阳极
材料科学
水溶液
电解质
电化学
锌
分子
钝化
电偶阳极
纳米技术
化学工程
无机化学
化学
冶金
电极
阴极保护
有机化学
图层(电子)
物理化学
工程类
作者
Huaming Yu,Dongping Chen,Tianyun Zhang,Meng Fu,Jinhao Cai,Weifeng Wei,Xiaobo Ji,Yuejiao Chen,Libao Chen
标识
DOI:10.1002/sstr.202200143
摘要
As promising candidates for aqueous metal batteries, aqueous zinc‐ion batteries (ZIBs) have attracted more attention due to their superior safety, low cost, and environmentally benign characteristics. Solvent water plays a double‐edged sword role that cannot be ignored in the electrochemical performance and long cycling stability of the batteries. The hydrated zinc ions of the solvated structure can boost the diffusion kinetics of zinc ions, whereas the released active water molecules during desolvation can lead to notorious hydrogen evolution reactions, dendrites growth, and surface passivation at the unstable interface between the electrolyte and the anode. Unlike previous reports that summarize recent research progress, this review focuses on the double‐edged sword role of water molecules in the anode during electrochemical processes in ZIBs. The influencing mechanism of water molecules on the stability of zinc anode during the energy storage process is systematically discussed, including the basic theory, water regulation strategies, and recent reports. The two‐faced identity of the water molecules in aqueous electrolyte is profoundly revealed herein, and some revelatory insights and possible strategies are provided for the future design on stable and durable zinc anodes of high‐performance ZIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI