Geometric phase effects in the coherent control of the branching ratio of photodissociation products of phenol

Abstract

Optimal control simulation is used to examine the control mechanisms in the photodissociation of phenol within a two-dimensional, three-electronic-state model with two conical intersections. This model has two channels for H-atom elimination, which correspond to the (2)pi and (2)sigma states of the phenoxyl radical. The optimal pulse that enhances (2)sigma dissociation initially generates a wave packet on the S(1) potential-energy surface of phenol. This wave packet is bifurcated at the S(2)-S(1) conical intersection into two components with opposite phases because of the geometric phase effect. The destructive interference caused by the geometric phase effect reduces the population around the S(1)-S(0) conical intersection, which in turn suppresses nonadiabatic transitions and thus enhances dissociation to the (2)sigma limit. The optimal pulse that enhances S(0) dissociation, on the other hand, creates a wave packet on the S(2) potential-energy surface of phenol via an intensity borrowing mechanism, thus avoiding geometric phase effects at the S(2)-S(1) conical intersection. This wave packet hits the S(1)-S(0) conical intersection directly, resulting in preferred dissociation to the (2)pi limit. The optimal pulse that initially prepares the wave packet on the S(1) potential-energy surface (PES) has a higher carrier frequency than the pulse that prepares the wave packet on the S(2) PES. This counterintuitive effect is explained by the energy-level structure and the S(2)-S(1) vibronic coupling mechanism.