Coupled Ion/Electron Hopping in LixNiO2: A 7Li NMR Study

化学 离子 非阻塞I/O 电子 结晶学 原子物理学 核物理学 物理 生物化学 催化作用 有机化学
作者
Cédric Chazel,Michel Ménétrier,Laurence Croguennec,Claude Delmas
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:45 (3): 1184-1191 被引量:26
标识
DOI:10.1021/ic051593n
摘要

Deintercalated "LixNiO2" materials (x = 0.25, 0.33, 0.50, 0.58, and 0.65) were obtained using the electrochemical route from the Li0.985Ni1.015O2 and Li0.993Ni1.007O2 compounds. Refinements of X-ray diffraction data using the Rietveld method show a good agreement with the phase diagram of the LixNiO2 system studied earlier in this laboratory. Electronic conductivity measurements show a thermally activated electron-hopping process for the deintercalated Li0.5NiO2 phase. In the LixNiO2 materials investigated (x = 0.25, 0.33, 0.50, and 0.58), 7Li NMR shows mobility effects leading to an exchanged signal at room temperature. A clear tendency for Li to be surrounded mainly by Ni3+ ions with the 180° configuration is observed, particularly, for strongly deintercalated materials with smaller Li+ and Ni3+ contents, even upon heating, when this mobility becomes very fast in the NMR time scale. This suggests that Li/vacancy hopping does occur on the NMR time scale but that Ni3+/Ni4+ hopping does not occur independently. The position of Li seems to govern the oxidation state of the Ni around it at any time; the electrons follow the Li ions to satisfy local electroneutrality and minimal energy configuration. The observed NMR shifts are compatible with the Li/vacancy and Ni3+/Ni4+ ordering patterns calculated by Arroyo y de Dompablo et al. for x = 0.25 and x = 0.50, but not for x = 0.33 and x = 0.58.
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