBURGH-The University of Pittsburgh has received a $5 million gift from alumnus John M. Petersen and his wife, Gertrude, to create an endowment supporting research in nanoscale science and technology at Pitt's Institute of NanoScience and Engineering, now the Gertrude E. and John M. Petersen Institute of NanoScience and Engineering.

Nanoengineering and nanotechnology use atoms and molecules as basic blocks to build minute machines, create new materials, and perform new molecular tasks. In a major push to advance the frontiers of the promising nanoscience field, which has energized researchers worldwide, Pitt enjoys a competitive edge through its newly endowed Petersen Institute. Pitt researchers in the institute, founded in 2002, focus at the “essentially nano” level (less than 10 nanometers, each nanometer approximately one eighty-thousandth of the width of a human hair), where the greatest breakthroughs in nanoscience are expected to occur, offering the potential for previously unimagined progress in a wide variety of areas. Work already done by institute researchers has resulted in the development of color-shifting paints, a contact lens-embedded sensor with the potential for noninvasive glucose-level monitoring for diabetes, and scaffolding to heal damaged hearts.

Within the last three years, Pitt-developed nanotechnology has been licensed to three start-up companies and one major corporation. The National Science Foundation predicts that the market for nanotech products and services will reach $1 trillion by the year 2015.

John Petersen, the retired president and chief executive officer of the Erie Insurance Group in Erie, Pa., earned the Bachelor of Business Administration degree at Pitt in 1951. He was among the first students to live on campus at Pitt, where he earned varsity athletics letters as a member of the swimming and diving team. The Petersens have maintained a strong relationship with the University through their support of a variety of University programs, including their gift to name Pitt's John M. and Gertrude E. Petersen Events Center, home of what is considered the nation's premier on-campus basketball arena. Both avid fans of Pitt athletics, the Petersens recently continued their longstanding support of the Department of Athletics with a gift of $600,000 to support baseball and swimming scholarships.

“John and Gertrude Petersen have been extraordinarily loyal and generous to the University over the years. Their gift to support the construction of the Petersen Events Center helped elevate both our men's and women's basketball programs to remarkable new heights and also gave us the chance to hold commencement on campus and to host such special events as the National Senior Olympics and the Jeopardy! College Championship,” said Pitt Chancellor Mark A. Nordenberg. “Their more recent gift to support our nanotechnology initiatives positions the newly named Petersen Institute to be an international leader in the field, to solve complex scientific and engineering challenges, and to develop new technologies with the potential for commercial applications.”

The scientists and engineers who make up Pitt's Petersen Institute are experts in designing, characterizing, and fabricating nanoscale materials, devices, and systems. The researchers, drawn from the University's Schools of Arts and Sciences, Engineering, and the Health Sciences, form flexible, cross-disciplinary teams to investigate major questions in nanoscience and engineering.

Fall 2006 will mark the opening of Pitt's 4,000-square-foot nanoscale fabrication and characterization facility, located in Benedum Hall, which will house the best available technology in a single location and allow researchers to observe and manipulate materials at the atomic level.

“Exciting advances are on the horizon through the study of phenomena at length scales of only a few nanometers,” said Pitt Provost James V. Maher. “The increased scientific understanding we gain will lead to technological breakthroughs, and the resulting improved technology will allow us to deepen our understanding of the science. This gift greatly enhances the sizeable commitment that Pitt is making to position ourselves as a leader in this field.”

 


 

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Pitt nanotech researcher devises versions of building blocks on a molecular scale

Sweating the very small stuff

Monday, November 21, 2005

By Byron Spice, Pittsburgh Post-Gazette
 

Nanotechnology is a buzzword that often brings to mind images of microscopic gears and springs etched into silicon wafers.

 

 

Tony Tye, Post-Gazette
Christian Schafmeister of the University of Pittsburgh has developed a system for building nanodevices using molecular building blocks.

 

 

 

But if you really want to build nanomachines, ones measured in billionths of meters, or nanometers, it makes sense to consider the nanomachines of nature -- proteins.

That's what Christian Schafmeister did.

"We've got 40,000 of these machines in our bodies that make us what we are," explained the University of Pittsburgh chemist. Proteins digest our food, move our arms and transport materials. And the beauty of it is that all are made from about 20 different types of building blocks, called amino acids.

