Single atom-based catalysts for electrochemical CO2 reduction

催化作用 电化学 纳米技术 金属 位阻效应 Atom(片上系统) 材料科学 化学 氧化还原 法拉第效率 化学工程 组合化学 电极 物理化学 有机化学 计算机科学 工程类 嵌入式系统 冶金
作者
Qian Sun,Chen Jia,Yong Zhao,Chuan Zhao
出处
期刊:Chinese Journal of Catalysis [Elsevier BV]
卷期号:43 (7): 1547-1597 被引量:64
标识
DOI:10.1016/s1872-2067(21)64000-7
摘要

Electrochemical CO2 reduction reaction (CO2RR), powered by renewable energy, emerges as a promising approach against environmental issues and energy crisis by converting CO2 into value-added chemicals. Single atom catalysts (SACs) with isolated metal atoms dispersed on supports exhibit outstanding performance for CO2 electroreduction, because of their strong single atom-support interactions, maximum metal utilization and excellent catalytic activity. However, SACs suffer from agglomeration of particles, low metal loading, and difficulty in large-scale production. In addition, molecular catalysts as another single atom-based catalyst, consisting of ligands molecules connected to metal ions, exhibited similar metal-nitrogen (M-N) active centers as that in metal-nitrogen-carbon (M-N-C) SACs, which were highly active to CO2 reduction due to their well-defined active sites and tunability over the steric and electronic properties of the active sites. Nonetheless, molecular catalysts are challenged by generally moderate activity, selectivity and stability, poor conductivity and aggregation. Many works have been devoted to overcoming these issues of SACs and molecular catalysts for efficient CO2RR, but only limited reviews for systematic summary of their fabrication, application, and characterizations, which were highlighted in this review. Firstly, we summarize recent advanced strategies in preparing SACs for CO2RR, including wet-chemistry approaches (defect engineering, spatial confinement, and coordination design), other synthetic methods and large-scale production of SACs. Besides, electrochemical applications of SACs and molecular catalysts on CO2RR are discussed, which involved the faradaic efficiency and partial current density of the desired product as well as the catalyst stability. In addition, ex-situ and in-situ/operando characterization techniques are briefly assessed, benefiting probing the active sites and understanding the CO2RR catalytic mechanisms. Finally, future directions for the development of single atom-based catalysts (SACs, molecular catalysts) are pointed out.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
阜睿发布了新的文献求助10
1秒前
4秒前
5秒前
周志轩66发布了新的文献求助10
6秒前
7秒前
村长夫人发布了新的文献求助10
8秒前
科研通AI5应助清脆四娘采纳,获得10
8秒前
Lucas应助骑羊采纳,获得10
10秒前
丰富的慕卉完成签到,获得积分10
11秒前
Felly发布了新的文献求助10
12秒前
李梦媛完成签到 ,获得积分10
14秒前
朱华彪完成签到,获得积分10
16秒前
周志轩66完成签到,获得积分20
16秒前
16秒前
19秒前
21秒前
热心的善愁完成签到,获得积分10
21秒前
高兴的斑马完成签到 ,获得积分10
22秒前
22秒前
24秒前
25秒前
三岁半完成签到 ,获得积分10
26秒前
28秒前
柚子肉发布了新的文献求助10
28秒前
29秒前
岁啦发布了新的文献求助10
31秒前
是小雨呀完成签到,获得积分10
32秒前
33秒前
1111完成签到 ,获得积分10
35秒前
莫里亚蒂完成签到,获得积分10
38秒前
斯文败类应助岁啦采纳,获得10
39秒前
qianqian发布了新的文献求助20
40秒前
41秒前
莫里亚蒂发布了新的文献求助20
41秒前
42秒前
夏时安发布了新的文献求助20
45秒前
zhzzhz应助科研通管家采纳,获得10
45秒前
充电宝应助科研通管家采纳,获得10
45秒前
深情安青应助科研通管家采纳,获得10
45秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
China—Art—Modernity: A Critical Introduction to Chinese Visual Expression from the Beginning of the Twentieth Century to the Present Day 360
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3776959
求助须知:如何正确求助?哪些是违规求助? 3322349
关于积分的说明 10209964
捐赠科研通 3037710
什么是DOI,文献DOI怎么找? 1666837
邀请新用户注册赠送积分活动 797676
科研通“疑难数据库(出版商)”最低求助积分说明 758003