催化作用
材料科学
质子交换膜燃料电池
化学工程
过渡金属
微波食品加热
间歇式反应器
钴
化学
冶金
有机化学
量子力学
物理
工程类
作者
Jiapeng Lu,Zhuangzhi Liu,Xianghui Zeng,Lingyun Zhang,Wei Fang,Weitao Gao,Yanan Yin,Xuejun Zhu,Tao Yang,Xing Du,Cheng Wang,Hui Chen,Lei Zhao
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2024-01-11
卷期号:38 (3): 2387-2395
被引量:2
标识
DOI:10.1021/acs.energyfuels.3c03762
摘要
Alloying Pt with 3d transition metals has proven to be the most attractive oxygen reduction reaction electrocatalysts for proton exchange membrane fuel cells with improved catalytic activity and stability; thus, their large-scale and cost-effective production is in high demand. Herein, we present a strategy for the batch preparation of PtCo/C with a highly uniform morphology and tiny PtCo dispersions of 2.48 nm using a continuous-flow microwave pipeline reactor. Due to its unique structure, which greatly facilitated the catalytic kinetics, the prepared PtCo/C catalyst exhibited an initial mass activity of 485.6 mA·mg–1pt at 0.9 V, which was 3.6 times higher than that of the commercial Pt/C catalysts. The as-obtained PtCo/C was able to maintain 74.6% of the initial activity after 30,000 accelerated cycle tests. Furthermore, a maximum power density of 1.76 W·cm–2 was attained in a single-cell test under 0.2 mg·cm–2 Pt loading conditions, far exceeding those of commercial Pt/C catalysts.
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