Giant enhancement of exciton radiative lifetime by ferroelectric polarization: The case of monolayer TiOCl2

Exciton binding energy and lifetime are the two most important parameters controlling exciton dynamics, and the general consensus is that the larger the former, the larger the latter. However, our first-principles study of monolayer ferroelectric TiOCl2 shows that this is not always the case. We find that ferroelectric polarization tends to weaken exciton binding but enhance exciton lifetime. This stems from the different effects of the induced built-in electric field and structural distortion by the spontaneous polarization: the former always destabilizes or even dissociates the exciton while the latter leads to a relaxation of the selection rule and activates excitons that are otherwise not optically active. Their combined effect leads to a halving of the exciton binding energy but a substantial increase in lifetime by 40 times. Our results deepen the understanding of the interaction of light with ferroelectric materials and provide new insights into the use of ferroelectricity to control exciton dynamics.