Using computational and experimental techniques, we examine the nature of the 2+ oxidation of Ti-doped CdSe. Through stoichiometry and confirmed through magnetization measurements, the weakly-doped material of Cd1-xTixSe (x = 0.0043) shows the presence of a robust spin-1 magnetic state of Ti, which is indicative of a 2+ oxidation state. Given the obscure nature of the Ti2+ state, we investigate the electronic and magnetic states using density functional theory. Using a generalized gradient approximation with an onsite potential, we determine the electronic structure, magnetic moment density, and optical properties for a supercell of CdSe with an ultra-low concentration of Ti. We find that, in order to reproduce the magnetic moment of spin-1, an onsite potential of 4-6 eV must be in included in the calculation. Furthermore, the electronic structure and density of states shows the presence of a Ti-d impurity band above the Fermi level and a weakly metallic state for a U = 0 eV. However, the evolution of the electronic properties as a function of the Hubbard U shows that the Ti-d drop below the Fermi around 4 eV with the onset of a semiconducting state. The impurity then mixes with the lower valence bands and produces the 2+ state for the Ti atom
