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Atlanta, GA, United States

The Georgia Institute of Technology is a public research university in Atlanta, Georgia, in the United States. It is a part of the University System of Georgia and has satellite campuses in Savannah, Georgia; Metz, France; Athlone, Ireland; Shanghai, China; and Singapore.The educational institution was founded in 1885 as the Georgia School of Technology as part of Reconstruction plans to build an industrial economy in the post-Civil War Southern United States. Initially, it offered only a degree in mechanical engineering. By 1901, its curriculum had expanded to include electrical, civil, and chemical engineering. In 1948, the school changed its name to reflect its evolution from a trade school to a larger and more capable technical institute and research university.Today, Georgia Tech is organized into six colleges and contains about 31 departments/units, with emphasis on science and technology. It is well recognized for its degree programs in engineering, computing, business administration, the science, architecture, and liberal arts.Georgia Tech's main campus occupies part of Midtown Atlanta, bordered by 10th Street to the north and by North Avenue to the south, placing it well in sight of the Atlanta skyline. In 1996, the campus was the site of the athletes' village and a venue for a number of athletic events for the 1996 Summer Olympics. The construction of the Olympic village, along with subsequent gentrification of the surrounding areas, enhanced the campus.Student athletics, both organized and intramural, are a part of student and alumni life. The school's intercollegiate competitive sports teams, the four-time football national champion Yellow Jackets, and the nationally recognized fight song "Ramblin' Wreck from Georgia Tech", have helped keep Georgia Tech in the national spotlight. Georgia Tech fields eight men's and seven women's teams that compete in the NCAA Division I athletics and the Football Bowl Subdivision. Georgia Tech is a member of the Coastal Division in the Atlantic Coast Conference. Wikipedia.


Wang Z.L.,Georgia Institute of Technology
Advanced Materials | Year: 2012

The fundamental principle of piezotronics and piezo-phototronics were introduced by Wang in 2007 and 2010, respectively. Due to the polarization of ions in a crystal that has non-central symmetry in materials such as the wurtzite structured ZnO, GaN and InN, a piezoelectric potential (piezopotential) is created in the crystal by applying a stress. Owing to the simultaneous possession of piezoelectricity and semiconductor properties, the piezopotential created in the crystal has a strong effect on the carrier transport at the interface/junction. Piezotronics is about the devices fabricated using the piezopotential as a "gate" voltage to tune/control charge carrier transport at a contact or junction. The piezo-phototronic effect is to use the piezopotential to control the carrier generation, transport, separation and/or recombination for improving the performance of optoelectronic devices, such as photon detector, solar cell and LED. This manuscript reviews the updated progress in the two new fields. A perspective is given about their potential applications in sensors, human-silicon technology interfacing, MEMS, nanorobotics and energy sciences. Piezotronics is about devices fabricated using the piezopotential as a "gate" voltage to tune/control charge carrier transport at a contact or junction. The piezo-phototronic effect is to use the piezopotential to control the carrier generation, transport, separation and/or recombination for improving the performance of optoelectronic devices, such as photon detectors, solar cells and LEDs. This manuscript reviews progress in these two new fields. A perspective is given about their potential applications in sensors, human-silicon technology interfacing, MEMS, nanorobotics, and energy sciences. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.


Merrill A.H.,Georgia Institute of Technology
Chemical Reviews | Year: 2011

There are several nomenclature systems for glycosphingolipids, and many compounds are still referred to by their historically assigned names. Some of the breakthroughs in understanding the functions of sphingolipids, especially with respect to cell signaling, have come from having the capacity to measure more than one bioactive subspecies so the correct signaling pathways can be sorted out, especially when the metabolites have opposite effects, such as ceramide versus S1P. The relationships are being explored as a way for cancer detection and targeting using Shiga toxin. The story for iGb3 is less clear because although it stimulates NKT cells and has been hypothesized to be a natural modulator of them, recent studies have found that the human iGb3 synthase gene contains several mutations that render its product nonfunctional. A number of physiological factors have also been found to modulate DES.


