Self-assembled SnO2/COF catalysts for improved electro-synthesis of hydrogen peroxide†

IF 9.2 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2025-01-14 DOI:10.1039/D4TA08190K
Guoliang Wang, Zhikang Bao, Yuanan Li, Yabing Wang, Xuejiao Cui, Haochong Zhong, Wenjuan Fang and Jianguo Wang
{"title":"Self-assembled SnO2/COF catalysts for improved electro-synthesis of hydrogen peroxide†","authors":"Guoliang Wang, Zhikang Bao, Yuanan Li, Yabing Wang, Xuejiao Cui, Haochong Zhong, Wenjuan Fang and Jianguo Wang","doi":"10.1039/D4TA08190K","DOIUrl":null,"url":null,"abstract":"<p >The electrochemical oxygen reduction reaction (ORR) <em>via</em> a two-electron pathway offers a sustainable route for on-site hydrogen peroxide (H<small><sub>2</sub></small>O<small><sub>2</sub></small>) production. However, achieving stable H<small><sub>2</sub></small>O<small><sub>2</sub></small> production at industrial-scale current densities continues to pose significant challenges. In this study, 10% SnO<small><sub>2</sub></small>/COF catalysts synthesized <em>via</em> the self-assembly approach exhibited both high performance and robust stability. In a neutral solution, a yield of 11 873 mg L<small><sup>−1</sup></small> h<small><sup>−1</sup></small> could be achieved at a high current density of 125 mA cm<small><sup>−2</sup></small>, with a Faraday efficiency exceeding 80% maintained throughout a 60 hour stability test. Through a series of experiments and <em>in situ</em> tests, it was concluded that the hierarchical porous structure of a COF enhances the mass transfer of oxygen, while the strong interaction between SnO<small><sub>2</sub></small> nanoparticles and the COF promotes the 2-electron (2e<small><sup>−</sup></small>) reaction pathway. This interaction also accelerates the desorption of hydrogen peroxide and enhances its accumulation rate. This research provides a method to design efficient catalysts for production of H<small><sub>2</sub></small>O<small><sub>2</sub></small><em>via</em> the electrochemical 2e<small><sup>−</sup></small> ORR.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 8","pages":" 6059-6066"},"PeriodicalIF":9.2000,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ta/d4ta08190k","RegionNum":2,"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

The electrochemical oxygen reduction reaction (ORR) via a two-electron pathway offers a sustainable route for on-site hydrogen peroxide (H2O2) production. However, achieving stable H2O2 production at industrial-scale current densities continues to pose significant challenges. In this study, 10% SnO2/COF catalysts synthesized via the self-assembly approach exhibited both high performance and robust stability. In a neutral solution, a yield of 11 873 mg L−1 h−1 could be achieved at a high current density of 125 mA cm−2, with a Faraday efficiency exceeding 80% maintained throughout a 60 hour stability test. Through a series of experiments and in situ tests, it was concluded that the hierarchical porous structure of a COF enhances the mass transfer of oxygen, while the strong interaction between SnO2 nanoparticles and the COF promotes the 2-electron (2e) reaction pathway. This interaction also accelerates the desorption of hydrogen peroxide and enhances its accumulation rate. This research provides a method to design efficient catalysts for production of H2O2via the electrochemical 2e ORR.

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
用于改进过氧化氢电合成的自组装 SnO2/COF 催化剂
通过双电子途径的电化学氧还原反应(ORR)为现场生产过氧化氢(H2O2)提供了一条可持续的途径。然而,在当前工业规模密度下实现稳定的H2O2产量仍然是一个重大挑战。在本研究中,通过自组装方法合成的10%SnO2/COF催化剂具有高性能和鲁棒稳定性。在中性溶液中,在125 mA/cm2的高电流密度下,产率可以达到11,873 mg/(L•h),在60小时的稳定性测试中,法拉第效率保持在80%以上。通过一系列的实验和原位测试,得出COF的分层多孔结构增强了氧的传质,而SnO2纳米粒子与COF的强相互作用促进了2电子(2e-)反应途径。这种相互作用还加速了过氧化氢的解吸,提高了过氧化氢的积累速率。本研究为设计电化学2e- ORR制H2O2的高效催化剂提供了思路。
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 Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
期刊最新文献
Modulated Stabilization of Cu 2+ /Cu + /Cu 0 Gradient Interfaces for Efficient Electrochemical CO 2 Reduction to C 2 H 4 Activating Reversible Multielectron Redox in Mg/Al Co-doped Na3V2(PO4)3 toward High-Performance Sodium-Ion Batteries Activating Lattice Oxygen via Proton-Decoupled Electron Transfer in Iron Chromium Phosphate for Efficient (Sea)Water Oxidation Carbon dioxide capture from air using ionic liquid hybrid metal–organic frameworks Metal-Free Supramolecularly Engineered Catalysis: Perylene Diimide-Amino Acid Conjugates for Photoelectrochemical Water Splitting
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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