Heterogeneous N-coordinated single-atom photocatalysts and electrocatalysts

电催化剂 光催化 催化作用 纳米技术 材料科学 Atom(片上系统) 化学 物理化学 计算机科学 电化学 电极 有机化学 嵌入式系统
作者
Rongchen Shen,Lei Hao,Yun Hau Ng,Peng Zhang,Arramel Arramel,Youji Li,Xin Li
出处
期刊:Chinese Journal of Catalysis [Elsevier BV]
卷期号:43 (10): 2453-2483 被引量:50
标识
DOI:10.1016/s1872-2067(22)64104-4
摘要

Single-atom catalysts (SACs) have been widely used in heterogeneous catalysis owing to the maximum utilization of metal-active sites with controlled structures and well-defined locations. Upon tailored coordination with nitrogen atom, the metal-nitrogen (M-N)-based SACs have demonstrated interesting physical, optical and electronic properties and have become intense in photocatalysis and electrocatalysis in the past decade. Despite substantial efforts in constructing various M–N-based SACs, the principles for modulating the intrinsic photocatalytic and electrocatalytic performance of their active sites and catalytic mechanism have not been sufficiently studied. Herein, the present review intends to shed some light on recent research made in studying the correlation between intrinsic electronic structure, catalytic mechanism, single-metal atom (SMA) confinement and their photocatalytic and electrocatalytic activities (conversion, selectivity, stability and etc). Based on the analysis of fundamentals of M–N-based SACs, theoretical calculations and experimental investigations, including synthetic methods and characterization techniques, are both included to provide an integral understanding of the underlying mechanisms behind improved coordination structure and observed activity. Finally, the challenges and perspectives for constructing highly active M–N based photocatalysis and electrocatalysis SACs are provided. In particular, extensive technical and mechanism aspects are thoroughly discussed, summarized and analyzed for promoting further advancement of M-N-based SACs in photocatalysis and electrocatalysis.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
SYLH应助无私诗云采纳,获得10
刚刚
1秒前
慕容博完成签到 ,获得积分0
2秒前
笑一笑完成签到,获得积分10
2秒前
3秒前
3秒前
3秒前
芳芳完成签到,获得积分10
4秒前
11111发布了新的文献求助10
4秒前
chen.完成签到,获得积分10
5秒前
Dan完成签到 ,获得积分10
5秒前
5秒前
淡定自中完成签到 ,获得积分10
6秒前
亲爱的冯老师完成签到 ,获得积分10
6秒前
tang完成签到,获得积分10
7秒前
与淇完成签到,获得积分10
7秒前
伊萨卡完成签到 ,获得积分10
7秒前
Khr1stINK完成签到,获得积分10
8秒前
酷波er应助qcl采纳,获得10
8秒前
1111111完成签到,获得积分10
8秒前
胖九完成签到,获得积分10
8秒前
烟花应助淡然鸡翅采纳,获得10
8秒前
逍遥自在发布了新的文献求助10
9秒前
luke17743508621完成签到 ,获得积分10
9秒前
麦客发布了新的文献求助10
9秒前
林深完成签到,获得积分10
9秒前
柠檬柚子晴完成签到,获得积分10
10秒前
总之发布了新的文献求助10
10秒前
77完成签到 ,获得积分10
10秒前
无私诗云完成签到,获得积分10
10秒前
fussguai完成签到,获得积分10
10秒前
11秒前
海蓝鲸完成签到 ,获得积分10
12秒前
杨小羊完成签到,获得积分10
12秒前
fujun完成签到,获得积分10
13秒前
GSY完成签到,获得积分20
13秒前
邱航完成签到,获得积分10
13秒前
ee完成签到,获得积分10
13秒前
怪兽小泥巴完成签到,获得积分10
14秒前
老实皮皮虾完成签到,获得积分10
15秒前
高分求助中
【提示信息,请勿应助】关于scihub 10000
The Mother of All Tableaux: Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 3000
Social Research Methods (4th Edition) by Maggie Walter (2019) 2390
A new approach to the extrapolation of accelerated life test data 1000
北师大毕业论文 基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 390
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
Robot-supported joining of reinforcement textiles with one-sided sewing heads 360
热门求助领域 (近24小时)
化学 材料科学 医学 生物 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 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4009004
求助须知:如何正确求助?哪些是违规求助? 3548719
关于积分的说明 11299835
捐赠科研通 3283284
什么是DOI,文献DOI怎么找? 1810333
邀请新用户注册赠送积分活动 886115
科研通“疑难数据库(出版商)”最低求助积分说明 811259