GIEC OpenIR

Efficient electrocatalytic reduction of N-2 to ammonia at ambient conditions with municipal sludge-derived porous carbon codoped with multiple heteroatoms

Deng, Lifang1,2,3; Wang, Lufeng3; Wei, Guoqiang1; Yuan, Haoran1,2,3; Xie, Jun1; Chen, Yong1,2,3
2022-03-10
发表期刊ELECTROCHIMICA ACTA
ISSN0013-4686
卷号408页码:10
通讯作者Yuan, Haoran(yuanhaoran81@gmail.com)
摘要Electrocatalytic reduction of N-2 to ammonia (NH3) at ambient conditions has attracted widespread attention, and revealing the mechanism has been a remarkably challenging problem for decades. This work developed a low-cost and efficient multiple heteroatom codoped porous carbon catalyst from municipal sludge (MSB-P), which demonstrated excellent electrochemical stability and selectivity for the electrochemical N-2 reduction reaction (N2RR). In 0.1 mol/L HCl solution, a high NH3 yield rate of 35.76 mu g.h(-1).mg(-1) cat. and an excellent Faraday Efficiency (FE) of 7.79% at-0.7 V vs. RHE (reversible hydrogen electrode) were obtained under ambient conditions. Furthermore, the electrocatalytic mechanism of MSB-P for N2RR was also revealed by in situ Fourier transform infrared spectroscopy (FTIR) data, and an associative route was identified. These findings provide an exciting new method for fabricating inexpensive and efficient carbon-based catalysts for production of NH3 at ambient conditions. (C)& nbsp;2022 Elsevier Ltd. All rights reserved.
关键词Municipal sludge Electrocatalytic reduction N 2 to ammonia Faraday efficiency
DOI10.1016/j.electacta.2022.139934
关键词[WOS]HYDROGEN STORAGE ; GRAPHENE ; NITROGEN ; CATALYST ; DEGRADATION ; WATER
收录类别SCI
语种英语
资助项目Key-Area Research and Devel-opment Program of GuangDong Province[2019B110209003] ; Guangdong Basic and Applied Basic Research Foundation[2019A1515010928] ; Guangdong Basic and Applied Basic Research Foundation[2021B1515020068] ; Key Special Project for Introduced Talents Team of Southern Marine Science and En-gineering Guangdong Laboratory (Guangzhou)[GML2019ZD0101] ; Guangdong Province Science and Technology Planning Project[2019B1102100 03]
WOS研究方向Electrochemistry
项目资助者Key-Area Research and Devel-opment Program of GuangDong Province ; Guangdong Basic and Applied Basic Research Foundation ; Key Special Project for Introduced Talents Team of Southern Marine Science and En-gineering Guangdong Laboratory (Guangzhou) ; Guangdong Province Science and Technology Planning Project
WOS类目Electrochemistry
WOS记录号WOS:000780756600011
出版者PERGAMON-ELSEVIER SCIENCE LTD
引用统计
被引频次:5[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.giec.ac.cn/handle/344007/36186
专题中国科学院广州能源研究所
通讯作者Yuan, Haoran
作者单位1.South China Agr Univ, Guangdong Engn Technol Res Ctr Agr & Forestry Bio, Key Lab Energy Plants Resource & Utilizat, Inst Biomass Engn,Minist Agr & Rural Affairs, Guangzhou 510642, Peoples R China
2.Southern Marine Sci & Engn Guangdong Lab Guangzho, Guangzhou 510650, Peoples R China
3.Chinese Acad Sci, Guangzhou Inst Energy Convers, Key Lab Renewable Energy, Guangzhou 510640, Peoples R China
第一作者单位中国科学院广州能源研究所
推荐引用方式
GB/T 7714
Deng, Lifang,Wang, Lufeng,Wei, Guoqiang,et al.

Efficient electrocatalytic reduction of N-2 to ammonia at ambient conditions with municipal sludge-derived porous carbon codoped with multiple heteroatoms

[J]. ELECTROCHIMICA ACTA,2022,408:10.
APA Deng, Lifang,Wang, Lufeng,Wei, Guoqiang,Yuan, Haoran,Xie, Jun,&Chen, Yong.(2022).

Efficient electrocatalytic reduction of N-2 to ammonia at ambient conditions with municipal sludge-derived porous carbon codoped with multiple heteroatoms

.ELECTROCHIMICA ACTA,408,10.
MLA Deng, Lifang,et al."

Efficient electrocatalytic reduction of N-2 to ammonia at ambient conditions with municipal sludge-derived porous carbon codoped with multiple heteroatoms

".ELECTROCHIMICA ACTA 408(2022):10.
条目包含的文件
条目无相关文件。
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Deng, Lifang]的文章
[Wang, Lufeng]的文章
[Wei, Guoqiang]的文章
百度学术
百度学术中相似的文章
[Deng, Lifang]的文章
[Wang, Lufeng]的文章
[Wei, Guoqiang]的文章
必应学术
必应学术中相似的文章
[Deng, Lifang]的文章
[Wang, Lufeng]的文章
[Wei, Guoqiang]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。