Modern battery electrolytes: Ion-ion interactions in Li+/Na+ conductors from DFT calculations

被引:81
作者
Jonsson, Erlendur [1 ]
Johansson, Patrik [1 ]
机构
[1] Chalmers, Dept Appl Phys, SE-41296 Gothenburg, Sweden
关键词
STABLE LITHIUM-SALTS; ELECTROCHEMICAL PROPERTIES; THERMOCHEMICAL KINETICS; NONAQUEOUS SOLUTIONS; DENSITY FUNCTIONALS; BASIS-SETS; ANIONS; CONDUCTIVITY; COMPLEXES; MOLECULES;
D O I
10.1039/c2cp40612h
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-ion batteries, the sodium counterpart of the ubiquitous lithium-ion batteries, are currently being developed as a complementary technology to assure resource availability. As battery electrolytes tend to be one of the more limiting parts of any battery for both performance and life-length, chemical and physical data on sodium-ion battery electrolytes are important for rational development. Here the cation-anion interaction, a key property of any salt used in an electrolyte, of a number of salts is probed using numerous DFT methods via the ion-pair dissociation reaction: AlkAn reversible arrow Alk(+) + An(-), where An(-) is any anion and Alk(+) is Na+ or Li+, the latter used here for a straight-forward literature and methodology comparison. Furthermore, the applicability of different DFT functionals for these types of calculations is benchmarked vs. a robust higher accuracy method (G4MP2).
引用
收藏
页码:10774 / 10779
页数:6
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