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Crystallography

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Full-Text Articles in Physical Sciences and Mathematics

Enhanced Piezoresponse And Nonlinear Optical Properties Of Fluorinated Self-Assembled Peptide Nanotubes, Soma Khanra, Sandra V. Vassiliades, Wendel A. Alves, Kaidi Yang, Rainer Glaser, Kartik Ghosh, Payal Bhattacharya, Ping Yu, Suchismita Guha Nov 2019

Enhanced Piezoresponse And Nonlinear Optical Properties Of Fluorinated Self-Assembled Peptide Nanotubes, Soma Khanra, Sandra V. Vassiliades, Wendel A. Alves, Kaidi Yang, Rainer Glaser, Kartik Ghosh, Payal Bhattacharya, Ping Yu, Suchismita Guha

Chemistry Faculty Research & Creative Works

Self-assembled L,L-diphenylalanine (FF) nanostructures offer an attractive platform for photonics and nonlinear optics. The nonlinear optical (NLO) coefficients of FF nanotubes depend on the diameter of the tube [S. Khanra et al. Phys. Chem. Chem. Phys. 19(4), 3084-3093 (2017)]. To further enhance the NLO properties of FF, we search for structural modifications. Here, we report on the synthesis of fluorinated FF dipeptides by replacing one ortho-hydrogen atom in each of the phenyl groups of FF by a fluorine atom. Density-functional theoretical calculations yield insights into minimum energy conformers of fluorinated FF (Fl-FF). Fl-FF self-assembles akin to FF into micron-length tubes. …


New Polyanion-Based Cathode Materials For Alkali-Ion Batteries, Hooman Yaghoobnejad Asl Jan 2016

New Polyanion-Based Cathode Materials For Alkali-Ion Batteries, Hooman Yaghoobnejad Asl

Doctoral Dissertations

"A number of new materials have been discovered through exploratory synthesis with the aim to be studied as the positive electrode (cathode) in Li-ion and Na-ion batteries. The focus has been set on the ease of synthesis, cost and availability of active ingredients in the battery, and decent cycle-life performance through a combination of iron and several polyanionic ligands. An emphasis has been placed also on phosphite (HPO32-) as a polyanionic ligand, mainly due to the fact that it has not been studied seriously before as a polyanion for cathode materials. The concept of mixed polyanions, for …


Slow Magnetic Relaxation And Electron Delocalization In An S = 9/2 Iron(Ii/Iii) Complex With Two Crystallographically Inequivalent Iron Sites, Susanta Hazra, Sujit Sasmal, Michel Fleck, Fernande Grandjean, Moulay T. Sougrati, Meenakshi Ghosh, T. David Harris, Pierre Bonville, Gary J. Long, Sasankasekhar Mohanta May 2011

Slow Magnetic Relaxation And Electron Delocalization In An S = 9/2 Iron(Ii/Iii) Complex With Two Crystallographically Inequivalent Iron Sites, Susanta Hazra, Sujit Sasmal, Michel Fleck, Fernande Grandjean, Moulay T. Sougrati, Meenakshi Ghosh, T. David Harris, Pierre Bonville, Gary J. Long, Sasankasekhar Mohanta

Chemistry Faculty Research & Creative Works

The magnetic, electronic, and Mössbauer spectral properties of Fe 2L(µ-OAc)2ClO4, 1, where L is the dianion of the tetraimino-diphenolate macrocyclic ligand, H2L, indicate that 1 is a class III mixed valence iron(II/III) complex with an electron that is fully delocalized between two crystallographically inequivalent iron sites to yield a [Fe2]V cationic configuration with a St 9/2 ground state. Fits of the dc magnetic susceptibility between 2 and 300K and of the isofield variable-temperature magnetization of 1 yield an isotropic magnetic exchange parameter, J, of -32(2) cm-1 for an …


A Mössbauer Spectral Study Of The Gdco₄₋ₓfeₓb Compounds, Fernande Grandjean, Raphäel P. Hermann, Eustachy S. Popiel, Gary J. Long Jan 2007

A Mössbauer Spectral Study Of The Gdco₄₋ₓfeₓb Compounds, Fernande Grandjean, Raphäel P. Hermann, Eustachy S. Popiel, Gary J. Long

Chemistry Faculty Research & Creative Works

The iron-57 Mössbauer spectra of the GdCo4-xFexB compounds, where x is 0.10, 0.15, 0.20, 0.25, 1, 2, 2.5, and 2.6, have been measured at room temperature and reveal relatively small iron hyperfine fields of approximately 12-18 T, relatively large quadrupole interactions of approximately +0.9 and -1 mm/s, and three very different types of spectra for x=0.10 and 0.15, x=0.25, 1, and 2, and x=2.5 and 2.6. The differences result from both the different easy magnetization directions in these compounds and the different cobalt and/or iron occupancies of the crystallographic 2c and 6i sites. The spectra have …


Properties Of A Mixed-Valent Iron Compound With The Kagomé Lattice, Chintamani Nagesa Ramachandra Rao, Geo L. Paul, Amitava Choudhury, Echur Varadadesikan Sampathkumaran, Arup Kumar R. Raychaudhuri, Suryanarayanasastry Ramasesha, Indranil Rudra Apr 2003

Properties Of A Mixed-Valent Iron Compound With The Kagomé Lattice, Chintamani Nagesa Ramachandra Rao, Geo L. Paul, Amitava Choudhury, Echur Varadadesikan Sampathkumaran, Arup Kumar R. Raychaudhuri, Suryanarayanasastry Ramasesha, Indranil Rudra

Chemistry Faculty Research & Creative Works

An organically templated iron sulfate of the formula [HN(CH2)6NH][FeIII Fe2 IIF6(SO4)2] ·[H3O] possessing the kagomé lattice has been prepared and characterized by single-crystal crystallography and other techniques. This mixed-valent iron compound shows complex magnetic properties including spin-glass behavior and magnetic hysteresis. The low-temperature specific heat data show deviation from the T2 behavior found in two-dimensional frustrated systems. Simple calculations have been carried out to understand the properties of this kagomé compound.


Magnetic And Mössbauer Spectral Study Of Erfe₁₁Ti And Erfe₁₁Tih, Cristina Piquer, Raphäel P. Hermann, Fernande Grandjean, Gary J. Long, Olivier Isnard Mar 2003

Magnetic And Mössbauer Spectral Study Of Erfe₁₁Ti And Erfe₁₁Tih, Cristina Piquer, Raphäel P. Hermann, Fernande Grandjean, Gary J. Long, Olivier Isnard

Chemistry Faculty Research & Creative Works

The influence of the insertion of hydrogen into the crystal lattice of ErFe11Ti upon its spin reorientation was investigated. It was found that the insertion of hydrogen into ErFe11Ti to form ErFe11TiH expanded the lattice by 1% and increased the Curie temperature by 56 K. The presence of one titanium near neighbor in the environment of an iron site decreased the hyperfine field by ~2T and changed the isomer shift by ~0.05 mm/s.