阳极
电解质
化学
水溶液
充电周期
锌
甘氨酸
化学工程
金属
电池(电)
电化学
材料科学
容量损失
无机化学
电流密度
储能
氢
位阻效应
能量密度
过渡金属
枝晶(数学)
氢气储存
电偶阳极
作者
Fengyuan Fu,Hong Yin,Yuliang Liu,Yifeng Zhu,Zhiping Xiong,Guanliang Xu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-12-25
卷期号:40 (1): 865-873
标识
DOI:10.1021/acs.energyfuels.5c04635
摘要
Among all kinds of energy storage systems, water-based zinc-ion batteries have attracted much attention due to their high theoretical capacity (820 mAh g–1), intrinsic safety, and low cost. However, zinc metal anodes are facing severe challenges in practical application, including parasitic reactions, dendrite growth, and hydrogen evolution, which significantly limit the application of aqueous zinc-ion batteries (AZIBs). Introducing trimethyl glycine (Tri) into the aqueous electrolyte forms a unique anode/electrolyte interface and enhances steric effects. Theoretical calculations elucidate the mechanism by which the Tri additive influences the Zn metal anode and electrolyte, while experimental results further confirm the critical role of Tri in simultaneously regulating anode interfacial chemistry and the electrolyte environment. Therefore, the cycle life of the Zn//Zn symmetrical battery is extended to 4000 h at 1 mA cm–2, and it can maintain a stable cycle for 600 h even at a high current density of 3 mA cm–2. In addition, the Zn//V2O5 battery assembled with the Tri additive also showed a stable cycle performance of more than 1500 cycles and a high residual discharge specific capacity of 185.8 mAh g–1. A novel and simple electrolyte additive strategy was put forward in this work, which realized dendrite-free zinc anodes and a stable full battery, providing a reference for surpassing the most advanced AZIBs.
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