Institute de Physique de Rennes , UMR 6251 University Rennes 1-CNRS, 35042 Rennes, France.
CNRS, Université de Bordeaux , ICMCB, 87 avenue du Dr. A. Schweitzer, Pessac 33608, France.
Struct Dyn. 2015 Nov 20;3(2):023605. doi: 10.1063/1.4936290. eCollection 2016 Mar.
We combine ultrafast optical spectroscopy with femtosecond X-ray absorption to study the photo-switching dynamics of the [Fe(PM-AzA)2(NCS)2] spin-crossover molecular solid. The light-induced excited spin-state trapping process switches the molecules from low spin to high spin (HS) states on the sub-picosecond timescale. The change of the electronic state (<50 fs) induces a structural reorganization of the molecule within 160 fs. This transformation is accompanied by coherent molecular vibrations in the HS potential and especially a rapidly damped Fe-ligand breathing mode. The time-resolved studies evidence a delayed activation of coherent optical phonons of the lattice surrounding the photoexcited molecules.
我们将超快光学光谱学与飞秒 X 射线吸收相结合,研究 [Fe(PM-AzA)2(NCS)2] 自旋交叉分子固体的光致开关动力学。光诱导激发态捕获过程将分子在亚皮秒时间尺度内从低自旋状态切换到高自旋 (HS) 状态。电子态的变化(<50 fs)在 160 fs 内引起分子的结构重排。这种转变伴随着 HS 势能中分子的相干振动,特别是快速阻尼的 Fe-配体呼吸模式。时间分辨研究证明,光激发分子周围晶格的相干光学声子的激活存在延迟。