Collision, Adhesion, and Oxidation of Single Ag Nanoparticles on a Polysulfide-Modified Microelectrode.

Abstract

We report the collision, adhesion, and oxidation behavior of single silver nanoparticles (Ag NPs) on a polysulfide-modified gold microelectrode. Despite its remarkable success in volume analysis for smaller Ag NPs, the method of NP-collision electrochemistry has failed to analyze particles greater than 50 nm due to uncontrollable collision behavior and incomplete NP oxidation. Herein, we describe the unique capability of an ultrathin polysulfide layer in controlling the collision behavior of Ag NPs by drastically improving their sticking probability on the electrode. The ultrathin sulfurous layer is formed on gold by sodium thiosulfate electro-oxidation and serves both as an adhesive interface for colliding NPs and as a preconcentrated reactive medium to chemically oxidize Ag to form Ag2S. Rapid particle dissolution is further promoted by the presence of bulk sodium thiosulfate serving as a Lewis base, which drastically improves the solubility of generated Ag2S by a factor of 1013. The combined use of polysulfide and sodium thiosulfate allows us to observe a 25× increase in NP detection frequency, a 3× increase in peak amplitude, and more complete oxidation for larger Ag NPs. By recognizing how volumetric analysis using transmission electron microscopy (TEM) may overestimate quasi-spherical NPs, we believe we can have full NP oxidation for particles up to 100 nm. By focusing on the electrode/solution interface for more effective NP-electrode contact, we expect that the knowledge learned from this study will greatly benefit future NP collision systems for mechanistic studies in single-entity electrochemistry as well as designing ultrasensitive biochemical sensors.