Theoretical study on the electrocatalytic CO2 reduction mechanisms using carbon-nanotube-supported carbon-based single metal atom catalysts

催化作用 碳纳米管 金属 碳纤维 还原(数学) Atom(片上系统) 碳原子 电催化剂 材料科学 纳米技术 化学工程 化学 无机化学 电化学 物理化学 电极 冶金 有机化学 计算机科学 工程类 复合数 戒指(化学) 复合材料 嵌入式系统 数学 几何学
作者
Shuang-Ling Qi,Xin-Long Zhang,Chao Fu,Yang Wu,Jiajia Yang,Laicai Li,Xiang‐Yang Liu
出处
期刊:Molecular Catalysis [Elsevier]
卷期号:558: 114003-114003 被引量:2
标识
DOI:10.1016/j.mcat.2024.114003
摘要

In this study, five Ni-doped carbon-based single metal atom catalysts supported by carbon nanotubes, which can be used for electrocatalytic CO2 reduction, were constructed. According to their structures, these catalysts include one Ni phthalocyanine (NiPc) molecule, two di- and tri-coordinated Ni-doped carbon nanoribbons, and two di-/tri-coordination Ni-doped graphene, which are denoted as NiPc/CNT, H2(H3)-Ni/CNT, 2(3)-Ni/CNT respectively. We first optimized their structures and studied the adsorption characteristics of CO2 on these catalysts with PBE+D3 method. Additionally, the electronic structure characteristics were then calculated, and the electrocatalytic mechanisms of CO2 reduction to CO, HCOOH, CH3OH and CH4 using these catalysts were studied in detail. It is found that the electrocatalytic activities of these five catalysts for reducing CO2 follow the order of 2-Ni/CNT>3-Ni/CNT>H3-Ni/CNT>H2-Ni/CNT>NiPc/CNT. As can be seen, the di-coordination catalysts perform best, followed by the tri-coordination catalysts, while the four-coordination NiPc-based catalyst performs worst. Moreover, graphene-based materials have stronger catalytic activities than their nanoribbon counterparts. Apart from these facts, these five catalytic materials may exhibit product selectivity at different limiting potentials, and specific reaction products can therefore be synthesized by controlling the potentials. We simultaneously investigated the mechanism of competing hydrogen evolution reactions in the electrocatalytic reduction of CO2 with five catalysts, and in order to inhibit the competing hydrogen evolution reactions and improve the efficiency of CO2 electrocatalytic reduction, the acidity of the solution can be appropriately reduced. We hope that our present work can provide a theoretical foundation for the future design and synthesis of novel carbon-based electrocatalyst for efficient CO2 reduction.
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
指纹抒写年轮完成签到,获得积分10
刚刚
1秒前
1秒前
超级真发布了新的文献求助10
1秒前
3秒前
5秒前
5秒前
爱笑的万天完成签到,获得积分20
5秒前
5秒前
脑洞疼应助柒陆采纳,获得10
7秒前
7秒前
鹌鹑蛋发布了新的文献求助10
10秒前
科研小白发布了新的文献求助10
10秒前
璐璐完成签到 ,获得积分10
11秒前
吉如天发布了新的文献求助10
11秒前
跳跃的黑猫完成签到,获得积分10
12秒前
13秒前
鲤鱼完成签到 ,获得积分10
13秒前
13秒前
龚薇发布了新的文献求助10
17秒前
在水一方应助monly采纳,获得10
18秒前
王珺完成签到,获得积分10
19秒前
乘风的法袍完成签到,获得积分10
20秒前
22秒前
打打应助超级真采纳,获得10
23秒前
飞快的万声完成签到,获得积分10
24秒前
24秒前
萧水白应助bear4f采纳,获得10
24秒前
24秒前
27秒前
32完成签到,获得积分10
27秒前
27秒前
28秒前
29秒前
30秒前
千里共婵娟应助牧无声采纳,获得10
32秒前
超级真完成签到,获得积分10
32秒前
微笑的芯完成签到 ,获得积分10
33秒前
是真的发布了新的文献求助10
34秒前
msd2phd完成签到,获得积分10
34秒前
高分求助中
The late Devonian Standard Conodont Zonation 2000
歯科矯正学 第7版(或第5版) 1004
Nickel superalloy market size, share, growth, trends, and forecast 2023-2030 1000
Semiconductor Process Reliability in Practice 1000
Smart but Scattered: The Revolutionary Executive Skills Approach to Helping Kids Reach Their Potential (第二版) 1000
Security Awareness: Applying Practical Cybersecurity in Your World 6th Edition 800
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 700
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3241437
求助须知:如何正确求助?哪些是违规求助? 2885871
关于积分的说明 8240942
捐赠科研通 2554412
什么是DOI,文献DOI怎么找? 1382503
科研通“疑难数据库(出版商)”最低求助积分说明 649598
邀请新用户注册赠送积分活动 625279