High-Resolution Spectroscopy of NO in Helium Droplets: A Prototype for Open Shell Molecular Interactions in a Quantum Solvent
- 1. Lehrstuhl fuer Physikalische Chemie II, Ruhr-Universitaet Bochum, Universitaetsstrasse 150, 44780 Bochum (Germany)
- 2. Lehrstuhl fuer Theoretische Chemie, Ruhr-Universitaet Bochum, Universitaetsstrasse 150, 44780 Bochum (Germany)
Description
We have measured the high-resolution infrared spectrum of the radical NO in the 2Π1/2 state in superfluid helium nanodroplets. The features are attributed to the Λ-doubling splitting and the hyperfine structure. The hyperfine interaction is found to be unaffected by the He solvation. For the Λ-doubling splitting, we find a considerable increase by 55% compared to the gas phase. This is explained by a confinement of the electronically excited NO states by the surrounding He. The rotational level spacing is decreased to 76% of the gas phase value. The IR transition to the J=1.5 state is found to be homogeneously broadened. We attribute both observations to the coupling between the molecular rotation and phonon/roton excitations in superfluid 4He droplets
Additional details
Identifiers
Publishing Information
- Journal Title
- Physical Review Letters
- Journal Volume
- 95
- Journal Issue
- 21
- Journal Page Range
- p. 215301-215301.4
- ISSN
- 0031-9007
- CODEN
- PRLTAO
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 37015587
- Subject category
- S74: ATOMIC AND MOLECULAR PHYSICS;
- Descriptors DEI
- CONFINEMENT; DROPLETS; EXCITATION; HELIUM 4; HYPERFINE STRUCTURE; INFRARED SPECTRA; NITRIC OXIDE; PHONONS; RADICALS; ROTATIONAL STATES; SOLVATION; SOLVENTS; SPECTROSCOPY; SUPERFLUIDITY
- Descriptors DEC
- CHALCOGENIDES; ENERGY LEVELS; ENERGY-LEVEL TRANSITIONS; EVEN-EVEN NUCLEI; EXCITED STATES; HELIUM ISOTOPES; ISOTOPES; LIGHT NUCLEI; NITROGEN COMPOUNDS; NITROGEN OXIDES; NUCLEI; OXIDES; OXYGEN COMPOUNDS; PARTICLES; QUASI PARTICLES; SPECTRA; STABLE ISOTOPES
Optional Information
- Notes
- (c) 2005 The American Physical Society