Electrocatalytic behaviour towards oxygen reduction reaction of carbon-supported PtxMyAuz (M = Ni, Cu, Co) binary and ternary catalysts. (10th July 2017)
- Record Type:
- Journal Article
- Title:
- Electrocatalytic behaviour towards oxygen reduction reaction of carbon-supported PtxMyAuz (M = Ni, Cu, Co) binary and ternary catalysts. (10th July 2017)
- Main Title:
- Electrocatalytic behaviour towards oxygen reduction reaction of carbon-supported PtxMyAuz (M = Ni, Cu, Co) binary and ternary catalysts
- Authors:
- Lankiang, Styven D.
Baranton, Stève
Coutanceau, Christophe - Abstract:
- Graphical abstract: Highlights: Order of activity of binary materials: Pt10-x Nix > Pt10-x Cox > Pt > Pt10-x Cux . Pt7 Ni3 /C catalysts display the higher activity amongst binary materials. Ternary systems: Au leads to increase the activity of Co and Cu containing catalysts. Ternary materials containing Ni still display the higher activities. Order of activity after durability test: Pt6 Au2 Cu2 > Pt6 Au2 Co2 > Pt6 Au2 Ni2 ≈ Pt. Abstract: Carbon-supported binary and ternary nanocatalysts based on Pt, Me (Me = Ni, Co, Cu) and Au were synthesized by a "water in oil" microemulsion method and characterized by atomic absorption spectrometry or energy dispersive spectroscopy, X-ray photoelectron spectroscopy, thermogravimetry, transmission electron microscopy, X-ray diffraction, and electrochemical methods. A comparative study of the oxygen reduction reaction on binary and ternary nanocatalysts has been performed. The catalytic activity and the selectivity of the nanocatalysts towards the ORR have been determined in O2 -saturated 0.1 M HClO4 electrolyte. For binary systems, it was shown that the addition of Ni and Co to Pt led to an improvement of the catalytic activity, whereas the addition of Cu was detrimental for the ORR. The higher activities were achieved for atomic ratios close to that of Pt3 Me defined compounds with Pt7 Ni3 /C displaying the highest activity. The modification of binary catalysts with gold led to increase the activity in the case of systems containingGraphical abstract: Highlights: Order of activity of binary materials: Pt10-x Nix > Pt10-x Cox > Pt > Pt10-x Cux . Pt7 Ni3 /C catalysts display the higher activity amongst binary materials. Ternary systems: Au leads to increase the activity of Co and Cu containing catalysts. Ternary materials containing Ni still display the higher activities. Order of activity after durability test: Pt6 Au2 Cu2 > Pt6 Au2 Co2 > Pt6 Au2 Ni2 ≈ Pt. Abstract: Carbon-supported binary and ternary nanocatalysts based on Pt, Me (Me = Ni, Co, Cu) and Au were synthesized by a "water in oil" microemulsion method and characterized by atomic absorption spectrometry or energy dispersive spectroscopy, X-ray photoelectron spectroscopy, thermogravimetry, transmission electron microscopy, X-ray diffraction, and electrochemical methods. A comparative study of the oxygen reduction reaction on binary and ternary nanocatalysts has been performed. The catalytic activity and the selectivity of the nanocatalysts towards the ORR have been determined in O2 -saturated 0.1 M HClO4 electrolyte. For binary systems, it was shown that the addition of Ni and Co to Pt led to an improvement of the catalytic activity, whereas the addition of Cu was detrimental for the ORR. The higher activities were achieved for atomic ratios close to that of Pt3 Me defined compounds with Pt7 Ni3 /C displaying the highest activity. The modification of binary catalysts with gold led to increase the activity in the case of systems containing Co and Cu, and led to maintain the activity in the case of Ni-containing catalysts. The order of initial activity is: Pt6 Ni2 Au2 /C > Pt6 Co2 Au2 /C > Pt6 Cu2 Au2 /C. Aging tests have been carried out on ternary catalysts, showing that a part of activity loss was due to gold segregation from the bulk to the surface of nanoparticles. After aging study for 1000 potential cycles between 0.6 and 1.05 V vs. RHE in O2 -saturated electrolyte, the order of activity was: Pt6 Cu2 Au2 /C > Pt6 Co2 Au2 /C > Pt6 Ni2 Au2 /C. … (more)
- Is Part Of:
- Electrochimica acta. Volume 242(2017)
- Journal:
- Electrochimica acta
- Issue:
- Volume 242(2017)
- Issue Display:
- Volume 242, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 242
- Issue:
- 2017
- Issue Sort Value:
- 2017-0242-2017-0000
- Page Start:
- 287
- Page End:
- 299
- Publication Date:
- 2017-07-10
- Subjects:
- Cobalt -- Copper -- Gold -- Nickel -- Platinum -- oxygen reduction reaction -- fuel cells
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2017.05.036 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2870.xml