Voltage-induced modulation of interfacial ionic liquids measured using surface plasmon resonant grating nanostructures

Author:

Aravind Indu1ORCID,Wang Yu2ORCID,Cai Zhi2ORCID,Li Ruoxi2ORCID,Shahriar Rifat3ORCID,Gibson George N.45ORCID,Guignon Ernest5,Cady Nathaniel C.6ORCID,Page William D.5ORCID,Pilar Arturo5,Cronin Stephen B.137ORCID

Affiliation:

1. Department of Physics and Astronomy 1 , University of Southern California, Los Angeles, California 90089, USA

2. Mork Family Department of Chemical Engineering and Materials Science 2 , University of Southern California, Los Angeles, California 90089, USA

3. Ming Hsieh Department of Electrical Engineering 3 , University of Southern California, Los Angeles, California 90089, USA

4. Department of Physics, University of Connecticut 4 , Storrs, Connecticut 06269, USA

5. Ciencia Inc. 5 , East Hartford, Connecticut 06108, USA

6. Colleges of Nanoscale Science and Engineering, SUNY Polytechnic Institute 6 , Albany, New York 12203, USA

7. Department of Chemistry, University of Southern California 7 , Los Angeles, California 90089, USA

Abstract

We have used surface plasmon resonant metal gratings to induce and probe the dielectric response (i.e., electro-optic modulation) of ionic liquids (ILs) at electrode interfaces. Here, the cross-plane electric field at the electrode surface modulates the refractive index of the IL due to the Pockels effect. This is observed as a shift in the resonant angle of the grating (i.e., Δϕ), which can be related to the change in the local index of refraction of the electrolyte (i.e., Δnlocal). The reflection modulation of the IL is compared against a polar (D2O) and a non-polar solvent (benzene) to confirm the electro-optic origin of resonance shift. The electrostatic accumulation of ions from the IL induces local index changes to the gratings over the extent of electrical double layer (EDL) thickness. Finite difference time domain simulations are used to relate the observed shifts in the plasmon resonance and change in reflection to the change in the local index of refraction of the electrolyte and the thickness of the EDL. Simultaneously using the wavelength and intensity shift of the resonance enables us to determine both the effective thickness and Δn of the double layer. We believe that this technique can be used more broadly, allowing the dynamics associated with the potential-induced ordering and rearrangement of ionic species in electrode–solution interfaces.

Funder

Army Research Office

U.S. Department of Energy

National Science Foundation

Air Force Office of Scientific Research

Publisher

AIP Publishing

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