A universal chemical potential for sulfur vapours. Issue 2 (12th November 2015)

• Record Type: Journal Article
• Authors: Jackson, Adam J.; Tiana, Davide; Walsh, Aron
• Is Part Of: Chemical science. Volume 7:Issue 2(2016:Feb.)
• Page Start: 1082
• Page End: 1092
• Publication Date: 2015-11-12
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5sc03088a
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : The equilibrium thermochemistry of mixed vapour-phase sulfur allotropes is computed and solved to obtain a single chemical potential function. Abstract : The unusual chemistry of sulfur is illustrated by the tendency for catenation. Sulfur forms a range of open and closed S n species in the gas phase, which has led to speculation on the composition of sulfur vapours as a function of temperature and pressure for over a century. Unlike elemental gases such as O2 and N2, there is no widely accepted thermodynamic potential for sulfur. Here we combine a first-principles global structure search for the low energy clusters from S2 to S8 with a thermodynamic model for the mixed-allotrope system, including the Gibbs free energy for all gas-phase sulfur on an atomic basis. A strongly pressure-dependent transition from a mixture dominant in S2 to S8 is identified. A universal chemical potential function, μ S ( T, P ), is proposed with wide utility in modelling sulfurisation processes including the formation and annealing of metal chalcogenide semiconductors.