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Ultrafast Electron-Lattice Coupling Dynamics in VO2 and V2O3 Thin Films

机译:VO2和V2O3薄膜的超快电子 - 晶格耦合动力学

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摘要

Ultrafast optical pump - optical probe and optical pump - terahertz probespectroscopy were performed on vanadium dioxide (VO2) and vanadium sesquioxide(V2O3) thin films over a wide temperature range. A comparison of theexperimental data from these two different techniques and two differentvanadium oxides, in particular a comparison of the electronic oscillationsgenerated by the photoinduced longitudinal acoustic modulation, reveals thestrong electron-phonon coupling that exists in the metallic state of bothmaterials. The low energy Drude response of V2O3 appears more susceptible thanVO2 to ultrafast strain control. Additionally, our results provide ameasurement of the temperature dependence of the sound velocity in bothsystems, revealing a four- to fivefold increase in VO2 and a three- to fivefoldincrease in V2O3 across the phase transition. Our data also confirmobservations of strong damping and phonon anharmonicity in the metallic phaseof VO2, and suggest that a similar phenomenon might be at play in the metallicphase of V2O3. More generally, our simple table-top approach provides relevantand detailed information about dynamical lattice properties of vanadium oxides,opening the way to similar studies in other complex materials.
机译:在较宽的温度范围内,对二氧化钒(VO2)和三氧化二钒(V2O3)薄膜进行了超快光泵-光学探针和光泵-太赫兹探针光谱学。来自这两种不同技术和两种不同钒氧化物的实验数据的比较,特别是对光致纵向声调制产生的电子振荡的比较,揭示了在两种材料的金属状态下均存在的强电子-声子耦合。 V2O3的低能量Drude响应似乎比VO2易受超快应变控制。此外,我们的结果提供了两种系统中声速对温度的依赖性的测量结果,表明在整个相变过程中,VO2的增加了4至5倍,V2O3的增加了3至5倍。我们的数据还证实了在VO2金属相中强阻尼和声子非谐性的观察,并表明在V2O3金属相中可能存在类似现象。更一般而言,我们的简单台式方法提供了有关钒氧化物动态晶格特性的相关和详细信息,从而为其他复杂材料中的类似研究开辟了道路。

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