Lévêque Camille, Taïeb Richard, Köppel Horst
Sorbonne Universités, UPMC Univ. Paris 06, Laboratoire de Chimie Physique-Matière et Rayonnement, UMR 7614, 11 Rue Pierre et Marie Curie, 75231 Paris Cedex 05, France.
Theoretische Chemie, Physikalisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 229, D-69120 Heidelberg, Germany.
J Chem Phys. 2014 Mar 7;140(9):091101. doi: 10.1063/1.4867252.
Even though the sulfur dioxide molecule has been extensively studied over the last decades, its photo-excitation dynamics is still unclear, due to its complexity, combining conical intersections, and spin-orbit coupling between a manifold of states. We present a comprehensive ab initio study of the intersystem crossing of the molecule in the low energy domain, based on a wave-packet propagation on the manifold of the lowest singlet and triplet states. Furthermore, spin-orbit couplings are evaluated on a geometry-dependent grid, and diabatized along with the different conical intersections. Our results show for the first time the primordial role of the triplet (3)B2 state and furthermore predict novel interference patterns due to the different intersystem crossing channels induced by the spin-orbit couplings and the shapes of the different potential energy surfaces. These give new insight into the coupled singlet-triplet dynamics of SO2.
尽管在过去几十年中二氧化硫分子已得到广泛研究,但其光激发动力学仍不明确,这是由于其复杂性,它结合了锥形交叉以及多个态之间的自旋轨道耦合。我们基于在最低单重态和三重态流形上的波包传播,对该分子在低能域的系间窜越进行了全面的从头算研究。此外,自旋轨道耦合是在依赖于几何结构的网格上进行评估的,并与不同的锥形交叉一起进行 diabatic 处理。我们的结果首次展示了三重态(3)B2 态的首要作用,并且进一步预测了由于自旋轨道耦合和不同势能面形状所诱导的不同系间窜越通道而产生的新型干涉图样。这些为二氧化硫的单重态 - 三重态耦合动力学提供了新的见解。