Constructing ultrafine Pt nanoparticles anchored on N-doped porous carbon nanofibers for efficient and stable oxygen reduction reaction

被引:9
作者
Li, Xuan [1 ]
Li, Guodong [2 ]
Deng, Chen [2 ]
Jing, Lingyan [2 ]
Feng, Chao [2 ]
Kong, Yan [1 ]
Jiang, Xingxing [2 ]
Zhou, Weiliang [2 ]
Chai, Xiaoyan [2 ]
Yang, Hengpan [2 ]
Hu, Qi [2 ]
He, Chuanxin [2 ]
机构
[1] Univ Sci & Technol China, Dept Chem Phys, Hefei 230026, Peoples R China
[2] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518071, Peoples R China
基金
中国国家自然科学基金;
关键词
oxygen reduction reaction; space confinement; Pt nanoparticles; porous carbon nanofibers (PCNFs); PLATINUM NANOPARTICLES; FUEL-CELL; CATALYSTS;
D O I
10.1007/s40843-023-2483-x
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Synthesis of ultrafine Pt nanoparticles with high metal utilization is essential to achieve efficient oxygen reduction reaction (ORR) with a low mass loading of Pt; however, it remains challenging. Here, we propose a facile yet robust strategy to construct ultrafine Pt nanoparticles (similar to 3 nm) anchored on porous carbon nanofibers (PCNFs) via electro-spinning. It is found that the porous architecture facilitates mass transport and active sites exposure, thereby providing highly accessible Pt sites. As a result, the synthesized Pt@PCNFs with low Pt loading (4.2 wt%) display excellent ORR activity with a mass activity of 41 and 51 A g(Pt)(-1) at 0.9 V in alkaline and acidic electrolytes, 8 times and 10 times that of the corresponding value for commercial Pt/C catalyst, respectively. More importantly, the strong metal-support interaction between Pt nanoparticles and N-doped carbon nanofibers, as well as carbon shell protection, significantly enhances the stability by suppressing the aggregation of Pt nanoparticles during ORR, and consequently the stability of Pt@PCNFs is much superior to that of the Pt/C benchmark in both alkaline and acid media at different temperatures. This work provides a facile approach to developing efficient and stable low-Pt-based electrocatalysts toward ORR.
引用
收藏
页码:3509 / 3519
页数:11
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