Recent experiments claimed that the catalysis of reaction rates in numerous bond-dissociation reactions occurs the decrease of activation barriers driven by non-equilibrium ("hot") electrons in illuminated plasmonic metal nanoparticles. Thus, these experiments identify plasmon-assisted photocatalysis as a promising path for enhancing the efficiency of various chemical reactions. Here, we argue that what appears to be photocatalysis is much more likely thermo-catalysis, driven by the well-known plasmon-enhanced ability of illuminated metallic nanoparticles to serve as heat sources. Specifically, we point to some of the most important papers in the field, and show that a simple theory of illumination-induced heating can explain the extracted experimental data to remarkable agreement, with minimal to no fit parameters. We further show that any small temperature difference between the photocatalysis experiment and a control experiment performed under external heating is effectively amplified by the exponential sensitivity of the reaction, and is very likely to be interpreted incorrectly as "hot" electron effects.
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http://dx.doi.org/10.1039/c9sc06480j | DOI Listing |
Nanophotonics
February 2024
School of Engineering, College of Engineering and Computer Science, Australian National University, Canberra, ACT 2601, Australia.
ACS Phys Chem Au
March 2024
Department of Chemistry, School of Science, Westlake University, Hangzhou, Zhejiang 310024, China.
Electron transfer (ET) at molecule-metal or molecule-semiconductor interfaces is a fundamental reaction that underlies all electrochemical processes and substrate-mediated surface photochemistry. In this study, we show that ET rates near a metal surface can be significantly manipulated by periodic driving (e.g.
View Article and Find Full Text PDFPhys Chem Chem Phys
April 2024
State Key laboratory of silicate Materials for Architectures, Wuhan University of Technology, Wuhan City, Hubei Province, P. R. China.
Electron transfer and its kinetics play a major role in the photocatalysis of metal/semiconductor systems. Using photoconductances, photoabsorption, and photoinduced spectroscopic techniques, the present research aimed to gain a deep insight into electron transfer pathways and their kinetics for Ag/TiO systems under sub-bandgap light illumination and gaseous conditions. The results revealed that electrons generated in TiO can transfer to Ag nanoparticles at fast rates, and plasmon-generated electrons in Ag nanoparticles can also transfer to TiO.
View Article and Find Full Text PDFACS Nano
September 2023
Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Plasmonic photocatalysis has attracted interest for its potential to generate energy-efficient reactions, but ultrafast internal conversion limits efficient plasmon-based chemistry. Resonance energy transfer (RET) to surface adsorbates offers a way to outcompete internal conversion pathways and also eliminate the need for sacrificial counter-reactions. Herein, we demonstrate RET between methylene blue (MB) and gold nanorods (AuNRs) using single-particle spectroelectrochemistry.
View Article and Find Full Text PDFJ Phys Chem Lett
June 2023
School of Physics and Information Technology, Shaanxi Normal University, Xi'an, Shaanxi 710119, China.
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