Solar-to-hydrogen conversion by water splitting in photoelectrochemical cells (PECs) is a promising approach to alleviate problems associated with intermittency in solar energy supply and demand. Several interfacial resistances in photoelectrodes limit the performance of such cells, while the properties of interfaces are not easy to analyze in situ. We applied photoconductive-AFM to analyze the performance of WO/pn Si photoanodes, containing an ultra-thin metal interface of either Au or Pt. The Au interface consisted of Au nanoparticles with well-ordered interspacing, while Pt was present in the form of a continuous film. Photoconductive-AFM data show that upon illumination significantly larger currents are measured for the WO/pn Si anode equipped with the Au interface, as compared to the WO/pn Si anode with the Pt interface, in agreement with the better performance of the former electrode in a photoelectrochemical cell. The remarkable performance of the Au-containing electrode is proposed to be the result of favorable electron-hole recombination rates induced by the Au nanoparticles in a plasmon resonance excited state.
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http://dx.doi.org/10.1088/1361-6528/aa752f | DOI Listing |
Nanoscale
December 2024
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
Solar fuel production involving the conversion of solar energy directly into chemical fuels such as hydrogen and valuable chemicals using photoelectrochemical (PEC) cells and photocatalysts (PCs) offers a promising avenue for sustainable energy while reducing carbon emissions. However, existing PEC cells and PCs fall short of economic viability due to their low solar-to-chemical (STC) conversion efficiency associated with the employed semiconductors, highlighting the clear need for identifying ideal semiconductor materials. Organic semiconductors (OSs), π-conjugated carbon-based materials, have emerged as promising candidates for enhancing STC conversion efficiency due to their remarkable optoelectrical properties, which can be readily adjustable through molecular engineering.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
December 2024
Department of Physics, Technical University of Denmark, Fysikvej 307, 2800 Kongens Lyngby, Denmark.
Heliyon
October 2024
Institute of Microengineering and Nanoelectronics (IMEN), Universiti Kebangsaan Malaysia (UKM), Bangi, 43600, Selangor, Malaysia.
J Am Chem Soc
December 2024
Institute of Photoelectronic Thin Film Devices and Technology, State Key Laboratory of Photovoltaic Materials and Cells, Tianjin Key Laboratory of Efficient Solar Energy Utilization, Ministry of Education Engineering Research Center of Thin Film Photoelectronic Technology, Nankai University, Tianjin 300350, China.
Chem Sci
December 2024
Shenzhen Key Laboratory of Advanced Thin Films and Applications, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, State Key Laboratory of Radio Frequency Heterogeneous Integration, College of Physics and Optoelectronic Engineering, Shenzhen University Shenzhen 518060 China
Antimony sulfoselenide (Sb(S,Se)) is a promising sunlight absorber material for solar energy conversion in photovoltaic (PV) cells and photoelectrochemical (PEC) photoelectrodes due to its excellent photoelectric properties. However, the obtained thin-film and back contact properties significantly influence the PEC performance of photocathodes, causing severe bulk recombination, carrier transport loss, and deteriorating half-cell solar-to-hydrogen (HC-STH) efficiency. This study introduces an intriguing dual back interface engineering strategy for Sb(S,Se) photocathodes by incorporating an intermediate MoO layer and a secondary carrier transport channel of Au to strengthen charge carrier dynamics.
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