电化学
兴奋剂
阴极
钠离子电池
电池(电)
空位缺陷
离子
化学工程
钠
材料科学
扩散
储能
化学
纳米技术
分析化学(期刊)
电极
光电子学
法拉第效率
物理化学
热力学
结晶学
工程类
有机化学
色谱法
物理
功率(物理)
冶金
作者
HanChi Hu,Hongxia Chen,Shuangwu Xu,Mengcheng Zhou,Xinyu Zhang,Tao Shen,HaiChen Li,Hongming Zhou
标识
DOI:10.1021/acsaem.4c01617
摘要
As a leading sodium-ion battery cathode material, O3-type layered oxides combine excellent theoretical specific capacity and cost-effectiveness, offering potential solutions for the large-scale energy storage industry. However, they still struggle with significant capacity degradation and inferior battery performance due to the narrow Na+ diffusion channels and complex phase. In this paper, we introduce Sb ions into the NaNi0.3Fe0.2Mn0.5O2 cathode material to improve its electrochemical performance. Our findings demonstrate that doping Sb results in an expansion of the Na layer spacing and cell volume, contributing to faster diffusion of Na+. Furthermore, the Na+/vacancy ordering and undesirable phase transition under high pressure are inhibited in the synthesized Na(Ni0.3Fe0.2Mn0.5)0.98Sb0.02O2 cathode material, which obtains a more boosting structure and advanced electrochemical performance. Within the voltage range of 2.0–4.2 V, the cathode material possesses an initial discharge specific capacity of 127.71 mAh g–1 and maintains a capacity retention of 82.34% (64.33% before doping) after 100 cycles. Moreover, at a 10 C current density, a high discharge specific capacity of 90.26 mAh g–1 is observed in the doped material. These results contribute essential insights for the design and advancement of cathode materials for sodium-ion batteries with outstanding properties.
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