The photoexcitation of plasmonic nanoparticles has been shown to drive multistep, multicarrier transformations, such as the conversion of CO into hydrocarbons. But for such plasmon-driven chemistry to be precisely understood and modeled, the critical photoinitiation step in the reaction cascade must be identified. We meet this goal by measuring H/D and C/ C kinetic isotope effects (KIEs) in plasmonic photosynthesis. In particular, we found that the substitution of H O with D O slows hydrocarbon production by a factor of 5-8. This primary H/D KIE leads to the inference that hole-driven scission of the O-H bond in H O is a critical, limiting step in plasmonic photosynthesis. This study advances mechanistic understanding of light-driven chemical reactions on plasmonic nanoparticles.
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http://dx.doi.org/10.1002/anie.202011805 | DOI Listing |
Nanophotonics
February 2024
School of Engineering, College of Engineering and Computer Science, Australian National University, Canberra, ACT 2601, Australia.
J Colloid Interface Sci
February 2025
School of Chemistry and Chemical Engineering, North Minzu University, Yinchuan 750021, PR China; Ningxia Key Laboratory of Solar Chemical Conversion Technology, North Minzu University, Yinchuan 750021, PR China; Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China. Electronic address:
Although traditional type II heterojunction designs for artificial photosynthesis show promise for photocatalytic hydrogen production, their redox capacity is somewhat limited due to the spatial separation of hydrogen evolution and oxidation reactions at less favorable sites. To overcome this limitation, ohmic junctions based on type II heterojunctions have been designed to enhance hydrogen evolution by transferring electrons to the metal component. In this study, a copper powder graphdiyne (Cu-GDY) composite catalyst with ohmic angle contact was synthesized by coupling copper foil with hexa-hexylbenzene.
View Article and Find Full Text PDFChemistry
January 2025
Université Paris-Saclay, UMR 8000 CNRS, Institut de Chimie Physique, 91405, Orsay, France.
Anal Chem
November 2024
Shenzhen Key Laboratory of Precision Measurement and Early Warning Technology for Urban Environmental Health Risks, School of Environmental Science and Engineering, Southern University of Science and Technology, Shenzhen 518055, China.
Despite its excellent efficiency in natural photosynthesis, the utilization of photosystem II (PSII)-based artificial photoelectrochemical (PEC) systems for analytical purposes is hindered due to the low enzyme loading density and ineffective electron transfer (ET) processes. Here, we present a straightforward and effective approach to prepare a PSII-based biohybrid photoanode with remarkable photoresponse, enabled by the use of a hierarchically structured inverse-opal tin oxide (IO-SnO) electrode combined with gold nanoparticles (Au NPs). The porous, carbon-containing IO-SnO structure allows for a high density and photoactivity loading of PSII complexes, while also providing strong electrical coupling between the protein film and the electrode.
View Article and Find Full Text PDFACS Nanosci Au
October 2024
Interdisciplinary Program Climate Studies, Indian Institute of Technology Bombay, Mumbai, Maharashtra 400076, India.
Significant endeavors have been dedicated to the advancement of materials for artificial photosynthesis, aimed at efficiently harvesting light and catalyzing reactions such as hydrogen production and CO conversion. The application of plasmonic nanomaterials emerges as a promising option for this purpose, owing to their excellent light absorption properties and ability to confine solar energy at the nanoscale. In this regard, coupling plasmonic particles with molecular catalysts offers a pathway to create high-performance hybrid catalysts.
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