等离子体子
材料科学
电子
热电子
光电子学
胶体金
等离子纳米粒子
纳米颗粒
热载流子注入
纳米技术
化学工程
物理
晶体管
量子力学
工程类
电压
作者
Daniel Ratchford,Adam D. Dunkelberger,I. Vurgaftman,Jeffrey C. Owrutsky,Pehr E. Pehrsson
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-08-29
卷期号:17 (10): 6047-6055
被引量:158
标识
DOI:10.1021/acs.nanolett.7b02366
摘要
Excitation of localized surface plasmons in metal nanostructures generates hot electrons that can be transferred to an adjacent semiconductor, greatly enhancing the potential light-harvesting capabilities of photovoltaic and photocatalytic devices. Typically, the external quantum efficiency of these hot-electron devices is too low for practical applications (<1%), and the physics underlying this low yield remains unclear. Here, we use transient absorption spectroscopy to quantify the efficiency of the initial electron transfer in model systems composed of gold nanoparticles (NPs) fully embedded in TiO2 or Al2O3 films. In independent experiments, we measure free carrier absorption and electron–phonon decay in the model systems and determine that the electron-injection efficiency from the Au NPs to the TiO2 ranges from about 25% to 45%. While much higher than some previous estimates, the measured injection efficiency is within an upper-bound estimate based on a simple approximation for the Au hot-electron energy distribution. These results have important implications for understanding the achievable injection efficiencies of hot-electron plasmonic devices and show that the injection efficiency can be high for Au NPs fully embedded within a semiconductor with dimensions less than the Au electron mean free path.
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