Yang Jie, Guehr Markus, Shen Xiaozhe, Li Renkai, Vecchione Theodore, Coffee Ryan, Corbett Jeff, Fry Alan, Hartmann Nick, Hast Carsten, Hegazy Kareem, Jobe Keith, Makasyuk Igor, Robinson Joseph, Robinson Matthew S, Vetter Sharon, Weathersby Stephen, Yoneda Charles, Wang Xijie, Centurion Martin
University of Nebraska-Lincoln, 855 N 16th Street, Lincoln, Nebraska 68588, USA.
PULSE, SLAC National Accelerator Laboratory, Menlo Park, California 94025, USA.
Phys Rev Lett. 2016 Oct 7;117(15):153002. doi: 10.1103/PhysRevLett.117.153002. Epub 2016 Oct 3.
Observing the motion of the nuclear wave packets during a molecular reaction, in both space and time, is crucial for understanding and controlling the outcome of photoinduced chemical reactions. We have imaged the motion of a vibrational wave packet in isolated iodine molecules using ultrafast electron diffraction with relativistic electrons. The time-varying interatomic distance was measured with a precision 0.07 Å and temporal resolution of 230 fs full width at half maximum. The method is not only sensitive to the position but also the shape of the nuclear wave packet.
在空间和时间上观察分子反应过程中核波包的运动,对于理解和控制光致化学反应的结果至关重要。我们利用相对论电子的超快电子衍射对孤立碘分子中振动波包的运动进行了成像。测量了随时间变化的原子间距离,精度为0.07 Å,半高宽的时间分辨率为230 fs。该方法不仅对核波包的位置敏感,而且对其形状也敏感。