Metal-Organic Framework-Derived N-Doped Carbon with Controllable Mesopore Sizes for Low-Pt Fuel Cells

被引:21
|
作者
Huang, Qirui [1 ]
Hu, Linyu [1 ,2 ]
Chen, Xianchun [1 ]
Cai, Wenjun [1 ]
Wang, Lu [1 ]
Wang, Bo [1 ]
机构
[1] Beijing Inst Technol, Adv Technol Res Inst Jinan, Frontiers Sci Ctr High Energy Mat, Sch Chem & Chem Engn,Beijing Key Lab Photoelect El, Beijing 100081, Peoples R China
[2] Southern Univ Sci & Technol, Sch Microelect, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysts; fuel cells; metal-organic frameworks; N-doped carbon; porosity; OXYGEN REDUCTION REACTION; CATALYST LAYERS;
D O I
10.1002/adfm.202302582
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mesoporous structure of carbon materials plays an important role in electrocatalyst design. Constructing carbon supports with tunable mesopores has long been a challenge. Herein, the elaborate regulation of mesopores in N-doped carbon materials is reported by pyrolyzing energetic metal-triazolate (MET) frameworks with different particle sizes and at different ramp rates. Higher thermal transfer rates brought about by smaller particle size and higher ramp rate lead to more violent decomposition with a large number of gases producing, which in turn result in larger mesopores in the derivatives. Consequently, a series of N-doped carbon materials with controllable mesopores are obtained. As a proof-of-concept, ultrafine Pt nanoparticles are enveloped inside these mesopores to acquire high-performance electrocatalysts for oxygen reduction reaction. The optimized catalyst achieves high mass activity of 1.52 A mg(Pt)(-1) at 0.9 ViR-free and peak power density of 0.8 W cm(-2) (H-2-Air) with an ultralow Pt loading of 0.05 mg(Pt) cm(-2) at cathode in fuel cells, highlighting the great advantages of MET-derived carbon materials with controllable mesopores in the preparation of advanced electrocatalysts.
引用
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页数:8
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