Flame-Made Ir–IrO2/TiO2 Particles as Anode Catalyst Support for Improved Durability in Polymer Electrolyte Fuel Cells

材料科学 电解质 氧化物 阳极 催化作用 化学工程 粒子(生态学) 氧化钛 纳米颗粒 电导率 无机化学 电极 纳米技术 化学 冶金 有机化学 物理化学 工程类 地质学 海洋学
作者
Thi Thanh Nguyen Ho,Tomoyuki Hirano,Ryosuke Narui,Hiroshi Tsutsumi,Masahito Kishi,Yusuke Yoshikawa,Kiet Le Anh Cao,Takashi Ogi
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:6 (11): 6064-6071 被引量:1
标识
DOI:10.1021/acsaem.3c00536
摘要

The development of metal oxide support with high electrical conductivity has attracted attention to improving the durability and performance of polymer electrolyte fuel cells. Iridium oxide–titanium oxide particles are outstanding candidates, owing to their excellent properties. In this study, catalyst support comprising titanium oxide particles with low-loading iridium–iridium oxide species (Ir–IrO2/TiO2) with a chain-like structure was synthesized by a flame aerosol process. The flame aerosol process is a versatile and one-step method allowing the production of metal-loaded metal oxide particles with a low amount of precious metal. The effect of the Ir loading contents on the morphology and electrical conductivity of the synthesized particles was investigated. The volume resistivity of Ir–IrO2/TiO2 particles containing 10 wt % IrO2 (Ir–IrO2/TiO2-10) (0.95 Ω cm) was much lower than that of TiO2 particles (108 Ω cm), which demonstrates the improvement of the conductivity of TiO2 particles resulting from the Ir loading. The electrochemical surface area of 20 wt % Pt-loaded Ir–IrO2/TiO2-10 particles was 42 m2 g–1-Pt, and Pt nanoparticles were distributed homogeneously on the Ir–IrO2/TiO2 particle surface. The performance of a membrane electrode assembly (MEA) based on the developed Ir–IrO2/TiO2 catalyst support as an anode shows no significant differences compared to that of MEA based on a carbon-supported Pt catalyst. MEA prepared from the Ir–IrO2/TiO2-10 particles exhibited remarkable stability after 20 min testing at a voltage of 1.7 V, whereas the cell potential of a carbon-supported Pt catalyst decreased dramatically under the same conditions.
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