Tuning functionalized hexagonal boron nitride quantum dots for full visible-light fluorescence emission.

Abstract

Tunable photoluminescence has been observed in hexagonal boron nitride quantum dots (BNQDs), but the underlying luminescence mechanism remains elusive. In this study, we examine excited-state properties of several functionalized BNQDs models using density functional theory (DFT), time-dependent DFT, and multistate complete active space second-order perturbation theory (MS-CASPT2) methods. Unlike reported graphene quantum dots, photoluminescence of BNQDs is not affected by their sizes (<2.5 nm). Instead, the embedded single sp3 carbon atom connecting different functional groups can tune emission colors of BNQDs, whose emission wavelength cover full range of visible light and even extend toward near-infrared region. Further analysis reveals that both exciton self-trapping and electron-hole separation decrease HOMO-LUMO energy gaps, leading to large Stokes shifts. Moreover, uneven and even hybridizations induce blue- and red-shifted emission spectra. These findings provide novel insights into full-spectrum emission of BNQDs modified with functional groups.