Fuel blends: Enhanced electro-oxidation of formic acid in its blend with methanol at platinum nanoparticles modified glassy carbon electrodes

被引:29
作者
El-Deab, Mohamed S. [1 ]
El-Nagar, Gumaa A. [1 ]
Mohammad, Ahmad M. [1 ]
El-Anadouli, Bahgat E. [1 ]
机构
[1] Cairo Univ, Fac Sci, Dept Chem, Cairo, Egypt
关键词
Fuel utilization; Catalytic enhancement; Platinum nanoparticles; Electrocatalysis; Carbon monoxide tolerance; FARADAIC ELECTROCHEMICAL MODIFICATION; ELECTROCATALYTIC OXIDATION; CATALYTIC-ACTIVITY; CELLS; PERFORMANCE;
D O I
10.1016/j.jpowsour.2015.04.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The current study addresses, for the first time, the enhanced direct electro-oxidation of formic acid (FA) at platinum-nanoparticles modified glassy carbon (nano-Pt/GC) electrode in the presence of methanol (Me0H) as a blending fuel. This enhancement is probed by: (i) the increase of the direct oxidation current of FA to CO2 (I-p(d), dehydrogenation pathway), (ii) suppressing the dehydration pathway (I-p(ind), producing the poisoning intermediate CO) and (iii) a favorable negative shift of the onset potential of I-p(d) with increasing the mole fraction of MeOH in the blend. Furthermore, the charge of the direct FA oxidation in 0.3 M FA + 0.3 M MeOH blend is by 14 and 21 times higher than that observed for 0.3 M FA and 0.3 M MeOH, respectively. MeOH is believed to adsorb at the Pt surface sites and thus disfavor the "nonfaradaic" dissociation of FA (which produces the poisoning CO intermediate), i.e., MeOH induces a high CO tolerance of the Pt catalyst. The enhanced oxidation activity indicates that FA/MeOH blend is a promising fuel system. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:504 / 509
页数:6
相关论文
共 27 条
[1]  
Adzic R, 1998, ELECTROCATALYSIS, V197
[2]   Kinetics and mechanism of the electrooxidation of formic acid - Spectroelectrochemical studies in a flow cell [J].
Chen, YX ;
Heinen, M ;
Jusys, Z ;
Behm, RJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (06) :981-985
[3]   Adsorbed formate: the key intermediate in the oxidation of formic acid on platinum electrodes [J].
Cuesta, Angel ;
Cabello, Gema ;
Gutierrez, Claudio ;
Osawa, Masatoshi .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (45) :20091-20095
[4]   Impact of acrylonitrile poisoning on oxygen reduction reaction at Pt/C catalysts [J].
El-Deab, Mohamed S. ;
Kitamura, Fusao ;
Ohsaka, Takeo .
JOURNAL OF POWER SOURCES, 2013, 229 :65-71
[5]   Enhanced electrocatalytic activity and stability of platinum, gold, and nickel oxide nanoparticles-based ternary catalyst for formic acid electro-oxidation [J].
El-Nagar, Gumaa A. ;
Mohammad, Ahmad M. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2014, 39 (23) :11955-11962
[6]   Acrylonitrile-contamination induced enhancement of formic acid electro-oxidation at platinum nanoparticles modified glassy carbon electrodes [J].
El-Nagar, Gumaa A. ;
Mohammad, Ahmad M. ;
El-Deab, Mohamed S. ;
Ohsaka, Takeo ;
El-Anadouli, Bahgat E. .
JOURNAL OF POWER SOURCES, 2014, 265 :57-61
[7]   Electrocatalysis by design: Enhanced electrooxidation of formic acid at platinum nanoparticles-nickel oxide nanoparticles binary catalysts [J].
El-Nagar, Gumaa A. ;
Mohammad, Ahmad M. ;
El-Deab, Mohamed S. ;
El-Anadouli, Bahgat E. .
ELECTROCHIMICA ACTA, 2013, 94 :62-71
[8]   Electrooxidation of small organic molecules on mesoporous precious metal catalysts II: CO and methanol on platinum-ruthenium alloy [J].
Jiang, JH ;
Kucernak, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2003, 543 (02) :187-199
[9]   The effect of pH on the electrocatalytic oxidation of formic acid/formate on platinum: A mechanistic study by surface-enhanced infrared spectroscopy coupled with cyclic voltammetry [J].
Joo, Jiyong ;
Uchida, Taro ;
Cuesta, Angel ;
Koper, Marc T. M. ;
Osawa, Masatoshi .
ELECTROCHIMICA ACTA, 2014, 129 :127-136
[10]   Importance of Acid-Base Equilibrium in Electrocatalytic Oxidation of Formic Acid on Platinum [J].
Joo, Jiyong ;
Uchida, Taro ;
Cuesta, Angel ;
Koper, Marc T. M. ;
Osawa, Masatoshi .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (27) :9991-9994