Enhanced catalytic activity of Au core Pd shell Pt cluster trimetallic nanorods for CO reduction.

Herein, Au core Pd shell Pt cluster nanorods (Au@Pd@Pt NRs) with enhanced catalytic activity were rationally designed for carbon dioxide (CO) reduction. The surface composition and Pd-Pt ratios significantly influenced the catalytic activity, and the optimized structure had only a half-monolayer equivalent of Pt ( = 0.5) with 2 monolayers of Pd, which could enhance the catalytic activity for CO reduction by 6 fold as compared to the Pt surface at -1.5 V SCE. A further increase in the loading of Pt actually reduced the catalytic activity; this inferred that a synergistic effect existed among the three different nanostructure components. Furthermore, these Au NRs could be employed to improve the photoelectrocatalytic activity by 30% at -1.5 V due to the surface plasmon resonance. An SERS investigation inferred that the Au@Pd@Pt NRs ( = 0.5) were less likely to be poisoned by CO because of the Pd-Pt bimetal edge sites; due to this reason, the proposed structure exhibited highest catalytic activity. These results play an important role in the mechanistic studies of CO reduction and offer a new way to design new materials for the conversion of CO to liquid fuels.