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用于固有光谱线宽的灵活高分辨率宽带和频产生振动光谱学。

Flexible high-resolution broadband sum-frequency generation vibrational spectroscopy for intrinsic spectral line widths.

机构信息

State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, People's Republic of China.

出版信息

J Chem Phys. 2019 Feb 21;150(7):074702. doi: 10.1063/1.5066580.

Abstract

The difficulty in achieving high spectral resolution and accurate line shape in sum-frequency generation vibrational spectroscopy (SFG-VS) has restricted its use in applications requiring precise detection and quantitative analysis. Recently, the development of high-resolution broadband sum-frequency generation vibrational spectroscopy (HR-BB-SFG-VS) with sub-wavenumber resolution generated by synchronizing two independent amplifier lasers have opened new opportunities for probing an intrinsic SFG response. Here, we present a new flexible approach to achieve HR-BB-SFG-VS. In this system, two regeneration amplifiers shared the same oscillator laser as the seed, and a time-asymmetric visible pulse with a nearly Lorentzian line shape filtered by an etalon was used to overlap with a femtosecond broadband infrared pulse. This Lorentzian line shape of the visible pulse can greatly simplify the spectral fitting and analysis. We also demonstrated that the single-sided long visible pulse provided both high spectral resolution (1.4 cm) and effective suppression of the non-resonant background by detuning the time delay between visible and infrared pulses in SFG-VS measurements. With this new SFG setup, a pair of spectral splittings by 3.1 ± 0.7 and 3 ± 0.2 cm for the symmetric and antisymmetric stretching of the CH group was resolved at the CHCN/TiO(110) surface, which are tentatively attributed to two different orientational methyl groups. These technological advancements can help broaden the applications of HR-BB-SFG-VS and provide solid ground for a better understanding of complex molecular structures and dynamics at interfaces.

摘要

在和频产生振动光谱学(SFG-VS)中实现高光谱分辨率和精确线宽的困难限制了其在需要精确检测和定量分析的应用中的使用。最近,通过同步两个独立的放大器激光产生具有亚波数分辨率的高分辨率宽带和频产生振动光谱学(HR-BB-SFG-VS)的发展为探测固有 SFG 响应开辟了新的机会。在这里,我们提出了一种新的实现 HR-BB-SFG-VS 的灵活方法。在该系统中,两个再生放大器共享同一振荡器激光作为种子,并用啁啾脉冲放大技术放大,并使用通过法布里-珀罗标准具滤波的具有近洛伦兹线形状的可见光脉冲与飞秒宽带红外脉冲重叠。该可见光脉冲的洛伦兹线形状可以大大简化光谱拟合和分析。我们还证明,通过在 SFG-VS 测量中调整可见光和红外脉冲之间的时间延迟,可以提供单边长可见光脉冲,从而实现高光谱分辨率(1.4cm)和对非共振背景的有效抑制。通过这种新的 SFG 装置,在 CHCN/TiO(110)表面上,CH 基团的对称和反对称伸缩的两个光谱分裂分别被分辨为 3.1±0.7 和 3±0.2cm,这两个光谱分裂可能归因于两个不同的取向甲基。这些技术进步可以帮助拓宽 HR-BB-SFG-VS 的应用,并为更好地理解界面处的复杂分子结构和动力学提供坚实的基础。

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