Challenges and opportunities of atomic-scales reactive sites in thriving electrochemical CO2 reduction reaction

催化作用 背景(考古学) 纳米技术 电化学 生化工程 经济短缺 化学 材料科学 计算机科学 工程类 有机化学 语言学 生物 哲学 物理化学 古生物学 政府(语言学) 电极
作者
Pengliang Sun,Sailin Liu,Xiong Zheng,Guangzhi Hu,Qingran Zhang,Xinchao Liu,Guanghong Zheng,Yinguang Chen
出处
期刊:Nano Today [Elsevier BV]
卷期号:55: 102152-102152 被引量:50
标识
DOI:10.1016/j.nantod.2024.102152
摘要

Electrochemical carbon dioxide reduction reaction (ECO2RR) converts CO2 into value-added chemicals or fuels to realize carbon recycling as means to solve the problems of renewable energy shortage and environmental pollution. The development of cost-effective CO2RR catalysts with high activity, stability and selectivity is the key that enables efficient conversion from CO2 to valuable products. It is also important to understand intrinsic mechanisms of the underlying active-site that affect the performances of catalysts, which can, in turn, facilitate the rational design of more active electrocatalysts. In this context, it is particularly important to understand the structure-activity relationship of catalyst active sites during the CO2RR process from different atomic-scales, which inspires to organize this review. Specifically, we focus on the atomic-level construction of active sites from single atoms, dual-site metal, clusters, or/and graphitic carbon materials: key approaches for tailoring coordination configurations to enhance target product selectivity, i.e., optimizing the interplay between the catalytic active center and reactants or intermediates, disrupting the linear correlation of intermediate adsorption energies, and promoting intricate cascading reactions involving multiple intermediates. Highlight the intricate correlation between the structure-activity of CO2RR catalysts, which govern the discerning refinement of catalysts and propel advances in their practical application. Then, the electrocatalytic reactors for ECO2R reactions are critically reviewed. The acquisition of key metrics, the challenges faced, and the most suitable solutions for electrocatalytic CO2RR are proposed. Finally, future research directions and strategies are anticipated to inspire revolutionary advancements.
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
刚刚
zeqian完成签到,获得积分10
1秒前
1秒前
露露娜娜完成签到 ,获得积分10
2秒前
Kil发布了新的文献求助10
2秒前
3秒前
小白发布了新的文献求助10
3秒前
kmm发布了新的文献求助10
3秒前
尚买办完成签到,获得积分20
4秒前
SciGPT的应助被科研通管家采纳,获得10
5秒前
wanci的应助被科研通管家采纳,获得10
5秒前
小马甲的应助被科研通管家采纳,获得10
5秒前
小蘑菇的应助被科研通管家采纳,获得10
5秒前
小禹的应助被科研通管家采纳,获得10
5秒前
molihuakai的应助被科研通管家采纳,获得10
5秒前
Nole的应助被科研通管家采纳,获得10
6秒前
慕青的应助被科研通管家采纳,获得10
6秒前
NexusExplorer的应助被科研通管家采纳,获得10
6秒前
小禹的应助被科研通管家采纳,获得10
6秒前
ding的应助被科研通管家采纳,获得10
6秒前
6秒前
6秒前
酷波er的应助被科研通管家采纳,获得10
6秒前
6秒前
精明严青发布了新的文献求助10
7秒前
跨材料发布了新的文献求助10
7秒前
8秒前
山野完成签到,获得积分10
9秒前
锅嘚硬发布了新的文献求助10
9秒前
10秒前
yy完成签到 ,获得积分10
12秒前
彭于晏的应助被Warren采纳,获得10
13秒前
大模型的应助被张三三采纳,获得10
13秒前
13秒前
蛋白工人完成签到,获得积分10
14秒前
海阔天空完成签到,获得积分10
15秒前
旅程完成签到 ,获得积分10
15秒前
小马甲的应助被人间由物采纳,获得10
15秒前
YangyTjjt发布了新的文献求助20
15秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
Production Logging: Theoretical and Interpretive Elements 400
CLSI C56QG Examples of Hemolyzed, Icteric, and Lipemic/Turbid Samples Quick Guide 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7815228
求助须知:如何正确求助?哪些是违规求助? 9344832
关于积分的说明 20526208
捐赠科研通 7407794
什么是DOI,文献DOI怎么找? 3330899
关于科研通互助平台的介绍 2477377
邀请新用户注册赠送积分活动 2350511