학술논문

Effects of rotational excitation on decay rates of long-lived Rydberg states in NO.
Document Type
Article
Source
Journal of Chemical Physics. 10/28/2023, Vol. 159 Issue 16, p1-7. 7p.
Subject
*RYDBERG states
*ELECTRIC field strength
*QUANTUM numbers
*DECAY constants
*NITRIC oxide
*EXCITED states
Language
ISSN
0021-9606
Abstract
Nitric oxide (NO) molecules in pulsed supersonic beams have been excited to long-lived Rydberg-Stark states in series converging to the lowest vibrational level in the ground electronic state of NO+ with rotational quantum numbers N+ = 2, 4, and 6. The molecules in these excited states were then guided, or decelerated and trapped in a chip-based Rydberg-Stark decelerator, and detected in situ by pulsed electric field ionization. Time constants, reflecting the decay of molecules in N+ = 2 Rydberg-Stark states, with principal quantum numbers n between 38 and 44, from the electrostatic traps were measured to be ∼ 300 μ s. Molecules in Rydberg-Stark states with N+ = 4 and 6, and the same range of values of n were too short-lived to be trapped, but their decay time constants could be determined from complementary sets of delayed pulsed electric field ionization measurements to be ∼100 and ∼25 μs, respectively. [ABSTRACT FROM AUTHOR]