Low-valence platinum single atoms in sulfur-containing covalent organic frameworks for photocatalytic hydrogen evolution

This study focuses on optimizing catalytic activity in photocatalytic hydrogen evolution reaction by precisely designing and modulating the electronic structure of metal single atoms. The catalyst, denoted as PtSA@S-TFPT, integrates low-valence platinum single atoms into sulfur-containing covalent organic frameworks. The robust asymmetric four-coordination between sulfur and platinum within the framework enables a high platinum loading of 12.1 wt%, resulting in efficient photocatalytic hydrogen production activity of 11.4 mmol g<sup>-1</sup> h<sup>-1</sup> and stable performance under visible light. These outcomes are attributed to a reduced hydrogen desorption barrier and enhanced photogenerated charge separation, as indicated by density functional theory calculations and dynamic carrier analysis. This work challenges traditional notions and opens an avenue for developing low-valence metal single atom-loaded covalent organic framework catalysts to advance photocatalytic hydrogen evolution.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2024-12-03
DOI
https://doi.org/10.1038/s41467-024-54959-8
Citations
66
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
6.76

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Low-valence platinum single atoms in sulfur-containing covalent organic frameworks for photocatalytic hydrogen evolution

Yongwu Peng, Guinan Chen, Chengtao Gong, Guodong Xu et al.
66 citations
Nature Communications
Advanced Photocatalysis Techniques
6.76
article

Low-valence platinum single atoms in sulfur-containing covalent organic frameworks for photocatalytic hydrogen evolution

Yongwu Peng, Guinan Chen, Chengtao Gong, Guodong Xu, Zhihao Xing, Jiahao Li, Yifei Zhang, Gao Li, Liangjun Chen
article en
66 citations

Abstract

This study focuses on optimizing catalytic activity in photocatalytic hydrogen evolution reaction by precisely designing and modulating the electronic structure of metal single atoms. The catalyst, denoted as PtSA@S-TFPT, integrates low-valence platinum single atoms into sulfur-containing covalent organic frameworks. The robust asymmetric four-coordination between sulfur and platinum within the framework enables a high platinum loading of 12.1 wt%, resulting in efficient photocatalytic hydrogen production activity of 11.4 mmol g<sup>-1</sup> h<sup>-1</sup> and stable performance under visible light. These outcomes are attributed to a reduced hydrogen desorption barrier and enhanced photogenerated charge separation, as indicated by density functional theory calculations and dynamic carrier analysis. This work challenges traditional notions and opens an avenue for developing low-valence metal single atom-loaded covalent organic framework catalysts to advance photocatalytic hydrogen evolution.

Nature CommunicationsVol. 15(1)
Dalian Institute of Chemical Physics (CN), Shenyang Normal University (CN), Yancheng Teachers University (CN), Zhejiang University of Technology (CN)
Salt Science Research Foundation, National Natural Science Foundation of China, Zhejiang University, Zhejiang University of Technology
Openalex Percentile: Top 2%
Advanced Photocatalysis Techniques
6.76
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.