过电位
材料科学
阳极
成核
化学工程
氢
锌
水溶液
电化学
电极
纳米技术
冶金
物理化学
热力学
化学
工程类
有机化学
物理
作者
Aosai Chen,Chenyang Zhao,Zhikun Guo,Xingyuan Lu,Nannan Liu,Yu Zhang,Lishuang Fan,Naiqing Zhang
标识
DOI:10.1016/j.ensm.2021.10.016
摘要
Metallic zinc has become one of the most potential anodes for aqueous zinc-ion batteries (ZIBs) due to its high capacity and safety. However, uneven Zn deposition and hydrogen evolution at zinc anode severely limit the development and commercialization of aqueous ZIBs. Here, we directly formed a uniform ridge-like ZnMoO4 layer on the Zn anode (denoted as [email protected]4) within 20 s by chemical deposition. Due to its special structure and strong binding energy to Zn adatoms, the modified layer can induce uniform zinc nucleation and inhibit dendrite growth. In addition, ZnMoO4 can significantly increase the adsorption free energy of H adatoms (ΔG(H*)), suppressing the evolution of hydrogen. With this synergy effect, [email protected]4 delivers strong hydrogen suppression capability that increases the hydrogen evolution overpotential from 27 mV to 137 mV, achieves exciting cycling stability for 10,000 cycles at a high current density of 10 mA cm−2. Meanwhile, the capacity retention rate of the [email protected]4/α-MnO2 full battery reaches 87% after 1000 cycles under 1A g − 1.
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