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A “movie” of ultrafast rotating molecules at a hundred billion per second

Quantum wave-like nature was successfully observed in rotating nitrogen molecules

Dr. Kenta Mizuse at Institute for Molecular Science, National Institutes of Natural Sciences, Professor Yasuhiro Ohshima at Tokyo Institute of Technology, and co-workers successfully took sequential “snapshots” of ultrafast unidirectionally rotating molecules at a hundred billion per second.  To visualize such an ultrafast molecular rotation, the research team developed a Coulomb explosion imaging setup with regulating rotational direction by a pair of time-delayed, polarization-skewed laser pulses.  In the sequential “snapshots”, the team successfully reported high-resolution direct imaging of direction-controlled rotational wave packets (RWPs) in nitrogen molecules, and the quantum wave-like nature was successfully observed.  The result will guide more sophisticated molecular manipulations, such as an ultrafast molecular “stopwatch”.  This result is published in Science Advance (July 3rd, 2015)

Rotational wave packets (RWPs) are time-varying states of motion of rotating microscopic objects like molecules, and change their shapes in an ultrafast time scale, typically some parts in a trillion second.  More importantly, because RWPs are governed by the fundamental microscopic physical laws, quantum mechanics, they show wave-like nature, much different from what macroscopic things exhibit.  So, RWPs are one of the ideal play grounds for examining the connection between quantum and classical worlds.

In the present study, such a RWP was created by using a pair of ultrafast laser pulses, of which mutual delay and polarization were properly adjusted.  In addition, by using a specially designed ion-imaging setup (Fig. 1), the team got images of unidirectional RWPs at a viewing angle that the previous 2D imaging studies could not adopt.  As a result, the team succeeded in recording a series of images of time-varying molecular angular distribution with high-spatial resolution, which is nothing but a “movie” on the RWPs with defined sense of rotation.  The movie shows clearly wave-like nature of the RWPs (Fig. 2).  Multiple running waves get together at some time to give a highly concentrated spatial orientation and split after a while into parts having different angular velocities, while the overall movement keeps rotating in one direction.  Such a kind of propagation of wave packets may be well expected as a pedantic example of a simple quantum system like rotating molecules in free space, for which the mutual interaction is essentially inoperative.  Nevertheless, it has never been visualized experimentally so far.


Fig. 1.  Experimental setup to take a “snapshot” of molecular rotation.


         Fig 2.  “Snapshots” of unidirectionally rotating nitrogen molecules.(femtosecond = a quadrillionth part of one second)  Quantum-wave nature of the molecular rotation is clearly seen.

There have been many proposals for novel application of unidirectional RWPs.  For instance, unidirectionally rotating molecular gas ensembles is expected to make sophisticated polarization shaping of ultrafast light pulses.  In addition, unidirectional RWPs exhibiting cogwheel like motion is expected to be used as a “stopwatch” to measure the precise time difference between pulses from two independent ultrafast laser systems.

In a purely fundamental point of view, on the other hand, it is so challenging to experimentalists to explore how the wave-like nature of RWPs is approaching to the particle-like behavior for a macroscopic object.  It is also of great interest to experimentally track the loss of the wave-like character by a mutual or external interaction.  The present high-resolution RWP imaging is applicable to take a movie on such crossovers from quantum to classical worlds.

  Quantum unidirectional rotation directly imaged with molecules
  Kenta Mizuse, Kenta Kitano, Hirokazu Hasegawa, and Yasuhiro Ohshima
  Science Advances, July 3rd, 2015
  DOI: 10.1126/sciadv.1400185

  Professor Yasuhiro Ohshima
  Department of Chemistry, Graduate School of Science and Engineering,
  Tokyo   Institute of Technology

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