Issue 48, 2014

One-step microwave synthesis of Pt (Pd)/Cu2O/GNs composites and their electro-photo-synergistic catalytic properties for methanol oxidation

Abstract

A facile one-pot method was used to synthesize Pt/Cu2O/GNs and Pd/Cu2O/GNs composites. Pt or Pd nanoparticles are deposited onto graphene sheets (GNs) and Cu2O via synchronous reduction of K2PtCl4 (K2PdCl4), Cu(OH)2 and graphene oxide (GO) with glucose as a reducing agent under microwave irradiation. The formation of Cu2O promotes the nucleation of Pt(0) or Pd(0) particles and favors more complete reduction of PtCl42− or PdCl42−. Catalytic properties of as-prepared composites for methanol oxidation reaction (MOR) were evaluated by cyclic voltammetry (CV), chronoamperometry, COads stripping voltammetry and electrochemical impedance spectrum (EIS). Electrochemical experiments showed that Pt/Cu2O/GNs and Pd/Cu2O/GNs had much higher catalytic activity and stability for MOR and better resistance to CO poisoning compared with the commercially available Johnson Matthey 20% Pt/C catalyst (Pt/C-JM) and Sigma-Aldrich 20% Pd/C catalyst (Pd/C-SA). Especially under the UV irradiation, the total peak current density and catalytic stability of Pt/Cu2O/GNs and Pd/Cu2O/GNs drastically increase, which may result from the synergistic effect between the electro-catalytic and photo-catalytic properties. In brief, the cooperation among Pt (Pd), Cu2O and GNs promotes remarkably the catalytic performance for MOR on Pt/Cu2O/GNs and Pd/Cu2O/GNs either without light or with UV irradiation.

Graphical abstract: One-step microwave synthesis of Pt (Pd)/Cu2O/GNs composites and their electro-photo-synergistic catalytic properties for methanol oxidation

Article information

Article type
Paper
Submitted
25 Sep 2014
Accepted
13 Oct 2014
First published
13 Oct 2014

J. Mater. Chem. A, 2014,2, 21010-21019

One-step microwave synthesis of Pt (Pd)/Cu2O/GNs composites and their electro-photo-synergistic catalytic properties for methanol oxidation

L. Ye, Z. Li, X. Zhang, F. Lei and S. Lin, J. Mater. Chem. A, 2014, 2, 21010 DOI: 10.1039/C4TA05094K

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