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Hot Electron-driven Photocatalysis and Transient Absorption Spectroscopy in Plasmon Resonant Grating Structures

Plasmon resonant grating structures provide an effective platform for distinguishing between the effects of plasmon resonant excitation and bulk metal absorption via interband transitions. By simply rotating the polarization of the incident light, we can switch between resonant excitation and non-re...

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Published in:Faraday discussions 2018-12, Vol.214
Main Authors: Wang, Yi, Shen, Lang, Wang, Yu, Hou, Bingya, Gibson, George N., Poudel, Nirakar, Chen, Jihan, Shi, Haotian, Guignon, Ernest, Cady, Nathaniel C., Page, William D., Pilar, Arturo, Dawlaty, Jahan, Cronin, Stephen B.
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container_title Faraday discussions
container_volume 214
creator Wang, Yi
Shen, Lang
Wang, Yu
Hou, Bingya
Gibson, George N.
Poudel, Nirakar
Chen, Jihan
Shi, Haotian
Guignon, Ernest
Cady, Nathaniel C.
Page, William D.
Pilar, Arturo
Dawlaty, Jahan
Cronin, Stephen B.
description Plasmon resonant grating structures provide an effective platform for distinguishing between the effects of plasmon resonant excitation and bulk metal absorption via interband transitions. By simply rotating the polarization of the incident light, we can switch between resonant excitation and non-resonant excitation, while keeping all other parameters of the measurement constant. With light polarized perpendicular to the lines in the grating (i.e., TE-polarization), the photocatalytic reaction rate (i.e., photocurrent) is measured as the angle of the incident laser light is tuned through the resonance with the grating. Here, hot holes photoexcited in the metal are used to drive the oxygen evolution reaction (OER), producing a measurable photocurrent. Using TE-polarized light, we observe sharp peaks in the photocurrent and sharp dips in the photoreflectance at approximately 9° from normal incidence, which corresponds to the conditions under which there is good wavevector matching between the incident light and the lines in the grating. With light polarized parallel to the grating (i.e., TM), we excite the grating structure non-resonantly and there is no angular dependence in the photocurrent or photoreflectance. In order to quantify the lifetime of these hot carriers, we performed transient absorption spectroscopy of these plasmon resonant grating structures. Here, we observe one feature in the spectra corresponding to interband transitions and another feature associated with the plasmon resonant mode in the grating. Both features decay over a time scale of 1–2 ps. Finally, the spectral responses of grating structures fabricated with Ag, Al, and Cu are also presented.
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title Hot Electron-driven Photocatalysis and Transient Absorption Spectroscopy in Plasmon Resonant Grating Structures
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