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Epitaxial and atomically thin graphene–metal hybrid catalyst films: the dual role of graphene as the support and the chemically-transparent protective cap

Abstract:
In this study, we demonstrate dual roles for graphene, as both a platform for large-area, fully-wetted growth of two-dimensional Pt films that are one monolayer to several multilayers thick, while also serving as a 'chemically transparent' barrier to catalytic deactivation wherein graphene does not restrict the access of the reactants but does block Pt from dissolution or agglomeration. Using these architectures, we show that it is possible to simultaneously achieve enhanced catalytic activity and unprecedented stability, retaining full activity beyond 1000 cycles, for the canonical oxygen reduction reaction (ORR). Using high resolution TEM, AFM, X-ray photoemission/absorption spectroscopy (XPS/XAS), Raman, and electrochemical methods, we show that, due to intimate graphene-Pt epitaxial contact, Pt-ML/GR hybrid architectures are able to induce a compressive strain on the supported Pt adlayer and increase catalytic activity for ORR. With no appreciable Pt loss or agglomeration observed with the GR/Pt-ML catalysts after 1000 ORR cycles, our results open the door to using similar graphene-templated/graphene-capped hybrid catalysts as means to improve catalyst lifetime without a necessary compromise to their activity. More broadly, the epitaxial growth made possible by the room-temperature, wetted synthesis approach, should allow for efficient transfer of charge, strain, phonons and photons, impacting not just catalysis, but also electronic, thermoelectric and optical materials.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1039/C8EE00539G

Authors


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Role:
Author
ORCID:
0000-0003-4270-6258
More by this author
Role:
Author
ORCID:
0000-0003-4980-5574
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Role:
Author
ORCID:
0000-0002-0528-4685


Publisher:
Royal Society of Chemistry
Journal:
Energy and Environmental Science More from this journal
Volume:
11
Issue:
6
Pages:
1610-1616
Publication date:
2018-04-20
Acceptance date:
2018-04-12
DOI:
EISSN:
1754-5706
ISSN:
1754-5692


Keywords:
Pubs id:
pubs:864497
UUID:
uuid:c4c8ba92-fdf2-40d9-9b58-d1a30287bca7
Local pid:
pubs:864497
Source identifiers:
864497
Deposit date:
2018-11-06

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