NiO/Nb2O5/C Hydrazine Electrooxidation Catalysts for Anion Exchange Membrane Fuel Cells

NiO/Nb2O5/C (8:1), (4:1), (2:1), NiO/C, and Ni/C catalysts for hydrazine electrooxidation were synthesized by an evaporation drying method followed by thermal annealing. Prepared catalysts were characterized by X-ray diffraction (XRD), high-angle annular dark field scanning transmission electron mic...

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Veröffentlicht in:Journal of the Electrochemical Society 2017-01, Vol.164 (4), p.F229-F234
Hauptverfasser: Sakamoto, Tomokazu, Masuda, Teruyuki, Yoshimoto, Koji, Kishi, Hirofumi, Yamaguchi, Susumu, Matsumura, Daiju, Tamura, Kazuhisa, Hori, Akihiro, Horiuchi, Yousuke, Serov, Alexey, Artyushkova, Kateryna, Atanassov, Plamen, Tanaka, Hirohisa
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container_issue 4
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container_title Journal of the Electrochemical Society
container_volume 164
creator Sakamoto, Tomokazu
Masuda, Teruyuki
Yoshimoto, Koji
Kishi, Hirofumi
Yamaguchi, Susumu
Matsumura, Daiju
Tamura, Kazuhisa
Hori, Akihiro
Horiuchi, Yousuke
Serov, Alexey
Artyushkova, Kateryna
Atanassov, Plamen
Tanaka, Hirohisa
description NiO/Nb2O5/C (8:1), (4:1), (2:1), NiO/C, and Ni/C catalysts for hydrazine electrooxidation were synthesized by an evaporation drying method followed by thermal annealing. Prepared catalysts were characterized by X-ray diffraction (XRD), high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM), energy dispersive X-ray spectrometry (EDS), and X-ray absorption fine structure (XAFS). Catalytic activity, durability, and selectivity in the reaction of hydrazine electrooxidation were evaluated in alkaline media. The highest catalytic activity in mentioned above reaction was found for Ni/C, followed by: NiO/Nb2O5/C (8:1), NiO/Nb2O5/C (4:1). NiO/Nb2O5/C (2:1) whiles NiO/C has almost no activity for hydrazine oxidation. NiO/Nb2O5/C (8:1) and (4:1) had a highest stability during electrooxidation of hydrazine at 60°C. It was explained by oxygen defect of NiO in NiO/Nb2O5/C from XAFS analysis. The selectivity hydrazine electrooxidation as measured by ammonia production resulted in observation that metallic Ni surface facilitates N-N bond breaking of hydrazine, which was confirmed by density functional theory (DFT) calculations.
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Prepared catalysts were characterized by X-ray diffraction (XRD), high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM), energy dispersive X-ray spectrometry (EDS), and X-ray absorption fine structure (XAFS). Catalytic activity, durability, and selectivity in the reaction of hydrazine electrooxidation were evaluated in alkaline media. The highest catalytic activity in mentioned above reaction was found for Ni/C, followed by: NiO/Nb2O5/C (8:1), NiO/Nb2O5/C (4:1). NiO/Nb2O5/C (2:1) whiles NiO/C has almost no activity for hydrazine oxidation. NiO/Nb2O5/C (8:1) and (4:1) had a highest stability during electrooxidation of hydrazine at 60°C. It was explained by oxygen defect of NiO in NiO/Nb2O5/C from XAFS analysis. The selectivity hydrazine electrooxidation as measured by ammonia production resulted in observation that metallic Ni surface facilitates N-N bond breaking of hydrazine, which was confirmed by density functional theory (DFT) calculations.</description><identifier>EISSN: 1945-7111</identifier><identifier>DOI: 10.1149/2.0281704jes</identifier><language>eng</language><publisher>The Electrochemical Society</publisher><ispartof>Journal of the Electrochemical Society, 2017-01, Vol.164 (4), p.F229-F234</ispartof><rights>The Author(s) 2017. 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Electrochem. Soc</addtitle><description>NiO/Nb2O5/C (8:1), (4:1), (2:1), NiO/C, and Ni/C catalysts for hydrazine electrooxidation were synthesized by an evaporation drying method followed by thermal annealing. Prepared catalysts were characterized by X-ray diffraction (XRD), high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM), energy dispersive X-ray spectrometry (EDS), and X-ray absorption fine structure (XAFS). Catalytic activity, durability, and selectivity in the reaction of hydrazine electrooxidation were evaluated in alkaline media. The highest catalytic activity in mentioned above reaction was found for Ni/C, followed by: NiO/Nb2O5/C (8:1), NiO/Nb2O5/C (4:1). NiO/Nb2O5/C (2:1) whiles NiO/C has almost no activity for hydrazine oxidation. NiO/Nb2O5/C (8:1) and (4:1) had a highest stability during electrooxidation of hydrazine at 60°C. It was explained by oxygen defect of NiO in NiO/Nb2O5/C from XAFS analysis. 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Electrochem. Soc</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>164</volume><issue>4</issue><spage>F229</spage><epage>F234</epage><pages>F229-F234</pages><eissn>1945-7111</eissn><abstract>NiO/Nb2O5/C (8:1), (4:1), (2:1), NiO/C, and Ni/C catalysts for hydrazine electrooxidation were synthesized by an evaporation drying method followed by thermal annealing. Prepared catalysts were characterized by X-ray diffraction (XRD), high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM), energy dispersive X-ray spectrometry (EDS), and X-ray absorption fine structure (XAFS). Catalytic activity, durability, and selectivity in the reaction of hydrazine electrooxidation were evaluated in alkaline media. The highest catalytic activity in mentioned above reaction was found for Ni/C, followed by: NiO/Nb2O5/C (8:1), NiO/Nb2O5/C (4:1). NiO/Nb2O5/C (2:1) whiles NiO/C has almost no activity for hydrazine oxidation. NiO/Nb2O5/C (8:1) and (4:1) had a highest stability during electrooxidation of hydrazine at 60°C. It was explained by oxygen defect of NiO in NiO/Nb2O5/C from XAFS analysis. The selectivity hydrazine electrooxidation as measured by ammonia production resulted in observation that metallic Ni surface facilitates N-N bond breaking of hydrazine, which was confirmed by density functional theory (DFT) calculations.</abstract><pub>The Electrochemical Society</pub><doi>10.1149/2.0281704jes</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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title NiO/Nb2O5/C Hydrazine Electrooxidation Catalysts for Anion Exchange Membrane Fuel Cells
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