Manipulating Quantum Interference in Two-Color (ω+3ω) Strong Laser Field Photodissociation Dynamics of D 2 .

In a strong field regime, exploring the molecular photodissociation process and revealing the underlying reaction mechanism remain challenging tasks due to the dramatic changes of molecular potentials caused by the applied fields. In this paper, we investigate the strong field photodissociation dynamics of D 2 + in a synthesized VUV + IR (266 + 800 nm) two-color laser field by solving the three-dimensional time-dependent Schrödinger equation. We show that the Aharonov-Bohm-like quantum interference in the photofragment angular distribution can be controlled by varying the ellipticity of the VUV light. We demonstrate that the interference phenomenon originates from the geometric phase accumulation of the nuclear wave function when it undergoes cyclic evolution on light-induced potential energy surfaces. This work has implications for the control of chemical reactions of a small molecular system through the geometric phase.