Littérature scientifique sur le sujet « Defects Chemistry »
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Articles de revues sur le sujet "Defects Chemistry"
Gabániová, Mária. « Surface Chemistry-Based Surface Defects Situated on Steel Strips Edges ». Defect and Diffusion Forum 405 (novembre 2020) : 199–204. http://dx.doi.org/10.4028/www.scientific.net/ddf.405.199.
Texte intégralIpser, Herbert. « A3B Intermetallics : Defect chemistry and nonstoichiometry ». Pure and Applied Chemistry 79, no 10 (1 janvier 2007) : 1675–89. http://dx.doi.org/10.1351/pac200779101675.
Texte intégralKovalevsky, Andrei V., Myriam H. Aguirre, Sascha Populoh, Sonia G. Patrício, Nuno M. Ferreira, Sergey M. Mikhalev, Duncan P. Fagg, Anke Weidenkaff et Jorge R. Frade. « Designing strontium titanate-based thermoelectrics : insight into defect chemistry mechanisms ». Journal of Materials Chemistry A 5, no 8 (2017) : 3909–22. http://dx.doi.org/10.1039/c6ta09860f.
Texte intégralMeggiolaro, Daniele, Silvia G. Motti, Edoardo Mosconi, Alex J. Barker, James Ball, Carlo Andrea Riccardo Perini, Felix Deschler, Annamaria Petrozza et Filippo De Angelis. « Iodine chemistry determines the defect tolerance of lead-halide perovskites ». Energy & ; Environmental Science 11, no 3 (2018) : 702–13. http://dx.doi.org/10.1039/c8ee00124c.
Texte intégralAyoub, Irfan, Vijay Kumar, Reza Abolhassani, Rishabh Sehgal, Vishal Sharma, Rakesh Sehgal, Hendrik C. Swart et Yogendra Kumar Mishra. « Advances in ZnO : Manipulation of defects for enhancing their technological potentials ». Nanotechnology Reviews 11, no 1 (1 janvier 2022) : 575–619. http://dx.doi.org/10.1515/ntrev-2022-0035.
Texte intégralGötze, Jens, Yuanming Pan et Axel Müller. « Mineralogy and mineral chemistry of quartz : A review ». Mineralogical Magazine 85, no 5 (28 septembre 2021) : 639–64. http://dx.doi.org/10.1180/mgm.2021.72.
Texte intégralLuo, Yang, et Yinghong Wu. « Defect Engineering of Nanomaterials for Catalysis ». Nanomaterials 13, no 6 (21 mars 2023) : 1116. http://dx.doi.org/10.3390/nano13061116.
Texte intégralChiodelli, G., U. Anselmi-Tamburini, M. Arimondi, G. Spinolo et G. Flor. « Defect Chemistry of “BaCuO2” II. Transport Properties and Nature of Defects ». Zeitschrift für Naturforschung A 50, no 11 (1 novembre 1995) : 1059–66. http://dx.doi.org/10.1515/zna-1995-1113.
Texte intégralWithers, Ray, Jeffrey Sellar, Michael O'Keeffe et Stephen Hyde. « Bruce Godfrey Hyde 1925–2014 ». Historical Records of Australian Science 26, no 2 (2015) : 179. http://dx.doi.org/10.1071/hr15006.
Texte intégralStemmer, S., G. Duscher, E. M. James, M. Ceh et N. D. Browning. « Atomic Scale Structure-Property Relationships of Defects and Interfaces in Ceramics ». Microscopy and Microanalysis 4, S2 (juillet 1998) : 556–57. http://dx.doi.org/10.1017/s143192760002290x.
Texte intégralThèses sur le sujet "Defects Chemistry"
Cromack, Keith Richard. « Photo-induced magnetic defects in conducting polymers ». The Ohio State University, 1991. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343059111.
Texte intégralJózefowicz, Mikolaj Edward. « Structure and long-lived defects in polyanilines ». The Ohio State University, 1991. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343400785.
Texte intégralCliffe, Matthew James. « Disorder and defects in functional molecular frameworks ». Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:cd827bc8-b3dd-4fda-bdb8-f0dc893d66c2.
Texte intégralLee, Lawrence Yoon Suk 1972. « Probing and controlling defects in self-assembled monolayers ». Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=102674.
Texte intégralThis characteristic electrochemical property of FcC12S-Au system allows for the quantification of defects in SAMs. This is important because coverage defects, or voids in alkylthiol SAMs, are a critical component of electron transfer mechanisms of soluble redox probes. Short time exposure of a defective SAM to FcC12SH leads to a quantifiable defect-related Fc coverage (GammaFc), with GammaFc < 1% being readily measurable. Using FcC12SH as a label, a number of alkylthiol SAM preparation conditions have been assessed.
