材料科学
剥离(纤维)
法拉第效率
锌
水溶液
电镀(地质)
离子键合
阳极
溴化物
溶剂化
化学工程
溶剂
无机化学
离子
复合材料
有机化学
电极
冶金
化学
工程类
物理化学
地球物理学
地质学
作者
Di Tang,Xinyue Zhang,Daliang Han,Changjun Cui,Zishan Han,Lu Wang,Zhiguo Li,Bingbo Zhang,Yingxin Liu,Zhe Weng,Quan‐Hong Yang
标识
DOI:10.1002/adma.202406071
摘要
Developing hydrophobic interface has proven effective in addressing dendrite growth and side reactions during zinc (Zn) plating in aqueous Zn batteries. However, this solution inadvertently impedes the solvation of Zn2+ with H2O and subsequent ionic transport during Zn stripping, leading to insufficient reversibility. Herein, an adaptive hydrophobic interface that can be switched "on" and "off" by ionic valves to accommodate the varying demands for interfacial H2O during both the Zn plating and stripping processes, is proposed. This concept is validated using octyltrimethyl ammonium bromide (C8TAB) as the ionic valve, which can initiatively establish and remove a hydrophobic interface in response to distinct electric-field directions during Zn plating and stripping, respectively. Consequently, the Zn anode exhibits an extended cycling life of over 2500 h with a high Coulombic efficiency of ≈99.8%. The full cells also show impressive capacity retention of over 85% after 1 000 cycles at 5 A g-1. These findings provide a new insight into interface design for aqueous metal batteries.
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