High-resolution vibrational predissociation spectroscopy of I-·H2O by single-mode CW infrared excitation in a 3D cryogenic ion trap
- Yale Univ., New Haven, CT (United States); Yale University
- Yale Univ., New Haven, CT (United States)
- Emory Univ., Atlanta, GA (United States)
- Univ. of Washington, Seattle, WA (United States). Dept. of Chemistry
We describe the integration of a tunable, single-mode, continuous wave infrared laser into a cryogenic ion spectroscopy experiment to measure the rovibrational spectrum of the I-∙H2O complex in the OH stretching region. These upper levels lie about 300 cm-1 above the dissociation threshold. The measurements are carried out by loading the ions in a radiofrequency ion trap at 10 Hz and cooling them to 5 K with pulsed He buffer gas. IR photodissociation (PD) of the I-∙H2O complex is monitored by recording the I- product yield by time-of-flight mass spectrometry as a function of laser wavelength. Very narrow (Δν~75 MHz) rotational lines are observed throughout the spectrum, indicating long (ca. 2 ns) lifetimes for the excited metastable rovibrational levels. Rotational analysis of the band arising from the K”=1 to K’=2 transition of the free OH stretching fundamental yields the structure of the complex for the first time. Over 50% of the trapped ion ensemble in the trap can be photodissociated upon excitation of a single rotational line. This enables very high signal-to-noise in the PD spectrum, and is traced to a mechanism in which the ground state rotational levels are rapidly equilibrated by collisions with the buffer gas.
- Research Organization:
- Yale Univ., New Haven, CT (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC)
- Grant/Contract Number:
- SC0021012
- OSTI ID:
- 1914098
- Journal Information:
- Molecular Physics, Journal Name: Molecular Physics Journal Issue: 1-2 Vol. 122; ISSN 0026-8976
- Publisher:
- Taylor & FrancisCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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