First-Principles Studies of Photoinduced Charge Transfer in Noncovalently Functionalized Carbon Nanotubes

TL;DR

This study uses first-principles calculations to explore how photoinduced charge transfer occurs in carbon nanotubes functionalized with dinitromethane, revealing insights into electronic states, adsorption energies, and relaxation dynamics relevant for optoelectronic applications.

Contribution

It provides the first detailed theoretical analysis of charge transfer and relaxation processes in noncovalently functionalized CNTs using DFT and reduced density matrix formalism.

Findings

Dinitromethane introduces localized states inside CNT band gaps.

Adsorption energy of dinitropentylpyrene on CNTs is approximately 75.26 kJ/mol.

Electron relaxation in CNTs is faster than hole relaxation, both with and without adsorbates.

Abstract

We have studied the energetics, electronic structure, optical excitation, and electron relaxation of dinitromethane molecules (CH$_{2}$N$_{2}$O$_{4}$) adsorbed on semiconducting carbon nanotubes (CNTs) of chiral index (n,0) (n=7, 10, 13, 16, 19). Using first-principles density functional theory (DFT) with generalized gradient approximations and van der Waals corrections, we have calculated adsorption energies of dinitropentylpyrene, in which the dinitromethane is linked to the pyrene via an aliphatic chain, on a CNT. A 75.26 kJ/mol binding energy has been found, which explains why such aliphatic chain-pyrene units can be and have been used in experiments to bind functional molecules to CNTs. The calculated electronic structures show that the dinitromethane introduces a localized state inside the band gap of CNT systems of n=10, 13, 16 and 19; such a state can trap an electron when the CNT is photoexcited. We have therefore investigated the dynamics of intra-band relaxations using the reduced density matrix formalism in conjunction with DFT. For pristine CNTs, we have found that the calculated charge relaxation constants agree well with the experimental time scales. Upon adsorption, these constants are modified, but there is not a clear trend for the direction and magnitude of the change. Nevertheless, our calculations predict that electron relaxation in the conduction band is faster than hole relaxation in the valence band for CNTs with and without molecular adsorbates.