The HER in alkaline media on Pt-modified three-dimensional Ni cathodes

被引:58
作者
Fiameni, Stefania [1 ]
Herraiz-Cardona, Isaac [2 ]
Musiani, Marco [1 ]
Perez-Herranz, Valentin [2 ]
Vazquez-Gomez, Lourdes [1 ]
Verlato, Enrico [1 ]
机构
[1] IENI CNR, Corso Stati Uniti 4, I-35127 Padua, Italy
[2] Univ Politecn Valencia, Dept Ingn Quim & Nucl, Valencia 46022, Spain
关键词
Electrocatalysis; Foam electrodes; Galvanic displacement; HER; Porous electrodes; Spontaneous deposition; HYDROGEN EVOLUTION REACTION; NICKEL FOAM CATHODE; SPONTANEOUS DEPOSITION; FUEL-CELLS; POROUS NI; ELECTRODE MORPHOLOGIES; GALVANIC DISPLACEMENT; COMPOSITE ELECTRODES; PLATINUM-ELECTRODES; RHODIUM ELECTRODES;
D O I
10.1016/j.ijhydene.2012.04.100
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
Electrodeposited porous Ni layers and commercial Ni foams were submitted to spontaneous deposition of Pt, achieved by immersing the Ni substrates in H2PtCl6 solutions, at open circuit, to produce Pt-modified 3D Ni electrodes. When using Ni foams, the immersion was prolonged until the whole amount of H2PtCl6 in the solution had reacted. Such an approach, which granted an easy control of the Pt loading, could not be used for Ni trodeposits, since they underwent significant corrosion. The true Pt surface area was determined by measuring, for each electrode, the hydrogen desorption charge according to methods described in the literature. The ratios between Pt surface area and Pt loading were higher for Ni foam electrodes than for porous Ni electrodeposits. Both kinds of Pt-modified Ni electrodes were used as cathodes for hydrogen evolution in 1 M KOH. Cathodes with Pt loading below 0.5 mg cm(-2) (referred to geometric surface area) evolved hydrogen at -100 mA cm(-2) with a -75 mV overpotential. The better activity of foam electrodes as compared to electrodeposits, especially at low Pt loading, was mainly due to their higher Pt surface area per unit Pt mass. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10507 / 10516
页数:10
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