Taking this cue from nature, Dr. Schafmeister and his students have spent the last five years concocting their own set of 14 building blocks -- the molecular equivalent of Lego pieces.

By his estimation, that's enough to make roughly 140 trillion structures. So creating different shapes is no longer the challenge; rather, "it's finding those sequences that do interesting things," he said.

New types of pharmaceuticals, chemical catalysts and sensors are all among the possibilities.

"We haven't made a big splash with this yet," acknowledged Dr. Schafmeister, an assistant professor of chemistry and a researcher at Pitt's Institute of NanoScience and Engineering. But that should change once applications are identified, something he hopes will occur within the next year.

Even so, the work already has drawn attention within the nanotech community. Last month, the Foresight Nanotech Institute, a nanotechnology think tank, awarded its Feynman Prize for experimental work to Dr. Schafmeister and its Distinguished Student Award to one of his graduate students, Christopher Levins, who developed one of the building blocks.

"It's the most impressive work we've seen on the pathway to building useful three-dimensional structures with atomic precision," said Christine Peterson, Foresight's founder and vice president for public policy. "The biggest payoffs across the board in nanotechnology . . . are from reaching the ultimate goal of atomic precision."

Controlling the position of each atom within a molecule would be difficult to achieve simply by trying to build molecules out of the same amino acids used so skillfully by nature.

Trouble is, as good as humans may be with their hands, they still lack the intellectual dexterity needed to build machines with amino acids. Arrange a set of amino acids one way and you've made an enzyme; rearrange the same amino acids and you've got a muscle component.

The reason for these dramatically different functions lies in what's called the protein folding problem. Proteins are more than just long, floppy chains of amino acids; their function depends in large part on their shape, how they fold themselves up. And the rules that govern that folding procedure are only dimly understood.

During four years of graduate school at the University of California, San Francisco, Dr. Schafmeister designed his own protein, called 4HB1, with 180 amino acids. "It's a molecular doorstop," he said wistfully, gazing at its structure on his computer monitor. "It doesn't do anything. But it is well-folded."

So he reasoned that to control the shape of his molecules -- and thus increase the chances of designing a molecule that does something -- he would need to eliminate the folding problem. And that meant developing molecular building blocks with rigid connections between them.

Rigid connections
Amino acids connect to each other with single bonds, creating chains with all of the rigidity of a string of plastic beads. He and his students devised blocks with a pair of bonds, creating rigid connections between the molecules much like those between Lego blocks.

Most of the blocks have been processed from 4-hydroxyproline, a form of the amino acid proline obtained commercially from chicken feathers; two are processed from the amino acid tyrosine. Making the building blocks "is boring chemistry, pedestrian chemistry," he said, and intentionally so. Though he and his students now make their own building blocks, he hopes that someday they will be churned out in large quantities by industry.

The building blocks each have a different shape, though they are not as simple as pieces of an Erector set -- no straight sections, or right angles. All twist a bit in three dimensions, but can be assembled to form a number of shapes.

Simply repeating the same building block will form something roughly rod-shaped. Alternating a block with a mirror-image block will form a horseshoe- or ring-shaped molecule. Dr. Schafmeister has devised a software program that can show a designer the options available for shaping a molecule with each of the available building blocks.

"You can sculpt almost anything," said William A. Goddard III, director of the Materials and Process Simulation Center at the California Institute of Technology. "Proteins are like a piece of string, but his structure is like having a wide ribbon" that can be used to build all sorts of three-dimensional objects.

This "bottom-up" approach to building nanotech devices still must be further developed, but eventually will be essentially for building nanomachines, he suggested.

The "top-down" approach, particularly that used by the semiconductor industry, may soon reach its limits, Dr. Goddard explained. Computer chip makers, who etch transistors and wires into silicon wafers, now are preparing to build devices measuring 130 nanometers and have begun to struggle with 90 nanometer devices.

Increasingly smaller component sizes have been the key to "Moore's Law," the concept that chip capabilities roughly double every year or so. On the horizon are 45- and 32-nanometer components. But within 10 years, he said, continued progress may depend on switching over from a top-down to a bottom-up strategy.

"There's a good chance that by 2015, this might be the only solution to maintaining Moore's Law," he added.

