阴极
法拉第效率
材料科学
锂(药物)
电池(电)
氧化还原
化学工程
能量密度
电压
阳极
电极
化学
工程物理
电气工程
物理化学
医学
功率(物理)
物理
工程类
量子力学
冶金
内分泌学
作者
Haotian Yang,Wei Wang,Yuqiang Li,Zengqing Zhuo,Tianhao Wu,Jie Liu,Ligang Xu,Haozhe Du,Shiqi Liu,Lingqiao Wu,Shu Zhao,Mingxue Tang,Wanli Yang,Haijun Yu
标识
DOI:10.1073/pnas.2412460121
摘要
Lithium-rich layered oxides (LLOs) hold the promise for high-energy battery cathodes. However, its application has been hindered by voltage decay associated with irreversible reactions at high voltages despite decades of intensive efforts. Here, we first theoretically studied the molecular orbitals of Mn-based Li-rich configurations. We found that the π -bond ring formed within the LiMn 6 structure could participate in stable redox reactions as one unit, but Co could disrupt its symmetry. We thus designed and synthesized Co-free concentration-gradient LLOs (CF-CG-LLOs) materials. The combination of concentration gradient and Co removal leads to exceptional capacity retention without any fading over 100 cycles of the pouch cell. More importantly, it exhibits an extraordinarily low voltage decay of 0.15 mV/cycle, accompanied by a high Coulombic efficiency of 99.86%. This concept and demonstration of CF-CG-LLO cathodes reveal a viable avenue toward low-cost, high-energy-density battery cathodes.
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