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

被引:43
作者
Humbert, C. [1 ]
Busson, B. [1 ]
Six, C. [1 ]
Gayral, A. [1 ]
Gruselle, M. [2 ]
Villain, F. [2 ]
Tadjeddine, A. [1 ]
机构
[1] Univ Paris 11, Chim Phys Lab, CNRS, F-91405 Orsay, France
[2] Univ Paris 06, Lab Chim Inorgan & Mat Mol, CNRS, F-75252 Paris, France
关键词
Cyanopolyynes; thiophenol; Interfaces; Gold; Silver; Nonlinear optics;
D O I
10.1016/j.jelechem.2008.02.008
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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.
引用
收藏
页码:314 / 321
页数:8
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