溶剂化
电解质
化学
锌
无机化学
盐(化学)
电化学
水溶液
离子
溶剂化壳
物理化学
有机化学
电极
作者
Yong Zhang,Gang Wan,Nicholas H. C. Lewis,Julian Mars,Sharon Bone,Hans‐Georg Steinrück,Maria R. Lukatskaya,Nicholas J. Weadock,Michal Bajdich,Oleg Borodin,Andrei Tokmakoff,Michael F. Toney,Edward J. Maginn
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-09-08
卷期号:6 (10): 3458-3463
被引量:63
标识
DOI:10.1021/acsenergylett.1c01624
摘要
Applications of aqueous zinc batteries for grid-scale energy storage are limited by their poor reversibility and the competing water splitting reaction. The recent invention of a water-in-salt (WIS) electrolyte concept provides a new route enabling a stable and highly reversible aqueous zinc battery chemistry. In the present work, a mixed zinc bis(trifluoromethane sulfonyl)imide (Zn(TFSI)2) and LiTFSI WIS electrolyte was studied using X-ray total scattering, X-ray absorption, and Fourier transform infrared spectroscopy in conjunction with classical molecular dynamics simulations. It was found that, in the highly concentrated WIS electrolyte consisting of 1 m Zn(TFSI)2 and 20 m LiTFSI, Zn2+ cations are mainly solvated by six waters in their first solvation shell, while the TFSI– anions are completely excluded. This ion solvation picture is fundamentally different from the previous understandings. The results suggest that additional studies are needed to fully understand the unusual stability and reversibility of zinc-WIS electrolyte-based batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI