A binder-driven cathode-electrolyte interphase via a displacement reaction for high voltage Na3V2(PO4)2F3 cathodes in sodium-ion batteries

被引:17
作者
Yun, Dae Hui [1 ]
Song, Jinju [1 ]
Kim, Jiseong [1 ]
Seo, Joon Kyo [1 ]
Kang, Joonhee [2 ]
Park, Sohyun [3 ]
Kim, Jaekook [3 ]
Yoo, Dong-Joo [4 ]
Choi, Sunghun [1 ]
机构
[1] Korea Inst Energy Res KIER, Gwangju Clean Energy Res Ctr, 270-25 Samso ro, Gwangju 27025, South Korea
[2] Korea Inst Energy Res KIER, Computat Sci & Engn Lab, 152 Gajeong ro, Daejeon 34129, South Korea
[3] Chonnam Natl Univ, Dept Mat Sci & Engn, Gwangju 61186, South Korea
[4] Korea Univ, Sch Mech Engn, 145 Anam ro, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
ELECTROCHEMICAL PROPERTIES; PERFORMANCE;
D O I
10.1039/d2ta07990a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Sodium super ionic conductor (NASICON)-structured Na3V2(PO4)(2)F-3 (NVPF) is a promising cathode for application in sodium-ion batteries (SIBs) because of its high working potential (3.7 V and 4.2 V vs. Na/Na+) and structural stability. Nonetheless, interfacial instability deteriorates its electrochemical performance. Therefore, to overcome this limitation, we introduced a sodium polyacrylate (NaPAA) binder for NVPF cathodes. The NaPAA binder effectively suppresses electrolyte decomposition by uniformly covering NVPF particles. Furthermore, the sodium carboxylate group of R-COONa in the NaPAA binder can react with the HPO2F2 intermediate generated by the hydrolysis of NaPF6 and be converted into R-COOH and NaPO(2)F(2)via the displacement of Na+ by H+. This results in the formation of a stable and Na-ion conductive NaPO2F2-rich cathode-electrolyte interphase (CEI) layer. In addition, the NaPAA-based electrode exhibits desirable cycling and rate performances compared to those of conventional poly(vinylidene difluoride)-based electrodes. This study provides new insights into the design of CEI layers by introducing chemical functional groups in the binder for high-performance SIB cathodes.
引用
收藏
页码:5540 / 5547
页数:9
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