A seaweed-inspired separator for high performance Zn metal batteries: Boosting kinetics and confining side-reactions

IF 13.1 1区 化学 Q1 Energy Journal of Energy Chemistry Pub Date : 2024-10-04 DOI:10.1016/j.jechem.2024.09.047
Qianzhi Gou , Horan Luo , Long Qu , Feilin Yu , Kaixin Wang , Sida Zhang , Ziga Luogu , Ben Zhang , Yujie Zheng , Bingye Song , John Wang , Meng Li
{"title":"A seaweed-inspired separator for high performance Zn metal batteries: Boosting kinetics and confining side-reactions","authors":"Qianzhi Gou ,&nbsp;Horan Luo ,&nbsp;Long Qu ,&nbsp;Feilin Yu ,&nbsp;Kaixin Wang ,&nbsp;Sida Zhang ,&nbsp;Ziga Luogu ,&nbsp;Ben Zhang ,&nbsp;Yujie Zheng ,&nbsp;Bingye Song ,&nbsp;John Wang ,&nbsp;Meng Li","doi":"10.1016/j.jechem.2024.09.047","DOIUrl":null,"url":null,"abstract":"<div><div>Uncontrolled dendrite growth, sluggish reaction kinetics, and drastic side reactions on the anode-electrolyte interface are the main obstacles that restrict the application prospect of aqueous zinc-ion batteries. Traditional glass fiber (GF) separator with chemical inertness is almost ineffective in restricting these challenges. Herein, inspired by the ionic enrichment behavior of seaweed plants, a facile biomass species, anionic sodium alginate (SA), is purposely decorated on the commercial GF separator to tackle these issues towards Zn anode. Benefiting from the abundant zincophilic functional groups and superior mechanical strength properties, the as-obtained SA@GF separator could act as ion pump to boost the Zn<sup>2+</sup> transference number (0.68), reduce the de-solvation energy barrier of hydrated Zn<sup>2+</sup>, and eliminate the undesired concentration polarization effect, which are verified by experimental tests, theoretical calculations, and finite element simulation, respectively. Based on these efficient modulation mechanisms, the SA@GF separator can synchronously achieve well-aligned Zn deposition and the suppression of parasitic side-reactions. Therefore, the Zn||Zn coin cell integrated with SA@GF separator could yield a prolonged calendar lifespan over 1230 h (1 mA cm<sup>−2</sup> and 1 mAh cm<sup>−2</sup>), exhibiting favorable competitiveness with previously reported separator modification strategies. Impressively, the Zn-MnO<sub>2</sub> full and pouch cell assembled with the SA@GF separator also delivered superior cycling stability and rate performance, further verifying its practical application effect. This work provides a new design philosophy to stabilize the Zn anode from the aspect of separator.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":"101 ","pages":"Pages 191-200"},"PeriodicalIF":13.1000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495624006715","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0

Abstract

Uncontrolled dendrite growth, sluggish reaction kinetics, and drastic side reactions on the anode-electrolyte interface are the main obstacles that restrict the application prospect of aqueous zinc-ion batteries. Traditional glass fiber (GF) separator with chemical inertness is almost ineffective in restricting these challenges. Herein, inspired by the ionic enrichment behavior of seaweed plants, a facile biomass species, anionic sodium alginate (SA), is purposely decorated on the commercial GF separator to tackle these issues towards Zn anode. Benefiting from the abundant zincophilic functional groups and superior mechanical strength properties, the as-obtained SA@GF separator could act as ion pump to boost the Zn2+ transference number (0.68), reduce the de-solvation energy barrier of hydrated Zn2+, and eliminate the undesired concentration polarization effect, which are verified by experimental tests, theoretical calculations, and finite element simulation, respectively. Based on these efficient modulation mechanisms, the SA@GF separator can synchronously achieve well-aligned Zn deposition and the suppression of parasitic side-reactions. Therefore, the Zn||Zn coin cell integrated with SA@GF separator could yield a prolonged calendar lifespan over 1230 h (1 mA cm−2 and 1 mAh cm−2), exhibiting favorable competitiveness with previously reported separator modification strategies. Impressively, the Zn-MnO2 full and pouch cell assembled with the SA@GF separator also delivered superior cycling stability and rate performance, further verifying its practical application effect. This work provides a new design philosophy to stabilize the Zn anode from the aspect of separator.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
用于高性能锌金属电池的海藻启发式隔膜:促进动力学和限制副反应
阳极-电解质界面不受控制的枝晶生长、缓慢的反应动力学和剧烈的副反应是限制锌离子水电池应用前景的主要障碍。具有化学惰性的传统玻璃纤维(GF)隔膜几乎无法有效限制这些挑战。本文受海藻植物离子富集行为的启发,特意在商用玻璃纤维隔膜上装饰了一种简便的生物质物种--阴离子海藻酸钠(SA),以解决锌阳极的这些问题。得益于丰富的亲锌官能团和优越的机械强度特性,所获得的 SA@GF 分离器可作为离子泵提高 Zn2+ 迁移数(0.68),降低水合 Zn2+ 的脱溶能障,并消除不希望出现的浓度极化效应,这些都分别通过实验测试、理论计算和有限元模拟得到了验证。基于这些高效的调制机制,SA@GF 分离器可以同步实现锌的均匀沉积和抑制寄生副反应。因此,集成了 SA@GF 分离器的 Zn||Zn 纽扣电池可延长日历寿命超过 1230 h(1 mA cm-2 和 1 mAh cm-2),与之前报道的分离器改性策略相比,表现出良好的竞争力。令人印象深刻的是,与 SA@GF 分离器组装在一起的 Zn-MnO2 全电池和袋式电池还具有优异的循环稳定性和速率性能,进一步验证了其实际应用效果。这项工作从分离器方面为稳定锌阳极提供了一种新的设计理念。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Energy Chemistry
Journal of Energy Chemistry CHEMISTRY, APPLIED-CHEMISTRY, PHYSICAL
CiteScore
19.10
自引率
8.40%
发文量
3631
审稿时长
15 days
期刊介绍: The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies. This journal focuses on original research papers covering various topics within energy chemistry worldwide, including: Optimized utilization of fossil energy Hydrogen energy Conversion and storage of electrochemical energy Capture, storage, and chemical conversion of carbon dioxide Materials and nanotechnologies for energy conversion and storage Chemistry in biomass conversion Chemistry in the utilization of solar energy
期刊最新文献
Catalytic production of high-energy-density spiro polycyclic jet fuel with biomass derivatives Metallized polymer current collector as “stress acceptor” for stable micron-sized silicon anodes Microdynamic modulation through Pt–O–Ni proton and electron “superhighway” for pH-universal hydrogen evolution High-areal-capacity and long-life sulfide-based all-solid-state lithium battery achieved by regulating surface-to-bulk oxygen activity Introducing strong metal–oxygen bonds to suppress the Jahn-Teller effect and enhance the structural stability of Ni/Co-free Mn-based layered oxide cathodes for potassium-ion batteries
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1