钾
成核
过电位
阴极
阳极
金属
电流密度
枝晶(数学)
材料科学
化学工程
电解质
电镀(地质)
二甲氧基乙烷
普鲁士蓝
化学
电化学
冶金
复合材料
物理化学
有机化学
电极
工程类
复合数
物理
几何学
数学
量子力学
地球物理学
地质学
作者
Fei Yi,Jiangmin Jiang,Lei Zhang,Ping Nie,Jiang Ye,Yaxin Chen,Quanchao Zhuang,Zhicheng Ju
标识
DOI:10.1016/j.cej.2024.151527
摘要
Potassium metal anodes are desirable for the advantages of low price, high abundance, and similar standard redox potential with metallic lithium. However, dendritic growth and large volume changes impede its practical application. Herein, a dendrite-free and stable potassium metal composite anode has realized by infusing metallic potassium into an α-MoC modified carbon cloth (α-MoC@CC). The prepared α-MoC@CC as a 3D host exhibits an intrinsic potassiophilicity based on experimental investigations and density functional theory (DFT) calculations, which not only facilitates fast molten potassium wetting but also reduces nucleation overpotential. In addition, the current density distribution of the composite anode carried out by COMSOL Multiphysics reveals that the 3D host can effectively reduce current density and inhibit dendrite growth. Consequently, the K@α-MoC@CC composite anode displays stable plating/stripping profiles for more than 2000 h with low polarization in symmetric batteries. As a practical device application, the K@α-MoC@CC composite anode demonstrates superior suitability when paired with Prussian blue cathode in a full battery. Significantly, this work represents an effective pathway to regulate potassium metal anode towards practical applications.
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