Loading…

A molecular view of single-atom catalysis toward carbon dioxide conversion

Carbon dioxide (CO 2 ) conversion has attracted much interest recently owing to its importance in both scientific research and practical applications, but still faces a bottleneck in selectivity control and mechanism understanding owing to diversified active sites. Single-atom catalysts (SACs) featu...

Full description

Saved in:
Bibliographic Details
Published in:Chemical science (Cambridge) 2024-03, Vol.15 (13), p.4631-478
Main Authors: Shang, Xin, Yang, Xiaofeng, Liu, Guodong, Zhang, Tianyu, Su, Xiong
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Carbon dioxide (CO 2 ) conversion has attracted much interest recently owing to its importance in both scientific research and practical applications, but still faces a bottleneck in selectivity control and mechanism understanding owing to diversified active sites. Single-atom catalysts (SACs) featuring isolated and well-defined active centers are proved to not only exhibit unparalleled performances in various processes of CO 2 conversion but also provide excellent research paradigms by circumventing the heterogeneity of active sites. Herein, we will not only critically review recent progress on the application of SACs in chemical CO 2 conversion based on previous comprehension of general thermodynamics and kinetics, but also try to offer a multi-level understanding of SACs from a molecular point of view in terms of the central atom, coordination environment, support effect and synergy with other active centers. Meanwhile, crucial scientific issues of research methods will be also identified and highlighted, followed by a future outlook that is expected to present potential aspects of further developments. We present critical advances in single-atom catalysis toward CO 2 transformation and address crucial issues about SACs from a molecular point of view.
ISSN:2041-6520
2041-6539
DOI:10.1039/d3sc06863c