Fugane Keisuke, Mori Toshiyuki, Yan Pengfei, Masuda Takuya, Yamamoto Shunya, Ye Fei, Yoshikawa Hideki, Auchterlonie Graeme, Drennan John
Global Research Center for Environmental and Energy Based on Nanomaterials Science (GREEN), National Institute for Materials Science (NIMS) , 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
ACS Appl Mater Interfaces. 2015 Feb 4;7(4):2698-707. doi: 10.1021/am507754w. Epub 2015 Jan 20.
Pt-CeOx/C (1.5 ≤ x ≤ 2) electro-catalyst is one of the most promising cathode materials for use in polymer membrane electrolyte fuel cells. To clarify the microstructure of Pt-CeOx heterointerface, we prepared Pt-loaded CeOx thin film on conductive SrTiO3 single crystal substrate by using a stepwise process of pulse laser deposition method for the preparation of epitaxial growth CeOx film followed by an impregnation method which loaded the Pt particles on the CeOx film. The electrochemistry observed for the Pt-loaded CeOx thin film on the conductive single crystal substrate was examined by using cyclic voltammetry in 0.5 M H2SO4 aqueous solution, and a cross-sectional image of the aforementioned Pt-CeOx thin film electrode was observed using a transmission electron microscope. The electrochemistry observed for Pt-CeOx thin film electrode clearly showed the promotion effect of CeOx. Also, the microanalysis indicated that unique, large clusters that consisted of C-type rare-earth-like structures were formed in the Pt-CeOx interface by a strong interaction between Pt and CeOx. The present combination analysis of the electrochemistry, microanalysis, and atomistic simulation indicates that the large clusters (i.e., 12 (PtCe''-Vo(••)) + 2 (PtCe''-2Vo(••)-2CeCe')) that were formed into the Pt-CeOx interface promoted the charge transfer between Pt surface and CeOx, suggesting that the oxygen reduction reaction activity on Pt can be maximized by fabrication of C-type rare-earth-like structure that consists of the aforementioned large clusters in the Pt-CeOx interfaces.
Pt-CeOx/C(1.5≤x≤2)电催化剂是用于聚合物膜电解质燃料电池最具前景的阴极材料之一。为了阐明Pt-CeOx异质界面的微观结构,我们通过脉冲激光沉积法的分步工艺在导电SrTiO3单晶衬底上制备了负载Pt的CeOx薄膜,该工艺先制备外延生长的CeOx薄膜,然后采用浸渍法将Pt颗粒负载在CeOx薄膜上。使用循环伏安法在0.5M H2SO4水溶液中研究了导电单晶衬底上负载Pt的CeOx薄膜的电化学性质,并使用透射电子显微镜观察了上述Pt-CeOx薄膜电极的横截面图像。Pt-CeOx薄膜电极的电化学性质清楚地显示了CeOx的促进作用。此外,微观分析表明,由于Pt与CeOx之间的强相互作用,在Pt-CeOx界面形成了由C型类稀土结构组成的独特大簇。目前对电化学、微观分析和原子模拟的联合分析表明,在Pt-CeOx界面形成的大簇(即12(PtCe''-Vo(••))+2(PtCe''-2Vo(••)-2CeCe'))促进了Pt表面与CeOx之间的电荷转移,这表明通过在Pt-CeOx界面制造由上述大簇组成的C型类稀土结构,可以使Pt上的氧还原反应活性最大化。