Abstract
Solid nitrogen doped with 0.1 % oxygen has been reinvestigated by using pulsed low-energy electron excitation. The resulting 0 atom emissions (ls)
2
(2s)
2
(2p)
4
β(0,
1
S -
1
D) and the associated vibrational sidebands β', β" and β'" have been examined by using a variable temperature liquid helium cryostat and photoelectric recording. This demonstrated that the electronic transition 0 (
1
S -
1
D) is split into three zero-phonon Tines’ (z.p.l.) by the crystalline field arising at a substitutional centro-symmetric trapping site in solid N
2
. However, little or no emission arises from the z.p.l. origins since the transition is still dipole forbidden, but strong electron-phonon coupling of the three components of the
1
D state takes place and the transition becomes dipole allowed owing to asymmetric inducing low energy lattice modes. β', β" and β'" arise from the transition of O atoms simultaneous with a vibrational step down or up in the ground state of a neighbouring N
2
molecule. For β" and β'" the weak vibron-electron coupling is to symmetric non-inducing modes. Thus these transitions are shifted by the vibrational ground-state spacing energy of N
2
(X
1
Σ, v" = 6±1 to v" = 5± 1 or v" = 7±1). The initial v" = 6 + 1 value corresponds to the maximum in the intensity distribution of β" and β'" after an N
2
triplet exciton is quenched by a ground state 0 (
3
P) atom. Since the vibron modes are non-inducing, the vibrational sidebands appear with an intensity distribution resembling the phonon induced electronic transition β.
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