Ambient Oxidation of Ultrasmall Platinum Nanoparticles on Microporous Carbon Catalyst Supports

被引:18
作者
Banerjee, Ritubarna [1 ]
Chen, Donna A. [2 ]
Karakalos, Stavros [1 ]
Piedboeu, Marie-Laure C. [3 ]
Job, Nathalie [3 ]
Regalbuto, John R. [1 ]
机构
[1] Univ South Carolina, Dept Chem Engn, Columbia, SC 29208 USA
[2] Univ South Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA
[3] Univ Liege, Dept Chem Engn Nanomat, Catalysis, Electrochem, B-4000 Liege, Belgium
来源
ACS APPLIED NANO MATERIALS | 2018年 / 1卷 / 10期
关键词
micropores; ambient oxidation; carbon supports; platinum nanoparticles; particle stabilization; ADSORPTION; OXIDE; SURFACE; XEROGELS; NITROGEN; XPS;
D O I
10.1021/acsanm.8b01548
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ultrasmall platinum nanoparticles on carbon catalyst supports undergo oxidation in ambient air. A systematic survey of carbon supports with controlled pore structures was conducted to isolate the effect of pore structure on particle size and resistance to oxidation. It was found that carbon supports with higher microporosity gave larger metal particles at high metal weight loadings, whereas the particle sizes remained independent of pore size at low weight loadings. It is the large particles that are most stable to oxidation; particles of average size less than 1.4 nm are more than 80% oxidized, while particles greater than 1.8 nm are less than 30% oxidized. The effect of micropores on the stabilization of Pt to oxidation is thus indirect; the larger particles formed in the micropores at high metal loadings do not oxidize. At lower loadings, the pore environment plays no role in stabilizing the Pt nanoparticles to oxidation.
引用
收藏
页码:5876 / 5884
页数:17
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