The F + HD (v = 0,1; j=1) reaction; Angular momenta correlations in the low (< 1 meV) collision energy regime.

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL Physical Chemistry Chemical Physics Pub Date : 2024-11-27 DOI:10.1039/d4cp02866j
V Saez-Rabanos, Guadalupe Sáez-Cano, Juan Enrique Verdasco, Francisco Javier Aoiz, Victor J. Herrero
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Abstract

A detailed analysis of the low energy (0.01-10 meV) integral reaction cross section has been carried out for the F + HD(v=0, 1; j=1) → HF(DF) + D(H) reaction using accurate, fully converged time-independent hyperspherical quantum dynamics. Particular attention has been paid to the shape (orbiting) resonances and their assignment to the orbital (L) and total (J) angular momenta, as well as to the product’s state resolved cross sections at the energies of the resonances. As in previous works, it has been found that the energy position of the resonances depends on the initial state, but is essentially the same for the two exit channels and the product’s rovibrational states. The analysis in terms of the orbital and total angular momenta showed that each resonance is characterised by a given value of L but is contributed by several J. The main resonances are due to L=3 and L=5 for both F + HD (v=0, j=1) and F + HD(v=1, j=1) reactions, although they appear at different collision energies. The product’s vibrationally resolved excitation functions are found to follow the same pattern than the integral cross section summed over all final states. A more detailed exam has been made of the rotationally resolved integral cross sections associated with L=3, which gives rise to the main resonance for the two reactions and both product channels, for different final j′ states, showing similar behaviour for all j′ states except for j′=0 due to parity conservation. The joint analysis of the final rotational and orbital angular momenta shows that L′ and j′ tend to have antiparallel orientation.
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F + HD (v = 0,1; j=1) 反应;低(< 1 meV)碰撞能量机制中的角矩相关性。
利用精确、完全收敛的时间无关超球量子动力学,对 F + HD(v=0, 1; j=1) → HF(DF) + D(H) 反应的低能(0.01-10 meV)积分反应截面进行了详细分析。我们特别关注了形状(轨道)共振及其对轨道(L)和总(J)角矩的分配,以及共振能量下的产物状态解析截面。与之前的研究一样,我们发现共振的能量位置取决于初始状态,但对于两个出口通道和产物的振荡态来说基本相同。根据轨道和总角矩进行的分析表明,每个共振的特征都是一个给定的 L 值,但却由多个 J 共同作用。研究发现,产物的振动解析激发函数与所有终态的积分截面总和遵循相同的模式。我们对与 L=3 相关的旋转分辨积分截面进行了更详细的研究,这引起了两个反应和两个产物通道的主共振,对于不同的最终 j′态,除了 j′=0(由于奇偶性守恒)外,所有 j′态都显示出相似的行为。对最终旋转角矩和轨道角矩的联合分析表明,L′和j′趋向于反平行取向。
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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