Laboratory studies of uv emissions ofH2by electron impact. The Werner- and Lyman-band systems

Abstract
We report a laboratory measurement of absolute emission cross sections of both the Lyman bands (BΣu+1XΣg+1) and Werner bands (CΠu1XΠg+1) of H2 by electron impact over the energy range from threshold to 400 eV with the same optical system. We find the emission cross section for the BΣu+1XΣg+1 transition at 100 eV to be (3.55±0.8) × 1017 cm2 (2.7 × 1017 cm2, direct excitation, 0.85 × 1017 cm2, cascading) and the emission cross section for the CΠu1XΣg+1 transition at 100 eV to be (3.1±0.6) × 1017 cm2 (cascading is estimated to be not present). The cross-section ratio QCQB for direct excitation is 1.21±0.30 at 300 eV in excellent agreement with published values for this ratio from theoretical calculations and experimental data of the optical oscillator strengths. We measure the cross section for cascading to the B state to be 24±10% of the total emission cross section both at 100 and 300 eV. We show that cascading increases to 51±20% of the total cross section of the B state at 20 eV. The vibrational population distribution of the B state is found to be a function of electron-impact energy as the importance of cascading relative to direct excitation changes with electron-impact energy.