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Electronic and Crystal Structure of Cu2−xS: Full-Potential Electronic Structure Calculations
Physical Review B (2007)
  • Pavel Lukashev, University of Northern Iowa
  • Walter R.L. Lambrecht, Case Western Reserve University
  • Takao Kotani, Arizona State University at the Tempe Campus
  • Mark Van Schilfgaarde, Arizona State University at the Tempe Campus
Abstract
Electronic structure calculations are presented for Cu2−xS using the full-potential linearized muffin-tin orbital method. In the simple cubic antifluorite structure, Cu2S is found to be semimetallic both in the local density approximation (LDA) and using the quasiparticle self-consistent GW (QSGW)method. This is because the Cud bands comprising the valence band maximum are degenerate at the Γ point and the fact that the Cus band, which can be considered to be the lowest conduction band, lies slightly below it at Γ. Small deviations from the ideal antifluorite positions for the Cu atoms, however, open a small gap between the Cud valence and Cus-like conduction bands because the symmetry breaking allows the Cus and Cud bands to hybridize. Supercell models are constructed for cubic and hexagonal chalcocite Cu2S as well as cubic digenite Cu1.8S by means of a weighted random number structure generating algorithm. This approach generates models with Wyckoff site occupancies adjusted to those obtained from experimental x-ray diffraction results and with the constraint that atoms should stay within reasonable distance from each other. The band structures of these models as well as of the low-chalcocite monoclinic structure (Cu96S48) are calculated in LDA with an additional Cus shift obtained from the QSGW-LDA difference for the antifluorite structure. Even with this correction, smaller band gaps of about 0.4–0.6eV (increasing from cubic to hexagonal to monoclinic) than experimentally observed (1.1–1.2eV) are obtained for the Cu2Scomposition. Decreasing the Cu content of Cu2−xS in the range 0.06<x<0.2 is found to essentially dope the p-type material by placing the Fermi level 0.2–0.3eV below the valence band maximum but also to increase the gap between highest partially filled valence band and lowest conduction bands to about 0.7–1.0eV. This results from a reduced Cud-band width. Thus, the optical band gap or onset of optical absorption increases in part but not exclusively due to the Moss-Burstein effect. The total energies of the structures are found to increase from monoclinic to hexagonal to cubic to antifluorite. This is consistent with the fact that the simple antifluorite structure is not observed and that the systems change from monoclinic to hexagonal to cubic with increasing temperature, under the assumption that the electronic energy of the system dominates the free energy. We find that Cu2S is unstable toward the formation of Cu vacancies even in thermodynamic equilibrium with bulk Cu metal. The experimental data on the band gaps and optical absorption are discussed. We find no evidence for indirect band gaps in the hexagonal materials and argue that the experimental results are consistent with this in spite of previous reports to the contrary. The presence of a second onset of absorption located about 0.5eV higher than the minimum band gap observed in experiment is explained by a rise in conduction band density of states at this energy in our calculations. The calculated increase in gap with decreasing Cu concentration is in agreement with experimental observations.
Disciplines
Publication Date
November 2, 2007
DOI
http://dx.doi.org/10.1103/PhysRevB.76.195202
Citation Information
Pavel Lukashev, Walter R.L. Lambrecht, Takao Kotani and Mark Van Schilfgaarde. "Electronic and Crystal Structure of Cu2−xS: Full-Potential Electronic Structure Calculations" Physical Review B Vol. 76 Iss. 19 (2007)
Available at: http://works.bepress.com/pavel-lukashev/16/