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Sum-frequency generation as a vibrational and electronic probe of the electrochemical interface and thin films

机译:和频生成作为电化学界面和薄膜的振动电子探针

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摘要

Standard vibrational sum-frequency generation (SFG) spectroscopy is performed to probe the electrochemical cyanoacetylene/Au(111) interface, enlightening at 20 cm(-1)/V Stark shift of the free CN vibration mode of this cyanopolyynes-class molecule. SFG data suggest an orientation for the adsorbed molecules with the CN moiety pointing out in a direction perpendicular to the metal surface. A newly developed two-colour SFG (2C-SFG) set-up based on the CLIO free electron laser synchronized with a tuneable visible laser source is used to probe simulaneously the vibrational and electronic fingerprint of a thiophenol/Ag(111) interface. Structural information on the adsorbed self-assembled monolayer is put in evidence as a function of the immersion time of the silver substrate in the thiophenol solution (24 h or 5 days). With a longer immersion time, the molecular packing is of better quality and more compact, with the carbon rings less tilted with respect to the surface normal. This new experimental set-up combines the advantages to have a higher spectral and temporal resolution with higher power energies at far infrared wavelengths than these presently available from tabletop infrared optical parametric oscillators. (c) 2008 Elsevier B.V. All rights reserved.
机译:执行标准振动和频生成(SFG)光谱以探测电化学氰基乙炔/ Au(111)界面,并以该氰基聚炔类分子的自由CN振动模式的20 cm(-1)/ V Stark位移启发。 SFG数据表明被吸附分子的取向,其中CN部分指向垂直于金属表面的方向。一种新开发的基于CLIO自由电子激光与可调谐可见激光源同步的双色SFG(2C-SFG)装置,用于同时探测硫酚/ Ag(111)界面的振动和电子指纹。吸附的自组装单分子层的结构信息已证明是银底物在苯酚溶液中的浸入时间(24小时或5天)的函数。浸泡时间较长时,分子堆积的质量更好,结构更紧凑,碳环相对于表面法线的倾斜程度较小。这种新的实验装置结合了以下优点:与目前的台式红外光学参量振荡器相比,在远红外波长具有更高的光谱和时间分辨率以及更高的能量。 (c)2008 Elsevier B.V.保留所有权利。

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