Radboud University Nijmegen, Institute for Molecules and Materials, Nijmegen, The Netherlands.
J Chem Phys. 2011 May 28;134(20):204308. doi: 10.1063/1.3589360.
State-to-state differential cross sections (DCSs) for rotationally inelastic scattering of H(2)O by H(2) have been measured at 71.2 meV (574 cm(-1)) and 44.8 meV (361 cm(-1)) collision energy using crossed molecular beams combined with velocity map imaging. A molecular beam containing variable compositions of the (J = 0, 1, 2) rotational states of hydrogen collides with a molecular beam of argon seeded with water vapor that is cooled by supersonic expansion to its lowest para or ortho rotational levels (J(KaKc) = 0(00) and 1(01), respectively). Angular speed distributions of fully specified rotationally excited final states are obtained using velocity map imaging. Relative integral cross sections are obtained by integrating the DCSs taken with the same experimental conditions. Experimental state-specific DCSs are compared with predictions from fully quantum scattering calculations on the most complete H(2)O-H(2) potential energy surface. Comparison of relative total cross sections and state-specific DCSs show excellent agreement with theory in almost all details.
在 71.2 meV(574 cm(-1)) 和 44.8 meV(361 cm(-1)) 碰撞能下,使用分子束交叉结合速度图成像技术,测量了 H(2)O 与 H(2)的旋转非弹性散射的态态差分截面 (DCS)。包含氢的 (J = 0,1,2) 转动态的可变组成的分子束与氩分子束碰撞,氩分子束中含有水蒸气,通过超音速膨胀冷却到其最低的 para 或 ortho 转动能级(分别为 J(KaKc) = 0(00) 和 1(01))。使用速度图成像获得完全指定的旋转激发终态的角速度分布。通过积分具有相同实验条件的 DCS 获得相对积分截面。实验态特异性 DCS 与最完整的 H(2)O-H(2)势能表面上的全量子散射计算的预测进行了比较。相对总截面和态特异性 DCS 的比较几乎在所有细节上都与理论非常吻合。