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Differential cross section for rotationally inelastic scattering of vibrationally excited NO(v=5) from Ar

机译:振动激发的NO(v = 5)从Ar的旋转非弹性散射的微分截面

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Rotationally inelastic scattering of vibrationally excited NO(v=5) from Ar was studied with a crossed molecular beam ion-imaging apparatus.Vibrationally excitd NO was generated at the exit of a pulsed nozzle by the photoinitiated reaction between O(~1D0 and N_2O.The results for rotational excitation in vibrationally excited NO were compared to those in the vibrational ground state at a collision energy of 1460 cm~(-1).The final rotational stage of NO,poulated by scattering from Ar,was detected by 1+1 REMPI via the A(~2sum~+)<-X(~2II_(1/2) electronic transition.TheR_(21) transition was used to probe the final scattered state in both cases.The rotational rainbow maxima are observed at slightly smaller angles in thescattering of vibrationally excited NO from Ar compared to the scattering of NO inthe vibrational ground state from Ar.A hard-ellipse potential model was used to investigate theeffect of initial vibrational excitation on the rotational energy-transfer process.The small shifts observedin the rainbow maxima are evidence for a slight enhancement in angular anisotropy in the intermolecular potential for NO(v=5)/Ar compared to that for NO(v=0)/Ar.
机译:用交叉分子束离子成像装置研究了Ar激发的NO(v = 5)的旋转非弹性散射,O(〜1D0和N_2O)之间的光引发反应在脉冲喷嘴的出口产生了振动激发的NO。在振动能量为1460 cm〜(-1)的情况下,将振动激发的NO的旋转激发结果与振动基态的旋转激发结果进行了比较.NO的最终旋转阶段是由Ar散射造成的,其结果是1 + 1通过A(〜2sum〜+)<-X(〜2II_(1/2)电子跃迁进行REMPI.R_(21)跃迁用于探测两种情况下的最终散射状态。在较小的情况下观察到旋转彩虹最大值相对于Ar振动基态中NO的散射,Ar激发NO的散射角有所不同。采用硬椭圆形势模型研究了初始振动激发对旋转能量传递过程的影响。 bservedin的彩虹最大值证明了NO(v = 5)/ Ar的分子间电势与NO(v = 0)/ Ar的分子间电势的角度各向异性略有增强。

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