T
Thomas E. Conry
Researcher at Lawrence Berkeley National Laboratory
Publications - 13
Citations - 936
Thomas E. Conry is an academic researcher from Lawrence Berkeley National Laboratory. The author has contributed to research in topics: Absorption spectroscopy & Lithium. The author has an hindex of 9, co-authored 13 publications receiving 878 citations. Previous affiliations of Thomas E. Conry include University of California, Berkeley & University of California.
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Journal ArticleDOI
Photovoltaic effects in BiFeO3
S. Y. Yang,Lane W. Martin,Byrnes Steven J,Byrnes Steven J,Thomas E. Conry,Thomas E. Conry,S. R. Basu,D. Paran,Lothar A. Reichertz,Jon F. Ihlefeld,Carolina Adamo,A. Melville,Ying-Hao Chu,Chan-Ho Yang,Janice L. Musfeldt,D. G. Schlom,Joel W. Ager,Ramamoorthy Ramesh,Ramamoorthy Ramesh +18 more
TL;DR: In this article, the photovoltaic effect in ferroelectric BiFeO3 thin films was reported and the all-oxide heterostructures with SrRuO3 bottom and tin doped indium oxide top electrodes were characterized by open-circuit voltages ∼08-09V and external quantum efficiencies up to ∼10% when illuminated with the appropriate light.
Journal ArticleDOI
Nanoporous spherical LiFePO4 for high performance cathodes
TL;DR: Micron sized, three dimensional (3D) nanoporous spherical LiFePO4/C synthesized by spray pyrolysis shows excellent cyclability and superior rate capability.
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Spherical Nanoporous LiCoPO4/C Composites as High Per-formance Cathode Materials for Rechargeable Lithium Bat-teries
TL;DR: In this paper, spherical nanoporous LiCoPO4/C composite microparticles were synthesized from soluble precursors by spray pyrolysis and achieved a reversible capacity of 123 mAh g−1 at C/10 rate, and showed excellent cycling behavior and rate capability.
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Structural Underpinnings of the Enhanced Cycling Stability upon Al-Substitution in LiNi0.45Mn0.45Co0.1–yAlyO2 Positive Electrode Materials for Li-ion Batteries
TL;DR: In situ X-ray diffraction revealed structural distortions in the transition metal layers of as-synthesized powders with high Al-contents, as well as a structural evolution seen in all materials after cycling.
Journal ArticleDOI
Structural and Electrochemical Investigation of Li ( Ni0.4Co0.15Al0.05Mn0.4 ) O2 Cathode Material
Christopher A. Rumble,Thomas E. Conry,Marca M. Doeff,Elton J. Cairns,Elton J. Cairns,James E. Penner-Hahn,Aniruddha Deb +6 more
Abstract: LiNi0.4Co0.15Al0.05Mn0.4O2 was investigated to understand the effect of replacement of the cobalt by aluminum on the structural and electrochemical properties. In situ X-ray absorption spectroscopy XAS was performed, utilizing a novel in situ electrochemical cell, specifically designed for long-term X-ray experiments. The cell was cycled at a moderate rate through a typical Li-ion battery operating voltage range. 1.0‐4.7 V XAS measurements were performed at different states of charge SOC during cycling, at the Ni, Co, and the Mn edges, revealing details about the response of the cathode to Li insertion and extraction processes. The extended X-ray absorption fine structure EXAFS region of the spectra revealed the changes of bond distance and coordination number of Ni, Co, and Mn absorbers as a function of the SOC of the material. The oxidation states of the transition metals in the system are Ni 2+ ,C o 3+ , and Mn 4+ in the as-made material fully discharged, while during charging the Ni 2+ is oxidized to Ni 4+ through an intermediate stage of Ni 3+ ,C o 3+ is oxidized toward Co 4+ , and Mn was found to be electrochemically inactive and remained as Mn 4+ . The EXAFS results during cycling show that the Ni‐O changes the most, followed by Co‐O, and Mn‐O varies the least. These measurements on this cathode material confirmed that the material retains its symmetry and good structural short-range order leading to the superior cycling reported earlier.