Platinum supported on pristine and nitrogen-doped bowl-like broken hollow carbon spheres as oxygen reduction reaction catalysts

被引:14
|
作者
Mashindi, Victor [1 ]
Mente, Pumza [1 ,4 ]
Mpofu, Nobuhle [3 ]
Phaahlamohlaka, Tumelo N. [1 ]
Makgae, Ofentse [2 ]
Kirkland, Angus I. [2 ]
Forbes, Roy [1 ]
Ozoemena, Kenneth I. [1 ]
Levecque, Pieter B. [3 ]
Coville, Neil J. [1 ,4 ]
机构
[1] Univ Witwatersrand, Mol Sci Inst, Sch Chem, ZA-2050 Johannesburg, South Africa
[2] Univ Oxford, Dept Mat, Parks Rd, Oxford OX1 3PH, England
[3] Univ Cape Town, Catalysis Inst, HySA Catalysis Ctr Competence, Dept Chem Engn, ZA-7701 Cape Town, South Africa
[4] Univ Witwatersrand, Sch Chem, DSI NRF Ctr Excellence Strong Mat, Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
Metal-support interactions; Broken bowl-like carbon; Oxygen reduction reaction; Nitrogen doping; Pore confinement; GRAPHITIZED CARBON; PT-ALLOY; ELECTROCATALYSTS; DURABILITY; NANOPARTICLES; MONODISPERSE; STABILITY; NANOTUBES; GRAPHENE; DEPOSITION;
D O I
10.1007/s10800-021-01554-0
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The development of active and durable proton exchange membrane fuel cell catalysts with high loading (ca. 40%) is critical for the commercialization of hydrogen fuel cells. Herein we report on the synthesis of a novel Pt/C catalyst using a novel bowl-like broken hollow carbon sphere (and N-doped sphere) support (carbon shell thickness similar to 4.6 nm). Highly dispersed Pt nanoparticles (d(Pt) similar to 4 nm) were deposited on both supports and within the carbon shell. The Pt particles in the pores were exposed on both sides of the shell, while the shell porosity ensured pore confinement of the Pt. Both catalysts exhibited high electrochemical surface areas (60-65 m(2) g(-1)) and cycling durability (6000 cycles) that was superior to a commercial benchmark Pt/C catalyst. These studies indicate that high loadings of confined small Pt particles on both sides of thin interconnected carbons can lead to high oxygen reduction reaction activities and durability. [GRAPHICS] .
引用
收藏
页码:991 / 1008
页数:18
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