The ability to control the orientation of small polar molecules is an important step toward experiments such as X-ray diffraction and high-harmonic generation, where structural information or ultrafast molecular dynamics can be reconstructed in the molecular frame. We present experiments where we have combined hexapole state-selection and the application of a strong DC electric field with the use of short, intense shaped laser pulses in order to demonstrate and optimize impulsive alignment and orientation of NO molecules under field-free conditions. Good agreement of the experimental results with theoretical predictions is found. In addition, impulsive alignment and orientation was investigated theoretically for a set of molecules that can be used state-selected by means of hexapole focusing.

Additional Metadata
Publisher Cham: Springer
Editor K. Yamanouchi , S. L. Chin , Pierre Agostini , G. Ferrante
Persistent URL dx.doi.org/10.1007/978-3-642-15054-8_3
Citation
Rouzée, A, Gijsbertsen, A, & Vrakking, M. J. J. (2010). Alignment and orientation of hexapole state-selected molecules. In K Yamanouchi, S. L Chin, Pierre Agostini, & G Ferrante (Eds.), Progress in Ultrafast Intense Laser Science VI (pp. 45–73). Cham: Springer. doi:10.1007/978-3-642-15054-8_3