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Ternary Pt/Re/SnO<sub>2</sub>/C catalyst for EOR: Electrocatalytic activity and durability enhancement

Autor
Drzymała, Elżbieta
Pawlyta, Miroslawa
Gruzeł, Grzegorz
Donten, Mikołaj
Parlińska-Wojtan, Magdalena
Depciuch-Czarny, Joanna
Data publikacji
2020
Abstrakt (EN)

Carbon-supported Pt/C, Pt/Re/C, Pt/SnO<sub>2</sub>/C and Pt/Re/SnO2/C, with 20 wt.% overall metal loading were prepared and their electrochemical activity towards ethanol oxidation reaction (EOR) was investigated. Transmission electron microscopy (TEM) combined with energy dispersive X-ray spectroscopy (EDS) revealed, that indeed binary and ternary combinations of the designed nanoparticles (NPs) were formed and successfully uniformly deposited on a carbon support. Fourier transform infrared spectroscopy (FTIR) allowed to assess the chemical composition of the nanocatalysts and X-ray diffraction (XRD) allowed to determine the catalyst structure. Potentiodynamic and chronoamperometric measurements were used to establish its catalytic activity and stability. The influence of Re addition on the electrochemical activity towards ethanol oxidation reaction (EOR) was verified. Indeed, the addition of Re to the binary Pt/SnO<sub>2</sub>/C catalyst leads to the formation of ternary Pt/Re/SnO<sub>2</sub>/C with physical contact between the individual NPs, enhancing the EOR. Furthermore, the onset potential of the synthesized ternary catalyst is shifted to more negative potentials and the current densities and specific activity are nearly 11 and 5 times higher, respectively, than for commercial Pt catalyst. Additionally ternary Pt/Re/SnO<sub>2</sub>/C catalyst retained 96% of its electrochemical surface area.

Słowa kluczowe EN
chemical synthesis
transmission electron microscopy (TEM) characterization
electrochemistry
ethanol oxidation reaction (EOR)
Pt
Re
SnO2
C catalysts
ternary catalysts
Dyscyplina PBN
nauki chemiczne
Czasopismo
Nano Research
Tom
13
Zeszyt
3
Strony od-do
832-842
ISSN
1998-0124
Data udostępnienia w otwartym dostępie
2020-02-26
Licencja otwartego dostępu
Uznanie autorstwa