FcC12SH is further used to probe the progress of the important alkylthiol-for-alkylthiol exchange reaction in SAMs. It is shown that variation of chain length, reaction temperature, terminal group, applied potential, and the initial defect density determines the extent and the rate of the exchange reaction. Kinetics studies of binary (FcC12S-/CH3RS-Au) SAM formation via co-incubation reveal that although csurfFc is initially close to the solution mole fraction of the FcC12 SH ( csolnFc ), the subsequent exchange reaction leads to a csurfFc which is often quite different from csolnFc .
Finally, the FcC12SH probe is used to further study the reductive voltammetric desorption of alkylthiol SAMs. Defects in a C14S-Au SAM created by excursions to desorptive reduction potentials were quantified by use of the FcC12SH label. A reductive desorption potential followed by re-adsorption, applied to a binary (FcC12S-/C14S-Au) SAM, results in mixing of the phase separated components of the binary SAM.
Pressé, Steve 1981. « Role of fluctuations and defects in select condensed matter problems ». Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43774.
Texte intégralPage 122 blank. Vita.
Includes bibliographical references.
Defects and fluctuations dominate both static and dynamical properties of systems in the condensed phase. In this work, we focus on three such examples. Firstly, we model the effect of proton fluctuations on the rate of electron transfer in the condensed phase through an electron donor-acceptor assembly linked via an H-bonding bridge. The model suggests that it is possible for the electron transfer rate through a deuterated H-bonding assembly to exceed the rate through a protonated H-bonding bridge at low temperature, consistent with experimental findings. Next, we consider the convergence properties of Jarzynski's non-equilibrium work relation. This relation expresses the free energy change of a system, onto which finite-time work is done, as an ensemble average over all possible trajectories of the system. We quantify the regime of applicability of this equality by considering the role of rare fluctuations which dominate the work average of entropy generating processes. Lastly, we consider fluorophore lifetime variations arising when single molecules are placed near non-planar metallic surfaces. We compute the exact first order self-fields of vertical dipoles located above locally curved perfectly conducting surfaces by invoking a small slope phase perturbation technique. The results suggest that smooth perturbations lead to deviations from the image theory results extensively used to interpret the experimentally observed single molecule lifetime changes.
by Steve Pressé.
Ph.D.
Mottishaw, Sinead. « Investigations of the nature, properties and distribution of defects in diamond ». Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/101511/.
Texte intégralRoy, Santanu. « Spectroscopic study of defects in cadmium selenide quantum dots (QDS) and cadmium selenide nanorods (NRS) ». Diss., Kansas State University, 2013. http://hdl.handle.net/2097/16118.
Texte intégralDepartment of Chemistry
Viktor Chikan
Ever depleting sources of fossil fuel has triggered more research in the field of alternate sources of energy. Over the past few years, CdSe nanoparticles have emerged as a material with a great potential for optoelectronic applications because of its easy exciton generation and charge separation. Electronic properties of CdSe nanoparticles are highly dependent on their size, shape and electronic environment. The main focus of this research is to explore the effect of different electronic environments on various spectroscopic properties of CdSe nanoparticles and link this to solar cell performance. To attain that goal, CdSe quantum dots (QDs) and nanorods (NRs) have been synthesized and either doped with metal dopants or embedded in polymer matrices. Electronic properties of these nanocomposites have been studied using several spectroscopic techniques such as absorption, photoluminescence, time-resolved photoluminescence, confocal microscopy and wide field microscopy. Indium and tin are the two metal dopants that have been used in the past to study the effect of doping on conductivity of CdSe QDs. Based on the photoluminescence quenching experiments, photoluminescence of both indium and tin doped samples suggest that they behave as n-type semiconductors. A comparison between theoretical and experimental data suggests that energy levels of indium doped and tin doped QDs are 280 meV and 100 meV lower than that of the lowest level of conduction band respectively. CdSe nanorods embedded in two different polymer matrices have been investigated using wide field fluorescence microscopy and confocal microscopy. The data reveals significant enhancement in bandedge luminescence of NRs in the vicinity of a conjugated polymer such as P3HT. Photoactive charge transfer from polymers to the surface traps of NRs may account for the observed behavior. Further study shows anti-correlation between bandedge and trap state emission of CdSe NRs. A recombination model has been proposed to explain the results. The origin of traps is also investigated and plausible explanations are drawn from the acquired data.
