Enhanced electrocatalytic activity and stability of platinum, gold, and nickel oxide nanoparticles-based ternary catalyst for formic acid electro-oxidation

被引:43
作者
El-Nagar, Gumaa A. [1 ]
Mohammad, Ahmad M. [1 ,2 ]
机构
[1] Cairo Univ, Fac Sci, Dept Chem, Cairo 12613, Egypt
[2] British Univ Egypt, Fac Engn, Dept Chem Engn, Cairo 11837, Egypt
关键词
Electrocatalysis; Gold nanoparticles; Platinum nanoparticles; Nickel oxide nanoparticles; Direct formic acid fuel cells; Third body; INFRARED-ABSORPTION SPECTROSCOPY; FUEL-CELLS; MODIFIED ELECTRODES; OXIDATION; TEMPERATURE;
D O I
10.1016/j.ijhydene.2014.06.028
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 global interest to realize and commercialize the direct formic acid fuel cells has motivated the development of efficient and stable anodes for the formic acid (FA) electrooxidation (FAO). In this investigation, a ternary catalyst composed of Pt nanoparticles (PtNPs), Au nanoparticles (AuNPs) and nickel oxide nanoparticles (nano-NiOx), all were sequentially electrodeposited onto the surface of a glassy carbon (GC) electrode, was recommended for this reaction. The surface morphology investigation revealed the deposition of grain-shaped PtNPs (25 nm average particle size), and flower-shaped nanospheres (less than 60 nm average particle size) of AuNPs and nano-NiOx. Interestingly, the ternary modified NiOx-Au-Pt/GC electrode has shown an outstanding electrocatalytic activity towards the direct FAO, concurrently with a complete suppression for the indirect route. It further exhibited excellent stability that extended for 7 h of continuous electrolysis. While PtNPs furnished a suitable base for FA adsorption, AuNPs played a significant role to interrupt the contiguity of the Pt surface sites, which is necessary for CO poisoning. On the other hand, nano-NiOx acted as a catalytic mediator facilitating the charge transfer of FAO and the oxidative removal of CO at a lower potential. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11955 / 11962
页数:8
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