Abstract
We introduce femtosecond wide-field transient absorption microscopy combining sub-10 fs pump and probe pulses covering the complete visible (500-650 nm) and near-infrared (650-950 nm) spectrum with diffraction-limited optical resolution. We demonstrate the capabilities of our system by reporting the spatially- and spectrally-resolved transient electronic response of MAPbI3-xClx perovskite films and reveal significant quenching of the transient bleach signal at grain boundaries. The unprecedented temporal resolution enables us to directly observe the formation of band-gap renormalization, completed in 25 fs after photoexcitation. In addition, we acquire hyperspectral Raman maps of TIPS pentacene films with sub-400 nm spatial and sub-15 cm-1 spectral resolution covering the 100-2000 cm-1 window. Our approach opens up the possibility of studying ultrafast dynamics on nanometer length and femtosecond time scales in a variety of two-dimensional and nanoscopic systems.
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CITATION STYLE
Schnedermann, C., Lim, J. M., Wende, T., Duarte, A. S., Ni, L., Gu, Q., … Kukura, P. (2016). Sub-10 fs Time-Resolved Vibronic Optical Microscopy. Journal of Physical Chemistry Letters, 7(23), 4854–4859. https://doi.org/10.1021/acs.jpclett.6b02387
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