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Constructing heterojunction photocatalysts with optimized architecture and components is an effective strategy for enhancing CO photoreduction by promoting photogenerated carrier separation, visible light absorption, and CO adsorption. Herein, defect-rich photocatalysts (NiP@Ce-BDC-CeO HOOs) with S-scheme heterojunction and hollowed-out octahedral architecture are prepared by decomposing Ce-BDC octahedrons embedded with NiP nanoparticles and subsequent lactic acid etching for CO photoreduction. The hollowed-out octahedral architecture with multistage pores (micropores, mesopores, and macropores) and oxygen vacancy defects are simultaneously produced during the preparation process. The S-scheme heterojunction boosts the quick transfer and separation of photoinduced charges. The formed hollowed-out multi-stage pore structure is favorable for the adsorption and diffusion of CO molecules and gaseous products. As expected, the optimized photocatalyst exhibits excellent performance, producing CO with a yield of 61.6 µmol h g, which is four times higher than that of the original Ce-BDC octahedrons. The X-ray photoelectron spectroscopy, scanning Kelvin probe, and electron spin resonance spectroscopy characterizations confirm the S-schematic charge-transfer route. The key intermediate species during the CO photoreduction process are detected by in situ Fourier transform infrared spectroscopy to support the proposed mechanism for CO photoreduction. This work presents a synthetic strategy for excellent catalysts with potential prospects in photocatalytic applications.
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http://dx.doi.org/10.1002/smll.202406487 | DOI Listing |
Int J Biol Macromol
September 2025
Department of Chemical Engineering, Faculty of Engineering, University of Isfahan, Isfahan, Iran.
The persistent presence of Metronidazole (MTZ), a commonly used antibiotic, in water bodies is a serious environmental and health concern because of its genotoxic and carcinogenic potential. Here, we report an effective visible-light photocatalyst system comprising an S-scheme glycine-modified TiO/FeO heterojunction immobilized on chitosan-polyacrylonitrile nanofibers. The photocatalyst nanocomposite was synthesized through a sol-gel and ultrasonication process coupled with electrospinning-assisted immobilization.
View Article and Find Full Text PDFChem Sci
August 2025
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Materials Science, Zhejiang Normal University Jinhua Zhejiang 321004 P. R. China
Selective photoreduction of CO with HO to hydrocarbons is challenged by inadequate and uncontrollable electron and proton feeding. Herein, this limitation is overcome by integrating HO dissociation, CO reduction, and O evolution catalysts into a dual S-scheme heterojunction and regulating exposed facets of the heterojunction supports. In this design, H and OH species generated by HO dissociation on the NH-MIL-125 support transfer to the T-COF shell and FeO insert for CO reduction and O evolution, respectively.
View Article and Find Full Text PDFLangmuir
September 2025
School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, China.
A simple solvothermal method was used in this paper. ZnCoS (ZCS) nanoparticles were smoothly synthesized by this method and loaded on the external surface of MnCd0S (MCS) to form an S-scheme heterojunction. A comparative evaluation was performed with two other single catalysts, and the compound catalyst MCS/ZCS achieved great gain in the process of catalytic action of H generated under sunlight.
View Article and Find Full Text PDFAdv Mater
September 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, 68 Jincheng St., Wuhan, 430078, P. R. China.
Photocatalysis enabled by step-scheme (S-scheme) heterojunction has emerged as a promising strategy for addressing the global energy crisis and achieving carbon neutrality. However, mechanisms regulating the interfacial charge transfer dynamics of S-scheme heterojunctions remain elusive. Herein, the electron transfer mechanisms are elucidated for a model S-scheme heterojunction composed of cadmium sulfide and a covalent organic framework material using synchrotron-based in situ soft X-ray absorption spectroscopy, substantiating the well-established in situ irradiated X-ray photoelectron spectroscopy.
View Article and Find Full Text PDFNanomicro Lett
September 2025
School of Microelectronics, Northwestern Polytechnical University, Xi'an, 710129, People's Republic of China.
Metal halide perovskites (MHPs) with striking electrical and optical properties have appeared at the forefront of semiconductor materials for photocatalytic redox reactions but still suffer from some intrinsic drawbacks such as inferior stability, severe charge-carrier recombination, and limited active sites. Heterojunctions have recently been widely constructed to improve light absorption, passivate surface for enhanced stability, and promote charge-carrier dynamics of MHPs. However, little attention has been paid to the review of MHPs-based heterojunctions for photocatalytic redox reactions.
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