Abstract
Single rotational states were populated in vibrationally excited hydrogen by stimulated Raman pumping. The population in H2 X 1+g(v″=0,1) and D2 X 1+g(v″=0,1) was probed state selectively by tunable vacuum ultraviolet (VUV) laser radiation around λ=110 nm, and the fluorescence induced when exciting the hydrogen molecules in the (0–0), (1–0), (2–0), (3–1), and (4–1) Lyman bands of the (B 1+uX 1+g) transition monitored. From a comparison of line heights, the stimulated Raman pumping efficiency is estimated to be 30%–50% in the focal volume. Rotational transitions in X 1+g(v″=1) were induced in collisions with H2, D2, and He. State‐to‐state rotational relaxation rates were measured for the (J″=1→J″=3) transition in H2(v″=1) and for the (J″=2→J″=0,4) transitions in D2(v″=1). These rates were found to be generally higher than the corresponding previously determined ones in ground state hydrogen, in qualitative accord with recent theoretical calculations. A comparison with available theoretical state‐to‐state cross sections shows that the rates obtained with these cross sections are generally lower than the relaxation rates directly measured in this work.