Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

In recent years, single-atom catalysts (SACs) with separated active centers and high atom utilization have grown significantly as a significant area of catalytic research. In catalytic applications, SACs of various kinds have demonstrated exceptional performance, so the study of the catalytic mechanism of SACs provides a clearer direction for the preparation of catalysts with high performance. Strong linkages between the single atoms and the support are necessary to overcome the tendency of single atoms to aggregate into clusters, which is called metal-support interaction (MSI). MSI affects not only the stability of individual atoms, but also the nature of the binding site and applicable reactions. Therefore, investigating the connection between MSI and the catalytic mechanism is crucial. This work describes the latest developments in the means of MSI and activity modulation in single-atom catalysis. First, the synthesis strategies of SACs are presented, including ALD, co-deposition, impregnation, and so on. Second, the catalytic mechanisms realized by using MSI in the loading of SACs with different types of supports are highlighted. Third, the strategies for the modulation of single-atom catalytic activity are discussed, including heterojunction strategy, ligand environment strategy, and dual-single-atom strategy. Finally, possible directions for future development in single-atom catalysis are suggested.

Download full-text PDF

Source
http://dx.doi.org/10.1002/smll.202410976DOI Listing

Publication Analysis

Top Keywords

single-atom catalysis
12
metal-support interaction
8
catalytic mechanism
8
single atoms
8
modulation single-atom
8
catalytic
6
single-atom
5
sacs
5
msi
5
regulation metal-support
4

Similar Publications

Engineering Brønsted Acidic Microenvironments via Strong Metal-Support Interaction in Single-Atom Pd/CeO for Acid-Free Acetalization Catalysis.

Inorg Chem

September 2025

College of Chemistry and Materials Science, The key Laboratory of Functional Molecular Solids, Ministry of Education, The Key Laboratory of Electrochemical Clean Energy of Anhui Higher Education Institutes, Anhui Provincial Engineering Laboratory for New-Energy Vehicle Battery Energy-Storage Materia

Conventional acid-catalyzed acetalization faces significant challenges in catalyst recovery and poses environmental concerns. Herein, we develop a CeO-supported Pd single-atom catalyst (Pd/CeO) that eliminates the reliance on liquid acids by creating a localized H-rich microenvironment through heterolytic H activation. X-ray absorption near-edge structure and extended X-ray absorption fine structure analyses confirm the atomic dispersion of Pd via Pd-O-Ce coordination, while density functional theory (DFT) calculations reveal strong metal-support interactions (SMSI) that facilitate electron transfer from CeO oxygen to Pd, downshifting the Pd d-band center and optimizing H activation.

View Article and Find Full Text PDF

Metal-organic frameworks (MOFs) are transformative platforms for heterogeneous catalysis, but distinguishing atomically dispersed metal sites from subnanometric clusters remains a major challenge. This often demands the integration of multiple characterization techniques, many of which either lack the resolving power to distinguish active sites from their surrounding environments (e.g.

View Article and Find Full Text PDF

Electronic Structure Reconfiguration of Zn-NB Sites for Enhanced Fenton-Like Catalysis.

Angew Chem Int Ed Engl

September 2025

College of Environmental Science and Engineering, Yangzhou University, Yangzhou, 225000, P.R. China.

Despite growing interest in single-atom catalysts (SACs) for Fenton-like reactions, zinc (Zn)-based SACs remain unexplored due to the inherent inertness of Zn, whose fully occupied 3d electronic configuration limits redox activity. Here, we overcome this limitation by introducing boron (B) atoms to reconfigure the electronic structure of Zn-N coordination sites, yielding an activated catalyst denoted as Zn-NBC. This electronic modulation transforms inert Zn-N sites into catalytically active centers (Zn-NB ), enabling significantly enhanced Fenton-like activity.

View Article and Find Full Text PDF

Selective Catalysis-Mediated Interface to Stabilize Antimony Atom-Cluster Anode for Robust Potassium-Ion Batteries.

Angew Chem Int Ed Engl

September 2025

State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, School of Physics and Electronics, Hunan Key Laboratory of Two-Dimensional Materials, Chongqing Research Institute, Hunan University, Changsha, 410082, P.R. China.

Controlling the electrode-electrolyte interfacial behavior is crucial for achieving a high-quality solid electrolyte interphase (SEI) and ensuring sustainable battery performance. Here, we propose a selective catalysis strategy to stabilize antimony atom-cluster (Sb) anode/electrolyte interface for robust potassium-ion batteries (PIBs). Specifically, the electrode featuring Sb in porous carbon (Sb/PC) as "electrocatalyst" unduly catalyzes the reduction of the dimethyl ether-based electrolyte, resulting in loose SEI layer and rapid capacity decay.

View Article and Find Full Text PDF

Single-atom nanozymes have made important progress in the field of sensors, but their catalytic performance as natural enzyme substitutes is far from satisfactory. We describe here a FeFe dual single-atom nanozyme (FeNCN) with a Fe loading of 0.89 wt %, and it shows a synergistic effect and a peroxidase (POD)-like activity.

View Article and Find Full Text PDF