Interplay between Electrostatic Properties of Molecular Adducts and Their Positions at Carbon Nanotubes
Braden M. Weight, Brendan J. Gifford, Sergei Tretiak, Svetlana Kilina
Abstract
Formation of the sp3-defect due to covalent functionalization of a single-walled carbon nanotube (SWCNT) results in a new red-shifted emissive excitons. Using density functional theory, we study the impact of the intrinsic molecular dipole moments and the local charges induced by various molecular adducts on the energy and localization properties of the optically active defect-based exciton in a (10,5) SWCNT. The interplay of two effects plays a role in the localization of the exciton and, therefore, its red shift, but at different scales: The source of the leading order contribution is the defect conformation, resulting in the red shift of the defect-associated exciton with respect to the E11 band of the pristine SWCNT on the order of ∼100 meV, while the individual dipoles and polarization properties of molecular adducts lead to significantly smaller red shifts on the order of ∼10 meV. While the species-dependent trends in defect-induced charges do not directly correlate to the exciton red shift, the charge at the sp3-defect exhibits a distinct behavior between ortho- and para-defect configurations and is relevant to the chemical reactivity of the defect position depending on the adduct type. Overall, our computational results may be helpful for diverse synthetic strategies to fine-tune emission of SWCNTs toward desired applications.