法拉第效率
阳极
溶剂化
电解质
电池(电)
水溶液
化学工程
酰胺
化学
锌
材料科学
枝晶(数学)
分子
氢
同种类的
过电位
吸附
无机化学
电极
束缚水
电化学
燃料电池
纳米技术
经济短缺
作者
Liang Huang,Xinxin Cai,Jingchen Tao,Huiquan Zhang,Dongmin Ma,Weixing Song
出处
期刊:
[Tsinghua University Press]
日期:2025-12-11
卷期号:5 (1): e9120213-e9120213
标识
DOI:10.26599/nre.2025.9120213
摘要
The Zn anode/electrolyte interface faces critical challenges, including hydrogen evolution reaction, corrosion, and dendrite growth that degrade battery performance. This study employs 1 mol% N-(2-hydroxyethyl) succinimide (NHS) as a multifunctional electrolyte additive to address these issues. The carbonyl groups (C=O) in NHS can strongly coordinate with Zn atoms and water molecules, selectively adhering to the Zn anode surface to displace H2O, thereby suppressing parasitic reactions while simultaneously reducing water activity in the electrolyte. The NHS can regulate Zn2+ solvation by replacing water molecules in the primary solvation sheath, thereby further facilitating Zn2+ desolvation by reducing the number of bound water molecules. Additionally, the NHS on the anode surface enables a homogeneous Zn2+ flux, resulting in uniform zinc deposition. As a result, the NHS enables a ZnZn symmetric cell to achieve 7,500 h cycling at 1 mA·cm−2, and a ZnCu cell to maintain 99.8% Coulombic efficiency over 3200 cycles. The ZnV2O5 full cell retains 82.5% capacity after 7,000 cycles. These findings highlight the proficiency of the NHS in securing Zn anodes for enhanced battery performance.
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