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dc.contributor.authorSeo, Jeongsuk
dc.contributor.authorZhao, Lan
dc.contributor.authorCha, Dong Kyu
dc.contributor.authorTakanabe, Kazuhiro
dc.contributor.authorKatayama, Masao
dc.contributor.authorKubota, Jun
dc.contributor.authorDomen, Kazunari
dc.date.accessioned2015-08-03T11:10:51Z
dc.date.available2015-08-03T11:10:51Z
dc.date.issued2013-05-22
dc.identifier.citationSeo, J., Zhao, L., Cha, D., Takanabe, K., Katayama, M., Kubota, J., & Domen, K. (2013). Highly Dispersed TaOx Nanoparticles Prepared by Electrodeposition as Oxygen Reduction Electrocatalysts for Polymer Electrolyte Fuel Cells. The Journal of Physical Chemistry C, 117(22), 11635–11646. doi:10.1021/jp4013703
dc.identifier.issn19327447
dc.identifier.doi10.1021/jp4013703
dc.identifier.urihttp://hdl.handle.net/10754/562804
dc.description.abstractBased on the chemical stability of group IV and V elements in acidic solutions, TaOx nanoparticles prepared by electrodeposition in an ethanol-based Ta plating bath at room temperature were investigated as novel nonplatinum electrocatalysts for the oxygen reduction reaction (ORR) in polymer electrolyte fuel cells (PEFCs). Electrodeposition conditions of Ta complexes and subsequent various heat treatments for the deposited TaOx were examined for the best performance of the ORR. TaOx particles on carbon black (CB), electrodeposited at a constant potential of -0.5 V Ag/AgCl for 10 s and then heat-treated by pure H2 flow at 523 K for 1 h, showed excellent catalytic activity with an onset potential of 0.93 VRHE (for 2 μA cm-2) for the ORR. Surface characterizations of the catalysts were performed by scanning transmission electron microscopy (STEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDS). The loading amounts of the electrodeposited material on the CB were determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES). All the physical results suggested that high dispersion of TaOx particles on the CB surface with 2-3 nm size was critical and key for high activity. The chemical identity and modified surface structure for the deposited TaOx catalysts before and after H 2 heat treatment were analyzed by X-ray photoelectron spectroscopy (XPS). The formation of more exposed active sites on the electrode surface and enhanced electroconductivity of the tantalum oxide promoted from the H 2 treatment greatly improved the ORR performance of the electrodeposited TaOx nanoparticles on CB. Finally, the highly retained ORR activity after an accelerated durability test in an acidic solution confirmed and proved the chemical stability of the oxide nanoparticles. The high utilization of the electrodeposited TaOx nanoparticles uniformly dispersed on CB for the ORR was comparable to that of commercial Pt/CB catalysts, visually demonstrating their catalytic potential for PEFC electrocatalysts. © 2013 American Chemical Society.
dc.description.sponsorshipThis work was supported in part by the Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST) of the Cabinet Office of Japan and "Elements Strategy Initiative for Catalysts & Batteries (ESICB)" supported by the MEXT program "Elements Strategy Initiative to Form Core Rersearch Center" (since 2012) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan. This work also contributes the international exchange program of the A3 Foresight Program of the Japan Society for the Promotion of Science (JSPS). One of authors, Seo, appreciates the support of the Global Centers of Excellence (GCOE) Program of JSPS for her work at the University of Tokyo.
dc.publisherAmerican Chemical Society (ACS)
dc.titleHighly dispersed TaOx nanoparticles prepared by electrodeposition as oxygen reduction electrocatalysts for polymer electrolyte fuel cells
dc.typeArticle
dc.contributor.departmentAdvanced Nanofabrication, Imaging and Characterization Core Lab
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentCatalysis for Energy Conversion (CatEC)
dc.contributor.departmentChemical Science Program
dc.contributor.departmentCore Labs
dc.contributor.departmentImaging and Characterization Core Lab
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalThe Journal of Physical Chemistry C
dc.contributor.institutionDepartment of Chemical System Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan
dc.contributor.institutionElements Strategy Initiative for Catalysts and Batteries (ESICB), Kyoto University, Katsura, Kyoto 615-8520, Japan
kaust.personCha, Dong Kyu
kaust.personTakanabe, Kazuhiro
kaust.personZhao, Lan
dc.date.published-online2013-05-22
dc.date.published-print2013-06-06


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