Wang Z.L.,Georgia Institute of Technology
Nano Today | Year: 2010

Due to the polarization of ions in a crystal that has non-central symmetry, a piezoelectric potential (piezopotential) is created in the crystal by applying a stress. For materials such as ZnO, GaN, and InN in the wurtzite structure family, the effect of piezopotential on the transport behavior of charge carriers is significant due to their multiple functionalities of piezoelectricity, semiconductor and photon excitation. By utilizing the advantages offered by these properties, a few new fields have been created. Electronics fabricated by using inner-crystal piezopotential as a "gate" voltage to tune/control the charge transport behavior is named piezotronics, with applications in strain/force/pressure triggered/controlled electronic devices, sensors and logic units. Piezo-phototronic effect is a result of three-way coupling among piezoelectricity, photonic excitation and semiconductor transport, which allows tuning and controlling of electro-optical processes by strain induced piezopotential. The objective of this review article is to introduce the fundamentals of piezotronics and piezo-phototronics and to give an updated progress about their applications in energy science and sensors. © 2010 Elsevier Ltd All rights reserved.


Heyde K.,Ghent University | Wood J.L.,Georgia Institute of Technology
Reviews of Modern Physics | Year: 2011

Shape coexistence in nuclei appears to be unique in the realm of finite many-body quantum systems. It differs from the various geometrical arrangements that sometimes occur in a molecule in that in a molecule the various arrangements are of the widely separated atomic nuclei. In nuclei the various "arrangements" of nucleons involve (sets of) energy eigenstates with different electric quadrupole properties such as moments and transition rates, and different distributions of proton pairs and neutron pairs with respect to their Fermi energies. Sometimes two such structures will "invert" as a function of the nucleon number, resulting in a sudden and dramatic change in ground-state properties in neighboring isotopes and isotones. In the first part of this review the theoretical status of coexistence in nuclei is summarized. Two approaches, namely, microscopic shell-model descriptions and mean-field descriptions, are emphasized. The second part of this review presents systematic data, for both even- and odd-mass nuclei, selected to illustrate the various ways in which coexistence is observed in nuclei. The last part of this review looks to future developments and the issue of the universality of coexistence in nuclei. Surprises continue to be discovered. With the major advances in reaching to extremes of proton-neutron number, and the anticipated new "rare isotope beam" facilities, guidelines for search and discovery are discussed. © 2011 American Physical Society.


Sherrill C.D.,Georgia Institute of Technology
Accounts of Chemical Research | Year: 2013

Fundamental features of biomolecules, such as their structure, solvation, and crystal packing and even the docking of drugs, rely on noncovalent interactions. Theory can help elucidate the nature of these interactions, and energy component analysis reveals the contributions from the various intermolecular forces: electrostatics, London dispersion terms, induction (polarization), and short-range exchange-repulsion. Symmetry-adapted perturbation theory (SAPT) provides one method for this type of analysis.In this Account, we show several examples of how SAPT pro-vides insight into the nature of noncovalent π-interactions. In cation-π interactions, the cation strongly polarizes electrons in π-orbitals, leading to substantially attractive induction terms. This polarization is so important that a cation and a benzene attract each other when placed in the same plane, even though a consideration of the electrostatic interactions alone would suggest otherwise. SAPT analysis can also support an understanding of substituent effects in π-π interactions. Trends in face-to-face sandwich benzene dimers cannot be understood solely in terms of electrostatic effects, especially for multiply substituted dimers, but SAPT analysis demonstrates the importance of London dispersion forces. Moreover, detailed SAPT studies also reveal the critical importance of charge penetration effects in π-stacking interactions. These effects arise in cases with substantial orbital overlap, such as in π-stacking in DNA or in crystal structures of π-conjugated materials. These charge penetration effects lead to attractive electrostatic terms where a simpler analysis based on atom-centered charges, electrostatic potential plots, or even distributed multipole analysis would incorrectly predict repulsive electrostatics. SAPT analysis of sandwich benzene, benzene-pyridine, and pyridine dimers indicates that dipole/induced-dipole terms present in benzene-pyridine but not in benzene dimer are relatively unimportant. In general, a nitrogen heteroatom contracts the electron density, reducing the magnitude of both the London dispersion and the exchange-repulsion terms, but with an overall net increase in attraction.Finally, using recent advances in SAPT algorithms, researchers can now perform SAPT computations on systems with 200 atoms or more. We discuss a recent study of the intercalation complex of proflavine with a trinucleotide duplex of DNA. Here, London dispersion forces are the strongest contributors to binding, as is typical for π-π interactions. However, the electrostatic terms are larger than usual on a fractional basis, which likely results from the positive charge on the intercalator and its location between two electron-rich base pairs. These cation-π interactions also increase the induction term beyond those of typical noncovalent π-interactions. © 2012 American Chemical Society.

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