Fundamentals and Rational Design of Heterogeneous C-N Coupling Electrocatalysts for Urea Synthesis at Ambient Conditions

IF 24.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Yuchi Wan, Muyun Zheng, Wei Yan, Jiujun Zhang, Ruitao Lv
{"title":"Fundamentals and Rational Design of Heterogeneous C-N Coupling Electrocatalysts for Urea Synthesis at Ambient Conditions","authors":"Yuchi Wan,&nbsp;Muyun Zheng,&nbsp;Wei Yan,&nbsp;Jiujun Zhang,&nbsp;Ruitao Lv","doi":"10.1002/aenm.202303588","DOIUrl":null,"url":null,"abstract":"<p>Electrocatalytic C-N coupling reaction is regarded as a promising strategy for achieving clean and sustainable urea production by coreducing CO<sub>2</sub> and nitrogen species, thus contributing to carbon neutrality and the artificial nitrogen cycle. However, restricted by the sluggish adsorption of reactants, competitive side reactions, and multistep reaction pathways, the electrochemical urea production suffers from a low urea yield rate and low selectivity so far. In order to comprehensively improve urea synthesis performance, it is crucial to develop highly efficient catalysts for electrochemical C-N coupling. In this article, the catalyst-designing strategies, C-N coupling mechanisms, and fundamental research methods are reviewed. For the coreduction of CO<sub>2</sub> and different nitrogen species, several prevailing reaction mechanisms are discussed. With the aim of establishing the standard research system, the fundamentals of electrocatalytic urea synthesis research are introduced. The most important catalyst-designing strategies for boosting the electrocatalytic urea production are discussed, including heteroatom doping, vacancy engineering, crystal facet regulation, atom-scale modulation, alloying and heterostructure construction. Finally, the challenges and perspectives are proposed for future industrial applications of electrochemical urea production by C-N coupling.</p>","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":"14 28","pages":""},"PeriodicalIF":24.4000,"publicationDate":"2024-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/aenm.202303588","RegionNum":1,"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

Electrocatalytic C-N coupling reaction is regarded as a promising strategy for achieving clean and sustainable urea production by coreducing CO2 and nitrogen species, thus contributing to carbon neutrality and the artificial nitrogen cycle. However, restricted by the sluggish adsorption of reactants, competitive side reactions, and multistep reaction pathways, the electrochemical urea production suffers from a low urea yield rate and low selectivity so far. In order to comprehensively improve urea synthesis performance, it is crucial to develop highly efficient catalysts for electrochemical C-N coupling. In this article, the catalyst-designing strategies, C-N coupling mechanisms, and fundamental research methods are reviewed. For the coreduction of CO2 and different nitrogen species, several prevailing reaction mechanisms are discussed. With the aim of establishing the standard research system, the fundamentals of electrocatalytic urea synthesis research are introduced. The most important catalyst-designing strategies for boosting the electrocatalytic urea production are discussed, including heteroatom doping, vacancy engineering, crystal facet regulation, atom-scale modulation, alloying and heterostructure construction. Finally, the challenges and perspectives are proposed for future industrial applications of electrochemical urea production by C-N coupling.

Abstract Image

Abstract Image

环境条件下尿素合成用异质 C-N 偶联电催化剂的基本原理与合理设计
电催化 C-N 偶联反应被认为是实现清洁和可持续尿素生产的一种有前途的策略,它通过核心生成二氧化碳和氮物种,从而促进碳中和和人工氮循环。然而,受反应物吸附缓慢、竞争性副反应和多步反应途径等因素的限制,迄今为止,电化学尿素生产存在尿素产率低、选择性低等问题。为了全面提高尿素合成性能,开发高效的电化学 C-N 偶联催化剂至关重要。本文综述了催化剂设计策略、C-N 偶联机理和基础研究方法。针对二氧化碳和不同氮种的核诱导,讨论了几种普遍的反应机理。以建立标准研究体系为目标,介绍了电催化尿素合成研究的基本原理。讨论了促进电催化尿素生产最重要的催化剂设计策略,包括杂原子掺杂、空位工程、晶面调节、原子尺度调控、合金化和异质结构构建。最后,提出了通过 C-N 偶联法电化学生产尿素的未来工业应用所面临的挑战和前景。
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 求助全文
来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信