Articles you may be interested inCollisional excitation of CO2(0111) by hot hydrogen atoms: Alternating intensities in stateresolved vibrational, rotational, and translational energy transfer J. Chem. Phys. 93, 445 (1990); 10.1063/1.459718 Stateresolved vibrational, rotational, and translational energy deposition in CO2(0001) excited by collisions with hot hydrogen atoms J. Chem. Phys. 92, 4876 (1990); 10.1063/1.457704 Rotationally resolved hot atom collisional excitation of CO2 0001 and 0002 stretching vibrations by time resolved diode laser spectroscopy J. Chem. Phys. 88, 6240 (1988); 10.1063/1.454463Rotationally resolved isotope effect in the hot atom collisional excitation of CO2 (0001) by timedependent diode laser spectroscopy Rotationally resolved hot atom collisional excitation of CO2(0001) by timeresolved diode laser spectroscopy Time domain tunable diode laser absorption spectroscopy has been used to measure rotationally resolved transient absorption line shapes and nascent rotational populations for CO 2 molecules excited into the (00°2) vibrational state by collisions with translation ally hot hydrogen atoms. The 00°2 rotational population distribution and rotationally resolved linewidths are remarkably similar to those previously obtained for 00°1. Within the context of a simple physical model used to interpret the data, the similar rotational distributions and translational recoils for 00°1 and 00°2 suggest that these two states are excited by similar collision trajectories, wherein asymmetric stretching excitation is optimized when H strikes near the end of the O-C-O molecule. The magnitude of population scattered into 00°2 is -21 times smaller than that scattered into 00°1.