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Articles 1 - 6 of 6
Full-Text Articles in Chemistry
Density Functional Theory Study On The Structures Of Solvent-Ion In The Electrolyte Of Lithium Ion Battery, Li-Dan Xing, Ru Yang, Xian-Wen Tang, Wen-Na Huang, Qi-Feng Liu, Qi-Peng Yu, Wei-Shan Li
Density Functional Theory Study On The Structures Of Solvent-Ion In The Electrolyte Of Lithium Ion Battery, Li-Dan Xing, Ru Yang, Xian-Wen Tang, Wen-Na Huang, Qi-Feng Liu, Qi-Peng Yu, Wei-Shan Li
Journal of Electrochemistry
In this work, the possible structures of solvent-ion complex, resulting from the electrostatic interaction in the propylene carbonate (PC) base electrolyte of lithium ion battery, have been investigated using the density functional theory. The calculated results show that the structure of solvent-ion complex depends on the solvent number. In the PC base electrolyte, maximum number of PC solvents that coexist in the Li+-solvent sheath is four. Additionally, the salt anion exists in a complex with the positively charged alkyl group of PC rather than in a free state. The calculated results give a good explanation to the reported …
Universal Two-Electron Correlation Operator On Excited States, Bryan Thomas Nichols
Universal Two-Electron Correlation Operator On Excited States, Bryan Thomas Nichols
Theses and Dissertations
Excited states of chemical systems are extremely important in understanding spectra, chemical phenomena, as well as how a particular compound behaves in reactions. Computationally, excited states are normally very expensive to calculate. The difficulty in calculating these states with wavefunction based methods can be mainly attributed to the calculation of large multi-determinant wavefunctions. One reason to use a complicated multi-determinant wavefunction is to include some of the effects of correlation energy. The quantity of correlation energy can most simply be defined as the reduction in energy caused by any two or more electrons trying to avoid each other. The most …
Effect Of Gamma Radiation On The Interfacial Reactions And Transfer Processes Of Phosphonium-Based Ionic Liquids With Carbon Steel, Ryan P. Morco
Effect Of Gamma Radiation On The Interfacial Reactions And Transfer Processes Of Phosphonium-Based Ionic Liquids With Carbon Steel, Ryan P. Morco
Electronic Thesis and Dissertation Repository
This thesis presents work on the effects of ionizing radiation on phosphonium-based ionic liquids (ILs). Ionic liquids are known for their tunable properties which make them attractive options for applications for the separation and sequestration of metal ions from spent nuclear fuels, and candidate lubricants for systems under severe conditions. The high radiation environment found in spent fuel processing may decompose the solvents (ILs) used in the process and affect their separation efficiency. The radiolytic decomposition products can also alter the physical and chemical properties of an IL in ways which can affect the potential corrosion of metal alloys in …
Advances In Molecular Quantum Chemistry Contained In The Q-Chem 4 Program Package, Yihan Shao, Zhengting Gan, Evgeny Epifanovsky, Andrew T. B. Gilbert, Michael Wormit, Shervin Fatehi
Advances In Molecular Quantum Chemistry Contained In The Q-Chem 4 Program Package, Yihan Shao, Zhengting Gan, Evgeny Epifanovsky, Andrew T. B. Gilbert, Michael Wormit, Shervin Fatehi
Chemistry Faculty Publications and Presentations
A summary of the technical advances that are incorporated in the fourth major release of the Q-CHEM quantum chemistry program is provided, covering approximately the last seven years. These include developments in density functional theory methods and algorithms, nuclear magnetic resonance (NMR) property evaluation, coupled cluster and perturbation theories, methods for electronically excited and open-shell species, tools for treating extended environments, algorithms for walking on potential surfaces, analysis tools, energy and electron transfer modelling, parallel computing capabilities, and graphical user interfaces. In addition, a selection of example case studies that illustrate these capabilities is given. These include extensive benchmarks of …
Electrochemical Catalysis: A Dft Study, Li Li, Zi-Dong Wei
Electrochemical Catalysis: A Dft Study, Li Li, Zi-Dong Wei
Journal of Electrochemistry
In this review, we focus on achievements in electro-catalysis based on the density function theory study. The relationships among the electrode potential, electronic structure of catalysts and electro-catalytic activity are summarized in three parts: the adsorption and desorption of species, electron transfer, and stability of catalysts. The electrode potential and the electronic structure (d-band center or Fermi (HOMO) energy) of catalysts significantly influence the formation, adsorption and desorption of surface species on electrode. The electro-catalytic activity can be improved by modulating the electrode potential and electronic structure of catalysts.
Coupling Ferrocene To Brominated Tetraazaporphyrin: Exploring An Alternative Synthetic Pathway For Preparation Of Ferrocene-Containing Tetraazaporphyrins, Victor N. Nemykin, Elena A. Makarova, Nathan R. Erickson, Pavlo V. Solntsev
Coupling Ferrocene To Brominated Tetraazaporphyrin: Exploring An Alternative Synthetic Pathway For Preparation Of Ferrocene-Containing Tetraazaporphyrins, Victor N. Nemykin, Elena A. Makarova, Nathan R. Erickson, Pavlo V. Solntsev
Turkish Journal of Chemistry
A Castro--Stephens coupling reaction between metal-free 3(2),8(7)-dibromo- 2(3),7(8),12(13),17(18)-tetra-tert-butyl-5,10,15,20-tetraazaporphyrin and (ferrocenylethynyl)copper resulted in the formation of copper 2(3),7(8),12(13), 17(18)-tetra-tert-butyl-3(2), 8(7)-di(ferrocenylethynyl)-5,10,15,20-tetraazaporphyrin and copper 2(3),7(8),12(13),17(18)-tetra-tert-butyl-3(2)-ferrocenylethynyl-5, 10,15,20-tetraazaporphyrin, which were separated in the form of 2 positional isomers along with copper 3(2)-bromo-2(3),7(8),12(13),17(18)-tetra-tert-butyl-5,10,15,20-tetraazaporphyrin and copper 2(3),7(8),12(13),17(18)-tetra-tert-butyl-5,10,15,20-tetraazaporphyrin. A similar reaction with metal-free 3(2),8(7),13(12), 18(17)-tetrabromo-2(3),7(8),12(13),17(18)-tetra-tert-butyl-5,10,15,20-tetraazaporphyrin resulted in only a trace amount of 3(2),8(7),13(12)-tribromo-2(3),7(8),12(13),17(18)-tetra-tert-butyl-18(17) -ferrocenylethynyl-5,10,15,20-tetraazaporphyrin, while no products with larger number of organometallic substituents were observed. Direct coupling between ferrocenelithium and 3(2),8(7)-dibromo-2(3),7(8),12(13),17(18)-tetra-tert-butyl-5,10,15,20-tetraazaporphyrin resulted in a debromination reaction accompanied by very minor dimerization of the tetraazaporphyrin core, which was explained based on the steric properties of the parent tetraazaporphyrin. The …