g-C3N4 promoted MOF derived hollow carbon nanopolyhedra doped with high density/fraction of single Fe atoms as an ultra-high performance non-precious catalyst towards acidic ORR and PEM fuel cells

被引:165
作者
Deng, Yijie [1 ,2 ]
Chi, Bin [1 ]
Tian, Xinlong [1 ]
Cui, Zhiming [1 ]
Liu, Ershuai [4 ]
Jia, Qingying [4 ]
Fan, Wenjun [1 ]
Wang, Guanghua [1 ]
Dang, Dai [1 ]
Li, Minsi [3 ]
Zang, Ketao [5 ]
Luo, Jun [5 ]
Hu, Yongfeng [6 ]
Liao, Shijun [1 ]
Sun, Xueliang [3 ]
Mukerjee, Sanjeev [4 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510641, Guangdong, Peoples R China
[2] Dongguan Univ Technol, Sch Environm & Civil Engn, Dongguan, Peoples R China
[3] Univ Western Ontario, Dept Mech & Mat Engn, 1151 Richmond St, London, ON N6A 3K7, Canada
[4] Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USA
[5] Tianjin Univ Technol, TUT FEI Joint Lab, Tianjin Key Lab Adv Funct Porous Mat,Sch Mat Sci, Ctr Electron Microscopy,Inst New Energy Mat & Low, Tianjin 300384, Peoples R China
[6] Canadian Light Source, 44 Innovat Blvd, Saskatoon, SK S7N 2V3, Canada
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION REACTION; METAL-ORGANIC FRAMEWORKS; POROUS CARBON; GRAPHITIC CARBON; FE/N/C-CATALYSTS; ELECTROCATALYSTS; SITES; IRON; NANOPARTICLES; NANOSTRUCTURES;
D O I
10.1039/c8ta11785c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report a hollow carbon nanopolyhedron catalyst doped with N and single Fe atoms, prepared by pyrolyzing hollow ZIF-8 with ferric acetylacetonate and g-C3N4. The catalyst retains the polyhedral morphology of its precursor and possesses exclusively Fe-N-4 moieties promoted by g-C3N4 nitriding, evidenced by multipronged microscopic and spectroscopic analyses. In rotating disk measurements, the catalyst exhibits superior ORR activity in both acidic and alkaline media, with a half-wave potential of 0.78 V in the former and 0.845 V in the latter. In addition, its ORR stability surpasses that of commercial Pt/C in acidic and alkaline media. Most notably, the catalyst exhibits ultra-high performance in a H-2/O-2 proton exchange membrane fuel cell (PEMFC), with a current density of 400 mA cm(-2) at 0.7 V and 133 mA cm(-2) at 0.8 V, and a maximum power density of 628 mW cm(-2). This is among the best PEMFC performances reported for cathodes free of platinum-group metals. We attribute this excellent-ORR activity to the integration of the high density Fe(ii)-N-4-H2O moiety (4.51956 x 10(13) sites cm(-2)) embedded in the carbon framework, identified by in situ X-ray absorption spectroscopy, and the well-balanced micro/meso/macroporous structure.
引用
收藏
页码:5020 / 5030
页数:11
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