Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation

© 2018 Elsevier Inc. The objective of our work is to improve low-temperature fuel cell catalysts by increasing the surface area to augment the efficiency of catalytic reactions. Reduced graphene oxide (rGO) supports were prepared by adding N-containing derivatives of polydopamine (PDA) and loading o...

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Main Authors: Suwaphid Themsirimongkon, Kontad Ounnunkad, Surin Saipanya
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/58385
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spelling th-cmuir.6653943832-583852018-09-05T04:30:47Z Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation Suwaphid Themsirimongkon Kontad Ounnunkad Surin Saipanya Chemical Engineering Materials Science © 2018 Elsevier Inc. The objective of our work is to improve low-temperature fuel cell catalysts by increasing the surface area to augment the efficiency of catalytic reactions. Reduced graphene oxide (rGO) supports were prepared by adding N-containing derivatives of polydopamine (PDA) and loading of Pt and Pt-based metal alloy nanoparticles were accomplished for catalyst preparation. To study the effects of surface modification on catalyst activity, the GO surfaces modified by addition of PDA (PDA-rGO) were richer in oxygen- and nitrogen-containing functional groups, which reduced the number of graphene defects. Reduction of metals (M = Pt, Pd, PtxPdywhere x and y = 1–3) by NaBH4produced M/GO (metal on GO) and M/PDA-rGO (metal on PDA-rGO) catalysts. Examination of morphology and chemical composition confirmed that the existence of particle size on M/PDA-rGO catalysts was smaller than that on M/GO catalysts in agreement with calculated electrochemically active surface areas (ECSA). Electrochemical analysis was conducted to evaluate the catalyst activity and stability. The prepared catalysts had significantly greater surface areas as a result of association between the metal nanoparticles and the oxygen and nitrogen functional groups on the rGO supports. The catalysts also exhibited lower onset potentials and greater current intensities, If/Ibvalues, and long-term stabilities for methanol and ethanol oxidation compared with those of commercial PtRu/C. Moreover, the diameter of the Nyquist plot of the catalysts on PDA-rGO were smaller than that of the catalysts M/GO. The results suggest that variation of the PtxPdyatomic ratio on carbon nanocomposites is an encouraging means of enhancing electrocatalytic performance in direct alcohol fuel cell applications. 2018-09-05T04:23:26Z 2018-09-05T04:23:26Z 2018-11-15 Journal 10957103 00219797 2-s2.0-85049320834 10.1016/j.jcis.2018.06.072 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85049320834&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/58385
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Chemical Engineering
Materials Science
spellingShingle Chemical Engineering
Materials Science
Suwaphid Themsirimongkon
Kontad Ounnunkad
Surin Saipanya
Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
description © 2018 Elsevier Inc. The objective of our work is to improve low-temperature fuel cell catalysts by increasing the surface area to augment the efficiency of catalytic reactions. Reduced graphene oxide (rGO) supports were prepared by adding N-containing derivatives of polydopamine (PDA) and loading of Pt and Pt-based metal alloy nanoparticles were accomplished for catalyst preparation. To study the effects of surface modification on catalyst activity, the GO surfaces modified by addition of PDA (PDA-rGO) were richer in oxygen- and nitrogen-containing functional groups, which reduced the number of graphene defects. Reduction of metals (M = Pt, Pd, PtxPdywhere x and y = 1–3) by NaBH4produced M/GO (metal on GO) and M/PDA-rGO (metal on PDA-rGO) catalysts. Examination of morphology and chemical composition confirmed that the existence of particle size on M/PDA-rGO catalysts was smaller than that on M/GO catalysts in agreement with calculated electrochemically active surface areas (ECSA). Electrochemical analysis was conducted to evaluate the catalyst activity and stability. The prepared catalysts had significantly greater surface areas as a result of association between the metal nanoparticles and the oxygen and nitrogen functional groups on the rGO supports. The catalysts also exhibited lower onset potentials and greater current intensities, If/Ibvalues, and long-term stabilities for methanol and ethanol oxidation compared with those of commercial PtRu/C. Moreover, the diameter of the Nyquist plot of the catalysts on PDA-rGO were smaller than that of the catalysts M/GO. The results suggest that variation of the PtxPdyatomic ratio on carbon nanocomposites is an encouraging means of enhancing electrocatalytic performance in direct alcohol fuel cell applications.
format Journal
author Suwaphid Themsirimongkon
Kontad Ounnunkad
Surin Saipanya
author_facet Suwaphid Themsirimongkon
Kontad Ounnunkad
Surin Saipanya
author_sort Suwaphid Themsirimongkon
title Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
title_short Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
title_full Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
title_fullStr Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
title_full_unstemmed Electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
title_sort electrocatalytic enhancement of platinum and palladium metal on polydopamine reduced graphene oxide support for alcohol oxidation
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85049320834&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/58385
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