锰
电化学
磷酸盐
阴极
氧化还原
钒
离子
材料科学
结构稳定性
动力学
掺杂剂
降级(电信)
快离子导体
电解质
无机化学
化学
电极
化学工程
兴奋剂
冶金
物理化学
光电子学
计算机科学
工程类
电信
物理
结构工程
量子力学
有机化学
作者
Chunliu Xu,Ruijuan Xiao,Junmei Zhao,Feixiang Ding,Yang Yang,Xiaohui Rong,Xiaodong Guo,Chao Yang,Huizhou Liu,Benhe Zhong,Yong‐Sheng Hu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-12-03
卷期号:7 (1): 97-107
被引量:129
标识
DOI:10.1021/acsenergylett.1c02107
摘要
A Mn-based NASICON-type Na4VMn(PO4)3 cathode is considered to be one of the most promising substitutions for Na3V2(PO4)3 due to the huge abundance and appropriate redox potential from Mn. However, the current Na4VMn(PO4)3/C cathode still delivers a limited electrochemical performance due to the sluggish kinetics and negative structural degradation caused by the Mn in the structure. Herein, a selective replacement of vanadium rather than manganese in the Na4VMn(PO4)3 system was developed to fully utilize the manganese element and enhance the structural stability. Both experimental and calculation results affirmed that the Al-substituted Na4V0.8Al0.2Mn(PO4)3 cathode shows favorable Na+ kinetics and structure stability. The resulting Na4V0.8Al0.2Mn(PO4)3 reveals a discharge capacity of ∼84 mA h g–1 at 40 C and renders a capacity retention of 92% after cycling 1000 times at 5 C. Inspired by the availability of Al dopants, we also demonstrated the Al-doped Mn-richer Na4.2V0.6Al0.2Mn1.2(PO4)3 to be a viable candidate for Mn-rich phosphate cathodes.
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