Six-dimensional quantum dynamics of an Eley–Rideal reaction between gaseous and adsorbed hydrogen atoms on Cu(111)

IF 3.4 3区 化学 Q2 Chemistry
Longlong Xiong, Liang Zhang, Bin Zhao and Bin Jiang
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引用次数: 0

Abstract

In the form of direct abstraction of a surface adsorbate by a gaseous projectile, the Eley–Rideal (ER) reaction at the gas–surface interface manifests interesting dynamics. Unfortunately, high-dimensional quantum dynamical (QD) studies for ER reactions remain very challenging, which demands a large configuration space and the coordinate transformation of wavefunctions. Here, we report the first six-dimensional (6D) fully coupled quantum scattering method for studying the ER reaction between gas phase H(D) atoms and adsorbed D(H) atoms on a rigid Cu(111) surface. Reaction probabilities and product rovibrational state distributions obtained by this 6D model are found to be quite different from those obtained by reduced-dimensional QD models, demonstrating the high-dimensional nature of the ER reaction. Using two distinct potential energy surfaces (PESs), we further discuss the influence of the PES on the calculated product vibrational and rotational state distributions, in comparison with experimental results. The lateral corrugation and the exothermicity of the PES are found to play a critical role in controlling the energy disposal in the ER reaction.

Abstract Image

Abstract Image

Cu(111)上气态氢原子与吸附氢原子之间埃利-里德尔反应的六维量子动力学。
在气体射弹直接吸附表面吸附物的形式下,气体-表面界面上的埃利-里德尔(ER)反应表现出有趣的动力学。遗憾的是,ER 反应的高维量子动力学(QD)研究仍然非常具有挑战性,这需要一个巨大的构型空间和波函数的坐标变换。在此,我们报告了第一种六维(6D)全耦合量子散射方法,用于研究气相 H(D)原子与刚性 Cu(111)表面上吸附的 D(H)原子之间的 ER 反应。研究发现,该 6D 模型得到的反应概率和产物振荡态分布与还原维 QD 模型得到的概率和产物振荡态分布大相径庭,这证明了 ER 反应的高维性质。利用两个不同的势能面(PES),我们进一步讨论了 PES 对计算产物振动和旋转状态分布的影响,并与实验结果进行了比较。研究发现,势能面的横向波纹和放热性在控制 ER 反应的能量处置方面起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Faraday Discussions
Faraday Discussions CHEMISTRY, PHYSICAL-
CiteScore
4.90
自引率
0.00%
发文量
259
审稿时长
2.8 months
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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