Design of efficient bimetallic Pt-Au nanoparticle-based anodes for direct formic acid fuel cells

被引:35
|
作者
Asal, Yaser M. [1 ]
Al-Akraa, Islam M. [1 ]
Mohammad, Ahmad M. [2 ]
El-Deab, Mohamed S. [2 ]
机构
[1] British Univ Egypt, Dept Chem Engn, Fac Engn, Cairo 11837, Egypt
[2] Cairo Univ, Fac Sci, Chem Dept, Cairo 12613, Egypt
关键词
Energy conversions; Fuel cells; Pt-Au nanocomposite; Poisoning; Co-electrodeposition; ELECTROCATALYTIC OXIDATION; ENHANCED ACTIVITY; BINARY CATALYSTS; ELECTROOXIDATION; PLATINUM; NANOCRYSTALS; GOLD; PERFORMANCE;
D O I
10.1016/j.ijhydene.2018.12.086
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
Formic acid (FA) electro-oxidation (FAO) was investigated at a binary catalyst composed of Pt (PtNPs) and Au (AuNPs) nanoparticles which were electrodeposited simultaneously onto a glassy carbon (GC) substrate. The catalytic activity of the binary modified catalyst toward FAO was significantly influenced by the relative molar ratio of PtNPs and AuNPs. Interestingly, the catalyst with a molar ratio (1:1) of PtNPs and AuNPs showed the highest activity toward the favorable pathway of FAO (ca. 26 times increase in the direct peak current concurrently with a ca. 133 mV negative shift in the onset potential). Such enhancement was believed originating from the outstanding improvement of charge transfer during FAO via the desirable "nonpoisoning" pathway along with a significant mitigation of CO poisoning at the electrode surface. The diversity of techniques (cyclic voltammetry, chronoamperometry, electrochemical impedance spectroscopy, field-emission scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray diffraction) employed in this investigation offered opportunities to assess and interpret the catalysts activity and stability and to possess a deliberated overview about its morphology, composition and structure. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3615 / 3624
页数:10
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