Electrocatalytic Oxygen Evolution Reaction (OER) on Ru, Ir, and Pt Catalysts: A Comparative Study of Nanoparticles and Bulk Materials

被引:2185
作者
Reier, Tobias [1 ]
Oezaslan, Mehtap [1 ]
Strasser, Peter [1 ]
机构
[1] Tech Univ Berlin, Electrochem Energy Catalysis & Mat Sci Lab, Dept Chem, D-10623 Berlin, Germany
来源
ACS CATALYSIS | 2012年 / 2卷 / 08期
关键词
oxygen evolution reaction (OER); water splitting; iridium; ruthenium; platinum; anodic oxidation; nanoparticles; PARTICLE-SIZE DEPENDENCE; X-RAY-DIFFRACTION; ACID-SOLUTIONS; SURFACE ELECTROCHEMISTRY; NANOCRYSTALLINE RUO2; OXIDE SURFACES; ELECTRODES; PLATINUM; WATER; RUTHENIUM;
D O I
10.1021/cs3003098
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
A comparative investigation was performed to examine the intrinsic catalytic activity and durability of carbon supported Ru, Ir, and Pt nanoparticles and corresponding bulk materials for the electrocatalytic oxygen evolution reaction (OER). The electrochemical surface characteristics of nanoparticles and bulk materials were studied by surface-sensitive cyclic voltammetry. Although basically similar voltammetric features were observed for nanoparticles and bulk materials of each metal, some differences were uncovered highlighting the changes in oxidation chemistry. On the basis of the electrochemical results, we demonstrated that Ru nanoparticles show lower passivation potentials compared to bulk Ru material. Ir nanoparticles completely lost their voltammetric metallic features during the voltage cycling, in contrast to the corresponding bulk material. Finally, Pt nanoparticles show an increased oxophilic nature compared to bulk Pt. With regard to the OER performance, the most pronounced effects of nanoscaling were identified for Ru and Pt catalysts. In particular, the Ru nanoparticles suffered from strong corrosion at applied OER potentials and were therefore unable to sustain the OER. The Pt nanoparticles exhibited a lower OER activity from the beginning on and were completely deactivated during the applied OER stability protocol, in contrast to the corresponding bulk Pt catalyst. We highlight that the OER activity and durability were comparable for Ir nanoparticles and bulk materials. Thus, Ir nanoparticles provide a high potential as nanoscaled OER catalyst.
引用
收藏
页码:1765 / 1772
页数:8
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