A Photochemical Reaction in Different Theoretical Representations

被引:17
|
作者
Ibele, Lea M. [1 ]
Curchod, Basile F. E. [1 ]
Agostini, Federica [2 ]
机构
[1] Univ Durham, Dept Chem, Durham DH1 3LE, England
[2] Univ Paris Saclay, CNRS, Inst Chim Phys, UMR8000, F-91405 Orsay, France
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2022年 / 126卷 / 07期
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
CONICAL INTERSECTIONS; DYNAMICS; ISOMERIZATION; PERSPECTIVE;
D O I
10.1021/acs.jpca.1c09604
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The Born-Oppenheimer picture has forged our representation and interpretation of photochemical processes, from photoexcitation down to the passage through a conical intersection, a funnel connecting different electronic states. In this work, we analyze a full in silico photochemical experiment, from the explicit electronic excitation by a laser pulse to the formation of photoproducts following a nonradiative decay through a conical intersection, by contrasting the picture offered by Born-Oppenheimer and that proposed by the exact factorization. The exact factorization offers an alternative understanding of photochemistry that does not rely on concepts such as electronic states, nonadiabatic couplings, and conical intersections. On the basis of nonadiabatic quantum dynamics performed for a two-state 2D model system, this work allows us to compare Born-Oppenheimer and exact factorization for (i) an explicit photoexcitation with and without the Condon approximation, (ii) the passage of a nuclear wavepacket through a conical intersection, (iii) the formation of excited stationary states in the Franck-Condon region, and (iv) the use of classical and quantum trajectories in the exact factorization picture to capture nonadiabatic processes triggered by a laser pulse.
引用
收藏
页码:1263 / 1281
页数:19
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