Dr. Schafmeister envisions using his building blocks, each measuring about half a nanometer, to build little boxes with lids that could serve as sensors; when a molecule of interest enters the box, the lid would shut and send a signal. The blocks might also be used as scaffolding to construct customized catalysts, which promote certain chemical reactions, or to build artificial antibodies.

He also is exploring the use of his building blocks for devising multivalent drugs -- drugs that bind to multiple receptors on the surface of cells, thus blocking toxins, such as cholera. Unlike the floppy molecules that now carry sugars designed to bind with these receptors, Dr. Schafmeister's rigid molecules could hold the sugars at the same precise distance as the spacing of the receptors on the cell.

"I have so many applications I want to try," he said. Though it's not clear which one is likely to prove itself first, he has encountered few limitations to the underlying building blocks themselves.

"If there are walls," he said, "we haven't hit them yet."

 

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Pitt Professor, Student Win Nanotechnology Prize for Work on "Molecular Lego(r) Set"

Molecules promising as nanoscale parts for atomically precise machines

PITTSBURGH-A University of Pittsburgh researcher has been awarded a prestigious prize from the Foresight Nanotech Institute for his work in developing a "molecular Lego(r) set" that will enable, for the first time, the quick manufacture of sturdy, predictable nanostructures.

Christian Schafmeister, assistant professor of chemistry at the University of Pittsburgh and a researcher in the University's Institute of NanoScience and Engineering (INSE), was awarded the 2005
Foresight Institute Feynman Prize for experimental work, named in honor of pioneer physicist Richard Feynman. He received the award at a banquet Oct. 26.

Schafmeister has designed 14 small molecules, each about 0.5 nanometers across. Each includes two removable molecular caps. Controlled chemical reactions strategically strip the caps away, causing the molecules to link together in predictable ways with pairs of stiff bonds-similar to Lego(r) blocks. He has snapped together 2.5-nanometer rods and 1.5-nanometer crescents, and has developed software that can aid in the construction of a wide variety of shapes.

With this method of nanofabrication, which he calls "a completely new field," Schafmeister is using his blocks to craft hinged, molecular traps that attract specific molecules, snap shut, and light up, serving as perfect chemical sensors-just one of an almost infinite number of possible uses. Molecules with customized cavities could serve as catalysts or biomedical agents. Because the molecules are
large enough to have interesting functions and rigid, designed shapes, they hold great promise as nanoscale parts for future atomically precise nanoscale machines.

"We're developing a new programming language for matter," said Schafmeister, "and we're writing, 'Hello, world.'"

Schafmeister's student Christopher Levins, a doctoral candidate in chemistry, received the Foresight Distinguished Student Award for work that he did within the umbrella of Schafmeister's research. "Chris
made some of the first breakthroughs-building blocks and larger structures-in our research," said Schafmeister.

"We're proud to see Dr. Schafmeister and his student awarded for nanotechnology research," said University Provost James V. Maher. "Pitt's program in nanoscience is focused on platform technologies,
like Dr. Schafmeister's, that will have a great affect on future research and applications."

The Foresight Nanotech Institute is the leading think tank and public interest organization focused on nanotechnology. Founded in 1986, its mission is to ensure the beneficial implementation of  nanotechnology.

The INSE is an integrated, multidisciplinary organization that brings coherence to the University's research efforts and resources in the fields of nanoscale science and engineering.


 

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New Nanofabrication Capability Makes Pitt Unique in United States

PITTSBURGH-The University of Pittsburgh recently became the only institution in the United States and only the second in the world to have a unique nanofabrication capability. Eight researchers in Pitt's Institute of NanoScience and Engineering (INSE) have just completed a week of training on the new Raith electron beam Lithography and Nano Engineering (eLiNE) workstation.

The eLiNE system allows researchers to create nanometer-scale structures using an electron beam that is focused to less than two nanometers. A unique feature of this instrument is an electron beam-induced deposition and etching capability that allows metals, insulators, and semiconductors to be added or removed, using the electrons as a nanocatalyst. This new capability only recently has become commercially available.

Pitt students and faculty from various disciplines, including electrical engineering, biomedical engineering, physics, and chemistry, are scheduled for training.

“In a sense, it's like having a machine shop, only a million times smaller,” said Jeremy Levy, Pitt professor of physics and astronomy and the faculty member in charge of training new users and maintaining the instrument.

“What is exciting is that researchers have come to the initial training session with some precursory ideas about what they want to do, but after seeing all of the capabilities, their outlooks change; completely new approaches now seem possible,” Levy added.

