亲爱的研友该休息了!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!身体可是革命的本钱,早点休息,好梦!

Revealing electrocatalytic C N coupling for urea synthesis with metal–free electrocatalyst

电催化剂 催化作用 化学 石墨烯 无机化学 电化学 材料科学 电极 纳米技术 有机化学 物理化学
作者
Yongyong Cao,Yuxiao Meng,Runzhi An,Xuhui Zou,Hongjie Huang,Weichan Zhong,Zhangfeng Shen,Qineng Xia,Xi Li,Yangang Wang
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:641: 990-999 被引量:35
标识
DOI:10.1016/j.jcis.2023.03.135
摘要

Urea is ubiquitous in agriculture and industry, but its production consumes a lot of energy. The conversion of nitrogen (N2) and carbon dioxide (CO2) into urea via an electrocatalytic CN coupling reaction under ambient conditions would be a major boon to sustainable development. However, designing a metal - free catalyst with high activity and selectivity for urea remains a major challenge. Herein, by means of density functional theory (DFT) and ab - initio molecular dynamics (AIMD) computations, the B12 cluster doped on nitrogenated graphene (C2N) substrate catalyst (B12@C2N) with superior stability was designed for electrocatalytic urea synthesis starting from the CO2 and N2 through four reaction mechanisms. The nature of the co-adsorption activation of CO2 and N2 on the B12@C2N catalyst was investigated, the electrochemical proton - electron transfer steps and the CN thermochemical coupling led to the synthesis of urea. The study showed that the B12@C2N catalyst exhibited high catalytic activity for urea synthesis with the lowest limiting potential of - 1.01 V following the *HNNH mechanism compared with other mechanisms. The potential - determining step (PDS) is the formation of the *CO+*NH2NH2 species. However, the two - step CN coupling barriers of *NCON species are 0.13 eV and 0.60 eV using AIMD and a "slow - growth" sampling approach in an explicit water molecules model. Calculations also showed that the byproducts of carbon monoxide (CO), methane (CH4), methanol (CH3OH), ammonia (NH3), and hydrogen (H2) can be inhibited on the B12@C2N catalyst. Therefore, the metal - free catalyst not only has a good performance for the hydrogenation of CO2 and N2 promoting the electrochemical reaction, but also facilitates CN thermochemical coupling for urea synthesis. This work provides new insights into the synthesis of urea via the CN coupling reaction on a metal - free electrocatalyst, a process that could contribute to greenhouse gas mitigation to help meet carbon neutrality targets.
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
1秒前
牙牙侠发布了新的文献求助10
3秒前
wxd发布了新的文献求助10
7秒前
隐形曼青应助牙牙侠采纳,获得10
10秒前
希望天下0贩的0应助www采纳,获得10
11秒前
wanci应助苏诗兰采纳,获得10
15秒前
rebron完成签到,获得积分10
16秒前
20秒前
Nn应助bakerwm采纳,获得10
21秒前
21秒前
26秒前
26秒前
wxd完成签到,获得积分20
28秒前
www发布了新的文献求助10
30秒前
32秒前
32秒前
顾先森发布了新的文献求助10
33秒前
Rita应助无敌喷火龙采纳,获得10
33秒前
35秒前
小二郎应助昏睡的金毛采纳,获得10
37秒前
娄十三完成签到 ,获得积分10
37秒前
苏诗兰发布了新的文献求助10
38秒前
眼睛大问柳完成签到 ,获得积分10
40秒前
nur完成签到,获得积分10
40秒前
合蒲发布了新的文献求助10
40秒前
烟花应助蓝02333采纳,获得10
44秒前
45秒前
molihuakai应助合蒲采纳,获得10
47秒前
小乖完成签到,获得积分10
47秒前
51秒前
可乐完成签到,获得积分10
54秒前
xiaoji发布了新的文献求助10
57秒前
asd1576562308完成签到 ,获得积分0
1分钟前
1分钟前
徐志豪完成签到,获得积分10
1分钟前
1分钟前
hwjhwj发布了新的文献求助10
1分钟前
英俊的铭应助过昼采纳,获得10
1分钟前
吕佳林完成签到,获得积分10
1分钟前
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
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
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 7297244
求助须知:如何正确求助?哪些是违规求助? 8915733
关于积分的说明 18878838
捐赠科研通 6962988
什么是DOI,文献DOI怎么找? 3210516
关于科研通互助平台的介绍 2379855
邀请新用户注册赠送积分活动 2186984