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A tight-binding based bond-order potential (BOP) has been constructed for the fcc transition metal iridium that includes explicitly only d orbitals in the evaluation of the total energy. We show that hybridization between the nearly free electron sp band and the unsaturated covalently bonded d orbitals is important in determining the relative stabilities of the close-packed structures and that this effect can be accurately captured through the use of a central force term. The BOP is found to provide an excellent description of the equilibrium properties of iridium, including its negative Cauchy pressure that is fitted using a many-body repulsive term. The transferability of the BOP is assessed by calculating energy differences between different crystal structures, the energetics of the tetragonal and trigonal deformation paths, the phonon spectra, stacking fault, and vacancy formation energies. Comparison of the results of these studies with either experiments or first principles calculations is found to be good. We also describe briefly the application of the constructed BOP to the atomistic simulation of the core structure of the screw dislocation that led to an explanation of the anomalous deformation and fracture behavior exhibited of iridium.
Cawkwell, M. J., Nguyen-Manh, D., Pettifor, D. G., & Vitek, V. (2006). Construction, assessment, and application of a bond-order potential for iridium. Retrieved from https://repository.upenn.edu/mse_papers/84
Date Posted: 29 June 2006
This document has been peer reviewed.