Nishida Jun, Johnson Samuel C, Chang Peter T S, Wharton Dylan M, Dönges Sven A, Khatib Omar, Raschke Markus B
Department of Physics and JILA, University of Colorado, Boulder, CO, 80309, USA.
Nat Commun. 2022 Feb 28;13(1):1083. doi: 10.1038/s41467-022-28224-9.
Ultrafast infrared nano-imaging has demonstrated access to ultrafast carrier dynamics on the nanoscale in semiconductor, correlated-electron, or polaritonic materials. However, mostly limited to short-lived transient states, the contrast obtained has remained insufficient to probe important long-lived excitations, which arise from many-body interactions induced by strong perturbation among carriers, lattice phonons, or molecular vibrations. Here, we demonstrate ultrafast infrared nano-imaging based on excitation modulation and sideband detection to characterize electron and vibration dynamics with nano- to micro-second lifetimes. As an exemplary application to quantum materials, in phase-resolved ultrafast nano-imaging of the photoinduced insulator-to-metal transition in vanadium dioxide, a distinct transient nano-domain behavior is quantified. In another application to lead halide perovskites, transient vibrational nano-FTIR spatially resolves the excited-state polaron-cation coupling underlying the photovoltaic response. These examples show how heterodyne pump-probe nano-spectroscopy with low-repetition excitation extends ultrafast infrared nano-imaging to probe elementary processes in quantum and molecular materials in space and time.
超快红外纳米成像已证明能够在半导体、关联电子或极化子材料的纳米尺度上获取超快载流子动力学信息。然而,所获得的对比度大多限于短寿命瞬态,仍然不足以探测重要的长寿命激发,这些激发源于载流子、晶格声子或分子振动之间的强扰动所引起的多体相互作用。在此,我们展示了基于激发调制和边带检测的超快红外纳米成像,以表征具有纳秒至微秒寿命的电子和振动动力学。作为量子材料的一个示例性应用,在对二氧化钒中光致绝缘体-金属转变的相分辨超快纳米成像中,定量了一种独特的瞬态纳米畴行为。在另一个应用于卤化铅钙钛矿的例子中,瞬态振动纳米傅里叶变换红外光谱在空间上解析了光伏响应背后的激发态极化子-阳离子耦合。这些例子展示了具有低重复激发的外差泵浦-探测纳米光谱如何将超快红外纳米成像扩展到在空间和时间上探测量子和分子材料中的基本过程。