Won‐Sub Yoon,Clare P. Grey,Mahalingam Balasubramanian,Xiao‐Qing Yang,J. McBreen
出处
期刊:Chemistry of Materials [American Chemical Society] 日期:2003-07-03卷期号:15 (16): 3161-3169被引量:229
标识
DOI:10.1021/cm030220m
摘要
We have investigated the local electronic and atomic structure of the LiMn0.5Ni0.5O2 electrode during the first charge and discharge process using in situ X-ray absorption spectroscopy (XAS) of the Mn and Ni K-edges. The Ni K-edge structure in the XANES spectrum shifts to higher energy during charge and shifts back reversibly during discharge in the higher voltage region of ∼4 V, whereas the Mn K-edge structure does not appear to exhibit a rigid edge shift. Further Li-ion intercalation during extended discharge in the 1-V plateau leads to the reduction of Mn4+ ions suggesting that the charge compensation in this region is achieved via the reduction of Mn4+ ions to Mn2+. Mn K-edge EXAFS results indicate that a small amount of Li is found in the Ni2+/Mn4+ layers. These Li ions in the transition metal layers are primarily present in the second coordination shell of Mn and not around Ni. Ni K-edge EXAFS fitting results suggest that the oxidation process upon Li deintercalation takes place in two steps: Ni2+ to Ni3+ first, and then Ni3+ to Ni4+.