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Metal atoms dispersed on the oxide supports constitute a large category of single-atom catalysts. In this review, oxide supported single-atom catalysts are discussed about their synthetic procedures, characterizations, and reaction mechanism in thermocatalysis, such as water-gas shift reaction, selective oxidation/hydrogenation, and coupling reactions. Some typical oxide materials, including ferric oxide, cerium oxide, titanium dioxide, aluminum oxide, and so on, are intentionally mentioned for the unique roles as supports in anchoring metal atoms and taking part in the catalytic reactions. The interactions between metal atoms and oxide supports are summarized to give a picture on how to stabilize the atomic metal centers, and rationally tune the geometric structures and electronic states of single atoms. Furthermore, several directions in fabricating single-atom catalysts with improved performance are proposed on the basis of state-of-the-art understanding in metal-oxide interactions.
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http://dx.doi.org/10.1021/acs.chemrev.0c00797 | DOI Listing |
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 PDFACS Appl Mater Interfaces
September 2025
Leibniz-Institut für Katalyse e.V. (LIKAT), Albert-Einstein-Str. 29a, Rostock 18059, Germany.
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 PDFAngew 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 PDFJ Colloid Interface Sci
September 2025
School of Material Electronics and Energy Storage, Zhongyuan University of Technology, Zhengzhou 450007, China. Electronic address:
Developing single-atom catalysts (SACs) with dense active sites and universal synthesis strategies remains a critical challenge. Herein, we present a scalable and universal strategy to synthesize high-density transition metal single-atom sites, anchored in nitrogen-doped porous carbon (M-SA@NC, M = Fe, Co, Ni) and investigate their oxygen reduction reaction (ORR) catalytic activity for flexible Zn-air batteries (ZABs). Using a facile coordination-pyrolysis strategy, atomically dispersed M-N sites with high metal loading are achieved.
View Article and Find Full Text PDFAnal Chem
September 2025
Anhui Key Laboratory of Biomedical Materials and Chemical Measurement, Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Key Laboratory of Molecule-Based Materials, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, P.R. China.
Current colorimetric sensing arrays for antioxidant detection often struggle with discrimination due to cross-reactive signals from individual nanozymes. These signals are typically modulated by external factors such as pH or chromogenic substrates, offering limited kinetic and mechanistic diversity. To overcome this, we present a novel triple-channel colorimetric sensing array utilizing two distinct single-atom nanozymes (Cu SA and Fe SA) and one dual-atom nanozyme (CuFe DA).
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