阴极
氧化还原
阳极
氧气
硼
钠离子电池
材料科学
氧化物
无机化学
析氧
离子
电化学
化学
化学工程
电极
法拉第效率
物理化学
冶金
有机化学
工程类
作者
Yu-Jie Guo,Pengfei Wang,Yubin Niu,Xu‐Dong Zhang,Qinghao Li,Xiqian Yu,Min Fan,Wan‐Ping Chen,Yang Yu,Xiangfeng Liu,Qinghai Meng,Sen Xin,Ya‐Xia Yin,Yu‐Guo Guo
标识
DOI:10.1038/s41467-021-25610-7
摘要
Abstract Na-ion cathode materials operating at high voltage with a stable cycling behavior are needed to develop future high-energy Na-ion cells. However, the irreversible oxygen redox reaction at the high-voltage region in sodium layered cathode materials generates structural instability and poor capacity retention upon cycling. Here, we report a doping strategy by incorporating light-weight boron into the cathode active material lattice to decrease the irreversible oxygen oxidation at high voltages (i.e., >4.0 V vs. Na + /Na). The presence of covalent B–O bonds and the negative charges of the oxygen atoms ensures a robust ligand framework for the NaLi 1/9 Ni 2/9 Fe 2/9 Mn 4/9 O 2 cathode material while mitigating the excessive oxidation of oxygen for charge compensation and avoiding irreversible structural changes during cell operation. The B-doped cathode material promotes reversible transition metal redox reaction enabling a room-temperature capacity of 160.5 mAh g −1 at 25 mA g −1 and capacity retention of 82.8% after 200 cycles at 250 mA g −1 . A 71.28 mAh single-coated lab-scale Na-ion pouch cell comprising a pre-sodiated hard carbon-based anode and B-doped cathode material is also reported as proof of concept.
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