The oxidation states of Thallium in FA1 Tl+n (n = 1,3) color centers at the (100) surface of NaCl play important role in laser light
generation and adsorbate–substrate interactions. Double-well potentials at these surfaces are investigated by using quantum mechanical
ab initio methods. Quantum clusters of variable sizes were embedded in the simulated Coulomb fields that closely approximate the
Madelung fields of the host surfaces, and ions that were the nearest neighbors to the FA1 Tl+n (n = 1,3) defect site were allowed to relax
to equilibrium.The calculated Stokes shifts suggest that laser light generation is sensitive to the oxidation states of Thallium. The relaxed
excited states of the defect-containing surface were deep below the lower edge of the conduction bands of the ground state defect-free
surface, suggesting that the FA1 Tl+n (n = 1,3) centers are suitable laser defects. The dependence of the orientational destruction and
recording sensitivity on the oxidation state of Thallium is clarified. The Glasner–Tompkins empirical rule is generalized to include
the oxidation state of the impurity cation. The adsorption energies of CO and OC over NaCl(100) was found to be sensitive to the oxidation
state of the impurity cation. FA1 Tl+n (n = 1,3) centers changed the physical adsorption of CO to chemical adsorption. While the
artificial flow of charge was significant in the case of Tl+1 impurity, it was negligible in the case of Tl+3 impurity, and the results were
explained in terms of the electrostatic potential curves.