Single-Particle Spectroelectrochemistry: Promoting the Electrocatalytic Activity of Gold Nanorods via Oxygen Plasma Treatment without Structural Deformation.

Abstract

Understanding of the electrocatalytic activity enhancement in gold nanoparticles is still limited. Herein, we present the effect of the oxygen plasma treatment on the electrochemical activity of gold nanorods (AuNRs). Oxygen plasma treatment resulted in the blueshift and line width narrowing of the localized surface plasmon resonance (LSPR) spectra obtained from individual AuNRs immobilized on an indium tin oxide (ITO) surface. These changes can be attributed to increases in the surface charges of the AuNRs. The formation of a Au-ITO heterojunction provided structural stability to the immobilized AuNRs regardless of the duration of oxygen plasma exposure. The electrocatalytic oxidation of hydrogen peroxide (H2O2) was induced by increases in the free-electron densities on the surfaces of these AuNRs owing to oxygen plasma treatment, and Au did not dissolve under the experimental conditions. However, the potential-dependent LSPR spectra of the individual AuNRs showed similar patterns of LSPR behavior, irrespective of the duration of oxygen plasma treatment and the concentration of H2O2. Therefore, this study based on single-particle spectroelectrochemistry and cyclic voltammetry improves the understanding of the role of oxygen plasma treatment in promoting the catalytic activity of structurally stable AuNRs immobilized on an ITO surface.