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Ultrafast electron crystallography of the cooperative reaction path in vanadium dioxide

机译:二氧化钒中协同反应路径的超快电子晶体学

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Time-resolved electron diffraction with atomic-scale spatial and temporal resolution was used to unravel the transformation pathway in the photoinduced structural phase transition of vanadium dioxide. Results from bulk crystals and single-crystalline thin-films reveal a common, stepwise mechanism: First, there is a femtosecond V?V bond dilation within 300 fs, second, an intracell adjustment in picoseconds and, third, a nanoscale shear motion within tens of picoseconds. Experiments at different ambient temperatures and pump laser fluences reveal a temperature-dependent excitation threshold required to trigger the transitional reaction path of the atomic motions.
机译:具有原子尺度的时空分辨的时间分辨电子衍射被用来揭示二氧化钒的光致结构相变中的转变途径。块状晶体和单晶薄膜的结果揭示了一种常见的逐步机制:首先,飞秒的VΔV键膨胀在300 fs内,其次,以微微秒为单位的细胞内调整,其次,在数十以内的纳米级剪切运动皮秒。在不同的环境温度和泵浦激光注量下进行的实验揭示了触发原子运动的过渡反应路径所需的依赖于温度的激发阈值。

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