98%
921
2 minutes
20
Electron spin at metal sites plays a critical role in surface/interface reaction activity. Herein, a series of metal (Fe, Co, Ni, Pd, Pt, Cu, Ag, and Au) single-atom catalysts as activity center and CO as a probe molecule, to systematically investigate the role of spin electrons by calculations of structure stability, orbital energy level, and electron transfer. Fe and Pt single-atom structures are most stable in low-spin states, while others are stable in high-spin states. The bond energy of CO influenced by spin state demonstrates the same trend, and the splitting degree of d-σ interaction determines the strength of bond energy. Furthermore, it is found that there is a quasi-linear relationship between frequency shift and bond length of adsorbed CO. This work offers an example of how spin electrons influence orbital interaction of molecular adsorption and helps to understand the role of electron spin at metal sites in reaction.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/cphc.202500516 | DOI Listing |
ACS 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).
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
School of Environmental Science and Engineering, Tianjin University/Tianjin Key Lab of Biomass/Wastes Utilization, Tianjin 300072, P.R. China.
Volatile organic compounds (VOCs) significantly impact air quality as photochemical smog precursors and health hazards. Catalytic oxidation is a leading VOC abatement method but suffers from catalyst deactivation due to metal sintering and competitive adsorption in complex mixtures. Strong metal-support interactions (SMSIs) provide atomic level control of interfacial electronic and geometric structures.
View Article and Find Full Text PDF