锂(药物)
尖晶石
锰
电化学
阴极
材料科学
相(物质)
磷酸钒锂电池
降级(电信)
单斜晶系
无机化学
阳极
化学工程
电池(电)
化学
电极
晶体结构
结晶学
冶金
物理化学
有机化学
功率(物理)
内分泌学
工程类
物理
电信
医学
量子力学
计算机科学
作者
Weibo Hua,Suning Wang,Michael Knapp,Steven Leake,Anatoliy Senyshyn,Carsten Richter,Murat Yavuz,Joachim R. Binder,Clare P. Grey,Helmut Ehrenberg,Sylvio Indris,Björn Schwarz
标识
DOI:10.1038/s41467-019-13240-z
摘要
One major challenge in the field of lithium-ion batteries is to understand the degradation mechanism of high-energy lithium- and manganese-rich layered cathode materials. Although they can deliver 30 % excess capacity compared with today's commercially- used cathodes, the so-called voltage decay has been restricting their practical application. In order to unravel the nature of this phenomenon, we have investigated systematically the structural and compositional dependence of manganese-rich lithium insertion compounds on the lithium content provided during synthesis. Structural, electronic and electrochemical characterizations of LixNi0.2Mn0.6Oy with a wide range of lithium contents (0.00 ≤ x ≤ 1.52, 1.07 ≤ y < 2.4) and an analysis of the complexity in the synthesis pathways of monoclinic-layered Li[Li0.2Ni0.2Mn0.6]O2 oxide provide insight into the underlying processes that cause voltage fading in these cathode materials, i.e. transformation of the lithium-rich layered phase to a lithium-poor spinel phase via an intermediate lithium-containing rock-salt phase with release of lithium/oxygen.
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