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The nature of photoinduced phase transition and metastable states in vanadium dioxide

机译:二氧化钒中光诱导相变和亚稳态的性质

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摘要

Photoinduced threshold switching processes that lead to bistability and the formation of metastable phases in photoinduced phase transition of VO2 are elucidated through ultrafast electron diffraction and diffusive scattering techniques with varying excitation wavelengths. We uncover two distinct regimes of the dynamical phase change: a nearly instantaneous crossover into an intermediate state and its decay led by lattice instabilities over 10 ps timescales. The structure of this intermediate state is identified to be monoclinic, but more akin to M2 rather than M1 based on structure refinements. The extinction of all major monoclinic features within just a few picoseconds at the above-threshold-level (~20%) photoexcitations and the distinct dynamics in diffusive scattering that represents medium-range atomic fluctuations at two photon wavelengths strongly suggest a density-driven and nonthermal pathway for the initial process of the photoinduced phase transition. These results highlight the critical roles of electron correlations and lattice instabilities in driving and controlling phase transformations far from equilibrium.
机译:通过超快电子衍射和具有不同激发波长的扩散散射技术,阐明了导致双稳态和在VO2的光致相变中形成亚稳相的光致阈值转换过程。我们发现了动态相变的两个不同的状态:几乎是瞬时过渡到中间状态,以及由10 ps时标上的晶格不稳定性导致的衰减。根据结构细化,该中间状态的结构被确定为单斜结构,但更类似于M2而不是M1。在高于阈值水平(〜20%)的光激发下,仅几皮秒内所有主要单斜晶特征的消失,以及代表两个光子波长处的中程原子涨落的扩散散射的独特动力学,强烈暗示了密度驱动和非热途径为光诱导相变的初始过程。这些结果突出了电子相关性和晶格不稳定性在驱动和控制远离平衡的相变中的关键作用。

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