Side Reaction Turned Positive: Synchronous OER Manipulating the Electrocatalytic Properties of Anodic Electrodeposited Lead Dioxide

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2025-01-22 DOI:10.1002/smll.202410556
Hua Guo, Xinyuan Li, Mingtao Li, Liu Yang, Wei Yan, Hao Xu
{"title":"Side Reaction Turned Positive: Synchronous OER Manipulating the Electrocatalytic Properties of Anodic Electrodeposited Lead Dioxide","authors":"Hua Guo, Xinyuan Li, Mingtao Li, Liu Yang, Wei Yan, Hao Xu","doi":"10.1002/smll.202410556","DOIUrl":null,"url":null,"abstract":"The preparation and modification of porous electrodes are an important component of the new generation electrochemical oxidation technology. Rapid preparation of porous electrodes can be easily achieved by synchronous oxygen bubble electrodeposition. However, according to the reaction mechanism of lead dioxide anodic electrodeposition, there is bound to be a competitive reaction of adsorbed hydroxyl radicals in the oxygen bubble template method, which means that synchronous OER impacts both the surface morphology and potentially the crystalline structure of the metal oxides. Clarifying the comprehensive influence of synchronous OER on the morphology and microstructure of the coating is important. In this work, the electrodeposition process of porous lead dioxide coating is regulated by the way of linear potential increase and realized the rapid preparation of high-performance porous lead dioxide coating within 40 s. The morphology and microstructure, electrical, and electrochemical properties are characterized, combined with theoretical calculation and orthogonal analysis, to investigate the regulatory mechanism of the rapid growth of the porous lead dioxide by the electric potential. It is demonstrated that synchronous OER confers porous morphology and a large number of defects to the coating in situ, and enhancing the electrocatalytic oxidation performance of the electrode.","PeriodicalId":228,"journal":{"name":"Small","volume":"10 1","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smll.202410556","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The preparation and modification of porous electrodes are an important component of the new generation electrochemical oxidation technology. Rapid preparation of porous electrodes can be easily achieved by synchronous oxygen bubble electrodeposition. However, according to the reaction mechanism of lead dioxide anodic electrodeposition, there is bound to be a competitive reaction of adsorbed hydroxyl radicals in the oxygen bubble template method, which means that synchronous OER impacts both the surface morphology and potentially the crystalline structure of the metal oxides. Clarifying the comprehensive influence of synchronous OER on the morphology and microstructure of the coating is important. In this work, the electrodeposition process of porous lead dioxide coating is regulated by the way of linear potential increase and realized the rapid preparation of high-performance porous lead dioxide coating within 40 s. The morphology and microstructure, electrical, and electrochemical properties are characterized, combined with theoretical calculation and orthogonal analysis, to investigate the regulatory mechanism of the rapid growth of the porous lead dioxide by the electric potential. It is demonstrated that synchronous OER confers porous morphology and a large number of defects to the coating in situ, and enhancing the electrocatalytic oxidation performance of the electrode.

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
副反应转为正反应:同步OER控制阳极电沉积二氧化铅的电催化性能
多孔电极的制备和改性是新一代电化学氧化技术的重要组成部分。通过同步氧泡电沉积,可以很容易地快速制备多孔电极。然而,根据氧化铅阳极电沉积的反应机理,在氧泡模板法中必然存在吸附羟基自由基的竞争反应,这意味着同步OER既影响金属氧化物的表面形貌,也可能影响金属氧化物的晶体结构。阐明同步OER对涂层形貌和显微组织的综合影响是很重要的。本工作通过线性电位增加的方式调节多孔二氧化铅涂层的电沉积过程,实现了在40 s内快速制备高性能多孔二氧化铅涂层。对多孔二氧化铅的形貌和微观结构、电学和电化学性能进行表征,结合理论计算和正交分析,探讨电势对多孔二氧化铅快速生长的调控机制。结果表明,同步OER使涂层在原位形成多孔形态和大量缺陷,提高了电极的电催化氧化性能。
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
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
期刊最新文献
Bioinspired Omnidirectional Interface Engineered Flexible Island for Highly Stretchable Electronics Synergistic Catalysis in Fe─In Diatomic Sites Anchored on Nitrogen‐Doped Carbon for Enhanced CO2 Electroreduction Highly Reversible Aqueous Zinc‐Ion Batteries via Multifunctional Hydrogen‐Bond‐Rich Dulcitol at Lower Temperature Enhanced Activity and Stability for Electrocatalytic Nitrate Reduction to Ammonia over Low‐Coordinated Cobalt Self‐Assembled Charge Bridge Path at the Sn‐Pb Perovskite/C60 Interface for High‐Efficiency All‐Perovskite Tandem Solar Cells
×
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