已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Rational Design of Ag‐Based Catalysts for the Electrochemical CO2 Reduction to CO: A Review

电催化剂 催化作用 纳米技术 电化学 可再生能源 材料科学 化学工程 化学 电极 生物化学 电气工程 工程类 物理化学
作者
Dalei Sun,Xiaomin Xu,Yanling Qin,San Ping Jiang,Zongping Shao
出处
期刊:Chemsuschem [Wiley]
卷期号:13 (1): 39-58 被引量:192
标识
DOI:10.1002/cssc.201902061
摘要

Abstract The selective electrochemical CO 2 reduction (ECR) to CO in aqueous electrolytes has gained significant interest in recent years due to its capability to mitigate the environmental issues associated with CO 2 emission and to convert renewable energy such as wind and solar power into chemical energy as well as its potential to realize the commercial use of CO 2 . In view of the thermodynamic stability and kinetic inertness of CO 2 molecules, the exploitation of active, selective, and stable catalysts for the ECR to CO is crucial to promote the reaction efficiency. Indeed, plenty of electrocatalysts for the selective ECR to CO have been explored, of which Ag is known as the most promising electrocatalyst for large‐scale ECR to CO due to several competitive advantages including high catalytic performance, low price, and rich reserves compared with other metal counterparts. To provide useful guidelines for the further development of efficient catalysts for the ECR to CO, a comprehensive summary of the recent progress of Ag‐based electrocatalysts is presented in this Review. Different modification strategies of Ag‐based electrocatalysts are highlighted, including exposure of crystal facets, tuning of morphology and size, introduction of support materials, alloying with other metals, and surface modification with functional groups. The reaction mechanisms involved in these different modification strategies of Ag‐based electrocatalysts are also discussed. Finally, the prospects for the development of next‐generation Ag‐based electrocatalysts are proposed in an effort to facilitate the industrialization of ECR to CO.
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
卢振杰完成签到,获得积分10
1秒前
awa606发布了新的文献求助10
4秒前
7秒前
不知道叫什么完成签到 ,获得积分10
8秒前
9秒前
11秒前
ok发布了新的文献求助10
12秒前
斯文弘文发布了新的文献求助10
13秒前
15秒前
17秒前
暗觉完成签到 ,获得积分10
17秒前
醉风琴完成签到 ,获得积分10
17秒前
宇儿发布了新的文献求助10
18秒前
王明磊完成签到 ,获得积分10
21秒前
23秒前
23秒前
是是是完成签到,获得积分10
25秒前
活力的bird完成签到,获得积分10
26秒前
27秒前
Doris发布了新的文献求助10
28秒前
susie发布了新的文献求助10
29秒前
顾矜应助zky采纳,获得10
29秒前
KeldonHuang发布了新的文献求助10
30秒前
30秒前
科研通AI6.3应助宇儿采纳,获得10
31秒前
31秒前
33秒前
斯文弘文发布了新的文献求助10
33秒前
吃茶去完成签到 ,获得积分10
34秒前
34秒前
唠叨的富完成签到,获得积分10
34秒前
戴亮发布了新的文献求助30
34秒前
章口就来完成签到 ,获得积分10
36秒前
37秒前
276868sxzz发布了新的文献求助10
37秒前
susie完成签到,获得积分10
39秒前
打打应助电磁场与电磁波采纳,获得10
39秒前
41秒前
qys发布了新的文献求助10
41秒前
Orange应助yusheng6688采纳,获得10
42秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7281128
求助须知:如何正确求助?哪些是违规求助? 8902081
关于积分的说明 18831377
捐赠科研通 6952786
什么是DOI,文献DOI怎么找? 3207496
关于科研通互助平台的介绍 2377700
邀请新用户注册赠送积分活动 2182620