POLARIZATION OF ATOMIC POTASSIUM FLUORESCENCE EXCITED BY LASER PHOTODISSOCIATION OF K2

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1988

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Ohio State University

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A tunable dye laser was used to excite K2 from the ground X(1Σg+) state into the continuum of the B(1Σu) state. This results in dissociation of the molecule producing an excited K2P3/2 atom which fluoresces. By monitoring the atomic D2 fluorescence under these molecular beam (collision-free) conditions, we were able to measure the pure bound-free absorption profile. At the same time, the polarization of the atomic fluorescence was measured for different laser excitation frequencies. We believe this to be the first observation of a large variation in the polarization, ranging from 15±2% to −6.3±0.4% as a function of laser excitation wave-length. The results are explained a) using the theory of Van Brunt and Zare1, which predicts a maximum polarization of 14.3% (axial recoil) and a minimum of -7.7% (transverse recoil) and b) the Rotating molecule theory2 where the polarization is a function of the angle of rotation of a half collision. Classical, semiclassical and quantum-mechanical calculations in the K2 case were also performed and a comparison with the experimental results is given.

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1 R. J. Van Brunt and R. N. Zare, J. Chem. Phys. 48, 4304 (1968). 2 J. Vigue, J. A. Beswick and M. Broyer, J. de Physique 44, 1225 (1983).


Author Institution: Iowa Laser Facility, University of Iowa

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