
Journal of Chemical Physics p. 6266 - 6275 (1987)
Update date:2022-08-11
Topics:
Becker, A. C.
Lodemann, K.-P.
Schurath, Ulrich
NBr in solid argon has been excited to the b1Σ+ state with a pulsed tunable dye laser.In addition to the well-known fluorescence spectrum of the b state, infrared emission from the vibrationally relaxed a 1Δ state was detected at 1086 nm.Three major trapping sites were resolved in absorption and fluorescence excitation spectra of the b-X system.Additional sites could be identified in the excitation spectrum of the a state, which is populated via the b state by internal conversion.There is a weak site elfect on the lifetime of the vibrationally relaxed b state, which varies between 40 and 30 μs.Vibrational relaxation rates in the b state show a stronger site dependence.Internal conversion from b 1Σ+ to a 1Δ accounts for < 0.1percent to at least 17percent of the decay rate of NBr b 1Σ+, v = 0.Orbitally forbidden transitions to the X10+ component of the ground state were identified 23.0 to 25.5 cm-1 on the high-energy side of the more intense a 1Δ <*> X21<*> transition of several sites.The lifetime of the a state varies between 152 <*> 12 ms in the least perturbed site and 121 <*> 15 ms in the site with the strongest a 1Δ <*>X10+ forbidden component.NBr trapped in double vacancies of pure fcc argon, of single stacking faults, and of multiple stacking faults ( hcp pockets ) in argon, can account for the sites.
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