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Single-atom catalysts show excellent catalytic performance because of their coordination environments and electronic configurations. However, controllable regulation of single-atom permutations still faces challenges. Herein, we demonstrate that a polarization electric field regulates single atom permutations and forms periodic one-dimensional Au single-atom arrays on ferroelectric BiTiO nanosheets. The Au single-atom arrays greatly lower the Gibbs free energy for CO conversion via Au-O=C=O-Au dual-site adsorption compared to that for Au-O=C=O single-site adsorption on Au isolated single atoms. Additionally, the Au single-atom arrays suppress the depolarization of BiTiO, so it maintains a stronger driving force for separation and transfer of photogenerated charges. Thus, BiTiO with Au single-atom arrays exhibit an efficient CO production rate of 34.15 µmol·g·h, ∼18 times higher than that of pristine BiTiO. More importantly, the polarization electric field proves to be a general tactic for the syntheses of one-dimensional Pt, Ag, Fe, Co and Ni single-atom arrays on the BiTiO surface.
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http://dx.doi.org/10.1038/s41467-023-44493-4 | DOI Listing |
Anal 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 PDFAnal Chem
September 2025
Department of Chemistry, Capital Normal University, Beijing 100048, China.
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 PDFAdv Mater
August 2025
Key Laboratory of Chemical Additives for China National Light Industry, College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.
Achieving efficient photothermal evaporation requires a synergistic integration of thermal management, water transport dynamics, and light trapping-key elements often challenging to harmonize. Herein, A high-entropy single-atomic metal doped porous carbon (HESA) with ultra-low metal content of 1.77 wt.
View Article and Find Full Text PDFNano Lett
July 2025
State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry, Fuzhou University, Fuzhou 350116, China.
Single-atom alloys (SAAs) are promising catalysts due to their unique electronic/geometric structures and high atomic efficiency, yet precise control of guest metal atoms and host nanoparticle dispersion remains challenging. This study develops a facile ion exchange-pyrolysis strategy to synthesize ultrafine NiRu SAA nanoparticles confined in porous carbon (NiRu/C) nanosheet arrays. Advanced characterization confirms isolated Ru atoms anchored on Ni nanoparticles with electron transfer from Ni to Ru, achieving uniform dispersion in ultrathin carbon.
View Article and Find Full Text PDFJ Phys Chem Lett
July 2025
School of Chemical Sciences, The University of Auckland, Auckland 1142, New Zealand.
Metal dual-atom nanozymes (DAzymes) with two sites commonly offer more advantages over single-atom nanozymes (SAzymes) in terms of electronic structure modification and synergy. However, the design of DAzymes remains challenging. Herein, we present a novel ion-imprinting strategy for preparing an axially coordinated Fe-Fe DAzyme (CNBFe-3-800) with an unreported configuration of FeNB active sites on a N,B-doped carbon support.
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