Srinivasan, K. « FDAS : a knowledge-based framework for analysis of defects in woven textile structures ». Thesis, Georgia Institute of Technology, 1990. http://hdl.handle.net/1853/8671.
Texte intégralRoberts, Sean T. (Sean Thomas). « Hydrogen bond rearrangements and the motion of charge defects in water viewed using multidimensional ultrafast infrared spectroscopy ». Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/57678.
Texte intégral"December 2009." Cataloged from PDF version of thesis. Vita.
Includes bibliographical references.
Compared with other molecular liquids, water is highly structured due to its ability to form up to four hydrogen bonds to its nearest neighbors, resulting in a tetrahedral network of molecules. However, this network is highly dynamic, exhibiting fluctuations and rearrangements that take place on femtosecond to picosecond time scales. The transport of excess protons and proton holes in water makes exclusive use of water's hydrogen bonding network. Compared to ions of similar size and charge density, both hydronium and hydroxide ions exhibit anomalously high diffusion rates due to the fact that water molecules that neighbor these ions can undergo a proton transfer reaction with the ion. This allows the structural diffusion of the ion to occur apart from the displacement of individual water molecules. In this thesis we adopt a joint experimental and theoretical approach to characterize the fluctuations of water's hydrogen bonding network and how these fluctuations act to drive the structural diffusion of the aqueous hydroxide ion. The experimental data that we present consists of a series of ultrafast nonlinear infrared spectroscopies, in particular two-dimensional infrared spectroscopy (2D IR), applied to the O-H stretching transition of a dilute solution of HOD in NaOD/D20. The frequency of the O-H stretch, (OH, is highly sensitive to the configuration of its hydrogen bonding partner. 2D IR spectroscopy allows us to measure rapid shifts in OH that reveal time scales for changes in the local environment of the HOD molecule.
(cont.) The calculation of 2D IR spectra from molecular dynamics simulations then allows us to make a direct connection between the results of our experiments and the underlying dynamics of the system that drive both hydrogen bond exchange and the structural diffusion of the hydroxide ion. 2D IR spectra recorded for dilute HOD in D20 show a strong asymmetry, preferentially broadening in the frequency region indicative of strained or broken hydrogen bonds, indicating that these configurations are unstable and quickly return to a hydrogen bond. The time scale over which the 2D spectra broaden, ~60 fs, is similar to the librational period of water and suggests that molecules exchange hydrogen bonding partners though rapid, large amplitude rotations. Molecular dynamics simulations find that the transition state for hydrogen bond exchange resembles a bifurcated hydrogen bond. In roughly half of the examined exchange events, a second solvation shell water molecule inserts across the breaking hydrogen bond. This suggests that hydrogen bond rearrangements are tied to the restructuring of a water molecule's solvation shell. Upon the addition of NaOD to HOD/D20 solution, a large absorption continuum appears to the low frequency side of the O-H stretch due to the formation of strong hydrogen bonds between HOD molecules and OD ions. At early waiting times, 2D IR spectra show large, offdiagonal intensity in this frequency range that rapidly relaxes within ~110 fs.
(cont.) Modeling using an empirical valence bond simulation (MS-EVB) model of aqueous NaOH suggests that as the 0-H stretching potential symmetrizes during proton transfer events, overtone transitions of the shared proton contribute strongly to 2D spectra. The rapid loss of offdiagonal intensity results from the spectral sweeping of these vibrational overtones as the solvent modulates the motion of the shared proton. The collective electric field of the solvent is found to be an appropriate reaction coordinate for the formation and modulation of shared proton states. Over picosecond waiting times, spectral features appear in the 2D IR spectra that are indicative of the exchange of population between OH~ ions and HOD molecules due to proton transfer. The construction of a spectral fitting model gives a lower bound of 3 ps for this exchange. Calculations of structural parameters following proton exchange using the MS-EVB simulation model suggest that the observed exchange process corresponds to the formation and breakage of hydrogen bonds donated by the HOD/OD~ pair formed as a result of the proton transfer. A full description of the structural diffusion of the hydroxide ion requires both a description of the local hydrogen bonding structure of the ion as well as the dielectric fluctuations of the surrounding solvent.
by Sean T. Roberts.
Ph.D.
Jensen, Stephen C. « The Role of Interstitials and Surface Defects on Oxidation and Reduction Reactions on Titania ». Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:10768.
Texte intégralChemistry and Chemical Biology
Livres sur le sujet "Defects Chemistry"
Tilley, R. J. D. Defect crystal chemistry and its applications. Glasgow : Blackie, 1987.
