A theoretical study of substitutional boron–nitrogen clusters in diamond. (27th September 2018)

• Record Type: Journal Article
• Authors: Croot, Alex; Othman, M Zamir; Conejeros, Sergio; Fox, Neil A; Allan, Neil L
• Is Part Of: Journal of physics. Volume 30:Number 42(2018)
• Publication Date: 2018-09-27
• Subjects: diamond -- DFT -- co-doping -- clusters -- hybrid; Condensed matter -- Periodicals; Matière condensée -- Périodiques; Vaste stoffen; Vloeistoffen; Natuurkunde; Electronic journals; Computer network resources; 530.4105
• DOI: 10.1088/1361-648X/aade16
• Languages: English
• ISSNs: 0953-8984

Abstract

Abstract: Substitutional clusters of multiple light element dopants are a promising route to the elusive shallow donor in diamond. To understand the behaviour of co-dopants, this report presents an extensive first principles study of possible clusters of boron and nitrogen. We use periodic hybrid density functional calculations to predict the geometry, stability and electronic excitation energies of a range of clusters containing up to five N and/or B atoms. Excitation energies from hybrid calculations are compared to those from the empirical marker method, and are in good agreement. When a boron-rich or nitrogen-rich cluster consists of three to five atoms, the minority dopant element—a nitrogen or boron atom respectively—can be in either a central or peripheral position. We find B-rich clusters are most stable when N sits centrally, whereas N-rich clusters are most stable with B in a peripheral position. In the former case, excitation energies mimic those of the single boron acceptor, while the latter produce deep levels in the band-gap. Implications for probable clusters that would arise in high-pressure high-temperature co-doped diamond and their properties are discussed.