位阻效应
溶剂化
水溶液
离子
锌
化学
无机化学
有机化学
作者
Haozhen Dou,Xinru Wu,Mi Xu,Renwu Feng,Qianyi Ma,Dan Luo,Kai Zong,Xin Wang,Zhongwei Chen
标识
DOI:10.1002/anie.202401974
摘要
Abstract Despite many additives have been reported for aqueous zinc ion batteries, steric‐hindrance effect of additives and its correlation with Zn 2+ solvation structure have been rarely reported. Herein, large‐sized sucrose biomolecule is selected as a paradigm additive, and steric‐hindrance electrolytes (STEs) are developed to investigate the steric‐hindrance effect for solvation structure regulation. Sucrose molecules do not participate in Zn 2+ solvation shell, but significantly homogenize the distribution of solvated Zn 2+ and enlarge Zn 2+ solvation shell with weakened Zn 2+ −H 2 O interaction due to the steric‐hindrance effect. More importantly, STEs afford the water‐shielding electric double layer and in situ construct the organic and inorganic hybrid solid electrolyte interface, which effectively boost Zn anode reversibility. Remarkably, Zn//NVO battery presents high capacity of 3.9 mAh ⋅ cm −2 with long cycling stability for over 650 cycles at lean electrolyte of 4.5 μL ⋅ mg −1 and low N/P ratio of 1.5, and the stable operation at wide temperature (−20 °C~+40 °C).
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