請用此 Handle URI 來引用此文件: http://hdl.handle.net/11455/42095
標題: Electrodeposition of Copper on a Pt(111) Electrode in Sulfuric Acid Containing Poly(ethylene glycol) and Chloride Ions as Probed by in Situ STM
作者: Fu, YunLin
Pao, Te
Chen, Sih-Zih
Yau, ShuehLin
Dow, Wei-Ping
Lee, Yuh-Lang
摘要: This study employed real-time in situ STM imaging to examine the adsorption of PEG molecules on Pt(111) modified by a monolayer of copper adatoms and the subsequent bulk Cu deposition in 1 M H2SO4 + 1 mM CuSO4+ 1 mM KCl + 88 μM PEG. At the end of Cu underpotential deposition (∼0.35 V vs Ag/AgCl), a highly ordered Pt(111)-(√3 × √7)-Cu + HSO4 − structure was observed in 1 M H2SO4 + 1 mM CuSO4. This adlattice restructured upon the introduction of poly(ethylene glycol) (PEG, molecular weight 200) and chloride anions. At the onset potential for bulk Cu deposition (∼0 V), a Pt(111)-(√3 × √3)R30°-Cu + Cl− structure was imaged with a tunneling current of 0.5 nA and a bias voltage of 100 mV. Lowering the tunneling current to 0.2 nA yielded a (4 × 4) structure, presumably because of adsorbed PEG200 molecules. The subsequent nucleation and deposition processes of Cu in solution containing PEG and Cl− were examined, revealing the nucleation of 2- to 3-nm-wide CuCl clusters on an atomically smooth Pt(111) surface at overpotentials of less than 50 mV. With larger overpotential (η > 150 mV), Cu deposition seemed to bypass the production of CuCl species, leading to layered Cu deposition, starting preferentially at step defects, followed by lateral growth to cover the entire Pt electrode surface. These processes were observed with both PEG200 and 4000, although the former tended to produce more CuCl nanoclusters. Raising [H2SO4] to 1 M substantiates the suppressing effect of PEG on Cu deposition. This STM study provided atomic- or molecular-level insight into the effect of PEG additives on the deposition of Cu.
URI: http://hdl.handle.net/11455/42095
文章連結: http://dx.doi.org/10.1021/la3011508
顯示於類別:化學工程學系所

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