Single Nanoparticle Electrocatalysis: Effect of Monolayers on Particle and Electrode on Electron Transfer

Abstract

The electrocatalytic properties of individual single Pt nanoparticles (NPs) can be studied electrochemically by measuring the current−time (i−t) responses during single NP collisions with a noncatalytic ultramicroelectrode (UME). The Pt NPs are capped with citrate ions or a self-assembled monolayer (SAM) of alkane thiols terminated with carboxylic acid that affect the observed i−t responses. By varying the length of the SAMs or the composition of a mixed monolayer, we have studied the effect of adsorbed molecules on the catalytic activity of Pt NPs at the single particle level through electrocatalytic amplification of single NP collisions. Collisions of single NPs were triggered and recorded as individual current steps whose amplitude represents the reactivity of single Pt NPs for the reaction of interest, here hydrazine oxidation, at a given electrode potential. The catalytic properties of Pt NPs are dependent not only on the nature of the interaction between the adsorbed monolayer and the catalytic NP surface, but also on the rate of electron transfer through the SAMs, governed by their length.