Bimetallic PtAg alloyed nanoparticles and 3-D mesoporous graphene nanosheet hybrid architectures for advanced oxygen reduction reaction electrocatalysts
Herein, three-dimensional mesoporous graphene conductive networks supporting bimetallic PtAg alloyed nanoparticles ( i.e. PtAg/3DMGS) with a superior composited nanostructure have been fabricated for advanced oxygen reduction reaction electrocatalysts. The unique architecture of 3D porous graphene e...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 5; no. 44; pp. 23158 - 23169 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
2017
|
Subjects | |
Online Access | Get full text |
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Summary: | Herein, three-dimensional mesoporous graphene conductive networks supporting bimetallic PtAg alloyed nanoparticles (
i.e.
PtAg/3DMGS) with a superior composited nanostructure have been fabricated for advanced oxygen reduction reaction electrocatalysts. The unique architecture of 3D porous graphene exhibits a high surface area (1382 m
2
g
−1
), a well-defined mesoporous structure (an average pore size of 3.28 nm), as well as an excellent electronic conductivity (1350 S m
−1
). Inside the PtAg/3DMGS, high-density and ultrafine PtAg NPs (∼2.5 nm) were well dispersed on the porous surface of 3DMGS. The combination of ultrafine PtAg NPs and 3DMGS conductive networks provides a relatively stable macroporous composite architecture, which offers convenient binary channels for both electron transport and ion diffusion. This promising PtAg/3DMGS composite material reveals an ultrahigh mass activity (at 0.9 V) of 392 mA mg
Pt
−1
, which is nearly 4 times that of Pt/C (TKK) (102 mA mg
Pt
−1
). After 1000 CV cycles, the retention rates of mass activity are 81.6% and 66.7% for PtAg/3DMGS and Pt/C (TKK), respectively. These results demonstrate that the PtAg/3DMGS composite material is a promising electrocatalyst with high catalytic activity and high stability for the oxygen reduction reaction. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2050-7488 2050-7496 2050-7496 |
DOI: | 10.1039/C7TA07525A |