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Dispersion effect in formic acid oxidation on PtAu/C nanocatalyst prepared by water-in-oil microemulsion method

Authorized Users Only
2019
Authors
Krstajic-Pajic, M. N.
Stevanović, Sanja I.
Radmilović, Velimir R
Gavrilovic-Wohlmuther, Aleksandra
Zabinski, P.
Elezović, Nevenka R.
Radmilović, Vuk V.
Gojković, Snežana Lj
Jovanović, V. M.
Article (Published version)
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Abstract
Low loading PtAu nanoparticles supported on high area carbon were synthesized by water-in-oil microemulsion method and examined for formic acid and methanol oxidation. Prepared catalyst powder was characterized by Xray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). These techniques revealed that the catalyst contains rather agglomerated quasi-spherical particles, similar to 4 nm diameter, composed of a solid solution of Pt and Au with only similar to 4 at% of Au. In spite of such low Au content, both onset and peak potentials for CO oxidation are shifted some 150 mV to more positive values in comparison to Pt synthesized in the same manner due to stronger binding of CO as a result of notable electronic effect. It is important that this small quantity of Au also significantly influences oxidation of formic acid promoting direct path and suppressing indirect path in formic acid oxidation in... a degree as expected by a much larger quantity of Au. Such improvement could be due exclusively by ensemble effect of high number of small Pt domains which formation could be possible only by very fine dispersion of such low Au quantity. High number of small Pt domains is corroborated by lower activity for methanol oxidation in comparison to Pt catalyst synthesized by the same procedure. These results emphasize the importance of the Au dispersion on the surface of Pt over its quantity in PtAu catalyst with regards to both, the ensemble and the electronic effects.

Keywords:
PtAu nanoparticles / Microemulsion method / Methanol electrooxidation / Formic acid electrooxidation
Source:
Applied Catalysis B-Environmental, 2019, 243, 585-593
Publisher:
  • Elsevier Science Bv, Amsterdam
Funding / projects:
  • New approach in designing materials for energy conversion and energy storage systems (RS-172060)
  • Serbian Academy of Sciences and Arts [F-141]
  • COST ActionEuropean Cooperation in Science and Technology (COST) [MP1407-STSM, COST-STSM-MP1407-35830]

