, Firstprinciples study of configurational disorder in B4C using a superatom-special quasirandom structure method, 2014, Physical Review B. Condensed Matter and Materials Physics, (90) Configurationally disordered crystalline boron carbide, with the composition B 4 C, is studied using firstprinciples calculations. We investigate both dilute and high concentrations of carbon-boron substitutional defects. For the latter purpose, we suggest a superatom's picture of the complex structure and combine it with a special quasirandom structure approach for disorder. In this way, we model a random distribution of high concentrations of the identified low-energy defects: (1) bipolar defects and (2) rotation of icosahedral carbon among the three polar-up sites. Additionally, the substitutional disorder of the icosahedral carbon at all six polar sites, as previously discussed in the literature, is also considered. Two configurational phase transitions from the ordered to the disordered configurations are predicted to take place upon an increase in temperature using a mean-field approximation for the entropy. The first transition, at 870 K, induces substitutional disorder of the icosahedral carbon atoms among the three polar-up sites; meanwhile the second transition, at 2325 K, reveals the random substitution of the icosahedral carbon atoms at all six polar sites coexisting with bipolar defects. Already the first transition removes the monoclinic distortion existing in the ordered ground-state configuration and restore the rhombohedral system (R3m). The restoration of inversion symmetry yielding the full rhombohedral symmetry (R3m) on average, corresponding to what is reported in the literature, is achieved after the second transition. Investigating the effects of high pressure on the configurational stability of the disordered B 4 C phases reveals a tendency to stabilize the ordered ground-state configuration as the configurationally ordering/disordering transition temperature increases with pressure exerted on B 4 C. The electronic density of states, obtained from the disordered phases, indicates a sensitivity of the band gap to the degree of configurational disorder in B 4 C.

Due to a large discrepancy between theory and experiment, the electronic character of crystalline boron carbide B 13 C 2 has been a controversial topic in the field of icosahedral boron-rich solids. We demonstrate that this discrepancy is removed when configurational disorder is accurately considered in the theoretical calculations. We find that while the ordered ground state B 13 C 2 is metallic, the configurationally disordered B 13 C 2 , modeled with a superatom-special quasirandom structure method, goes through a metal to nonmetal transition as the degree of disorder is increased with increasing temperature. Specifically, one of the chain-end carbon atoms in the CBC chains substitutes a neighboring equatorial boron atom in a B 12 icosahedron bonded to it, giving rise to a B 11 C e (BBC) unit. The atomic configuration of the substitutionally disordered B 13 C 2 thus tends to be dominated by a mixture between B 12 (CBC) and B 11 C e (BBC). Due to splitting of valence states in B 11 C e (BBC), the electron deficiency in B 12 (CBC) is gradually compensated.

No abstract