煅烧
结晶度
电化学
共沉淀
兴奋剂
材料科学
热液循环
溶解
降水
碳酸盐
水热合成
矿物学
分析化学(期刊)
核化学
无机化学
化学工程
化学
电极
冶金
物理化学
催化作用
物理
工程类
气象学
生物化学
复合材料
光电子学
色谱法
作者
Shaoxiong Fu,Yuan Zhang,Yuhan Bian,Jiahao Xu,Li Wang,Guangchuan Liang
标识
DOI:10.1021/acs.iecr.2c04037
摘要
An Fe3+/PO43– codoped LiNi0.5Mn1.4667Fe0.02P0.0133O4 sample has been prepared by a coprecipitation–hydrothermal method followed by two-step calcination. A novel wet chemical route, using FeSO4 rather than Fe2(SO4)3 as the Fe3+ source and NaH2PO4 as the PO43– source, is adopted to obtain uniform codoping of Fe3+ and PO43– ions in a carbonate precursor according to the precipitation–dissolution–transformation mechanism. For comparison, Fe3+-doped and PO43–-doped samples have been also synthesized via the same route. The effects of Fe3+/PO43– codoping and single doping on the crystalline structure, morphology, and electrochemical performance of LiNi0.5Mn1.5O4 are investigated. Compared with pristine and single doped samples, the codoped sample shows better electrochemical performance, with a specific discharge capacity of 125.2 mAh g–1 at 10 C and a capacity retention rate of 85.9% after 200 cycles at 1 C, under the synergy of Fe3+/PO43– codoping, including enhanced crystallinity, decreased Mn3+ content, significantly reduced primary particle size and secondary agglomeration, as well as the appearance of (110) surfaces in truncated octahedral primary particles.
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