Platinum Nanocatalysts Supported on Defective Hollow Carbon Spheres: Oxygen Reduction Reaction Durability Studies

被引:9
|
作者
Mashindi, Victor [1 ]
Mente, Pumza [1 ]
Phaahlamohlaka, Tumelo N. [1 ]
Mpofu, Nobuhle [2 ]
Makgae, Ofentse A. [3 ]
Moreno, Beatriz D. [4 ]
Barrett, Dean H. [1 ]
Forbes, Roy P. [1 ]
Levecque, Pieter B. [2 ]
Ozoemena, Kenneth I. [1 ,2 ]
Coville, Neil J. [1 ,2 ]
机构
[1] Univ Witwatersrand, Mol Sci Inst, Sch Chem, Johannesburg, South Africa
[2] Univ Cape Town, Catalysis Inst, HySA Catalysis Ctr Competence, Dept Chem Engn, Cape Town, South Africa
[3] Lund Univ, Natl Ctr High Resolut Electron Microscopy nCHREM, Ctr Anal & Synth NanoLund, Lund, Sweden
[4] Canadian Light Source Inc, Saskatoon, SK, Canada
来源
FRONTIERS IN CHEMISTRY | 2022年 / 10卷
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
platinum; hollow carbon spheres; oxygen reduction (ORR); nanocarbon; pair distribution function; catalysis; RADIAL-DISTRIBUTION FUNCTION; CATALYST DEGRADATION; NANOPARTICLES; MEMBRANE; BLACK; ELECTROCATALYSTS; PERFORMANCE; GRAPHENE;
D O I
10.3389/fchem.2022.839867
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The durability and long-term applicability of catalysts are critical parameters for the commercialization and adoption of fuel cells. Even though a few studies have been conducted on hollow carbon spheres (HCSs) as supports for Pt in oxygen reduction reactions (ORR) catalysis, in-depth durability studies have not been conducted thus far. In this study, Pt/HCSs and Pt/nitrogen-doped HCSs (Pt/NHCSs) were prepared using a reflux deposition technique. Small Pt particles were formed with deposition on the outside of the shell and inside the pores of the shell. The new catalysts demonstrated high activity (>380 mu A cm(-2) and 240 mA g(-1)) surpassing the commercial Pt/C by more than 10%. The catalysts demonstrated excellent durability compared to a commercial Pt/C in load cycling, experiencing less than 50% changes in the mass-specific activity (MA) and surface area-specific activity (SA). In stop-start durability cycling, the new materials demonstrated high stability with more than 50% retention of electrochemical active surface areas (ECSAs). The results can be rationalised by the high BET surface areas coupled with an array of meso and micropores that led to Pt confinement. Further, pair distribution function (PDF) analysis of the catalysts confirmed that the nitrogen and oxygen functional groups, as well as the shell curvature/roughness provided defects and nucleation sites for the deposition of the small Pt nanoparticles. The balance between graphitic and diamond-like carbon was critical for the electronic conductivity and to provide strong Pt-support anchoring.
引用
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页数:15
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