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Photodissociation of D+3 in an intense, femtosecond laser field

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J D Alexander1, C R Calvert1, R B King1, O Kelly1, L Graham1, W A Bryan2, G R A J Nemeth2, W R Newell3, C A Froud4, I C E Turcu4, E Springate4, I D Williams1 and J B Greenwood1

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FAST TRACK COMMUNICATION

H+3 is the simplest triatomic molecule and plays an important role in laboratory and astrophysical plasmas. It is very stable both in terms of its electronic and nuclear degrees of freedom but is difficult to study in depth in the laboratory due to its ionic nature. In this communication, experimental results are presented for the strong field dissociation of the isotopic analogue D+3, using 30 fs, 800 nm laser pulses with intensities up to 1016 W cm−2. By employing a novel experimental set-up, ions were confined in an electrostatic ion trap so that dissociation of the molecule could be studied as it radiatively cools. It was determined that dissociation could only be observed for molecules in ro-vibrational states relatively close to the dissociation limit, while more tightly bound states demonstrated remarkable stability in even the strongest fields.


PACS

33.80.Gj Diffuse spectra; predissociation, photodissociation

98.58.Bz Atomic, molecular, chemical, and grain processes

42.65.Re Ultrafast processes; optical pulse generation and pulse compression

33.20.Vq Vibration-rotation analysis

37.10.Mn Slowing and cooling of molecules

Subjects

Atomic and molecular physics

Optics, quantum optics and lasers

Astrophysics and astroparticles

Dates

Issue 14 (28 July 2009)

Received 21 April 2009, in final form 22 May 2009

Published 24 June 2009



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