正交晶系
电化学
钒
阴极
氧化还原
粉末衍射
离子
材料科学
扩散
锂(药物)
磷酸铁锂
衍射
磷酸钒锂电池
电极
无机化学
化学工程
化学
结晶学
物理
晶体结构
物理化学
冶金
热力学
工程类
内分泌学
有机化学
光学
医学
作者
Christian Jakobsen,Kasper Skovgaard Nielsen,P. Morgen,Espen D. Bøjesen,Dorthe Bomholdt Ravnsbæk
标识
DOI:10.1021/acs.jpcc.1c05494
摘要
Lithium vanadyl phosphate, LiVOPO4, holds interest as a Li-ion battery electrode due to the multiple active redox states of vanadium (V5+ ⇋ V4+ ⇋ V3+) and the high redox potential induced by vanadyl phosphate. The orthorhombic β-LiVOPO4 polymorph is of special interest owing to its low Li-ion diffusion barrier and high stability. In this work, we synthesize β-LiVOPO4 and investigate the polymorphic purity under different synthesis conditions and show that high-energy ball milling without postsintering can alter the sample morphology and thereby dramatically increase the electrochemical performance of β-LiVOPO4. Through operando powder X-ray diffraction (PXRD), the structural evolution of β-LiVOPO4 during charge and discharge is unraveled and unexpected solid solution behavior in the Li-poor β-VOPO4 is revealed.
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