DOI: 10.1016/j.apcatb.2018.10.064

ISSN: 0926-3373

WoS: 000453616800060

Scopus: 2-s2.0-85056487106
[ Google Scholar ]
31
22
URI
http://rimsi.imsi.bg.ac.rs/handle/123456789/1218
Collections
  • Radovi istraživača / Researchers’ publications
Institution/Community
Institut za multidisciplinarna istraživanja
TY  - JOUR
AU  - Krstajic-Pajic, M. N.
AU  - Stevanović, Sanja I.
AU  - Radmilović, Velimir R
AU  - Gavrilovic-Wohlmuther, Aleksandra
AU  - Zabinski, P.
AU  - Elezović, Nevenka R.
AU  - Radmilović, Vuk V.
AU  - Gojković, Snežana Lj
AU  - Jovanović, V. M.
PY  - 2019
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1218
AB  - Low loading PtAu nanoparticles supported on high area carbon were synthesized by water-in-oil microemulsion method and examined for formic acid and methanol oxidation. Prepared catalyst powder was characterized by Xray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). These techniques revealed that the catalyst contains rather agglomerated quasi-spherical particles, similar to 4 nm diameter, composed of a solid solution of Pt and Au with only similar to 4 at% of Au. In spite of such low Au content, both onset and peak potentials for CO oxidation are shifted some 150 mV to more positive values in comparison to Pt synthesized in the same manner due to stronger binding of CO as a result of notable electronic effect. It is important that this small quantity of Au also significantly influences oxidation of formic acid promoting direct path and suppressing indirect path in formic acid oxidation in a degree as expected by a much larger quantity of Au. Such improvement could be due exclusively by ensemble effect of high number of small Pt domains which formation could be possible only by very fine dispersion of such low Au quantity. High number of small Pt domains is corroborated by lower activity for methanol oxidation in comparison to Pt catalyst synthesized by the same procedure. These results emphasize the importance of the Au dispersion on the surface of Pt over its quantity in PtAu catalyst with regards to both, the ensemble and the electronic effects.
PB  - Elsevier Science Bv, Amsterdam
T2  - Applied Catalysis B-Environmental
T1  - Dispersion effect in formic acid oxidation on PtAu/C nanocatalyst prepared by water-in-oil microemulsion method
EP  - 593
SP  - 585
VL  - 243
DO  - 10.1016/j.apcatb.2018.10.064
ER  - 
@article{
author = "Krstajic-Pajic, M. N. and Stevanović, Sanja I. and Radmilović, Velimir R and Gavrilovic-Wohlmuther, Aleksandra and Zabinski, P. and Elezović, Nevenka R. and Radmilović, Vuk V. and Gojković, Snežana Lj and Jovanović, V. M.",
year = "2019",
abstract = "Low loading PtAu nanoparticles supported on high area carbon were synthesized by water-in-oil microemulsion method and examined for formic acid and methanol oxidation. Prepared catalyst powder was characterized by Xray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). These techniques revealed that the catalyst contains rather agglomerated quasi-spherical particles, similar to 4 nm diameter, composed of a solid solution of Pt and Au with only similar to 4 at% of Au. In spite of such low Au content, both onset and peak potentials for CO oxidation are shifted some 150 mV to more positive values in comparison to Pt synthesized in the same manner due to stronger binding of CO as a result of notable electronic effect. It is important that this small quantity of Au also significantly influences oxidation of formic acid promoting direct path and suppressing indirect path in formic acid oxidation in a degree as expected by a much larger quantity of Au. Such improvement could be due exclusively by ensemble effect of high number of small Pt domains which formation could be possible only by very fine dispersion of such low Au quantity. High number of small Pt domains is corroborated by lower activity for methanol oxidation in comparison to Pt catalyst synthesized by the same procedure. These results emphasize the importance of the Au dispersion on the surface of Pt over its quantity in PtAu catalyst with regards to both, the ensemble and the electronic effects.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Applied Catalysis B-Environmental",
title = "Dispersion effect in formic acid oxidation on PtAu/C nanocatalyst prepared by water-in-oil microemulsion method",
pages = "593-585",
volume = "243",
doi = "10.1016/j.apcatb.2018.10.064"
}
Krstajic-Pajic, M. N., Stevanović, S. I., Radmilović, V. R., Gavrilovic-Wohlmuther, A., Zabinski, P., Elezović, N. R., Radmilović, V. V., Gojković, S. L.,& Jovanović, V. M.. (2019). Dispersion effect in formic acid oxidation on PtAu/C nanocatalyst prepared by water-in-oil microemulsion method. in Applied Catalysis B-Environmental
Elsevier Science Bv, Amsterdam., 243, 585-593.
https://doi.org/10.1016/j.apcatb.2018.10.064
Krstajic-Pajic MN, Stevanović SI, Radmilović VR, Gavrilovic-Wohlmuther A, Zabinski P, Elezović NR, Radmilović VV, Gojković SL, Jovanović VM. Dispersion effect in formic acid oxidation on PtAu/C nanocatalyst prepared by water-in-oil microemulsion method. in Applied Catalysis B-Environmental. 2019;243:585-593.
doi:10.1016/j.apcatb.2018.10.064 .
Krstajic-Pajic, M. N., Stevanović, Sanja I., Radmilović, Velimir R, Gavrilovic-Wohlmuther, Aleksandra, Zabinski, P., Elezović, Nevenka R., Radmilović, Vuk V., Gojković, Snežana Lj, Jovanović, V. M., "Dispersion effect in formic acid oxidation on PtAu/C nanocatalyst prepared by water-in-oil microemulsion method" in Applied Catalysis B-Environmental, 243 (2019):585-593,
https://doi.org/10.1016/j.apcatb.2018.10.064 . .

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