Bi-Doped In2O3 Nanofiber for Efficient Electrocatalytic CO2 Reduction

IF 3.8 3区 化学 Q2 CHEMISTRY, PHYSICAL ChemCatChem Pub Date : 2024-10-09 DOI:10.1002/cctc.202401399
Yuanxiang Zhao, Xinchun Lv, Zifan Zhu, Chen Yang, Xintao Ma, Yifei Sun, Abdullah N. Alodhayb, Xiaodong Yi, Wei Shi, Zhou Chen
{"title":"Bi-Doped In2O3 Nanofiber for Efficient Electrocatalytic CO2 Reduction","authors":"Yuanxiang Zhao,&nbsp;Xinchun Lv,&nbsp;Zifan Zhu,&nbsp;Chen Yang,&nbsp;Xintao Ma,&nbsp;Yifei Sun,&nbsp;Abdullah N. Alodhayb,&nbsp;Xiaodong Yi,&nbsp;Wei Shi,&nbsp;Zhou Chen","doi":"10.1002/cctc.202401399","DOIUrl":null,"url":null,"abstract":"<p>Electrocatalytic carbon dioxide reduction reaction (CO<sub>2</sub>RR) to formic acid (HCOOH) is attracted for superfluous CO<sub>2</sub> removal and HCOOH production under ambient conditions. Indium-based catalysts has considered as a good candidate material for CO<sub>2</sub>RR to HCOOH due to their environmentally friendly features. However, the catalytic efficiency is limited by the poor HCOOH Faradaic efficiency (FE) and high reaction overpotential of electrocatalyst, and the activity and stability of indium-based catalysts are unsatisfactory, especially in industrial current density that is critical for commercialization. Herein, a fiber Bi-doped In<sub>2</sub>O<sub>3</sub> was synthesized through electrospinning method, and it demonstrate a FE<sub>HCOOH</sub> of 88.2% at −1.5 V versus RHE (reversible hydrogen electrode) with partial current density of −21.8 mA cm<sup>−2</sup> in H type cell. Specially, the Bi-In electrocatalyst also reach the industrial current density standard, which can work at −400 mA cm<sup>−2</sup> current density with FE<sub>HCOOH</sub> of 92.7% (yield of HCOOH is 6.9 mmol h<sup>−1</sup>) in home-made Flow cell. Importantly, Bi-In shows 24 h long-term stability test in −300 mA cm<sup>−2</sup>. The improvement catalytic activity of Bi-In catalyst is ascribed to the optimized electronic structure of In site, and the reduced work function value of Bi-In is beneficial for reducing the formation energy of the key *OCHO intermediates.</p>","PeriodicalId":141,"journal":{"name":"ChemCatChem","volume":"17 2","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemCatChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cctc.202401399","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Electrocatalytic carbon dioxide reduction reaction (CO2RR) to formic acid (HCOOH) is attracted for superfluous CO2 removal and HCOOH production under ambient conditions. Indium-based catalysts has considered as a good candidate material for CO2RR to HCOOH due to their environmentally friendly features. However, the catalytic efficiency is limited by the poor HCOOH Faradaic efficiency (FE) and high reaction overpotential of electrocatalyst, and the activity and stability of indium-based catalysts are unsatisfactory, especially in industrial current density that is critical for commercialization. Herein, a fiber Bi-doped In2O3 was synthesized through electrospinning method, and it demonstrate a FEHCOOH of 88.2% at −1.5 V versus RHE (reversible hydrogen electrode) with partial current density of −21.8 mA cm−2 in H type cell. Specially, the Bi-In electrocatalyst also reach the industrial current density standard, which can work at −400 mA cm−2 current density with FEHCOOH of 92.7% (yield of HCOOH is 6.9 mmol h−1) in home-made Flow cell. Importantly, Bi-In shows 24 h long-term stability test in −300 mA cm−2. The improvement catalytic activity of Bi-In catalyst is ascribed to the optimized electronic structure of In site, and the reduced work function value of Bi-In is beneficial for reducing the formation energy of the key *OCHO intermediates.

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
求助全文
约1分钟内获得全文 去求助
来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
期刊最新文献
Front Cover: Heterogeneous Asymmetric Hydrogenation of C═C and C═O Double Bonds (ChemCatChem 4/2025) Cover Feature: Coupling Conversion of CO2 and High-Carbon Alkane to CO and Gasoline (ChemCatChem 4/2025) Front Cover: Visible-Light-Induced Desulfurative Coupling of Alkyl Benzothiazolyl Sulfides with Electron-Deficient Alkenes/Alkynes: Dual Role of Base-Activated Hantzsch Esters (ChemCatChem 3/2025) Correction to “Durable Electrooxidation of Acidic Water Catalysed by a Cobalt-Bismuth-based Oxide Composite: An Unexpected Role of the F-doped SnO2 Substrate” Front Cover: Silica-Mediated Incorporation of Lipase into the Bulk of a Deep Eutectic Solvent: An Efficient Biocatalytic Phase for Esters Synthesis (ChemCatChem 2/2025)
×
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