Inducing SERS activity at graphitic carbon using graphene-covered Ag nanoparticle substrates: Spectroelectrochemical analysis of a redox-active adsorbed anthraquinone

Graphitic carbon electrodes are central to many electrochemical energy storage and conversion technologies. Probing the behavior of molecular species at the electrochemical interfaces they form is paramount to understanding redox reaction mechanisms. Combining surface-enhanced Raman scattering (SERS) with electrochemical methods offers a powerful way to explore such mechanisms, but carbon itself is not a SERS activating substrate. Here, we report on a hybrid substrate consisting of single- or few-layer graphene sheets deposited over immobilized silver nanoparticles, which allows for simultaneous SERS and electrochemical investigation. To demonstrate the viability of our substrate, we adsorbed anthraquinone-2,6-disulfonate to graphene and studied its redox response simultaneously using SERS and cyclic voltammetry in acidic solutions. We identified spectral changes consistent with the reversible redox of the quinone/hydroquinone pair. The SERS intensities on bare silver and hybrid substrates were of the same order of magnitude, while no discernible signals were observed over bare graphene, confirming the SERS effect on adsorbed molecules. This work provides new prospects for exploring and understanding electrochemical processes in situ at graphitic carbon electrodes.

Automated summary

Graphitic carbon electrodes are crucial for electrochemical energy storage and conversion technologies. By combining surface-enhanced Raman scattering (SERS) with electrochemical methods using a hybrid substrate of graphene sheets and silver nanoparticles, the reversible redox response of adsorbed anthraquinone-2,6-disulfonate was observed. The SERS effect was confirmed, providing new opportunities for studying electrochemical processes on graphitic carbon electrodes.