Design of catalytically active Pt-based catalysts with minimizing the usage of Pt is a major issue in fuel cells. Herein, for the first time, we have developed a Au catalytic reduction strategy to synthesize a Au@Pt core-shell electrocatalyst with a quasi-monolayer Pt skin spontaneously formed from the gold surface catalysis. In the presence of presynthesized gold nanocrystals (used as the catalyst and Au seeds) and 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffer (used as reductant), under the Au surface catalysis, platinum ions can be reduced and deposited on the gold nanocrystals to form a Pt skin surface with a quasi-monatomic thickness. In the present strategy, Pt ions can be reduced only under the catalysis of gold surface and thus when the surface of Au NPs is covered by a monatomic Pt layer, the reduction reaction of Pt ions will be spontaneously turned off. Therefore, the significant advantage of this synthesis strategy is that the formation of quasi-monolayer Pt skin surface can be self-controlled and is completely free of controlling the dosage of platinum ions and the size distribution of Au cores. The synthesized Au@Pt core@shell structure exhibited enhanced electrocatalytic activities for oxygen reduction reaction and methanol oxidation reaction, which are 6.87 and 10.17 times greater than those of Pt/C catalyst, respectively. The present study provides a new strategy for obtaining high-performance bimetallic/multimetallic electrocatalysts with high utilization of precious metals.
Keywords: Pt skin; catalytic reduction strategy; electrocatalyst; methanol oxidation reaction; oxygen reduction reaction.