A quick and versatile one step metal–organic chemical deposition method for supported Pt and Pt-alloy catalysts
A quick and versatile one step metal–organic chemical deposition method for supported Pt and Pt-alloy catalysts
A simple, modified Metal–Organic Chemical Deposition (MOCD) method for Pt, PtRu and PtCo nanoparticle deposition onto a variety of support materials, including C, SiC, B4C, LaB6, TiB2, TiN and a ceramic/carbon nanofiber, is described. Pt deposition using Pt(acac)2 as a precursor is shown to occur via a mixed solid/liquid/vapour precursor phase which results in a high Pt yield of 90–92% on the support material. Pt and Pt alloy nanoparticles range 1.5–6.2 nm, and are well dispersed on all support materials, in a one-step method, with a total catalyst preparation time of ∼10 hours (2.4–4× quicker than conventional methods). The MOCD preparation method includes moderate temperatures of 350 °C in a tubular furnace with an inert gas supply at 2 bar, a high pressure (2–4 bar) compared to typical MOCVD methods (∼0.02–10 mbar). Pt/C catalysts with Pt loadings of 20, 40 and 60 wt% were synthesised, physically characterised, electrochemically characterised and compared to commercial Pt/C catalysts. TEM, XRD and ex situ EXAFS show similar Pt particle sizes and Pt particle shape identifiers, namely the ratio of the third to first Pt coordination numbers modelled from ex situ EXAFS, between the MOCD prepared catalysts and commercial catalysts. Moreover, electrochemical characterisation of the Pt/C MOCD catalysts obtained ORR mass activities with a maximum of 428 A gPt−1 at 0.9 V, which has similar mass activities to the commercial catalysts (80–160% compared to the commercial Pt/C catalysts).
19982–19996
Jackson, Colleen
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Smith, Graham T.
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Mpofu, Nobuhle
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Dawson, Jack M.S.
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Khoza, Thulile
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September, Caelin
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Taylor, Susan M.
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Inwood, David W.
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Leach, Andrew
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Kramer, Denis
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Russell, Andrea E.
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Kucernak, Anthony R.
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Levecque, Pieter
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27 May 2020
Jackson, Colleen
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Smith, Graham T.
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Mpofu, Nobuhle
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Dawson, Jack M.S.
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Khoza, Thulile
a5c07b99-7bce-4f08-a76f-6061bf4ec450
September, Caelin
2df06869-72a3-4d80-a996-7f00c6ab91cb
Taylor, Susan M.
fe950a9c-7d8f-4179-a774-ca364d2d5144
Inwood, David W.
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Leach, Andrew
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Kramer, Denis
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Russell, Andrea E.
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Kucernak, Anthony R.
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Levecque, Pieter
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Jackson, Colleen, Smith, Graham T., Mpofu, Nobuhle, Dawson, Jack M.S., Khoza, Thulile, September, Caelin, Taylor, Susan M., Inwood, David W., Leach, Andrew, Kramer, Denis, Russell, Andrea E., Kucernak, Anthony R. and Levecque, Pieter
(2020)
A quick and versatile one step metal–organic chemical deposition method for supported Pt and Pt-alloy catalysts.
RSC Advances, 10 (34), .
(doi:10.1039/D0RA03001E).
Abstract
A simple, modified Metal–Organic Chemical Deposition (MOCD) method for Pt, PtRu and PtCo nanoparticle deposition onto a variety of support materials, including C, SiC, B4C, LaB6, TiB2, TiN and a ceramic/carbon nanofiber, is described. Pt deposition using Pt(acac)2 as a precursor is shown to occur via a mixed solid/liquid/vapour precursor phase which results in a high Pt yield of 90–92% on the support material. Pt and Pt alloy nanoparticles range 1.5–6.2 nm, and are well dispersed on all support materials, in a one-step method, with a total catalyst preparation time of ∼10 hours (2.4–4× quicker than conventional methods). The MOCD preparation method includes moderate temperatures of 350 °C in a tubular furnace with an inert gas supply at 2 bar, a high pressure (2–4 bar) compared to typical MOCVD methods (∼0.02–10 mbar). Pt/C catalysts with Pt loadings of 20, 40 and 60 wt% were synthesised, physically characterised, electrochemically characterised and compared to commercial Pt/C catalysts. TEM, XRD and ex situ EXAFS show similar Pt particle sizes and Pt particle shape identifiers, namely the ratio of the third to first Pt coordination numbers modelled from ex situ EXAFS, between the MOCD prepared catalysts and commercial catalysts. Moreover, electrochemical characterisation of the Pt/C MOCD catalysts obtained ORR mass activities with a maximum of 428 A gPt−1 at 0.9 V, which has similar mass activities to the commercial catalysts (80–160% compared to the commercial Pt/C catalysts).
Text
RSC Adv 2020 MOCD
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Accepted/In Press date: 20 May 2020
e-pub ahead of print date: 27 May 2020
Published date: 27 May 2020
Additional Information:
Funding Information:
This work was supported by the Royal Society in the form of a Royal Society-Newton Advanced Fellowship (P. L.; grant no. NA140367). C. J. acknowledges the University of Cape Town for nancial support through a UCT PhD Mobility Grant. D. K. and G. T. S. thank the EPSRC H2FC SUPERGEN (grant no. EP/ J016454/1) for nancial support. G. T. S. thanks the HySA/ Catalysis Programme for a postdoctoral fellowship. D. K. acknowledges support from STFC (ST/K00171X/1 and ST/ N002385/1). P. L., N. M., T. K., C. S. and S. M. T. acknowledge support from the HySA/Catalysis Programme.
Publisher Copyright:
© The Royal Society of Chemistry 2020.
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Local EPrints ID: 441082
URI: http://eprints.soton.ac.uk/id/eprint/441082
ISSN: 2046-2069
PURE UUID: cd7621de-fb4a-4c38-a9ac-0ad0a0407212
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Date deposited: 29 May 2020 16:31
Last modified: 06 Jun 2024 01:37
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Contributors
Author:
Colleen Jackson
Author:
Graham T. Smith
Author:
Nobuhle Mpofu
Author:
Jack M.S. Dawson
Author:
Thulile Khoza
Author:
Caelin September
Author:
Susan M. Taylor
Author:
David W. Inwood
Author:
Andrew Leach
Author:
Anthony R. Kucernak
Author:
Pieter Levecque
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