Electrodeposition of multilayered bimetallic nanoclusters of ruthenium and platinum via surface-limited redox-replacement reactions for electrocatalytic applications

Langmuir. 2010 Jan 5;26(1):570-80. doi: 10.1021/la902219t.

Abstract

An electrochemical synthesis of multilayered bimetallic Ru|Pt nanoclusters, supported on glassy carbon, is reported for the first time. The novel nanoclusters were synthesized via surface-limited redox-replacement reactions involving sacrificial Cu, deposited prior to the formation of each individual noble metal layer, in a sequential fashion. It has been shown that the Cu adlayers control the morphology and electrochemical properties of the resultant nanostructures. Sequentially deposited Ru|Pt nanoclusters exhibited superior electrocatalytic activity (when compared to equivalent monometallic Pt and an alloy-type codeposited Pt-Ru nanostructures) with respect to methanol electrooxidation in an acidic medium. Moreover, it has been established that the electrochemical process taking place at the Ru|Pt nanoclusters followed the bifunctional mechanism. Electrokinetic studies of the oxygen reduction reaction (ORR) were also performed. Analysis of hydrodynamic linear sweep voltammetric experiments, performed at various flow rates on oxygen-saturated acidic medium, revealed that the Pt and Ru|Pt nanoclusters exhibited direct four- and two-electron ORR pathways, respectively. A specially designed electrochemical flow-cell was used for automated sequential electrodeposition of the multilayered nanoclusters of predefined composition and electrochemical and electrocatalytic investigations.