Nuclear-Electronic Orbital Quantum Dynamics of Plasmon-Driven H 2 Photodissociation.

Leveraging localized surface plasmon resonances of metal nanoparticles to trigger chemical reactions is a promising approach for heterogeneous catalysis. First-principles modeling of such processes is challenging due to the large number of electrons and electronic excited states as well as the significance of nuclear quantum effects when hydrogen is involved. Herein, the nonadiabatic nuclear-electronic quantum dynamics of plasmon-induced H 2 photodissociation near an Al 13 - cluster is simulated with real-time nuclear-electronic orbital time-dependent density functional theory (RT-NEO-TDDFT). This approach propagates the nonequilibrium quantum dynamics of both electrons and protons. The plasmonic oscillations are shown to inject hot electrons into the antibonding orbital of H 2 , thereby inducing H 2 dissociation. The quantum mechanical treatment of the hydrogen nuclei leads to faster H 2 photodissociation and slightly larger isotope effects. Analysis of the nonequilibrium electronic density suggests that these findings stem from enhanced excited-state electronic coupling between the plasmonic mode and the H 2 antibonding orbital due to proton delocalization or zero-point energy effects. Given the low computational overhead for including nuclear quantum effects with the RT-NEO-TDDFT approach, this work paves the way for simulating nonadiabatic nuclear-electronic quantum dynamics in other plasmonic systems.