The eLiNE system is the first of three major pieces of instrumentation available at INSE. The other two instruments, a focused ion beam system and a transmission electron microscope, are scheduled for delivery in early 2006.

The INSE is an integrated, multidisciplinary organization that brings coherence to the University's research efforts and resources in the fields of nanoscale science and engineering
.
 

 

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UCLA Scientist to Present Provost Lecture on "Nano Meccano" Oct. 7 at Science2005

The research of this third-most-cited chemist has led to breakthroughs in product synthesis and nanotechnology

PITTSBURGH--An internationally recognized pioneer in the field of supramolecular chemistry--the chemistry beyond the molecule-from the University of California, Los Angeles (UCLA), will present the Provost Lecture at the University of Pittsburgh's fifth annual showcase of science and technology, Science2005: The New Research Ecology.

J. Fraser Stoddart, the Fred Kavli Chair of NanoSystems Sciences and director of the California NanoSystems Institute at UCLA, will speak at 11 a.m. Friday, Oct. 7, in the 7th floor auditorium of Alumni Hall at the University of Pittsburgh. The title of his lecture is "Nano Meccano: An Integrated Systems-Oriented Approach to Molecular Electronics."

Stoddart's work focuses on elucidating the natural processes of molecular recognition and self-assembly and applying that dynamic to directed activities in both the life and materials sciences, leading to a number of breakthroughs in product synthesis and nanotechnology. According to the Institute for Scientific Information, Stoddart is currently the third most cited chemist in academia.

Stoddart's research has given scientists a much better understanding of the information and instructions stored in the covalent frameworks of supramolecular architectures. By learning from existing supramolecular systems that use weak noncovalent bonding to undergo self-organization, Stoddart has developed unique mechanical interlocked molecules, often involving interlocking rings and dumbbells that function as molecular switches on the nanoscale. (A nanometer is one-billionth of a meter, or
10,000 times smaller than the thickness of a human hair.) These molecules are not only useful in and of themselves, but they represent the beginning of a series of developments that may give researchers
unprecedented control over the structural and dynamic organization of matter.

"Building artificial molecular machines and getting them to operate is where airplanes were a century ago," said Stoddart. "We have come a long way in the last decade, but we have a very, very long way to go yet to realize the full potential of artificial molecular machines." However, a number of futuristic-sounding concepts and materials already have been inspired by his work, including nanofibers that can improve sensor response, an artificial molecular machine that can move up and down between two levels like an elevator, and a molecule-trapping nanovalve that could potentially be used as a drug delivery system.

Stoddart received the Ph.D. and D.Sc. degrees from Edinburgh University in Scotland. In 1997, he arrived at UCLA as the Saul Winstein Professor of Chemistry. Stoddart has published more than 725 scientific papers. He is an associate editor of Organic Letters and is currently on the international advisory boards of numerous journals, including Angewandte Chemie and the Journal of Organic Chemistry. Among his many honors are the Carnegie Centenary Professorship at the Universities of Scotland (2005), the Nagoya Gold Medal in Organic Chemistry (2004), the American Chemical Society's Cope Scholar Award (1999), and the International Izatt-Christensen Award in Macrocyclic Chemistry (1993). Stoddart was elected to fellowship in the Royal Society of London in 1994 and to
membership in the German Academy of Natural Sciences Leopoldina in 1999.

The Provost Lecture is presented by Pitt's Office of the Provost. "The University is keenly interested in nanotechnology, and the provost has allocated considerable resources to this exciting new venture," said George Klinzing, Pitt vice provost for research.

Science2005 will explore some of today's leading areas of research at the University of Pittsburgh and throughout the region that are characterized by increasingly interrelated disciplines working together
to shed light on new pathways to discovery. The free, public program, which will take place Oct. 6-7 in Alumni Hall, will feature keynote lectures by some of America's leading scientists and symposium sessions on timely research topics as diverse as neuroimaging, whole genome analysis, nanoscience, the science of aging, structural biology, Einsteinian principles, and more. For more information or advance registration, go to www.science2005.pitt.edu.

