Micro-Cu Doped Co3O4 as an Effective Oxygen Reduction Nano-flower-like Catalyst to Enhance the Power Output of Air Cathode Microbial Fuel Cell

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL Catalysis Letters Pub Date : 2024-08-12 DOI:10.1007/s10562-024-04779-8
Cheng Li, Yao Yang, Jinrong Lu, Linde Ren, Xiayan Zhang, Cong Li, Xuan Yang, Yao Xiang, Hua Liu
{"title":"Micro-Cu Doped Co3O4 as an Effective Oxygen Reduction Nano-flower-like Catalyst to Enhance the Power Output of Air Cathode Microbial Fuel Cell","authors":"Cheng Li,&nbsp;Yao Yang,&nbsp;Jinrong Lu,&nbsp;Linde Ren,&nbsp;Xiayan Zhang,&nbsp;Cong Li,&nbsp;Xuan Yang,&nbsp;Yao Xiang,&nbsp;Hua Liu","doi":"10.1007/s10562-024-04779-8","DOIUrl":null,"url":null,"abstract":"<div><p>Air cathode microbial fuel cell (MFC) can use the biological activities of microorganisms to convert organic matter into ideal electrical energy, but this efficiency has not been satisfactory. The air cathode requires an optimal catalyst to enhance the power output of the MFC by improving its low oxygen reduction reaction (ORR) activity. Micro Cu-doped Co<sub>3</sub>O<sub>4</sub> nano-flower-like catalyst is successfully synthesized in this study using a metal-organic framework as the precursor material. The addition of 5% Cu induces a higher concentration of oxygen vacancies, thereby optimizing the local electronic state of the active site and enhancing the catalytic performance for oxygen reduction in the 5% Cu-Co<sub>3</sub>O<sub>4</sub> material. Consequently, when equipped with this material, the power output of the air cathode MFC is approximately 2.85 times greater than that achieved with pure Co<sub>3</sub>O<sub>4</sub>. This provides a novel design idea for the application of nano-flower-like transition metal oxygen reduction catalysts in MFC.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":508,"journal":{"name":"Catalysis Letters","volume":"154 11","pages":"6080 - 6093"},"PeriodicalIF":2.3000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Letters","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10562-024-04779-8","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Air cathode microbial fuel cell (MFC) can use the biological activities of microorganisms to convert organic matter into ideal electrical energy, but this efficiency has not been satisfactory. The air cathode requires an optimal catalyst to enhance the power output of the MFC by improving its low oxygen reduction reaction (ORR) activity. Micro Cu-doped Co3O4 nano-flower-like catalyst is successfully synthesized in this study using a metal-organic framework as the precursor material. The addition of 5% Cu induces a higher concentration of oxygen vacancies, thereby optimizing the local electronic state of the active site and enhancing the catalytic performance for oxygen reduction in the 5% Cu-Co3O4 material. Consequently, when equipped with this material, the power output of the air cathode MFC is approximately 2.85 times greater than that achieved with pure Co3O4. This provides a novel design idea for the application of nano-flower-like transition metal oxygen reduction catalysts in MFC.

Graphical Abstract

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
微掺铜 Co3O4 作为一种有效的氧还原纳米花状催化剂提高空气阴极微生物燃料电池的功率输出
空气阴极微生物燃料电池(MFC)可以利用微生物的生物活性将有机物转化为理想的电能,但这种效率并不令人满意。空气阴极需要一种最佳催化剂,通过改善其低氧还原反应(ORR)活性来提高 MFC 的功率输出。本研究以金属有机框架为前驱材料,成功合成了微掺铜 Co3O4 纳米花状催化剂。5%Cu 的添加诱导了更高浓度的氧空位,从而优化了活性位点的局部电子状态,提高了 5%Cu-Co3O4 材料的氧还原催化性能。因此,当使用这种材料时,空气阴极 MFC 的功率输出大约是使用纯 Co3O4 时的 2.85 倍。这为纳米花状过渡金属氧还原催化剂在 MFC 中的应用提供了一种新的设计思路。
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
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
期刊最新文献
Visible Light Induced Eosin Y Catalysed Green Synthesis of Substituted Pyrroles Correction to: In Silico Models for Prediction of Methanol Yield in CO2 Hydrogenation Reaction Using CuBased Catalysts Promotional Catalytic Activity of Bifunctional Ru-Ce-Zr Catalysts forNH3-SCO by Deposition Order of Dual Active Components Palladium-Based Catalyst on L-Histidine-Modified Boron Nitride Nanosheets: A Novel, Stable, and Highly Efficient Heterogeneous Catalyst for Suzuki–Miyaura Reaction M-BTC as Efficient Catalyst for the Synthesis of Cyclic Organic Carbonates Assisted Tandem by Olefin Epoxidation and CO2 Cycloaddition
×
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