Browsing by Author "Rodriguez, EE"
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- ItemHigh temperature magnetic ordering in the 4d perovskite SrTcO3(American Physical Society, 2011-02-07) Rodriguez, EE; Poineau, F; Llobet, A; Kennedy, BJ; Avdeev, M; Thorogood, GJ; Carter, ML; Seshadri, R; Singh, DJ; Cheetham, AKWe present evidence for possibly the highest magnetic ordering temperature in any compound without 3d transition elements. Neutron powder diffraction measurements, at both time-of-flight and constant wavelength sources, were performed on two independently prepared SrTcO3 powders. SrTcO3 adopts a distorted perovskite structure with G-type antiferromagnetic ordering and has a moment of 1.87(4)μB per Tc cation at room temperature with an extraordinarily high Néel point close to 750°C. Electronic structure calculations reveal extensive mixing between the technetium 4d states and oxygen states proximal to the Fermi level. This hybridization leads to a close relationship between magnetic ordering temperature and moment formation in SrTcO3. © 2011, American Physical Society
- ItemOn the electrochemical phase evolution of anti-PbO-type CoSe in alkali ion batteries(American Chemical Society, 2021-04-26) Gillard, CHR; Zhou, XQ; Avdeev, M; Rodriguez, EE; Sharma, NThe reaction mechanism of anti-PbO type CoSe in Li, Na, and K ion half cells is studied. Ex situ X-ray diffraction data is analyzed with the Rietveld method, in conjunction with discharge profiles and extended cycling data. These indicate that intercalation followed by a conversion reaction occur in all systems. For the case of Na, the intercalation reaction was associated with a contraction in the stacking axis lattice parameter, whereas Li and K exhibited expansion. Magnetic susceptibility versus temperature measurements of Li- and Na-intercalated CoSe samples produce unusual results, and several explanations are proposed, including the formation of a superconductive phase. Extended cycling experiments are also performed, and high initial capacities of 937, 657, and 972 mAh/g are observed for Li, Na, and K, respectively. However, all systems exhibit significantly lower second discharge capacities of 796, 530, and 515 mAh/g. The capacities continue to decline during extended cycling, with the systems exhibiting tenth cycle capacity fades of 52, 85, and 95% and Li half cells exhibit capacities over 150 mAh/g at 15 mA/g after 50 cycles. The capacity fade is likely attributable to volume changes and irreversibility associated with conversion and intercalation reactions. This work correlates electrochemical features to the structural evolution, magnetic properties, and reaction mechanisms. © 2021 American Chemical Society