化学
等离子体子
亚铁氰化物
纳米颗粒
表面增强拉曼光谱
胶体金
拉曼光谱
表面等离子体子
解吸
等离子纳米粒子
光谱学
纳米技术
分析化学(期刊)
光化学
吸附
拉曼散射
物理化学
光电子学
电极
有机化学
光学
材料科学
量子力学
物理
作者
Yue Qi,Vitor Brasiliense,Tyler W. Ueltschi,Ji Eun Park,Michael R. Wasielewski,George C. Schatz,Richard P. Van Duyne
摘要
The plasmon-driven chemistry of ferri-/ferrocyanide ions inside surface-enhanced Raman spectroscopy (SERS) active hot spots associated with gold nanoparticle oligomers is studied with continuous wave (CW) pump-probe SERS. By comparing with solution-phase normal Raman spectra, the characteristic spectral variations observed upon 532 nm optical pumping can be attributed to an oxidation process that occurs on the surface species followed by desorption of the oxidized surface species from the gold nanoparticles. Interrogating the plasmon-driven processes over a wide range of temperatures reveals that neither process is purely driven by the thermal effects associated with the optical pumping, and the apparent activation energies of both steps are estimated based on semiquantitative SERS analysis. Our observation identifies a more detailed reaction pathway for this classic model system under considerably simplified reaction conditions, adding to the current mechanistic background for future plasmon-driven chemistry studies and applications.
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