In situ scanning tunneling microscopy imaging self-assembled monolayers of mercaptoacetic acid and cupric ion on Au(111) electrode

Please use this identifier to cite or link to this item: https://ir.lib.ncu.edu.tw/handle/987654321/100996

Title:	In situ scanning tunneling microscopy imaging self-assembled monolayers of mercaptoacetic acid and cupric ion on Au(111) electrode
Authors:	姚學麟;Lai, Chao-Shan;Chen, Yu-Ying;Yau, Shuehlin;Dow, Wei-Ping;Lee, Yuh-Lang
Contributors:	理學院化學學系
Date:	2014-01-01
Issue Date:	2026-04-21 14:20:31 (UTC+8)
Publisher:	Electrochemical Society, Inc.;The Electrochemical Society
Abstract:	摘要： We employed voltammetry and scanning tunneling microscopy (STM) to study the coadsorption of mercaptoacetic acid (MAA) and cupric ions (Cu2+) on Au(111) electrode from 0.5 M sulfuric acid + 0.8 M CuSO4 + 0.03 mM MAA. Irreversibly adsorbed Cu2+ ions were reduced at 0.27 V first then at −0.2 V (vs. Ag/AgCl), ascribed to the underpotential and overpotential deposition processes, respectively. Counting the amount of charge involved in the stripping peak of the Cu deposit rendered quantification of Cu2+ ions codeposited with MAA on the Au(111) electrode, which yielded roughly 7.7 × 1014 Cu2+ ions/cm2. MAA alone and MAA + Cu2+ were adsorbed in Au(111) - (3 × √13) and (p × √3) structures, respectively. Cu2+ could be imaged by the STM, but their high mobility made it difficult to obtain high - quality STM results needed to quantify the amount of adsorbed Cu2+. Spatial structures of MAA molecules segregated onto the Cu deposit were found to vary with potential. They returned to the Au(111) electrode once the Cu deposit was oxidized at E > 0.4 V, yielding MAA + Cu2+ structures different from those seen at the pristine sample. 其他題名： J. Electrochem. Soc 出版者： The Electrochemical Society 出版日期： 2014-01-01 出處： Journal of the Electrochemical Society, 2014-01, Vol.161 (14), p.D742-D748 資源來源： Institute of Physics Journals 版權： 2014 The Electrochemical Society 識別號： ISSN: 0013-4651 識別號： EISSN: 1945-7111 識別號： DOI: 10.1149/2.0281414jes
Appears in Collections:	[Department of Chemistry] journal & Dissertation

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