HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product
Само за регистроване кориснике
2013
Чланак у часопису (Објављена верзија)

Метаподаци
Приказ свих података о документуАпстракт
The oxidation of HCOOH has been investigated on thin Pd layers ranging from 1 to 17 ML equivalents electrodeposited on polycrystalline Au substrate (Pd"Au). The results are compared to those on Pd black. Potentiodynamic polarization curves suggest that on both types of catalyst HCOOH oxidizes through dehydrogenation path. The high current densities achieved on 4-17 ML Pd"Au surpass more than three times the activity of Pd black. Chronoamperometric test reveals that the Pd"Au electrodes lose their activity faster than Pd black. In the stripping experiment performed after the chronoamperometry COads is detected on all the surfaces. On the 4 ML Pd"Au, which exhibits the highest deactivation rate, the COads coverage is the largest. After the chronoamperometric test repeated in the CO2 saturated supporting electrolyte, the anodic stripping shows that COads is present on all the electrodes, again with the highest coverage on 4 ML Pd"Au. It is concluded that deactivation of Pd surfaces is cau...sed by the COads formed in the electrochemical reduction of CO2, which is the product of HCOOH oxidation. Electronic modification of Pd by Au substrate causes stronger interactions of Pd with HCOOH and CO, which increases HCOOH oxidation rate, but also accelerates the poisoning by COads.
Кључне речи:
Formic acid electrooxidation / Carbon-dioxide electroreduction / Palladium / Gold / Fuel cellИзвор:
Electrochimica Acta, 2013, 88, 384-389Издавач:
- Oxford : Pergamon-Elsevier Science Ltd
Финансирање / пројекти:
DOI: 10.1016/j.electacta.2012.10.033
ISSN: 0013-4686
WoS: 000315076300051
Scopus: 2-s2.0-84870334684
Институција/група
IHTMTY - JOUR AU - Obradović, Maja AU - Gojković, Snežana Lj. PY - 2013 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/1279 AB - The oxidation of HCOOH has been investigated on thin Pd layers ranging from 1 to 17 ML equivalents electrodeposited on polycrystalline Au substrate (Pd"Au). The results are compared to those on Pd black. Potentiodynamic polarization curves suggest that on both types of catalyst HCOOH oxidizes through dehydrogenation path. The high current densities achieved on 4-17 ML Pd"Au surpass more than three times the activity of Pd black. Chronoamperometric test reveals that the Pd"Au electrodes lose their activity faster than Pd black. In the stripping experiment performed after the chronoamperometry COads is detected on all the surfaces. On the 4 ML Pd"Au, which exhibits the highest deactivation rate, the COads coverage is the largest. After the chronoamperometric test repeated in the CO2 saturated supporting electrolyte, the anodic stripping shows that COads is present on all the electrodes, again with the highest coverage on 4 ML Pd"Au. It is concluded that deactivation of Pd surfaces is caused by the COads formed in the electrochemical reduction of CO2, which is the product of HCOOH oxidation. Electronic modification of Pd by Au substrate causes stronger interactions of Pd with HCOOH and CO, which increases HCOOH oxidation rate, but also accelerates the poisoning by COads. PB - Oxford : Pergamon-Elsevier Science Ltd T2 - Electrochimica Acta T1 - HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product VL - 88 SP - 384 EP - 389 DO - 10.1016/j.electacta.2012.10.033 ER -
@article{ author = "Obradović, Maja and Gojković, Snežana Lj.", year = "2013", abstract = "The oxidation of HCOOH has been investigated on thin Pd layers ranging from 1 to 17 ML equivalents electrodeposited on polycrystalline Au substrate (Pd"Au). The results are compared to those on Pd black. Potentiodynamic polarization curves suggest that on both types of catalyst HCOOH oxidizes through dehydrogenation path. The high current densities achieved on 4-17 ML Pd"Au surpass more than three times the activity of Pd black. Chronoamperometric test reveals that the Pd"Au electrodes lose their activity faster than Pd black. In the stripping experiment performed after the chronoamperometry COads is detected on all the surfaces. On the 4 ML Pd"Au, which exhibits the highest deactivation rate, the COads coverage is the largest. After the chronoamperometric test repeated in the CO2 saturated supporting electrolyte, the anodic stripping shows that COads is present on all the electrodes, again with the highest coverage on 4 ML Pd"Au. It is concluded that deactivation of Pd surfaces is caused by the COads formed in the electrochemical reduction of CO2, which is the product of HCOOH oxidation. Electronic modification of Pd by Au substrate causes stronger interactions of Pd with HCOOH and CO, which increases HCOOH oxidation rate, but also accelerates the poisoning by COads.", publisher = "Oxford : Pergamon-Elsevier Science Ltd", journal = "Electrochimica Acta", title = "HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product", volume = "88", pages = "384-389", doi = "10.1016/j.electacta.2012.10.033" }
Obradović, M.,& Gojković, S. Lj.. (2013). HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product. in Electrochimica Acta Oxford : Pergamon-Elsevier Science Ltd., 88, 384-389. https://doi.org/10.1016/j.electacta.2012.10.033
Obradović M, Gojković SL. HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product. in Electrochimica Acta. 2013;88:384-389. doi:10.1016/j.electacta.2012.10.033 .
Obradović, Maja, Gojković, Snežana Lj., "HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product" in Electrochimica Acta, 88 (2013):384-389, https://doi.org/10.1016/j.electacta.2012.10.033 . .