成核
枝晶(数学)
材料科学
法拉第效率
化学工程
扩散
锌
阳极
剥离(纤维)
水溶液
离子
电镀(地质)
纳米技术
冶金
复合材料
物理化学
化学
热力学
电极
有机化学
工程类
几何学
地质学
物理
数学
地球物理学
作者
Mingchang Zhang,Weidong Xu,Xuefei Han,Huiqing Fan,Tao Chen,Yaxiong Yang,Yong Gao,Chao Zheng,Yi Yan Yang,Ting Xiong,Yong‐Wei Zhang,Wee Siang Vincent Lee,Weijia Wang,Hongge Pan,Zhi Gen Yu,Junmin Xue
标识
DOI:10.1002/aenm.202303737
摘要
Abstract Aqueous zinc ion batteries (ZIBs) exhibit great potential for next‐generation energy storage devices. However, significant challenges exist, including the uncontrollable formation of Zn dendrite and side reactions during zinc stripping and plating. The mechanism of Zn dendrite nucleation has yet to be fully understood. In this work, the first principles simulations are used to investigate the Zn dendrite formation process. The unintentionally adsorbed O 2− and OH − ions are the inducing factors for Zn dendrite nucleation and growth on the Zn (0001) plane due to significantly increased Zn diffusion barriers. A top‐down method is demonstrated to suppress the dendrite using delaminated V 2 CT x to capture O 2− and OH − ions thanks to reduced Zn diffusion barriers. The experimental results revealed significantly suppressed Zn dendrite nucleation and growth, resulting in a layer‐by‐layer deposit/stripping of Zn. Based on the electrochemical evaluations, the V 2 CT x ‐coated Zn composite delivers a high coulombic efficiency of 99.3% at 1.0 mAh cm −2 . Furthermore, the full cell achieves excellent cyclic performance of 93.6% capacity retention after 2000 cycles at 1 A g −1 . This strategy has broad scalability and can be widely applied in designing metallic anodes for rechargeable batteries.
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