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dc.contributor.authorRowley-Neale, Samuel J.*
dc.contributor.authorRatova, Marina*
dc.contributor.authorFugita, Lucas*
dc.contributor.authorSmith, Graham C.*
dc.contributor.authorGaffar, Amer*
dc.contributor.authorKulczyk-Malecka, Justyna*
dc.contributor.authorKelly, Peter J.*
dc.contributor.authorBanks, Craig E.*
dc.date.accessioned2018-11-19T15:59:55Z
dc.date.available2018-11-19T15:59:55Z
dc.date.issued2018-07-03
dc.identifier.citationRowley-Neale, S. J., Ratova, M., Fugita, L. T. N., Smith, G. C., Gaffar, A., Kulczyk-Malecka, Kelly, J., P. J. & Banks, C. E. (2018). Magnetron sputter coated nanoparticle MoS2 supported upon nanocarbon: A highly efficient electrocatalyst towards the Hydrogen Evolution Reaction, ACS Omega 3(7), 7235-7242.en
dc.identifier.issn2470-1343
dc.identifier.doi10.1021/acsomega.8b00258
dc.identifier.urihttp://hdl.handle.net/10034/621573
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Omega, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acsomega.8b00258en
dc.description.abstractThe design and fabrication of inexpensive highly efficient electrocatalysts for the production of hydrogen via the hydrogen evolution reaction (HER) underpin a plethora of emerging clean energy technologies. Herein, we report the fabrication of highly efficient electrocatalysts for the HER based on magnetron-sputtered MoS2 onto a nanocarbon support, termed MoS2/C. Magnetron sputtering time is explored as a function of its physiochemical composition and HER performance; increased sputtering times give rise to materials with differing compositions, i.e., Mo4+ to Mo6+ and associated S anions (sulfide, elemental, and sulfate), and improved HER outputs. An optimized sputtering time of 45 min was used to fabricate the MoS2/C material. This gave rise to an optimal HER performance with regard to its HER onset potential, achievable current, and Tafel value, which were −0.44 (vs saturated calomel electrode (SCE)), −1.45 mV s−1, and 43 mV dec−1, respectively, which has the highest composition of Mo4+ and sulfide (MoS2). Electrochemical testing toward the HER via drop casting MoS2/C upon screen-printed electrodes (SPEs) to electrically wire the nanomaterial is found to be mass coverage dependent, where the current density increases up to a critical mass (ca. 50 μg cm−2), after which a plateau is observed. To allow for a translation of the bespoke fabricated MoS2/C from laboratory to new industrial applications, MoS2/C was incorporated into the bulk ink utilized in the fabrication of SPEs (denoted as MoS2/C-SPE), thus allowing for improved electrical wiring to the MoS2/C and resulting in the production of scalable and reproducible electrocatalytic platforms. The MoS2/C-SPEs displayed far greater HER catalysis with a 450 mV reduction in the HER onset potential and a 1.70 mA cm−2 increase in the achievable current density (recorded at −0.75 V (vs SCE)), compared to a bare/unmodified graphitic SPE. The approach of using magnetron sputtering to modify carbon with MoS2 facilitates the production of mass-producible, stable, and effective electrode materials for possible use in electrolyzers, which are cost competitive to Pt and mitigate the need to use time-consuming and low-yield exfoliation techniques typically used to fabricate pristine MoS2.
dc.language.isoenen
dc.publisherAmerican Chemical Societyen
dc.relation.urlhttps://pubs.acs.org/doi/10.1021/acsomega.8b00258en
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectHydrogen evolution reactionen
dc.subjectMagnetron sputteringen
dc.subjectNanoparticle MoS2en
dc.subjectElectrocatalysten
dc.subjectXPSen
dc.titleMagnetron Sputter-Coated Nanoparticle MoS2 Supported on Nanocarbon: A Highly Efficient Electrocatalyst toward the Hydrogen Evolution Reactionen
dc.typeArticleen
dc.contributor.departmentManchester Metropolitan University; University of Chester; University of São Paulaen
dc.identifier.journalACS Omega
or.grant.openaccessYesen
rioxxterms.funderunfundeden_US
rioxxterms.identifier.projectunfundeden_US
rioxxterms.versionAMen
rioxxterms.versionofrecordhttps://doi.org/10.1021/acsomega.8b00258
rioxxterms.licenseref.startdate2018-07-03
rioxxterms.publicationdate2018-07-03
dc.dateAccepted2018-06-07
dc.date.deposited2018-11-19


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