Influence of elevated radiative lifetime on efficiency of CdSe/CdTe Type II colloidal quantum dot based solar cells

Colloidal quantum dots (CQDs) are promising materials for solar cells because their optoelectronic properties are easily adjusted by control of their size, structure and composition. We present calculations of the band gap and radiative lifetime for varying core diameter and shell thickness of CdSe/CdTe core/shell Type II CQDs using a combination of single particle (2,6)-band k·pk·p and many-electron configuration interaction (CI) Hamiltonians. These calculations are validated by comparison with experimental absorption spectra and photoluminescence decay data. The results are then incorporated into a model of photovoltaic efficiency which demonstrates how the overall performance of a solar cell based on Type II CQDs is affected by changes in the core/shell geometry. The largest effect on photovoltaic efficiency is found to be due to the longer radiative lifetime produced by increasing the shell thickness

Visible spectrum quantum light sources based on InxGa1–xN/GaN Quantum Dots

We present a method for designing quantum light sources, emitting in the visible band, using wurtzite InxGa1−xN quantum dots (QDs) in a GaN matrix. This system is significantly more versatile than previously proposed arsenide- and phosphide-based QDs, having a tuning range exceeding 1 eV. The quantum mechanical configuration interaction method, capturing the fermionic nature of electrons and associated quantum effects explicitly, is used to find shapes and compositions of dots to maximize the excitonic dipole matrix element and optimize the biexciton binding energy. These results provide QD morphologies tailored for either bright single-photon emission or entangledphoton- pair emission at any given wavelength in the visible spectrum

Effect of correlation and dielectric confinement on 1S1/2(e)nS3/2(h)Excitons in CdTe/CdSe and CdSe/CdTe Type-II quantum dots

Controlled reduction of graphene oxide is an alternative and promising method to tune the electronic and optically active energy gap of this two-dimensional material in the energy range of the visible light spectrum. By means of ab initio calculations, based on hybrid density functional theory, that combine the Hartree–Fock method with the generalized gradient approximation (GGA), we investigated the electronic, optical, and radiative recombination properties of partially reduced graphene oxide, modelled as small islands of pristine graphene formed in an infinite sheet of graphene oxide. We predict that tuning of optically active gaps, in the wide range from ∼6.5 eV to ∼0.25 eV, followed by the electron radiative transition times in the range from ns to μs, can be effected by controlling the level of oxidization