溶剂化
锌
电解质
甲醇
水溶液
结晶
无机化学
电化学
电极
化学
材料科学
化学工程
分子
有机化学
物理化学
工程类
作者
Junnan Hao,Libei Yuan,Chao Ye,Dongliang Chao,Kenneth Davey,Zhanhu Guo,Shi Zhang Qiao
标识
DOI:10.1002/anie.202016531
摘要
Abstract Antisolvent addition has been widely studied in crystallization in the pharmaceutical industries by breaking the solvation balance of the original solution. Here we report a similar antisolvent strategy to boost Zn reversibility via regulation of the electrolyte on a molecular level. By adding for example methanol into ZnSO 4 electrolyte, the free water and coordinated water in Zn 2+ solvation sheath gradually interact with the antisolvent, which minimizes water activity and weakens Zn 2+ solvation. Concomitantly, dendrite‐free Zn deposition occurs via change in the deposition orientation, as evidenced by in situ optical microscopy. Zn reversibility is significantly boosted in antisolvent electrolyte of 50 % methanol by volume (Anti‐M‐50 %) even under harsh environments of −20 °C and 60 °C. Additionally, the suppressed side reactions and dendrite‐free Zn plating/stripping in Anti‐M‐50 % electrolyte significantly enhance performance of Zn/polyaniline coin and pouch cells. We demonstrate this low‐cost strategy can be readily generalized to other solvents, indicating its practical universality. Results will be of immediate interest and benefit to a range of researchers in electrochemistry and energy storage.
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