†Department of Applied Physics, Chalmers University of Technology, Göteborg SE-412 96, Sweden.
‡Beijing Computational Science Research Center, Zhongguancun Software Park II, No. 10 Dongbeiwang West Road, Haidian District, Beijing 100094, China.
Nano Lett. 2015 Jun 10;15(6):4059-65. doi: 10.1021/acs.nanolett.5b01070. Epub 2015 May 6.
Emission of photoexcited hot electrons from plasmonic metal nanostructures to semiconductors is key to a number of proposed nanophotonics technologies for solar harvesting, water splitting, photocatalysis, and a variety of optical sensing and photodetector applications. Favorable materials and catalytic properties make systems based on gold and TiO2 particularly interesting, but the internal photoemission efficiency for visible light is low because of the wide bandgap of the semiconductor. We investigated the incident photon-to-electron conversion efficiency of thin TiO2 films decorated with Au nanodisk antennas in an electrochemical circuit and found that incorporation of a Au mirror beneath the semiconductor amplified the photoresponse for light with wavelength λ = 500-950 nm by a factor 2-10 compared to identical structures lacking the mirror component. Classical electrodynamics simulations showed that the enhancement effect is caused by a favorable interplay between localized surface plasmon excitations and cavity modes that together amplify the light absorption in the Au/TiO2 interface. The experimentally determined internal quantum efficiency for hot electron transfer decreases monotonically with wavelength, similar to the probability for interband excitations with energy higher than the Schottky barrier obtained from a density functional theory band structure simulation of a thin Au/TiO2 slab.
从等离子体金属纳米结构到半导体发射光激发的热电子,是许多用于太阳能收集、水分解、光催化以及各种光学传感和光电探测器应用的拟议纳米光子学技术的关键。具有有利的材料和催化性质的金和 TiO2 基系统尤其有趣,但由于半导体的宽带隙,可见光的内光电子发射效率较低。我们研究了在电化学回路中用 Au 纳米盘天线修饰的 TiO2 薄膜的入射光子到电子的转换效率,发现与没有反射镜组件的相同结构相比,在半导体下方掺入 Au 反射镜可将波长为 λ=500-950nm 的光的光响应放大 2-10 倍。经典的电动力学模拟表明,增强效应是由局域表面等离激元激发和腔模之间的有利相互作用引起的,这两者共同放大了 Au/TiO2 界面的光吸收。实验确定的热电子转移的内量子效率随波长单调下降,与从薄的 Au/TiO2 薄片的密度泛函理论能带结构模拟中获得的能量高于肖特基势垒的能带间激发的概率相似。