Investigation of V-doped TiO2 as an anodic catalyst support for SPE water electrolysis

被引:41
作者
Hao, Chuanpu [1 ,2 ]
Lv, Hong [1 ,2 ]
Zhao, Qiang [3 ]
Li, Bing [1 ,2 ]
Zhang, Cunman [1 ,2 ]
Mi, Cangen [4 ]
Song, Yukun [1 ,2 ]
Ma, Jianxin [1 ,2 ]
机构
[1] Tongji Univ, Sch Automot Studies, Shanghai 201804, Peoples R China
[2] Tongji Univ, Clean Energy Automot Engn Ctr, Shanghai 201804, Peoples R China
[3] China Elect Power Res Inst, Beijing 100192, Peoples R China
[4] Hunan Univ, Coll Mat & Engn, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
SPE water electrolysis; Titania support; IrO2; V-doped titania; Oxygen evolution reaction (OER); OXYGEN EVOLUTION; TITANIA; ELECTROCATALYSTS; HYDROGEN; OXIDE; SNO2; NB; SB; NANOPARTICLES; STABILITY;
D O I
10.1016/j.ijhydene.2017.02.131
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
A modified evaporation-induced self-assembly (EISA) method was employed to prepare titania samples doped with different amounts of vanadium (0, 10, 20, 30 at.%), which were further evaluated as catalyst supports for the oxygen evolution reaction (OER) catalyst IrO2 in the solid polymer electrolyte water electrolyzer (SPEWE). The effects of V dopant on titania supports are proved to be twofold: i) enhancing the simplification of phase composition and consequently improving the homogeneity of porous morphology; ii) introducing redox couple V (IV)/V (V) to the surface of titania. As a result, the catalyst's OER activity is improved with the increase of V dopant in the titania support after loading IrO2 via Adams fusion method. In single cells, the OER performance gradually increases with V dopant from 0 to 20 at.%, followed by a performance deterioration with V amount reaching 30 at.% due to the corrodible V2O5 precipitate. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:9384 / 9395
页数:12
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