A noble silver nanoflower on nitrogen doped carbon nanotube for enhanced oxygen reduction reaction

被引:34
|
作者
Yasmin, Sabina [1 ,2 ]
Ahmed, Mohammad Shamsuddin [1 ,2 ]
Jeon, Seungwon [1 ,2 ]
机构
[1] Chonnam Natl Univ, Dept Chem, Gwangju 500757, South Korea
[2] Chonnam Natl Univ, Inst Basic Sci, Gwangju 500757, South Korea
基金
新加坡国家研究基金会;
关键词
Oxygen reduction reaction; Nitrogen doping; Fuel cell; Silver nanoflowers; Electrochemical deposition; HIGH CATALYTIC-ACTIVITY; ALKALINE FUEL-CELLS; GRAPHENE OXIDE; ELECTROCHEMICAL DEPOSITION; ELECTROCATALYTIC PROPERTY; NANOFIBER ELECTRODES; HYDROGEN EVOLUTION; OXIDATION; PERFORMANCE; MEDIA;
D O I
10.1016/j.ijhydene.2016.09.145
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
An electrodeposition-approach for the synthesis of silver nanoflowers (AgNFs) on nitrogen doped carbon nanotubes (NCNTs) for the oxygen reduction reaction (ORR) in alkaline media has been developed. The as prepared material (NCNTs-AgNFs) has been characterized by various instrumental methods. The morphological analysis shows the unique rose-like AgNFs are placed onto the NCNTs with better dispersion. The higher population of AgNFs has also been observed onto NCNTs coated glassy carbon (GC) rather than bare GC plate. The X-ray photoelectron spectroscopy shows chemical reduction and N-doping has done successfully with the restoring sp(2) domain in carbon network. The electrocatalytic activities have been verified using cyclic voltammetry (CV) and hydrodynamic voltammetry techniques in 0.1 M KOH electrolyte. The resulting catalyst system, NCNT-AgNFs, surpasses the performance of Pt/C, in terms of a kinetic current density, better fuel selectivity and durability. It is also noteworthy that the NCNT-AgNFs exhibits a four electron reduction pathway for ORR with lowering H2O2 yield. The admirable performance of NCNT-AgNFs catalyst along with higher durability holds great potential for application in various fuel cells as cathode catalyst. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1075 / 1084
页数:10
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