首页> 外文期刊>The Journal of Chemical Physics >Quantum dynamics of the N(~4S)+O_2 reaction on the X~2A' and a ~4A' surfaces: Reaction probabilities, cross sections, rate constants, and product distributions
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Quantum dynamics of the N(~4S)+O_2 reaction on the X~2A' and a ~4A' surfaces: Reaction probabilities, cross sections, rate constants, and product distributions

机译:X〜2A'和〜4A'表面上N(〜4S)+ O_2反应的量子动力学:反应概率,截面,速率常数和产物分布

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We report real wave packet (WP) calculations of reaction probabilities, cross sections, rate constants, and product distributions of the reaction N(~4S)+O_2(X~3SIGMA_g~-)->NO(X~2II)+O(~3P). We propagate initial WPs corresponding to several O_2 levels, and employ reactant coordinates and a flux method for calculating initial-state-resolved obseervables, or product coordinates and an asymptotic analysis for calculating state-to-resolved observables, or product coordinates and an asymptotic analysis for calculating state-to-state quantities. Exact or J-shifting calculations are carried out at total angular momentum J=0 or J>0, respectively. We employ the recent X~2A' S3 otential energy surface (PES) by Sayos et al. and the earlier a ~4A' PES by Duff et al. In comparing S3 results with the WP ones of a previous X ~2A' S2 PES, we find lower S3 energy thresholds and larger S3 probabilities, despite the higher S3 barrier. This finding is due to the different features of the doublet PESs in the reactant and product channels, at the transition state, and in the NO_2 equilibrium region. We analyze the effects of the O_2 initial level and show that tunneling through the S3 barrier enhance the room-temperature rate constant by approx 3.7 times with respect to the previous S2 WP rate. The agreement with the room-temperature experimental result is thus notably improved. The NO vibrational distribution is inverted and the rotational ones are strongly oscillating. We explain these nonstatistical results showing that the reaction partners approach each other with a large impact parameter. The WP vibrational distribution is however different from that observed, which is oscillating. WP calculations show that the new S3 PES describes accurately several features of the X ~2A' state, although a lowering of its barrier height by approx 0.56 kcal/mol should bring calculated and observed rate constants in full agreement.
机译:我们报告了反应概率,截面,速率常数和反应产物分布的实波包(WP)计算N(〜4S)+ O_2(X〜3SIGMA_g〜-)-> NO(X〜2II)+ O( 〜3P)。我们传播对应于几个O_2水平的初始WP,并采用反应物坐标和通量方法计算初始状态可分辨的可观物,或乘积坐标和渐近分析以计算状态至可分辨的可观物,或乘积坐标和渐近分析用于计算状态间的数量。分别在总角动量J = 0或J> 0时进行精确或J位移计算。我们使用了Sayos等人最近的X〜2A'S3势能面(PES)。 Duff等人则是较早的〜4A'PES。通过比较S3结果与先前X〜2A'S2 PES的WP结果,我们发现尽管S3势垒较高,但S3能量阈值较低,S3概率较大。该发现是由于在反应物和产物通道中,在过渡态和在NO_2平衡区中双峰PES的不同特征。我们分析了O_2初始水平的影响,并表明通过S3势垒的隧穿使室温速率常数相对于先前的S2 WP速率提高了约3.7倍。因此,显着改善了与室温实验结果的一致性。 NO的振动分布反转,而旋转的振动强烈振荡。我们解释了这些非统计结果,这些结果表明反应伙伴彼此接近且影响参数很大。但是,WP的振动分布与观察到的振动不同。 WP计算表明,新的S3 PES准确地描述了X〜2A'状态的几个特征,尽管将其势垒高度降低了约0.56 kcal / mol,这应该使计算得出的速率常数和观测到的速率常数完全一致。

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