Department of Chemistry , University of Wisconsin , Madison , Wisconsin 53706 , United States.
J Phys Chem A. 2019 Dec 19;123(50):10824-10836. doi: 10.1021/acs.jpca.9b09099. Epub 2019 Dec 6.
The dynamics of electronic transitions in solid-state materials are closely linked to microscopic morphology, but it is challenging to simultaneously characterize their spectral and temporal response with high spatial resolution. We present a time-resolved nonlinear microscopy system using white-light supercontinuum pulses as a broadband light source. This system is capable of correlating nanometer scale sample morphology determined from atomic force topography measurements with broadband transient absorption hyperspectral images and ultrafast 2D white-light spectra, all with a spatial resolution of ≤1 μm. The experimental apparatus is described with a focus on the dispersion management strategies necessary to minimize the duration of optical pulses when implementing an AOM based pulse-shaping system covering a broad-spectral range in the VIS/NIR. Experiments on TIPS-pentacene organic semiconductor microcrystals are used to demonstrate the unique capabilities of this technique.
固态材料中电子跃迁的动力学与微观形态密切相关,但同时以高空间分辨率对其光谱和时间响应进行表征具有挑战性。我们提出了一种基于白光超连续脉冲的时间分辨非线性显微镜系统,该系统能够将原子力形貌测量确定的纳米级样品形态与宽带瞬态吸收高光谱图像和超快 2D 白光光谱相关联,所有这些都具有≤1μm 的空间分辨率。本文介绍了实验装置,重点介绍了在实施基于声光调制器的脉冲整形系统时,为了在可见/近红外光谱范围内实现最小光脉冲持续时间所需的色散管理策略。TIPS-五苯有机半导体微晶体的实验证明了该技术的独特功能。