材料科学
法拉第效率
溶剂化
相间
电解质
阳极
化学工程
溶剂化壳
吸附
电池(电)
枝晶(数学)
水溶液
过电位
电化学
氢键
无机化学
溶解
纳米孔
电化学电位
化学物理
容量损失
分子
图层(电子)
溶剂
电容器
电镀
相(物质)
阳极氧化
阴极
作者
D. WANG,Jingtian Zeng,Ying Tang,Kaifa Dong,Xin Wang,Zhe Zhang,Hui Peng,Guofu Ma
摘要
ABSTRACT Constructing a stable solid electrolyte interphase (SEI) layer on the Zn anode is crucial for suppressing dendrite growth and side reactions in aqueous zinc‐ion storage devices. However, current SEI engineering still lacks precise control over composition, gradient structure, dynamic interface stability construction of water‐deficient solvation sheath. Here, we developed a mixed electrolyte containing N‐aminocarbonylmethyl ethanesulfonic acid (ACES), which in situ forms a dynamic zwitterionic adsorption interphase (DZAI) layer. The DZAI has a gradient structure with strong Zn‐based groups and a robust hydrogen bond network, leading to dendrite‐free, planar Zn deposition, which is consistent with a highly uniform Zn 2+ flux at the interface. In addition, the ACES molecules effectively reconfigure the primary solvation shell of Zn 2+ into a water‐deficient complex [Zn(H 2 O) 2 (ACES) 4 ] 2+ , significantly reducing water‐induced side reactions. Therefore, the Zn||Zn symmetric battery incorporating the DZAI layer achieved excellent cycling stability of over 760 h at 50 mA cm −2 and 25 mAh cm −2 , with a cumulative electroplating capacity (CPC) of 19.5 Ah cm −2 . The average Coulombic efficiency (CE) of the Zn||Cu battery was also as high as 99%. Moreover, the zinc‐ion capacitors with the DZAI exhibited excellent rate performance and long‐term durability in 10 000 cycles.
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