水溶液
氢键
锌
离子
材料科学
无机化学
氢
化学工程
化学
有机化学
分子
冶金
工程类
作者
Ya Shan He,Zhuo Chen,Junrun Feng,Jian Wang,Lun Zhang,Hao Gu,Lin Sheng,Pengfei Yao,Feng Ryan Wang,Zhangxiang Hao
出处
期刊:Small
[Wiley]
日期:2025-01-31
卷期号:21 (11): e2411755-e2411755
被引量:15
标识
DOI:10.1002/smll.202411755
摘要
Abstract Aqueous zinc‐ion batteries (AZIBs) are considered one of the most promising next‐generation energy storage devices due to cost‐effectiveness and high safety. However, the uncontrolled dendrite growth and the intolerance against low temperatures hinder the application of AZIBs. Herein, hydrogen‐bonding‐rich dulcitol (DOL) is introduced into the ZnSO 4 , which reshaped the hydrogen‐bond network in the electrolyte and optimized the solvation sheath structure, effectively reducing the amount of active water molecules and inhibiting hydrogen evolution and the parasitic reaction at the zinc anode. In addition, higher adsorption energy DOL preferentially adsorbs on the surface of the zinc anode, guiding the uniform deposition of Zn 2+ and inhibiting the formation of dendrites. DOL also enhances the interaction between free and free water and improves the resistance to freeze of the electrolyte. Consequently, the Zn//Zn symmetric cells assembled with DOL are extremely stable cycled for 2000 h at 2 mA cm −2 . The NH 4 V 4 O 10 (NVO)//Zn full cell showed more excellent specific capacity of 183.07 mAh g −1 after 800 cycles. Even at the low temperature of −10 °C, the cell still maintains 155.95 mAh g −1 capacity after 600 cycles. This work provides a new strategy for the subsequent study of AZIBs with high stability at low temperatures.
科研通智能强力驱动
Strongly Powered by AbleSci AI