V-doped TiO2 supported Pt as a promising oxygen reduction reaction catalyst: Synthesis, characterization and in-situ evaluation in proton exchange membrane fuel cell

被引:27
作者
Bharti, Abha [1 ]
Cheruvally, Gouri [2 ]
机构
[1] Vikram Sarabhai Space Ctr, Energy Syst Div, Thiruvananthapuram 695022, Kerala, India
[2] Vikram Sarabhai Space Ctr, Polymers & Special Chem Grp, Thiruvananthapuram 695022, Kerala, India
关键词
V-TiO2; support; ORR catalyst; PEM fuel cell; In-situ electrochemical technique; Catalyst durability; PHOTOCATALYTIC PROPERTY; ENHANCED ACTIVITY; LAYER DEPOSITION; VISIBLE-LIGHT; ELECTROCATALYSTS; DURABILITY; NANOPARTICLES; PARTICLES; ANATASE; FE;
D O I
10.1016/j.jpowsour.2017.07.111
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
This study deals with the synthesis and characterization of V-doped, TiO2 supported Pt catalyst (Pt/V-TiO2) for oxygen reduction reaction (ORR) and its in-situ performance investigation in proton exchange membrane (PEM) fuel cell. Pt/V-TiO2 nanocomposite catalyst is prepared via a facile sol-gel and microwave assisted, modified chemical reduction route and its performance is compared with the undoped TiO2 supported catalyst, Pt/TiO2 prepared in an identical way. The prepared Pt/V-TiO2 and Pt/TiO2 catalysts are employed as cathode catalyst in PEM fuel cell and compared with standard Pt/C catalyst. Their comparative studies are conducted with physical and" electrochemical techniques. In-situ electrochemical characterization studies show improved ORR catalytic activity of Pt/V-TiO2 compared to Pt/TiO2. Furthermore, both Pt/TiO2 and Pt/V-TiO2 are more stable than Pt/C when subjected to 6000 voltammetric cycles in the range of 0.2-1.2 V vs. standard hydrogen electrode in operating fuel cell conditions, losing only <20% of its electrochemical surface area as compared to 50% loss exhibited by Pt/C. This study thus demonstrates Pt/V-TiO2 nanocomposite material as a potential cathode catalyst for PEM fuel cell with immense scope for further investigation. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:413 / 421
页数:9
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