电解质
材料科学
阳极
化学工程
锌
电化学
分子
电极
化学
有机化学
冶金
物理化学
工程类
作者
Yuting Xu,Sheng‐Jia Dai,Ming‐Jun Gong,Ji‐Zun Zhang,Hai Xu,Aijun Li,Shin‐ichi Sasaki,Xian‐Xiang Zeng,Xiongwei Wu,Xiaofeng Wang
出处
期刊:Small
[Wiley]
日期:2023-08-30
卷期号:20 (1)
被引量:10
标识
DOI:10.1002/smll.202304463
摘要
Abstract The high activity of water molecules results in a series of awful parasitic reaction, which seriously impede the development of aqueous zinc batteries. Herein, a new gel electrolyte with multiple molecular anchors is designed by employing natural biomaterials from chitosan and chlorophyll derivative. The gel electrolyte firmly anchors water molecules by ternary hydrogen bonding to reduce the activity of water molecules and inhibit hydrogen evolution reaction. Meanwhile, the multipolar charged functional groups realize the gradient induction and redistribution of Zn 2+ , which drives oriented Zn (002) plane deposition of Zn 2+ and then achieves uniform Zn deposition and dendrite‐free anode. As a result, it endows the Zn||Zn cell with over 1700 h stripping/plating processes and a high efficiency of 99.4% for the Zn||Cu cell. In addition, the Zn||V 2 O 5 full cells also exhibit capacity retention of 81.7% after 600 cycles at 0.5 A g −1 and excellent long‐term stability over 1600 cycles at 2 A g −1 , and the flexible pouch cells can provide stable power for light‐emitting diodes even after repeated bending. The gel electrolyte strategy provides a reference for reversible zinc anode and flexible wearable devices.
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