Trouver le texte intégralKosuge, Kōji. Chemistry of non-stoichiometric compounds. Oxford : Oxford University Press, 1994.
Trouver le texte intégralN, Schock Robert, dir. Point defects in minerals. Washington, D.C : American Geophysical Union, 1985.
Trouver le texte intégralGutoff, Edgar B. Coating and Drying Defects. New York : John Wiley & Sons, Ltd., 2006.
Trouver le texte intégralNowotny, J. Non-Stoichiometric Compounds : Surfaces, Grain Boundaries and Structural Defects. Dordrecht : Springer Netherlands, 1989.
Trouver le texte intégralD, Cohen Edward, et Kheboian Gerald I, dir. Coating and drying defects : Troubleshooting operating problems. 2e éd. Hoboken, N.J : John Wiley & Sons, 2006.
Trouver le texte intégralGutoff, Edgar B. Coating and drying defects : Troubleshooting operating problems. New York : Wiley, 1995.
Trouver le texte intégralFrank-Kamenetskaya, O. V. Atomic defects and crystal structure of minerals. Sous la direction de Rozhdestvenskaya, I. V. (Ira V.) et Frank-Kamenet︠s︡kiĭ V. A. 2e éd. Saint Petersburg : Yanus, 2004.
Trouver le texte intégralSohar, Christian Rudolf. Lifetime Controlling Defects in Tool Steels. Berlin, Heidelberg : Springer-Verlag Berlin Heidelberg, 2011.
Trouver le texte intégralMcCluskey, Matthew D. Dopants and defects in semiconductors. Boca Raton, FL : Taylor & Francis, 2012.
Trouver le texte intégralChapitres de livres sur le sujet "Defects Chemistry"
Ubic, Rick. « Point Defects ». Dans Crystallography and Crystal Chemistry, 347–72. Cham : Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-49752-0_16.
Texte intégralUbic, Rick. « Line Defects ». Dans Crystallography and Crystal Chemistry, 373–95. Cham : Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-49752-0_17.
Texte intégralMoore, Elaine A., et Lesley E. Smart. « Defects and Nonstoichiometry ». Dans Solid State Chemistry, 187–224. Fifth edition. | Boca Raton : CRC Press, [2021] : CRC Press, 2020. http://dx.doi.org/10.1201/9780429027284-5.
Texte intégralSmart, Lesley, et Elaine Moore. « Defects and non-stoichiometry ». Dans Solid State Chemistry, 159–218. Boston, MA : Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-6830-2_5.
Texte intégralCerofolini, Gianfranco, et Laura Meda. « Equilibrium Defects ». Dans Physical Chemistry of, in and on Silicon, 15–24. Berlin, Heidelberg : Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-73504-2_3.
Texte intégralZhu, Xuefeng, et Weishen Yang. « Defects and Diffusion ». Dans Green Chemistry and Sustainable Technology, 11–48. Berlin, Heidelberg : Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-53534-9_2.
Texte intégralCarter, C. Barry, et M. Grant Norton. « Characterizing Structure, Defects, and Chemistry ». Dans Ceramic Materials, 159–83. New York, NY : Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3523-5_10.
Texte intégralKröger, F. A. « Point Defects in Solids : Physics, Chemistry, and Thermodynamics ». Dans Point Defects in Minerals, 1–17. Washington, D. C. : American Geophysical Union, 2013. http://dx.doi.org/10.1029/gm031p0001.
Texte intégralKleman, M. « Defects in Quasicrystals ». Dans Physics and Chemistry of Finite Systems : From Clusters to Crystals, 199–210. Dordrecht : Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-017-2645-0_23.
Texte intégralChadwick, A. V., et J. Corish. « Defects and Matter Transport in Solid Materials ». Dans New Trends in Materials Chemistry, 285–318. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5570-0_10.
Texte intégralActes de conférences sur le sujet "Defects Chemistry"
Sharia, Onise, Maija M. Kuklja, Mark Elert, Michael D. Furnish, William W. Anderson, William G. Proud et William T. Butler. « EFFECT OF DEFECTS ON INITIATION OF CHEMISTRY IN HMX ». Dans SHOCK COMPRESSION OF CONDENSED MATTER 2009 : Proceedings of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2009. http://dx.doi.org/10.1063/1.3295142.
Texte intégralDean, B. E., C. J. Johnson, S. C. McDevitt, G. T. Neugebauer, J. L. Sepich, R. C. Dobbyn, M. Kuriyama, J. Elllsworth, H. R. Vydyanath et J. J. Kennedy. « Correlation of HgCdTe epilayer defects with underlying substrate defects by synchrotron x-ray topography ». Dans Physics and chemistry of mercury cadmium telluride and novel IR detector materials. AIP, 1991. http://dx.doi.org/10.1063/1.41061.
