纳米线
催化作用
质子交换膜燃料电池
电化学
兴奋剂
材料科学
铂金
氧还原反应
纳米技术
化学工程
氧气
氧还原
燃料电池
电极
化学
光电子学
物理化学
有机化学
工程类
作者
Zhiwei Hu,Jiajia Yang,Lei Tang,Haibo Jiang,Yihua Zhu,R. Li,Cui Liu,Jianhua Shen
标识
DOI:10.1002/smtd.202401138
摘要
Abstract The structural tailoring of Pt‐based catalysts into 1D nanowires for oxygen reduction reactions (ORR) has been a focus of research. Mo(CO) 6 is commonly used as a morphological modifier to form nanowires, but it is found that it inevitably leads to Mo doping. This doping introduces unique electrochemical signals not seen in other Pt‐based catalysts, which can directly reflect the stability of the catalyst. Through experiments, it is demonstrated that Mo doping is detrimental to ORR performance, and theoretical calculations have shown that Mo sites that are inherently inactive also poison the ORR activity of the surrounding Pt. Therefore, a novel gas‐assisted technique is proposed to replace Mo(CO) 6 with CO, which forms ultrafine nanowires with an order of magnitude increase in length, ruling out the effect of Mo. The catalyst performs at 1.24 A mg Pt −1 , 7.45 times greater than Pt/C, demonstrating significant ORR mass activity, and a substantial improvement in stability. The proton exchange membrane fuel cell using this catalyst provides a higher power density (0.7 W cm −2 ). This study presents a new method for the preparation of ultra‐long nanowires, which opens up new avenues for future practical applications of low‐Pt catalysts in PEMFC.
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