Compressive strain as the main origin of enhanced oxygen reduction reaction activity for Pt electrocatalysts on chromium-doped titania support

被引:54
作者
Kim, Jun-Hyuk [1 ]
Chang, Seohyoung [2 ]
Kim, Yong-Tae [1 ]
机构
[1] Pusan Natl Univ, Sch Mech Engn, Pusan 609735, South Korea
[2] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
基金
新加坡国家研究基金会;
关键词
Pt-based fuel cell electrocatalysts; Oxide supports; Charge transfer; Lattice strain; Oxygen reduction reaction; CATALYST SUPPORT; ALLOY CATALYSTS; TIO2; PLATINUM; EXCHANGE; SIZE; ELECTROREDUCTION; NANOPARTICLES; INSTABILITY; MONOLAYER;
D O I
10.1016/j.apcatb.2014.04.003
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
In this study, we have attempted to clarify the origin of the enhanced oxygen reduction reaction (ORR) activity of Pt on titania supports, which has been the subject of significant debate. To date, it has been claimed in several studies that the charge transfer from titania to Pt is the main origin of the enhanced ORR activity, while the theoretical adsorption model suggested that such charge transfer to Pt could lead to stronger OH adsorption and therefore a negative effect on ORR activity. We resolve this controversy by considering a lattice strain effect induced by the strong metal support interaction. EXAFS studies clearly show that a compressive strain leading to a lower d-band center is exerted on the Pt lattice on the titania-based supports. Hence, we strongly suggest that the main origin for the enhanced ORR activity is the compressive strain rather than the charge transfer. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 118
页数:7
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