阳极
扩散
枝晶(数学)
材料科学
电解质
化学工程
锌
水溶液
级联
化学
电极
冶金
有机化学
物理化学
热力学
工程类
物理
数学
几何学
作者
Jie Feng,Xinyang Li,Yuxin Ouyang,Hongyang Zhao,Hongyang Zhao,Na Li,Kai Xi,Junyan Liang,Shujiang Ding
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-05-31
卷期号:63 (41): e202407194-e202407194
被引量:48
标识
DOI:10.1002/anie.202407194
摘要
Abstract Parasitic side reactions and dendrite growth on zinc anodes are formidable issues causing limited lifetime of aqueous zinc ion batteries (ZIBs). Herein, a spontaneous cascade optimization strategy is first proposed to regulate Zn 2+ migration‐diffusion behavior. Specifically, PAPE@Zn layer with separation‐reconstruction properties is constructed in situ on Zn anode. In this layer, well‐soluble poly(ethylene oxide) (PEO) can spontaneously separation to bulk electrolyte and weaken the preferential coordination between H 2 O and Zn 2+ to achieve primary optimization. Meanwhile, poor‐soluble polymerized‐4‐acryloylmorpholine (PACMO) is reconstructed on Zn anode as hydrophobic flower‐like arrays with abundant zincophilic sites, further guiding the de‐solvation and homogeneous diffusion of Zn 2+ to achieve the secondary optimization. Cascade optimization effectively regulates Zn 2+ migration‐diffusion behavior, dendrite growth and side reactions of Zn anode are negligible, and the stability is significantly improved. Consequently, symmetrical cells exhibit stability over 4000 h (1 mA cm −2 ). PAPE@Zn//NH 4 + −V 2 O 5 full cells with a high current density of 15 A g −1 maintains 72.2 % capacity retention for 12000 cycles. Even better, the full cell demonstrates excellent performance of cumulative capacity of 2.33 Ah cm −2 at ultra‐low negative/positive (N/P) ratio of 0.6 and a high mass‐loading (~17 mg cm −2 ). The spontaneous cascade optimization strategy provides novel path to achieve high‐performance and practical ZIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI