电解质
磷酸
溶解
电化学
水溶液
电池(电)
储能
材料科学
腐蚀
化学工程
电极
无机化学
化学
冶金
有机化学
热力学
物理化学
工程类
功率(物理)
物理
作者
Bin Su,J. Deng,Zhouxiang Wu,Xinran Li,Jing Li,Haoxiang Yu,Peng Li,Hui Li,Lei Yan,Liyuan Zhang,Ting‐Feng Yi,Tianyi Ma,Jie Shu
标识
DOI:10.1002/anie.202505769
摘要
Aqueous proton batteries, leveraging the intrinsic advantages of protons such as minimal hydrated radius, natural abundance, and rapid transport kinetics, have emerged as promising candidates for next‐generation energy storage. However, conventional strong acid electrolytes like H2SO4 suffer from critical limitations including electrode dissolution and incompatibility with battery components. To circumvent these challenges, weak acids (e.g., HCOOH and H3PO4) have been strategically selected as alternative electrolytes due to their non‐corrosive characteristics. Particularly, the implementation of a high‐concentration "water‐in‐acid" (WIA) effectively suppresses undesirable interactions between electrode materials and free water molecules. Through electrolyte engineering, we developed a 9.5 M H3PO4 WIA system that synergizes with a molybdenum trioxide electrode, achieving remarkable electrochemical performance: a high reversible capacity of 229.8 mAh g‐1 at 3 A g‐1 and exceptional cycling stability with 83.86% capacity retention after 1,000 cycles at 5 A g‐1, surpassing conventional H2SO4‐based systems by both capacity and cyclability. This innovative approach establishes a new paradigm for developing high‐performance aqueous energy storage systems through acid‐dominated electrolyte design.
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