催化作用
多孔性
材料科学
电解质
退火(玻璃)
化学工程
耐久性
纳米颗粒
纳米技术
复合材料
化学
电极
有机化学
物理化学
工程类
作者
Tomoyuki Hirano,Takama Tsuboi,Thi Thanh Nguyen Ho,Eishi Tanabe,Aoi Takano,Mikihiro Kataoka,Takashi Ogi
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2023-12-08
卷期号:6 (24): 12364-12370
被引量:4
标识
DOI:10.1021/acsaem.3c02165
摘要
Recently, the emphasis on hydrogen-fuel utilization technologies─particularly polymer–electrolyte fuel cells (PEFCs)─has recently shifted from light-duty to heavy-duty vehicles. There is consequently an urgent need to develop a catalyst with excellent durability. In this study, we have endeavored to improve the power-generating performance of PEFCs by using high-durability Nb–SnO2 (NTO) nanoparticles and by controlling the porosity of the catalyst layer. We tuned the fused-aggregate network structure of the NTO nanoparticles by annealing them at 1000 or 1200 °C. This treatment promoted the development of aggregated structures of the NTO nanoparticles, which resulted in an increase in the porosity of the catalyst layer. In these catalysts, the maximum current density increased with increasing porosity. The gas-diffusion resistance calculated from the current–voltage (I–V) characteristics decreased from 148 m/s for NTO nanoparticles before annealing, to 113 m/s after annealing at 1000 °C, and to 102 m/s after annealing at 1200 °C. This study thus demonstrates that high-performance catalysts with high durability for PEFCs can be achieved by precisely engineering the porosity of the catalyst layer.
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