Plasma-assisted Pt and Pt-Pd nano-particles deposition on carbon carriers for application in PEM electrochemical cells

被引:30
作者
Fedotov, A. A. [1 ]
Grigoriev, S. A. [1 ,2 ,3 ]
Millet, P. [4 ]
Fateev, V. N. [1 ,2 ,3 ]
机构
[1] Kurchatov Inst, Natl Res Ctr, Moscow 123182, Russia
[2] Natl Res Univ, Moscow Power Engn Inst, Moscow 111250, Russia
[3] Moscow State Tech Univ Radio Engn Elect & Automat, Moscow 119454, Russia
[4] Univ Paris 11, Inst Chim Mol & Mat, UMR CNRS 8182, F-91405 Orsay, France
关键词
Plasma-assisted deposition; Magnetron sputtering; Carbon-supported platinum nano-particles; Proton-exchange membrane; Bimetallic electrocatalysts; FUEL-CELL; CATALYSTS; ELECTRODE; PLATINUM; NANOTUBES;
D O I
10.1016/j.ijhydene.2012.10.042
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Plasma-assisted deposition of platinum and platinum-palladium nano-particles at the surface of carbonaceous electronic carriers for application in proton-exchange membrane (PEM) electrochemical cells has been carried out using a conventional DC magnetron sputtering system. Different types of carrier have been used for that purpose: carbon powder (Vulcan XC-72), carbon nanotubes and carbon nano-fibers. The interest of initial chemical pretreatment or metallization of the electronic carrier to improve surface adhesion of catalyst nano-particles has been analyzed. Nanostructured catalytic powders thus obtained have been analyzed and characterized using TGA, SEM, TEM, XRD, XRF and cyclic voltammetry. The electrochemical performances of Pt/C and Pt-Pd/C electrodes have been measured in single-cell PEM fuel cell (PEMFC), water electrolyzer (PEMWE) and unitized regenerative fuel cell (URFC). Results show a high active surface area (up to 44 m(2) g(-1)) and high electrochemical activity for a number of synthesized samples. A qualitative correlation has been established between sputtering parameters, type of carbon carrier and performances as electrocatalyst. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8568 / 8574
页数:7
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