General synthesis and definitive structural identification of MN4C4 single-atom catalysts with tunable electrocatalytic activities

催化作用 合理设计 石墨烯 电化学 过渡金属 部分 组合化学 材料科学 纳米技术 密度泛函理论 Atom(片上系统) 化学 计算机科学 无机化学 计算化学 物理化学 嵌入式系统 有机化学 电极 立体化学
作者
Huilong Fei,Juncai Dong,Yexin Feng,Christopher S. Allen,Chengzhang Wan,Boris Volosskiy,Mufan Li,Zipeng Zhao,Yiliu Wang,Hongtao Sun,Pengfei An,Wenxing Chen,Zhiying Guo,Chain Lee,Dongliang Chen,Imran Shakir,Mingjie Liu,Tiandou Hu,Yadong Li,Angus I. Kirkland
出处
期刊:Nature Catalysis [Springer Nature]
卷期号:1 (1): 63-72 被引量:1908
标识
DOI:10.1038/s41929-017-0008-y
摘要

Single-atom catalysts (SACs) have recently attracted broad research interest as they combine the merits of both homogeneous and heterogeneous catalysts. Rational design and synthesis of SACs are of immense significance but have so far been plagued by the lack of a definitive correlation between structure and catalytic properties. Here, we report a general approach to a series of monodispersed atomic transition metals (for example, Fe, Co, Ni) embedded in nitrogen-doped graphene with a common MN4C4 moiety, identified by systematic X-ray absorption fine structure analyses and direct transmission electron microscopy imaging. The unambiguous structure determination allows density functional theoretical prediction of MN4C4 moieties as efficient oxygen evolution catalysts with activities following the trend Ni > Co > Fe, which is confirmed by electrochemical measurements. Determination of atomistic structure and its correlation with catalytic properties represents a critical step towards the rational design and synthesis of precious or nonprecious SACs with exceptional atom utilization efficiency and catalytic activities. Atomically dispersed metal catalysts are of increasing importance in many catalytic processes, but clear structural identification is challenging. Here, a general synthesis of metal (nickel, iron and cobalt) single-atom catalysts on nitrogen-doped graphene allows the authors to identify a common structure and furthermore correlate structure with electrocatalytic activity.
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
所所应助Claudia采纳,获得10
刚刚
桐桐应助文文娴采纳,获得10
刚刚
天天快乐应助zxy采纳,获得10
刚刚
濮阳灵竹完成签到,获得积分10
1秒前
聪明勇敢幸运虾完成签到,获得积分10
1秒前
1秒前
大力的灵雁应助XiaoYU采纳,获得10
2秒前
MaoXinLei发布了新的文献求助10
2秒前
领导范儿应助LioXH采纳,获得10
2秒前
上官若男应助Lin采纳,获得10
4秒前
5秒前
重要涔雨完成签到,获得积分10
5秒前
桐桐应助随便采纳,获得10
5秒前
脑洞疼应助西西采纳,获得10
6秒前
丘比特应助稳重盼夏采纳,获得10
6秒前
香蕉觅云应助科研通管家采纳,获得10
6秒前
6秒前
6秒前
Orange应助科研通管家采纳,获得10
6秒前
6秒前
乐乐应助科研通管家采纳,获得10
6秒前
Hello应助科研通管家采纳,获得10
6秒前
在水一方应助科研通管家采纳,获得10
6秒前
liao应助科研通管家采纳,获得10
7秒前
搜集达人应助hanyy采纳,获得10
7秒前
科目三应助科研通管家采纳,获得10
7秒前
小二郎应助科研通管家采纳,获得10
7秒前
Ava应助科研通管家采纳,获得10
7秒前
7秒前
充电宝应助科研通管家采纳,获得10
7秒前
wanci应助科研通管家采纳,获得10
7秒前
liao应助科研通管家采纳,获得10
7秒前
机灵柚子应助科研通管家采纳,获得20
7秒前
小蘑菇应助科研通管家采纳,获得30
7秒前
CipherSage应助科研通管家采纳,获得10
7秒前
7秒前
Lucas应助科研通管家采纳,获得10
7秒前
琉璃草梦给琉璃草梦的求助进行了留言
9秒前
居居侠完成签到 ,获得积分10
10秒前
顾矜应助叽里咕噜采纳,获得10
10秒前
高分求助中
(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
Aerospace Standards Index - 2026 ASIN2026 3000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Social Work and Social Welfare: An Invitation(7th Edition) 410
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6049477
求助须知:如何正确求助?哪些是违规求助? 7838056
关于积分的说明 16263564
捐赠科研通 5194963
什么是DOI,文献DOI怎么找? 2779669
邀请新用户注册赠送积分活动 1762873
关于科研通互助平台的介绍 1644874