Crystal Step‐Induced Uniform and Rapid Deposition on Zinc Anodes

IF 24.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Advanced Energy Materials Pub Date : 2024-09-17 DOI:10.1002/aenm.202403860
Mengdie Yan, Xuesong Zhao, Diancheng Chen, Wanxia Li, Liqi Liu, Yang Sun, Shuhong Jiao, Huilin Pan
{"title":"Crystal Step‐Induced Uniform and Rapid Deposition on Zinc Anodes","authors":"Mengdie Yan, Xuesong Zhao, Diancheng Chen, Wanxia Li, Liqi Liu, Yang Sun, Shuhong Jiao, Huilin Pan","doi":"10.1002/aenm.202403860","DOIUrl":null,"url":null,"abstract":"Aqueous Zn‐ion batteries have emerged as promising candidates for large‐scale energy storage owing to their high safety and low cost. However, dendrite growth and side reactions compromise the stability of the Zn anode in practical applications. Here, a novel Zn anode featuring well‐designed crystal steps along the (002) facets, referred to as Step‐Zn is introduced. The intersections of the (002) and (100) planes in these crystal steps create preferential adsorption sites for Zn<jats:sup>2</jats:sup>⁺ ions, promoting initial electro‐epitaxial growth of Zn that uniformly covers the crystal steps. This process effectively regulates subsequent Zn deposition, ensuring fast reaction kinetics and smooth morphology without dendrite formation. Consequently, the unique Step‐Zn anode exhibits excellent cycle life over 6000 times at 3 mA cm<jats:sup>−2</jats:sup> and low greatly reduced polarization voltage under high areal currents and capacities. Integrated with activated carbon (AC) cathode, the Step‐Zn||AC full cell demonstrates excellent durability over 10 000 cycles at 5 A g<jats:sup>−1</jats:sup>. This work offers valuable insights into controlling Zn deposition modes by engineering the surface microstructure of Zn anodes with greatly extended cycling stability.","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":null,"pages":null},"PeriodicalIF":24.4000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/aenm.202403860","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Aqueous Zn‐ion batteries have emerged as promising candidates for large‐scale energy storage owing to their high safety and low cost. However, dendrite growth and side reactions compromise the stability of the Zn anode in practical applications. Here, a novel Zn anode featuring well‐designed crystal steps along the (002) facets, referred to as Step‐Zn is introduced. The intersections of the (002) and (100) planes in these crystal steps create preferential adsorption sites for Zn2⁺ ions, promoting initial electro‐epitaxial growth of Zn that uniformly covers the crystal steps. This process effectively regulates subsequent Zn deposition, ensuring fast reaction kinetics and smooth morphology without dendrite formation. Consequently, the unique Step‐Zn anode exhibits excellent cycle life over 6000 times at 3 mA cm−2 and low greatly reduced polarization voltage under high areal currents and capacities. Integrated with activated carbon (AC) cathode, the Step‐Zn||AC full cell demonstrates excellent durability over 10 000 cycles at 5 A g−1. This work offers valuable insights into controlling Zn deposition modes by engineering the surface microstructure of Zn anodes with greatly extended cycling stability.
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
晶体阶跃诱导锌阳极均匀快速沉积
由于安全性高、成本低,锌离子水电池已成为大规模储能的理想候选电池。然而,枝晶生长和副反应影响了锌阳极在实际应用中的稳定性。本文介绍了一种新型锌阳极,它具有沿(002)面精心设计的晶体阶梯,被称为阶梯锌(Step-Zn)。在这些晶阶中,(002) 面和 (100) 面的交点为 Zn2⁺ 离子创造了优先吸附位点,促进了锌的初始电外延生长,使其均匀地覆盖晶阶。这一过程可有效调节后续的锌沉积,确保快速的反应动力学和平滑的形态,而不会形成枝晶。因此,这种独特的阶跃锌阳极在 3 mA cm-2 电流条件下具有超过 6000 次的出色循环寿命,并且在高等电流和高容量条件下极化电压大大降低。Step-Zn||AC 全电池与活性炭(AC)阴极集成后,在 5 A g-1 的条件下可循环使用 10,000 次,表现出卓越的耐用性。这项研究为通过设计锌阳极的表面微结构来控制锌沉积模式提供了宝贵的见解,从而大大提高了循环稳定性。
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
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
期刊最新文献
Recent Advances in the Large-Scale Production of Photo/Electrocatalysts for Energy Conversion and beyond Toward Practical Li–S Batteries: On the Road to a New Electrolyte High-Capacity, Long-Life All-Solid-State Lithium–Selenium Batteries Enabled by Lithium Iodide Active Additive A Fluorinated Lewis Acidic Organoboron Tunes Polysulfide Complex Structure for High‐Performance Lithium–Sulfur Batteries Rational Construction of Heterostructures with n‐Type Anti‐Barrier Layer for Enhanced Electrochemical Energy Storage
×
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