Baum Peter, Yang Ding-Shyue, Zewail Ahmed H
Physical Biology Center for Ultrafast Science and Technology, Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena, CA 91125, USA.
Science. 2007 Nov 2;318(5851):788-92. doi: 10.1126/science.1147724.
Complex systems in condensed phases involve a multidimensional energy landscape, and knowledge of transitional structures and separation of time scales for atomic movements is critical to understanding their dynamical behavior. Here, we report, using four-dimensional (4D) femtosecond electron diffraction, the visualization of transitional structures from the initial monoclinic to the final tetragonal phase in crystalline vanadium dioxide; the change was initiated by a near-infrared excitation. By revealing the spatiotemporal behavior from all observed Bragg diffractions in 3D, the femtosecond primary vanadium-vanadium bond dilation, the displacements of atoms in picoseconds, and the sound wave shear motion on hundreds of picoseconds were resolved, elucidating the nature of the structural pathways and the nonconcerted mechanism of the transformation.
凝聚态中的复杂系统涉及多维能量景观,了解过渡结构以及原子运动的时间尺度分离对于理解其动力学行为至关重要。在此,我们利用四维(4D)飞秒电子衍射报告了晶体二氧化钒中从初始单斜相到最终四方相的过渡结构的可视化;这种变化是由近红外激发引发的。通过揭示3D中所有观测到的布拉格衍射的时空行为,解析了飞秒级的钒 - 钒主键膨胀、皮秒级的原子位移以及数百皮秒级的声波剪切运动,阐明了结构路径的本质以及转变的非协同机制。