Issue 61, 2016, Issue in Progress

A green synthesis of “naked” Pt and PtPd catalysts for highly efficient methanol electrooxidation

Abstract

Up to now, green synthesis of “naked” nanoobjects with clean surfaces is still a great challenge since structure-directing agents such as surfactants are usually used to induce the anisotropic particle growth for interesting nanostructures in solution. Here, a green synthesis approach for preparing “naked” Pt nanoparticles (NPs) in acetic acid solution was reported. Interestingly, Pt NPs with different morphologies (well-defined polyhedrons, irregular polyhedron-constructed chain networks and nanoflower-constructed chain networks) could be successfully synthesized at different concentrations of acetic acid without adding additional structure-directing agents and reducing agents. The acetic acid itself works both as structure-directing agent and reducing agent for the formation of these interesting Pt NPs. Specifically; the synthesized NPs are “naked” with clean surfaces since the acetic acid is a weakly-capping agent which can be easily removed after the washing process. The versatility of this method is further demonstrated by preparation of “naked” PtPd alloy NPs. In particular, the as-prepared “naked” Pt_5.20 and Pt3Pd1_5.20 NPs are demonstrated to be excellent catalysts with much higher electroactivity and better durability than the commercial Pt black catalyst (Hispec™ 1000) for the methanol oxidation reaction. The method reported in this work may pave the way for simple, low-cost, green and eco-friendly synthesis of “naked” metal catalysts for advanced electrocatalytic applications.

Graphical abstract: A green synthesis of “naked” Pt and PtPd catalysts for highly efficient methanol electrooxidation

Supplementary files

Article information

Article type
Paper
Submitted
13 Apr 2016
Accepted
03 Jun 2016
First published
06 Jun 2016

RSC Adv., 2016,6, 56083-56090

A green synthesis of “naked” Pt and PtPd catalysts for highly efficient methanol electrooxidation

B. Zhang, Y. Xue, H. Sun, A. Jiang, Z. Li and J. Hao, RSC Adv., 2016, 6, 56083 DOI: 10.1039/C6RA09516J

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