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Metallic multilayered films electrodeposited over titanium as catalysts for methanol electro-oxidation

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Metallic multilayered films electrodeposited over titanium as catalysts for methanol electro-oxidation. / Zulke, Alana A.; Matos, Roberto; Pereira, Ernesto C.
In: Electrochimica Acta, Vol. 105, 30.08.2013, p. 578-583.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Zulke AA, Matos R, Pereira EC. Metallic multilayered films electrodeposited over titanium as catalysts for methanol electro-oxidation. Electrochimica Acta. 2013 Aug 30;105:578-583. doi: 10.1016/j.electacta.2013.05.027

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Zulke, Alana A. ; Matos, Roberto ; Pereira, Ernesto C. / Metallic multilayered films electrodeposited over titanium as catalysts for methanol electro-oxidation. In: Electrochimica Acta. 2013 ; Vol. 105. pp. 578-583.

Bibtex

@article{61110edb316f469bafeb41aca671ec54,
title = "Metallic multilayered films electrodeposited over titanium as catalysts for methanol electro-oxidation",
abstract = "Multilayered Pt/Ir/Pt films were electrodeposited over titanium substrates, controlling the film thickness by the deposition charge. Two probe molecules were used to perform the evaluation of catalytic activity, CH3OH and CO. Using a 22 factorial design with a central point, optimized intrinsic catalytic activity was obtained over the Ti/Pt25mC/Ir6mC/Pt electrode. An enhancement of the current density of up to 2.76 times was observed for the methanol oxidation reaction (MOR) compared with the reference sample (Ti/Pt electrodes), even though both samples had the same electroactive area. In addition to the methanol oxidation voltammetry, CO stripping voltammetry suggests that MM-like systems are less susceptible to the catalyst-poisoning phenomenon compared to the Ti/Pt ones. Impedance spectroscopy was mainly used to monitor the charge transference resistance (Rct), whose results showed a clear Rct reduction for the MOR process over MMs compared with Ti/Pt electrodes, corroborating the previous observations regarding the general catalytic improvement.",
author = "Zulke, {Alana A.} and Roberto Matos and Pereira, {Ernesto C.}",
year = "2013",
month = aug,
day = "30",
doi = "10.1016/j.electacta.2013.05.027",
language = "English",
volume = "105",
pages = "578--583",
journal = "Electrochimica Acta",
issn = "0013-4686",
publisher = "Elsevier Ltd",

}

RIS

TY - JOUR

T1 - Metallic multilayered films electrodeposited over titanium as catalysts for methanol electro-oxidation

AU - Zulke, Alana A.

AU - Matos, Roberto

AU - Pereira, Ernesto C.

PY - 2013/8/30

Y1 - 2013/8/30

N2 - Multilayered Pt/Ir/Pt films were electrodeposited over titanium substrates, controlling the film thickness by the deposition charge. Two probe molecules were used to perform the evaluation of catalytic activity, CH3OH and CO. Using a 22 factorial design with a central point, optimized intrinsic catalytic activity was obtained over the Ti/Pt25mC/Ir6mC/Pt electrode. An enhancement of the current density of up to 2.76 times was observed for the methanol oxidation reaction (MOR) compared with the reference sample (Ti/Pt electrodes), even though both samples had the same electroactive area. In addition to the methanol oxidation voltammetry, CO stripping voltammetry suggests that MM-like systems are less susceptible to the catalyst-poisoning phenomenon compared to the Ti/Pt ones. Impedance spectroscopy was mainly used to monitor the charge transference resistance (Rct), whose results showed a clear Rct reduction for the MOR process over MMs compared with Ti/Pt electrodes, corroborating the previous observations regarding the general catalytic improvement.

AB - Multilayered Pt/Ir/Pt films were electrodeposited over titanium substrates, controlling the film thickness by the deposition charge. Two probe molecules were used to perform the evaluation of catalytic activity, CH3OH and CO. Using a 22 factorial design with a central point, optimized intrinsic catalytic activity was obtained over the Ti/Pt25mC/Ir6mC/Pt electrode. An enhancement of the current density of up to 2.76 times was observed for the methanol oxidation reaction (MOR) compared with the reference sample (Ti/Pt electrodes), even though both samples had the same electroactive area. In addition to the methanol oxidation voltammetry, CO stripping voltammetry suggests that MM-like systems are less susceptible to the catalyst-poisoning phenomenon compared to the Ti/Pt ones. Impedance spectroscopy was mainly used to monitor the charge transference resistance (Rct), whose results showed a clear Rct reduction for the MOR process over MMs compared with Ti/Pt electrodes, corroborating the previous observations regarding the general catalytic improvement.

U2 - 10.1016/j.electacta.2013.05.027

DO - 10.1016/j.electacta.2013.05.027

M3 - Journal article

VL - 105

SP - 578

EP - 583

JO - Electrochimica Acta

JF - Electrochimica Acta

SN - 0013-4686

ER -