溶剂化
材料科学
电解质
成核
离子电导率
聚合物
多孔性
分子动力学
化学工程
化学物理
离子键合
电导率
图层(电子)
电阻率和电导率
聚合物电解质
亥姆霍兹自由能
电池(电)
动力学(音乐)
离子液体
纳米技术
电镀(地质)
多孔介质
热传导
复合材料
作者
Pengfei Sun,Shu Zhang,Chengdong Fang,Qingquan Lin,Liubin Feng,Jiajia Chen
出处
期刊:Small methods
[Wiley]
日期:2026-01-24
卷期号:10 (4): e02253-e02253
被引量:3
标识
DOI:10.1002/smtd.202502253
摘要
ABSTRACT In this work, an agarose‐polyacrylamide hydrogel electrolyte (APE) with an interpenetrating and hierarchically porous network is introduced to reconstruct solvation and interface dynamics for a high‐performance Zn‐S batteries. This structure results in a high ionic conductivity of 42.1 mS cm −1 and a Zn 2+ transference number of 0.64. Molecular dynamics reveal that most H 2 O and SO 4 2− are excluded from the outer Helmholtz plane, forming an optimized electric double layer on Zn surface. Consequently, a prolonged 1200 h Zn plating/stripping behavior is obtained with 1 mAh cm −2 at 1 mA cm −2 , and a high Zn plating of 20 mAh cm −2 at 5 mA cm −2 . Furthermore, APE modulates the nucleation mode of ZnS, converting the originally sluggish and non‐uniform progressive nucleation into a rapid and uniform instantaneous nucleation. As a result, this hydrogel Zn‐S batteries deliver a capacity of 895 mAh g −1 and 91% capacity retention within 300 cycles at 5 A g −1 .
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