实现(概率)
电解质
质子
电池(电)
图层(电子)
化学
无机化学
化学工程
材料科学
纳米技术
物理
工程类
电极
物理化学
热力学
量子力学
功率(物理)
统计
数学
作者
Peilin Liang,Shuanlong Di,Yuxin Zhu,Zhongbiao Li,Shulan Wang,Li Li
标识
DOI:10.1002/ange.202409871
摘要
Abstract Proton batteries have attracted increasing interests because of their potential for grid‐scale energy storage with high safety and great low‐temperature performances. However, their development is significantly retarded by electrolyte design due to free water corrosion. Herein, we report a layer intercalatable electrolyte (LIE) by introducing trimethyl phosphate (TMP) into traditional acidic electrolyte. Different from conventional role in batteries, the presence of TMP intriguingly achieves co‐intercalation of solvent molecules into the interlayer of anode materials, enabling a new working mechanism for proton reactions. The electrode corrosion was also strongly retarded with expanded electrochemical stability window. The half‐cell therefore showed an outstanding long‐term cycling stability with 91.0 % capacity retention at 5 A g −1 after 5000 cycles. Furthermore, the assembled full batteries can even deliver an ultra‐long lifetime with a capacity retention of 74.9 % for 2 months running at −20 °C. This work provides new opportunities for electrolyte design of aqueous batteries.
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