Reaction Stoichiometry and Mechanism of Pt Deposition via Surface Limited Redox Replacement of Copper UPD Layer on Au(111)

被引:8
|
作者
Yuan, Qiuyi [1 ]
Wakisakai, Yuki [1 ]
Uemura, Yohei [2 ]
Wada, Takahiro [3 ]
Ariga-Miwa, Hiroko [1 ]
Takakusagi, Satoru [1 ]
Asakura, Kiyotaka [1 ]
Brankovic, Stanko R. [4 ]
机构
[1] Hokkaido Univ, Intitute Catalysis, Kita Ku, Kita 21 Nishi 10, Sapporo, Hokkaido 0010021, Japan
[2] Inst Mol Sci, Okazaki, Aichi 4440867, Japan
[3] Tokyo Med & Dent Univ, Bunkyo Ku, 1-5-45 Yushima, Tokyo 1138549, Japan
[4] Univ Houston, Dept Elect & Comp Engn, Houston, TX 77204 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2018年 / 122卷 / 29期
关键词
X-RAY-ABSORPTION; OXYGEN-REDUCTION; MONOLAYER ELECTROCATALYSTS; REACTION-KINETICS; METAL-DEPOSITION; FINE-STRUCTURE; E-ALD; PLATINUM; GROWTH; GOLD;
D O I
10.1021/acs.jpcc.8b02218
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
The stoichiometry and reaction mechanism of Pt deposition via surface limited redox replacement (SLRR) of Cu underpotential-deposited (UPD) monolayer on Au(111) was studied using in situ polarization dependent total reflection fluorescence X-ray absorption fine structure (PTRF-XAFS), scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV). We proposed that Pt deposition via SLRR of Cu UPD monolayer leads to formation/deposition of Pt-surface species mainly consisting of Pt(II) chloride with a square planar local structure [PtCl4] parallel to the Au surface (60%) which has a strong interaction of the Pt complex with the Au substrate. The rest (40%) was one-monolayer Pt metal cluster. This result provides a new understanding into the mechanism and stoichiometry of the SLRR reaction, which has a wide application for synthesis of monolayer catalysts.
引用
收藏
页码:16664 / 16673
页数:10
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