4.8 Article

Effect of Nanoparticle Size on Plasmon-Driven Reaction Efficiency

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 3, 页码 4163-4169

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c21441

关键词

plasmon-driven reaction; hot charge carrier; perfect gold nanosphere; nanoparticle-on-mirror; SERS

资金

  1. National Research Foundation (NRF) of Korea [2019R1A2C1084078, 2020R1A5A1018052]
  2. National Research Foundation of Korea [2019R1A2C1084078] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Hot electron chemistry has great significance in photocatalytic reactions, solar energy conversion, and waste decomposition. This study investigates the relationship between the size of gold nanoparticles (AuNPs) and plasmon-induced reaction yield, providing insights for the design of efficient plasmonic photocatalysts and photovoltaic devices.
Hot electron chemistry is of paramount significance because of its applicability to photocatalytic reactions, solar energy conversion, and waste decomposition. The nonradiative decay of excited plasmons in gold nanoparticles (AuNPs) generates highly energetic nonthermal electrons and holes that can induce chemical reactions when transferred to nearby molecules. In this study, we explore the relationship between AuNP size (26-133 nm) and the plasmon-induced reaction yield. To isolate the size from other structural parameters, we prepare perfectly round gold nanospheres (AuNSs) with narrow size distributions. The use of a nanoparticle-on-mirror configuration, in which the reactant molecules (4-mercaptobenzoic acid) are positioned in nanogaps between the AuNSs and a Au film, promotes the generation of hot carriers and allows the highly sensitive detection of the reaction products (benzenethiol) using surface-enhanced Raman spectroscopy. We show that the reaction yield increases as the AuNS size increases up to 94 nm and then decreases for larger AuNSs. This peculiar.-shaped size-dependent reactivity can be explained by considering both the plasmonic absorption efficiency of AuNSs and the decay rate of plasmons via electron-surface scattering. The product of the calculated absorption cross section and the inverse of the AuNS size reproduces our experimental results remarkably well. These findings will contribute to the design of highly efficient plasmonic photocatalysts and photovoltaic devices.

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