Electrochemical Profile of LiTi2(PO4)3 and NaTi2(PO4)3 in Lithium, Sodium or Mixed Ion Aqueous Solutions

被引:44
作者
Chen, Long [1 ]
Liu, Jingyuan [1 ]
Guo, Zhaowei [1 ]
Wang, Yonggang [1 ]
Wang, Congxiao [1 ]
Xia, Yongyao [1 ]
机构
[1] Fudan Univ, iChEM Collaborat Innovat Ctr Chem Energy Mat, Inst New Energy, Dept Chem,Shanghai Key Lab Mol Catalysis & Innova, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
ANODE MATERIAL; TITANIUM PHOSPHATES; RECHARGEABLE LI; HIGH-POWER; BATTERY; INTERCALATION; INSERTION; PERFORMANCE; STABILITY; OXYGEN;
D O I
10.1149/2.0531606jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
Carbon-coated LiTi2(PO4)(3) and NaTi2(PO4)(3) were prepared using the sol-gel method, followed by solid-state reaction and thermal decomposition vapor deposition process. The electrochemical profile of both compounds were examined in three different aqueous electrolytes, including 1 M Li2SO4, 1 M Na2SO4 and 1 M Li2SO4/Na2SO4 mixed solutions (1:1 in the volume ratio). Both Li and Na ions can successfully inserted into these NASCION materials, and the two materials deliver a similar higher discharge potential in the Li2SO4 solution (-0.76 V vs. Ag/AgCl) compared to that in the Na2SO4 solution (-0.8 V vs. Ag/AgCl) after several charge/discharge cycles. The XRD analysis demonstrate that LiTi2(PO4)(3) is converted to NaTi2(PO4)(3) in the Na2SO4 and mixed solutions, and NaTi2(PO4)(3) was transformed to LiTi2(PO4)(3) in the Li2SO4 solution after cycling. It suggests that the Li or Na ions in the M1 sites of the NASCION materials are replaced by the ions from the electrolyte, but Na ions prefer to occupy the M1 sites compared with Li ions. (C) 2016 The Electrochemical Society.
引用
收藏
页码:A904 / A910
页数:7
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