 

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"Wet" Electrons Provide Easiest Way to Transport Charge,
Pitt Researchers Find

Technology has potential to produce clean fuel "if we could make it more efficient"

PITTSBURGH- The task of transporting electrical charges between metal-oxide and water phases is critical in such technologies as catalysis, sensors, and electrochemistry. In a paper published in this week's issue of the journal Science, University of Pittsburgh researchers report that "wet"electrons afford the lowest energy pathway for transporting electrons between solid and liquid states.

In their paper, titled "Wet electrons at the H2O/TiO2(110) Surface," Hrvoje Petek, Pitt professor of physics and codirector of Pitt's Institute of NanoScience and Engineering, and Kenneth Jordan, professor and chair of Pitt'ss Department of Chemistry, extend Jordan's previous work on the structure of electrons in small water clusters, which was named one of the top 10 breakthroughs of 2004 by Science.

Wet electrons, which occur on metal oxide surfaces, represent a transition point for electrons between solid and liquid states of matter. A tiny amount of water from the atmosphere sticks to the surfaces of the oxides and forms hydroxide molecules, which then act like "molecular-scale Velcro" said Petek. In the presence of energy, their positively charged hydrogen atoms attract negatively charged electrons. Those so-called "wet" electrons then determine how other molecules interact with the surfaces of metal oxides.

The researchers gave the electrons sufficient energy to achieve the wet state by directing short bursts of laser light at titanium dioxide. Titanium dioxide was used because it is a photocatalyst: Exposure to light excites its electrons, which split water molecules into hydrogen and oxygen. Because of this potential for making hydrogen from water, it is possible that titanium dioxide could be used to make a clean fuel-but the process remains inefficient, said Petek. "If we could find out how to make it more efficient by observing how electrons interact with hydrogen atoms, it would have a huge economic impact," he added.
Petek's research could also illuminate the interaction between protons and electrons in such biological processes as photosynthesis, in which the light energy is converted to chemical energy through correlated transport of protons and electrons, which Petek calls similar to a wet electron system "on a fundamental level."

Petek plans to continue research on the properties of other oxide materials. In their paper, the researchers note that conditions exist to support similar states on all oxide surfaces in contact with water or with a humid atmosphere.

The paper's other authors are Ken Onda, Bin Li, and Jin Zhao, graduate students and postdoctoral researchers in Pitt's Department of Physics and Astronomy, and Jinlong Yang, a professor at the University of Science and Technology of China.

This research was supported by the U.S. Department of Defense Multidisciplinary University Research Initiative program, the New Energy and Industrial Technology Development Organization (Japan), and the National Science Foundation.

 

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Pitt Researcher, Colleagues Create Self-Assembling Nanoparticle/Polymer Mixtures

New findings represent significant advance toward manufacture of nanodevices, researchers announce in Nature

PITTSBURGH ---- A University of Pittsburgh researcher and her colleagues announced today in the journal Nature that they have created self-assembling mixtures of nanoparticles and polymer layers that spontaneously assume different orientations. Their findings have applications in such areas as chemical sensing, data storage, and photonic materials.

In a paper titled "Self-Directed Self-Assembly of Nanoparticle/Copolymer Mixtures," Anna Balazs, Robert Von der Luft Professor in the Department of Chemical and Petroleum Engineering in Pitt's School of Engineering and a researcher in Pitt's Institute for NanoScience and Engineering, Thomas Russell of the University of Massachusetts Amherst, and their colleagues described a method with significant advantages over previous research.

While self-assembling processes are common in biological systems, such multiple-step processes are difficult to engineer synthetically. Previous research required intervention at each step of the process, but Balazs and her colleagues created a two-step process that only requires one intervention.

"What is unique about this study is that it has two interlocking self-assembling steps," said Balazs. "This is one-stop shopping."

The researchers began with thin films of copolymers-two types of polymer joined together-spread onto a surface. When equal amounts of each polymer are present, the copolymers arrange themselves into layers. If one polymer has an affinity for the surface the film is on, the layers will run parallel to the surface (horizontally); if neither of them "likes" that substrate, the layers will be vertical.

Then, to a horizontally layered copolymer film, the researchers added particles coated in a substance the polymers would not like. They found that the copolymer chains pushed the particles out to the edges of the film, essentially creating a new surface that was now unattractive to the polymers. Simultaneously, this new surface caused the horizontal polymer layers to change their orientation and become vertical.

This method of a self-assembling, interlocking two-step process provides remarkable control and flexibility over the fabrication of nanostructured materials. "The fact that you can put these chains and particles tens of nanometers apart and they assemble themselves will enable the next generation of nanoscale devices," said Balazs.