Texte intégralWang, Chenwei, Yue Li, Guoqiang Song, Zhaoqing Huo, Jia Liu et Yuling Liu. « Role of Slurry Chemistry for Defects Reduction During Barrier CMP ». Dans 2020 China Semiconductor Technology International Conference (CSTIC). IEEE, 2020. http://dx.doi.org/10.1109/cstic49141.2020.9282561.
Texte intégralWright, John C. « Site selective laser spectroscopy of defects in solids ». Dans OSA Annual Meeting. Washington, D.C. : Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.mgg3.
Texte intégralStashans, Arvids, Jean-Louis Calais et Eugene Kotomin. « Quantum-chemical simulations of point defects in α-Al2O3 ». Dans The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47655.
Texte intégralWang, YuHuang. « Organic color center quantum defects in carbon nanotube semiconductors : progresses, challenges, and opportunities ». Dans Physical Chemistry of Semiconductor Materials and Interfaces XXII, sous la direction de Andrew J. Musser et Derya Baran. SPIE, 2023. http://dx.doi.org/10.1117/12.2677676.
Texte intégralSarma, Ch Amarnatha, Bollem Vamsi Krishna, L. M. L. Narayana Reddy et P. Sree Lakshmi. « An inter-dıgıtal band-pass fılter wıth dual vıas in resonator and defects in ground sheet for S-band applıcatıons ». Dans CHEMISTRY BEYOND BORDERS : INTERNATIONAL CONFERENCE ON PHYSICAL CHEMISTRY : The 1st Annual Meeting of the Physical Chemistry Division of the Indonesian Chemical Society. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0166041.
Texte intégralMeggiolaro, Daniele. « A Theoretical Tour of Metal-Halide Perovskites Defects Chemistry : from Lead to Tin ». Dans MATSUS23 & Sustainable Technology Forum València (STECH23). València : FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.matsus.2023.376.
Texte intégralKONONENKO, V. K., D. V. USHAKOV et H. W. KUNERT. « EFFECTS OF DOPING AND NONRADIATIVE DEFECTS IN GaAs SUPERLATTICES ». Dans Physics, Chemistry and Application of Nanostructures - Reviews and Short Notes to Nanomeeting 2003. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812796738_0010.
Texte intégralMoro, Stefania, Giovanni Costantini et Michael Sommer. « Quantitative characterisation of conjugated polymers : mass distribution and polymerisation defects determined by molecular scale imaging ». Dans Physical Chemistry of Semiconductor Materials and Interfaces XXII, sous la direction de Andrew J. Musser et Derya Baran. SPIE, 2023. http://dx.doi.org/10.1117/12.2677311.
Texte intégralRapports d'organisations sur le sujet "Defects Chemistry"
Ballance, Joan B., Mitsuo Kawabe, Timothy D. Sands, Eicke R. Weber et R. S. Williams. Chemistry and Defects in Semiconductor Heterostructures. Materials Research Society Symposium Proceedings. Volume 148. Fort Belvoir, VA : Defense Technical Information Center, mai 1990. http://dx.doi.org/10.21236/ada229585.
Texte intégralMaxey. L51427 ERW Weld Zone Characteristics. Chantilly, Virginia : Pipeline Research Council International, Inc. (PRCI), juin 1992. http://dx.doi.org/10.55274/r0011187.
Texte intégralSingel, David J. Electron Transfer Chemistry in Optical Materials : An EPR Investigation of Radiation-Induced Defects in Chemically Modified Materials. Fort Belvoir, VA : Defense Technical Information Center, janvier 2001. http://dx.doi.org/10.21236/ada387336.
Texte intégralHarmer, Martin P., et Donald M. Smyth. Nanostructure and Defect Chemistry of Relaxor Ferroelectrics. Fort Belvoir, VA : Defense Technical Information Center, juillet 1988. http://dx.doi.org/10.21236/ada207217.
Texte intégralAnil V. Virkar. Electrically Conductive, Corrosion-Resistant Coatings Through Defect Chemistry for Metallic Interconnects. Office of Scientific and Technical Information (OSTI), décembre 2006. http://dx.doi.org/10.2172/920189.
Texte intégralKerr, Lei L., David C. Look et Zhaoqiang Fang. Defect Chemistry Study of Nitrogen Doped ZnO Thin Films. Final report. Office of Scientific and Technical Information (OSTI), novembre 2009. http://dx.doi.org/10.2172/1060189.
Texte intégral