4.6 Article

A rapid synthesis of high surface area PdRu nanosponges: Composition-dependent electrocatalytic activity for formic acid oxidation

Journal

JOURNAL OF ENERGY CHEMISTRY
Volume 26, Issue 4, Pages 703-711

Publisher

ELSEVIER
DOI: 10.1016/j.jechem.2017.02.009

Keywords

Palladium-ruthenium; Nanosponge; Nanoparticle networks; Methanol oxidation; Green synthesis

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Here, PdRu nanoparticle networks (NPNs) with various compositions were synthesized through an inexpensive method in water as a green solvent, at different ratios of the H2PdCl4 and RuCl3 precursors. This is a fast, room temperature and surfactant free strategy which is able to form high surface area metal nanosponges with a three-dimensional (3D) porous structure. The structure of as-prepared nanosponges was characterized using the techniques of field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS) and cyclic voltammetry (CV). Then, the electrocatalytic activities of PdRu NPNs towards formic acid oxidation were examined by electrochemical measurements including CV, chronoamperometry, and electrochemical impedance spectroscopy (EIS). Based on studies, it was found that the current density of formic acid oxidation (FAO) is strongly dependent on the composition of PdRu NPNs. The best performance was realized for Pd4Ru1 NPNs compared to monometallic Pd counterpart and other bimetallic NPNs which might be ascribed to the role of Ru in the decrease of CO adsorption strength on the catalyst and consequently the priority of formic acid oxidation through the direct pathway. The Pd4Ru1 NPNs also showed the maximum current density and stability in chronoampero-metric measurements. In addition, comparative studies were performed between as-prepared NPNs and CNTs-supported Pd nanoparticles (Pd NPs/CNTs). The present results demonstrated the unique structural advantages of NPNs compared to individual Pd NPs supported on the CNT which leads to the promising performance of NPNs as supportless catalysts for the oxidation of formic acid. (C) 2017 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.

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