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Oxygen reduction reaction and proton exchange membrane fuel cell performance of pulse electrodeposited Pt–Ni and Pt–Ni–Mo(O) nanoparticles

Eiler, Konrad (författare)
Department de Física, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain
Mölmen, Live (författare)
RISE,Elektrifiering och pålitlighet,Jönköping University, Sweden,JTH, Material och tillverkning,Department of Electrification and Reliability, RISE Research Institutes of Sweden, Borås, Sweden
Fast, Lars (författare)
RISE,Elektrifiering och pålitlighet,Department of Electrification and Reliability, RISE Research Institutes of Sweden, Borås, Sweden
visa fler...
Leisner, Peter (författare)
Jönköping University,JTH, Material och tillverkning
Sort, Jordi (författare)
Universitat Autònoma de Barcelona, Spain; ICREA, Spain,Department de Física, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain
Pellicer, Eva (författare)
Department de Física, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain
visa färre...
 (creator_code:org_t)
Elsevier Ltd, 2022
2022
Engelska.
Ingår i: Materials Today Energy. - : Elsevier Ltd. - 2468-6069. ; 27
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Proton exchange membrane fuel cells (PEMFCs) are an important alternative to fossil fuels and a complement to batteries for the electrification of vehicles. However, their high cost obstructs commercialization, and the catalyst material, including its synthesis, constitutes one of the major cost components. In this work, Pt–Ni and Pt–Ni–Mo(O) nanoparticles (NPs) of varying composition have been synthesized in a single step by pulse electrodeposition onto a PEMFC's gas diffusion layer. The proposed synthesis route combines NP synthesis and their fixation onto the microporous carbon layer in a single step. Both Pt–Ni and Pt–Ni–Mo(O) catalysts exhibit extremely high mass activities at oxygen reduction reaction (ORR) with very low Pt loadings of around 4 μg/cm2 due to the favorable distribution of NPs in contact with the proton exchange membrane. Particle sizes of 40–50 nm and 40–80 nm were obtained for Pt–Ni and Pt–Ni–Mo(O) systems, respectively. The highest ORR mass activities were found for Pt67Ni33 and Pt66Ni32–MoOx NPs. The feasibility of a single-step electrodeposition of Pt–Ni–Mo(O) NPs was successfully demonstrated; however, the ternary NPs are of more amorphous nature in contrast to the crystalline, binary Pt–Ni particles, due to the oxidized state of Mo. Nevertheless, despite their heterogeneous nature, the ternary NPs show homogeneous behavior even on a microscopic scale. © 2022 The Author(s)

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Materialteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering (hsv//eng)

Nyckelord

Electrocatalysis
Electrosynthesis
Hydrogen energy
PEM fuel cell
Pulse electrodeposition
Binary alloys
Catalysts
Diffusion in gases
Electrodeposition
Electrodes
Electrolytic reduction
Fossil fuels
Microporosity
Molybdenum oxide
Nanoparticles
Oxygen
Proton exchange membrane fuel cells (PEMFC)
Synthesis (chemical)
Fuel cell performance
Mass activity
Oxygen reduction reaction
Proton-exchange membranes fuel cells
Single-step
Ternary nanoparticles

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Eiler, Konrad
Mölmen, Live
Fast, Lars
Leisner, Peter
Sort, Jordi
Pellicer, Eva
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Kemi
TEKNIK OCH TEKNOLOGIER
TEKNIK OCH TEKNO ...
och Materialteknik
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Materials Today ...
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RISE
Jönköping University

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