Carbon monoxide promoted deposition of ordered pt adlayer on Au(111) and its electrocatalytic properties

Please use this identifier to cite or link to this item: https://ir.lib.ncu.edu.tw/handle/987654321/101382

Title:	Carbon monoxide promoted deposition of ordered pt adlayer on Au(111) and its electrocatalytic properties
Authors:	姚學麟;Liao, Weicheng;Liao, Weichen;Yau, Shuehlin
Contributors:	理學院化學學系
Date:	2015-01-01
Issue Date:	2026-04-21 14:32:12 (UTC+8)
Publisher:	Electrochemical Society, Inc.;The Electrochemical Society
Abstract:	摘要： In situ scanning tunneling microscopy (STM) was used to examine the microstructures of platinum (Pt) deposited on ordered Au(111) substrate in aqueous Na2PtCl6 solution saturated with carbon monoxide (CO) with and without potential control at room temperature. PtCl62− complexes were reduced to Pt atoms by CO molecules and deposited on Au(111) in a hexagonal array without potential control. The adsorption of CO molecules first mobilized and rearranged Pt adatoms on Au(111) from disordered Pt aggregates to 0.9 nm wide tortuous stripes, and then to patches of ordered Pt adatoms at 0.1 V (versus reversible hydrogen electrode). Electrodeposition of Pt in the presence of CO ceased with a monatomic Pt film capped with CO molecules arranged in a (2 × 2) array at 0.1 V. The CO monolayer adsorbed on Pt/Au(111) was stripped off at 0.96 V in 0.1 M H2SO4, as compared with 0.83 V observed with Pt(111). The E1/2 potential for oxygen reduction reaction (ORR) observed with the Pt-modified Au(111) electrode was 0.81 V in sulfuric acid, which is 0.16 V more positive than that of Pt(111). The microstructures of the as-prepared Pt monolayer on Au(111) changed with potential cycling between 0.05 and 1.0 V. 其他題名： J. Electrochem. Soc 出版者： The Electrochemical Society 出版日期： 2015-01-01 出處： Journal of the Electrochemical Society, 2015-01, Vol.162 (10), p.H767-H773 資源來源： Institute of Physics Journals 版權： 2015 The Electrochemical Society 識別號： ISSN: 0013-4651 識別號： EISSN: 1945-7111 識別號： DOI: 10.1149/2.1101509jes
Appears in Collections:	[Department of Chemistry] journal & Dissertation

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