This research was supported by the U.S. Department of Energy, the National Science Foundation (NSF)-supported Materials Research Science and Engineering Center at the University of Massachusetts Amherst, the NSF Collaborative Research in Chemistry Program, the NSF Career Award, the Army Research Office through a Multidisciplinary University Research Initiative, and the Max Kade Foundation.

Pitt's Institute of NanoScience and Engineering is an integrated, multidisciplinary organization that brings coherence to the University's research efforts and resources in the fields of nanoscale science and engineering.

 

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University of Pittsburgh Announces Construction of New $6.1 Million Nanotechnology Facility, Increase in Nano Faculty


At today's virtual groundbreaking, Provost James V. Maher reveals Pitt's
new commitment to nanoscience research


PITTSBURGH- The University of Pittsburgh today made a major commitment to boost its already-formidable efforts in the burgeoning field of nanotechnology by announcing its intentions to construct a new $6.1 million nanofabrication facility and to increase nanoscience and engineering faculty by almost 25 percent in the next few years.

At a virtual groundbreaking today in Alumni Hall, Pitt Provost James V. Maher announced the construction of the new 4,000-square-foot NanoScale Fabrication and Characterization Facility, to be part of Pitt's Institute of NanoScience and Engineering. The facility is scheduled to open in late 2005 and will be housed in Benedum Hall.

Pitt's Institute of NanoScience and Engineering currently includes approximately 40 faculty researchers, and Maher announced the addition of nine more. The added faculty will comprise basic scientists, chemists, biologists, and physicists, as well as engineers.

Pitt intends to be a leader in this emerging field that should change the way we think about and live our lives, said Maher.  Our number one asset is that our nanoscience program is based on our core strengths in the basic sciences, where we are focused at the essentially nano-level. That's where the greatest breakthroughs are expected to occur, and from there we can spawn potential applications over a broad range through our engineering capabilities.

Science and technology are very interdependent in this field, and it's an exciting time for Pitt because we do both,  Maher added. The new facility will promote multidisciplinary research, scholarship, and education among Pitt's School of Engineering, School of Arts and Sciences, and Schools of the Health Sciences.

Maher also pointed out that in the last three years, three start-up companies and one major corporation have licensed nanotechnology developed by Pitt researchers. He said he hopes the new facility will help attract top-level talent and garner more grants, as well as facilitate partnerships with industry.

The University has long acquired and even constructed state-of-the-art nanoscience equipment. With the opening of this facility, the best available technology will be housed in a single location, and the new equipment will allow researchers to see and change materials and structure on the atomic level. Key technologies available and their capabilities will be:

-Transmission electron microscope: Directs a beam of electrons at a material and  reads  the reflected and scattered electrons to create an atomic-level image of the surface;
-Scanning-probe microscope: A tiny tip hovers above the material and reacts to changes in voltage of electrons jumping between itself and the surface; this allows for mapping at the atomic level;
-Modular X-ray diffraction system: X-rays nanostructures to reveal their density, crystallinity, and the presence of impurities or structural defects;
-Inductively coupled plasma reactive ion etching system: A beam of charged particles cuts nanometer-wide grooves, pits, or holes in materials;
-Electron-beam lithography system: A beam of electrons  writes  nanometer-sized patterns on materials;
-Dual-beam nanopatterning system: Beams of electrons and/or other charged particles cut nanometer-wide patterns in materials; and
-Multisource e-beam deposition system and plasma-enhanced chemical vapor deposition: Deposition system for metals, semiconductors, insulators, and organic materials.

Combining many different tools of analysis, we can understand better what the entire picture is down to the atomic scale,  said Hong Koo Kim, Pitt professor of electrical and computer engineering and codirector of the Institute of NanoScience and Engineering.  The true payoff of this approach will be the resulting science.

 We're quickly approaching the scale at which the laws of classical physics don't apply, and that opens up a completely different realm of opportunity,  added Hrvoje Petek, Pitt professor of physics and astronomy and Kim's fellow codirector of the institute.

The University's focus at the  essentially nano  level, where the greatest breakthroughs in nanoscience are expected to occur, offers the potential for a broad range of applications, including environment and energy, materials and computation, biomedical and health care, and devices and systems.


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