In Situ Activation of Amorphous NiFeMo Oxide Cocatalyst To Improve the Photoelectrochemical Water Splitting Performance of BiVO4
Source abstract
Abstract
Amorphous NiFeMo oxides (a-NiFeMo) synthesized via a simple supersaturated coprecipitation method are explored as a cocatalyst to improve the photoelectrochemical water splitting performance of BiVO4. The performance of the composite photoelectrode is found to be further enhanced through a cyclic-voltammetry-related in situ activation process, and a photocurrent of 5.0 mA/cm2 is achieved at 1.23 VRHE with improved photoelectrochemical stability. X-ray photoelectron spectroscopy (XPS), Raman, and electron spin resonance (ESR) characterization results indicate that the surface-loaded a-NiFeMo cocatalyst undergoes a rapid surface reconstruction during the in situ activation process, which results in an incorporation of phosphate ions in the surface-loaded a-NiFeMo, along with an increased oxidation state of Ni ions and enriched oxygen vacancies. These combined effects lead to an improved oxygen evolution reaction performance and finally result in a reduced charge-transfer resistance at the solid/liquid interface, causing the interfacial charge-injection efficiency to be enormously enhanced from the original 25.1% in pure BiVO4 to 83.3% in BiVO4/a-NiFeMo after being in situ activated. Our result indicates that the rapid surface-reconstruction phenomenon shown in the amorphous materials may provide a promising strategy for designing a highly efficient cocatalyst for photoelectrodes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, College of New Energy and Materials, China University of Petroleum Beijing, No. 18 Fuxue Road, Beijing 102249, P. R. China
Research Center of New Energy, Research Institute of Petroleum Exploration & Development, PetroChina, No. 20 Xueyuan Road, Beijing 100083, P. R. China
Funding
National Natural Science Foundation of China · Science Foundation of China University of Petroleum, Beijing
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