Cammarata Marco, Bertoni Roman, Lorenc Maciej, Cailleau Hervé, Di Matteo Sergio, Mauriac Cindy, Matar Samir F, Lemke Henrik, Chollet Matthieu, Ravy Sylvain, Laulhé Claire, Létard Jean-François, Collet Eric
Institut de Physique de Rennes, UMR CNRS 6251, Université Rennes 1, 35042 Rennes Cedex, France.
CNRS, Université de Bordeaux, ICMCB, 87 Avenue du Dr. A. Schweitzer, Pessac 33608, France.
Phys Rev Lett. 2014 Nov 28;113(22):227402. doi: 10.1103/PhysRevLett.113.227402. Epub 2014 Nov 26.
We study the basic mechanisms allowing light to photoswitch at the molecular scale a spin-crossover material from a low- to a high-spin state. Combined femtosecond x-ray absorption performed at LCLS X-FEL and optical spectroscopy reveal that the structural stabilization of the photoinduced high-spin state results from a two step structural trapping. Molecular breathing vibrations are first activated and rapidly damped as part of the energy is sequentially transferred to molecular bending vibrations. During the photoswitching, the system follows a curved trajectory on the potential energy surface.
我们研究了在分子尺度上使光将自旋交叉材料从低自旋态光开关到高自旋态的基本机制。结合在LCLS X射线自由电子激光装置上进行的飞秒X射线吸收和光谱学研究表明,光诱导高自旋态的结构稳定性源于两步结构捕获。分子呼吸振动首先被激活,随着部分能量依次转移到分子弯曲振动上,分子呼吸振动迅速衰减。在光开关过程中,系统在势能面上沿着一条弯曲的轨迹运动。