法拉第效率
阴极
氧化还原
电解质
阳极
溶解
材料科学
氧气
电池(电)
锂(药物)
氧化物
化学工程
电极
无机化学
化学物理
纳米技术
化学
物理化学
热力学
内分泌学
功率(物理)
有机化学
冶金
工程类
物理
医学
作者
Qingyuan Li,De Ning,Deniz Wong,Ke An,Yuxin Tang,Dong Zhou,Götz Schuck,Zhenhua Chen,Nian Zhang,Xiangfeng Liu
标识
DOI:10.1038/s41467-022-28793-9
摘要
Abstract The oxygen redox reaction in lithium-rich layered oxide battery cathode materials generates extra capacity at high cell voltages (i.e., >4.5 V). However, the irreversible oxygen release causes transition metal (TM) dissolution, migration and cell voltage decay. To circumvent these issues, we introduce a strategy for tuning the Coulombic interactions in a model Li-rich positive electrode active material, i.e., Li 1.2 Mn 0.6 Ni 0.2 O 2 . In particular, we tune the Coulombic repulsive interactions to obtain an adaptable crystal structure that enables the reversible distortion of TMO 6 octahedron and mitigates TM dissolution and migration. Moreover, this strategy hinders the irreversible release of oxygen and other parasitic reactions (e.g., electrolyte decomposition) commonly occurring at high voltages. When tested in non-aqueous coin cell configuration, the modified Li-rich cathode material, combined with a Li metal anode, enables a stable cell discharge capacity of about 240 mAh g −1 for 120 cycles at 50 mA g −1 and a slower voltage decay compared to the unmodified Li 1.2 Mn 0.6 Ni 0.2 O 2 .
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