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Solar-driven photocatalytic reactions offer a promising route to clean and sustainable energy, and the spatial separation of photogenerated charges on the photocatalyst surface is the key to determining photocatalytic efficiency. However, probing the charge-separation properties of photocatalysts is a formidable challenge because of the spatially heterogeneous microstructures, complicated charge-separation mechanisms and lack of sensitivity for detecting the low density of separated photogenerated charges. Recently, we developed surface photovoltage microscopy (SPVM) with high spatial and energy resolution that enables the direct mapping of surface-charge distributions and quantitative assessment of the charge-separation properties of photocatalysts at the nanoscale, potentially providing unprecedented insights into photocatalytic charge-separation processes. Here, this protocol presents detailed procedures that enable researchers to construct the SPVM instruments by integrating Kelvin probe force microscopy with an illumination system and the modulated surface photovoltage (SPV) approach. It then describes in detail how to perform SPVM measurements on actual photocatalyst particles, including sample preparation, tuning of the microscope, adjustment of the illuminated light path, acquisition of SPVM images and measurements of spatially resolved modulated SPV signals. Moreover, the protocol also includes sophisticated data analysis that can guide non-experts in understanding the microscopic charge-separation mechanisms. The measurements are ordinarily performed on photocatalysts with a conducting substrate in gases or vacuum and can be completed in 15 h.
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http://dx.doi.org/10.1038/s41596-024-00992-2 | DOI Listing |
Chem
July 2025
Department of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
The selective reduction of to formate using molecular catalysts immobilized on high surface area porous silicon is described. Manganese complexes of the form (bpy)Mn(CO)Br (bpy = 2,2'-bipyridine) were prepared with silatrane groups on the bpy ligand for attachment to oxide-coated porous silicon (SiO-porSi). SiO-porSi wafers were formed by heating hydrogen-terminated p-type porous silicon wafers under air and the manganese complexes were immobilized on SiO-porSi by heating at 80 °C.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
School of Chemistry and Chemical Engineering, Yangzhou University, 180 Siwangting Road, Yangzhou 225002, People's Republic of China.
Surface state modulation has emerged as a promising strategy to reduce rapid carrier recombination in photocatalytic reactions. However, surface states can paradoxically serve as indirect recombination centers due to sluggish interfacial reaction kinetics. Herein, the charge separation function of Ni-mediated surface states is reactivated Z-scheme charge transfer engineering in FeO/CuO heterojunctions, where the surface states spontaneously accumulate photoinduced electrons for efficient photocatalytic hydrogen production.
View Article and Find Full Text PDFAdv Mater
August 2025
School of Physics and Electronic Science, East China Normal University, Shanghai, 200241, China.
Perovskite solar cells (PSCs) suffer from severe nonradiative recombination-induced photovoltage loss, limiting the device overall performance. To address this key issue, an efficient strategy via a dual-site anchoring bridge is developed to engineer the heterointerface between perovskite and PCBM electron transport layer. The resulting reinforced and homogeneous passivation by forming strong dual-site P─O─Pb covalent bonds, effectively decreases perovskite surface defect density.
View Article and Find Full Text PDFChemSusChem
August 2025
School of Chemistry and Chemical Engineering, Yangzhou University, 180 Si-Wang-Ting Road, Yangzhou, 225002, P. R. China.
In recent years, p-type CuFeO delafossite has attracted considerable interest as a cost-effective H evolution photocatalyst. However, the intrinsic alternating CuO/FeO layered architecture creates a high energy barrier for interlayer charge transfer, which causes rapid bulk recombination of photogenerated electron-hole pairs, severely limiting their photocatalytic reactivity. In this study, CuFeO nanosheets are designed with electron-rich Co sites, which induced enhancement of dipole moment and thereby built-in electric field driving charge separation efficiently.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States.
Interfacial charge transfer at electrocatalyst/semiconductor (EC/SC) junctions is central to the performance of photo(electro)catalysts, yet the influence of the reactive environment on these processes remains poorly understood. This is particularly the case for unburied EC/SC junctions, such as EC nanoparticles anchored on a SC (np-EC/SC), where reacting molecules readily access the EC surface sites and the np-EC/SC interfaces. Herein, we uncover a dynamic, chemically driven mechanism by which the local reaction environment modulates charge transfer at Pt/p-Si interfaces under solar water splitting conditions.
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