Regulating Zn2+ Migration-Diffusion Behavior by Spontaneous Cascade Optimization Strategy for Long-Life and Low N/P Ratio Zinc Ion Batteries.

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2024-10-07 Epub Date: 2024-07-19 DOI:10.1002/anie.202407194
Jie Feng, Xinyang Li, Yuxin Ouyang, Hongyang Zhao, Na Li, Kai Xi, Junyan Liang, Shujiang Ding
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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 Zn2+ 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 H2O and Zn2+ 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 Zn2+ to achieve the secondary optimization. Cascade optimization effectively regulates Zn2+ 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//NH4 +-V2O5 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.

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通过自发级联优化策略调节 Zn2+ 迁移-扩散行为,实现长寿命和低 N/P 比锌离子电池。
锌阳极上的寄生副反应和枝晶生长是导致锌离子水电池(ZIB)寿命受限的严重问题。本文首次提出了一种自发级联优化策略来调节 Zn2+ 迁移-扩散行为。具体来说,在锌阳极上原位构建了具有分离-重构特性的 PAPE@Zn 层。在该层中,溶解性好的聚环氧乙烷(PEO)可自发分离到体电解质中,并削弱 H2O 与 Zn2+ 之间的优先配位,从而实现初级优化。同时,贫溶性聚合-4-丙烯酰吗啉(PACMO)在 Zn 阳极重构为疏水性花状阵列,具有丰富的亲锌位点,进一步引导 Zn2+ 的去溶解和均匀扩散,实现二次优化。级联优化有效地调节了 Zn2+ 的迁移扩散行为,使 Zn 阳极的枝晶生长和副反应变得微不足道,并显著提高了稳定性。因此,对称电池的稳定性超过了 4000 小时(1 mA cm-2)。电流密度为 15 A g-1 的 PAPE@Zn//NH4+-V2O5 全电池在 12000 次循环后仍能保持 72.2% 的容量。更妙的是,在负极/正极(N/P)比为 0.6 的超低条件和高负载(约 17 毫克/厘米-2)下,全电池表现出了累积容量为 2.33 Ah cm-2 的优异性能。自发级联优化策略为实现高性能和实用的 ZIB 提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
期刊最新文献
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