A Pt/MnV2O6 nanocomposite for the borohydride oxidation reaction

Pt nanoparticles anchoring on MnV2O6 led to electrocatalyst with high performance for the direct borohydride fuel cell anode at low Pt loading along with remarkable stability shown by both experiments and DFT calculations. [Display omitted] Problems associated with carbon support corrosion under ope...

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Published inJournal of energy chemistry Vol. 55; pp. 428 - 436
Main Authors Milikić, Jadranka, Martins, Marta, Dobrota, Ana S., Bozkurt, Gamze, Soylu, Gulin S.P., Yurtcan, Ayşe B., Skorodumova, Natalia V., Pašti, Igor A., Šljukić, Biljana, Santos, Diogo M.F.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.04.2021
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Abstract Pt nanoparticles anchoring on MnV2O6 led to electrocatalyst with high performance for the direct borohydride fuel cell anode at low Pt loading along with remarkable stability shown by both experiments and DFT calculations. [Display omitted] Problems associated with carbon support corrosion under operating fuel cell conditions require the identification of alternative supports for platinum-based nanosized electrocatalysts. Platinum supported on manganese vanadate (Pt/MnV2O6) was prepared by microwave irradiation method and characterized using X-ray diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy with energy dispersive spectroscopy, and transmission electron microscopy. The borohydride oxidation reaction (BOR) on Pt/MnV2O6 was studied in highly alkaline media using voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. BOR electrocatalytic activity of Pt/MnV2O6 was also compared with that of commercial Pt/C (46 wt% Pt) electrocatalyst. The apparent activation energy of BOR at Pt/MnV2O6 was estimated to be 32 kJ mol−1 and the order of reaction to be 0.51, indicating that borohydride hydrolysis proceeds in parallel with its oxidation. Long-term stability of Pt/MnV2O6 under BOR typical conditions was observed. A laboratory-scale direct borohydride fuel cell assembled with a Pt/MnV2O6 anode reached a specific power of 274 W g−1. Experimental results on Pt/MnV2O6 were complemented by DFT calculations, which indicated good adherence of Pt to MnV2O6, beneficial for electrocatalyst stability.
AbstractList Pt nanoparticles anchoring on MnV2O6 led to electrocatalyst with high performance for the direct borohydride fuel cell anode at low Pt loading along with remarkable stability shown by both experiments and DFT calculations. [Display omitted] Problems associated with carbon support corrosion under operating fuel cell conditions require the identification of alternative supports for platinum-based nanosized electrocatalysts. Platinum supported on manganese vanadate (Pt/MnV2O6) was prepared by microwave irradiation method and characterized using X-ray diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy with energy dispersive spectroscopy, and transmission electron microscopy. The borohydride oxidation reaction (BOR) on Pt/MnV2O6 was studied in highly alkaline media using voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. BOR electrocatalytic activity of Pt/MnV2O6 was also compared with that of commercial Pt/C (46 wt% Pt) electrocatalyst. The apparent activation energy of BOR at Pt/MnV2O6 was estimated to be 32 kJ mol−1 and the order of reaction to be 0.51, indicating that borohydride hydrolysis proceeds in parallel with its oxidation. Long-term stability of Pt/MnV2O6 under BOR typical conditions was observed. A laboratory-scale direct borohydride fuel cell assembled with a Pt/MnV2O6 anode reached a specific power of 274 W g−1. Experimental results on Pt/MnV2O6 were complemented by DFT calculations, which indicated good adherence of Pt to MnV2O6, beneficial for electrocatalyst stability.
Problems associated with carbon support corrosion under operating fuel cell conditions require the identification of alternative supports for platinum-based nanosized electrocatalysts. Platinum supported on manganese vanadate (Pt/MnV2O6 ) was prepared by microwave irradiation method and characterized using X-ray diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy with energy dispersive spectroscopy, and transmission electron microscopy. The borohydride oxidation reaction (BOR) on Pt/MnV2O6 was studied in highly alkaline media using voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. BOR electrocatalytic activity of Pt/MnV2O6 was also compared with that of commercial Pt/C (46 wt% Pt) electrocatalyst. The apparent activation energy of BOR at Pt/MnV2O6 was estimated to be 32 kJ mol(-1) and the order of reaction to be 0.51, indicating that borohydride hydrolysis proceeds in parallel with its oxidation. Long-term stability of Pt/MnV2O6 under BOR typical conditions was observed. A laboratory-scale direct borohydride fuel cell assembled with a Pt/MnV2O6 anode reached a specific power of 274 W g(-1). Experimental results on Pt/MnV2O6 were complemented by DFT calculations, which indicated good adherence of Pt to MnV2O6, beneficial for electrocatalyst stability.
Author Martins, Marta
Bozkurt, Gamze
Santos, Diogo M.F.
Skorodumova, Natalia V.
Šljukić, Biljana
Soylu, Gulin S.P.
Dobrota, Ana S.
Yurtcan, Ayşe B.
Milikić, Jadranka
Pašti, Igor A.
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Manganese vanadate
Borohydride oxidation reaction
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Snippet Pt nanoparticles anchoring on MnV2O6 led to electrocatalyst with high performance for the direct borohydride fuel cell anode at low Pt loading along with...
Problems associated with carbon support corrosion under operating fuel cell conditions require the identification of alternative supports for platinum-based...
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StartPage 428
SubjectTerms Borohydride oxidation reaction
Density functional theory
Manganese vanadate
Platinum-based electrocatalyst
Title A Pt/MnV2O6 nanocomposite for the borohydride oxidation reaction
URI https://dx.doi.org/10.1016/j.jechem.2020.07.029
https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-434435
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