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Title: Investigation of methanol oxidation on a highly active and stable Pt–Sn electrocatalyst supported on carbon–polyaniline composite for application in a passive direct methanol fuel cell

Abstract

Highlights: • PtSn/C-PANI performed superior in the MOR compared with a commercial PtRu/C. • Catalytic activity of PtRu/C was highly reduced during the accelerated durability test. • Anode of the PtSn/C-PANI in a passive DMFC lowered methanol crossover by 30%. - Abstract: Polyaniline fiber (PANI) was synthesized and utilized to fabricate a vulcan–polyaniline (C-PANI) composite. Pt/C-PANI and PtSn/C-PANI electro-catalysts with different Pt:Sn atomic ratios were prepared by the impregnation method. These electro-catalysts, along with commercial PtRu/C (Electrochem), were characterized with respect to their structural and electrochemical properties in methanol oxidation reaction (MOR). PtSn(70:30)/C-PANI showed excellent performance in MOR, the obtained maximum current density being about 40% and 50% higher than that for PtRu/C and Pt/C-PANI, respectively. It was also found that the CO tolerance and stability of PtSn(70:30)/C-PANI was considerably higher than that of PtRu/C. Finally, the performance of these two materials was compared in a passive direct methanol fuel cell (DMFC). The DMFC test results demonstrated that the membrane electrode assembly (MEA) prepared using PtSn(70:30)/C-PANI anode catalyst performed more satisfactorily in terms of maximum power density and lower methanol crossover.

Authors:
 [1];  [2];  [3];  [1];  [3];  [4]
  1. Department of Chemical Engineering, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)
  2. Department of Chemical and Petroleum Engineering, Sharif University of Technology, Tehran (Iran, Islamic Republic of)
  3. Department of Chemistry, Faculty of Science, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)
  4. (United States)
Publication Date:
OSTI Identifier:
22475843
Resource Type:
Journal Article
Resource Relation:
Journal Name: Materials Research Bulletin; Journal Volume: 68; Other Information: Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
36 MATERIALS SCIENCE; ANODES; CARBON; COMPARATIVE EVALUATIONS; COMPOSITE MATERIALS; CURRENT DENSITY; DIRECT METHANOL FUEL CELLS; ELECTROCATALYSTS; FIBERS; HARDNESS; MEMBRANES; NANOSTRUCTURES; OXIDATION; PLATINUM COMPOUNDS; POWER DENSITY; STABILITY; TIN COMPOUNDS; TOLERANCE; WEAR RESISTANCE

Citation Formats

Amani, Mitra, Kazemeini, Mohammad, Hamedanian, Mahboobeh, Pahlavanzadeh, Hassan, Gharibi, Hussein, E-mail: h.gharibi@utah.edu, and Department of Material Science & Engineering, 122 S Campus Drive, University of Utah, Salt Lake City, UT 84112. Investigation of methanol oxidation on a highly active and stable Pt–Sn electrocatalyst supported on carbon–polyaniline composite for application in a passive direct methanol fuel cell. United States: N. p., 2015. Web. doi:10.1016/J.MATERRESBULL.2015.02.053.
Amani, Mitra, Kazemeini, Mohammad, Hamedanian, Mahboobeh, Pahlavanzadeh, Hassan, Gharibi, Hussein, E-mail: h.gharibi@utah.edu, & Department of Material Science & Engineering, 122 S Campus Drive, University of Utah, Salt Lake City, UT 84112. Investigation of methanol oxidation on a highly active and stable Pt–Sn electrocatalyst supported on carbon–polyaniline composite for application in a passive direct methanol fuel cell. United States. doi:10.1016/J.MATERRESBULL.2015.02.053.
Amani, Mitra, Kazemeini, Mohammad, Hamedanian, Mahboobeh, Pahlavanzadeh, Hassan, Gharibi, Hussein, E-mail: h.gharibi@utah.edu, and Department of Material Science & Engineering, 122 S Campus Drive, University of Utah, Salt Lake City, UT 84112. Sat . "Investigation of methanol oxidation on a highly active and stable Pt–Sn electrocatalyst supported on carbon–polyaniline composite for application in a passive direct methanol fuel cell". United States. doi:10.1016/J.MATERRESBULL.2015.02.053.
@article{osti_22475843,
title = {Investigation of methanol oxidation on a highly active and stable Pt–Sn electrocatalyst supported on carbon–polyaniline composite for application in a passive direct methanol fuel cell},
author = {Amani, Mitra and Kazemeini, Mohammad and Hamedanian, Mahboobeh and Pahlavanzadeh, Hassan and Gharibi, Hussein, E-mail: h.gharibi@utah.edu and Department of Material Science & Engineering, 122 S Campus Drive, University of Utah, Salt Lake City, UT 84112},
abstractNote = {Highlights: • PtSn/C-PANI performed superior in the MOR compared with a commercial PtRu/C. • Catalytic activity of PtRu/C was highly reduced during the accelerated durability test. • Anode of the PtSn/C-PANI in a passive DMFC lowered methanol crossover by 30%. - Abstract: Polyaniline fiber (PANI) was synthesized and utilized to fabricate a vulcan–polyaniline (C-PANI) composite. Pt/C-PANI and PtSn/C-PANI electro-catalysts with different Pt:Sn atomic ratios were prepared by the impregnation method. These electro-catalysts, along with commercial PtRu/C (Electrochem), were characterized with respect to their structural and electrochemical properties in methanol oxidation reaction (MOR). PtSn(70:30)/C-PANI showed excellent performance in MOR, the obtained maximum current density being about 40% and 50% higher than that for PtRu/C and Pt/C-PANI, respectively. It was also found that the CO tolerance and stability of PtSn(70:30)/C-PANI was considerably higher than that of PtRu/C. Finally, the performance of these two materials was compared in a passive direct methanol fuel cell (DMFC). The DMFC test results demonstrated that the membrane electrode assembly (MEA) prepared using PtSn(70:30)/C-PANI anode catalyst performed more satisfactorily in terms of maximum power density and lower methanol crossover.},
doi = {10.1016/J.MATERRESBULL.2015.02.053},
journal = {Materials Research Bulletin},
number = ,
volume = 68,
place = {United States},
year = {Sat Aug 15 00:00:00 EDT 2015},
month = {Sat Aug 15 00:00:00 EDT 2015}
}