| Abstrakt: |
Aiming at a fundamental understanding of the defect chemistry of pure ZnSe for optical and quantum applications, systematic density functional theory calculations with hybrid exchange-correlation functionals were performed to build an accurate database of native defects in ZnSe, including isolated defects and first nearest-neighbor defect–defect complexes. From the defect formation energies, zinc vacancy is found to be the most prevalent defect as the Fermi level approaches the conduction band edge, while zinc interstitial in the selenium tetrahedron and selenium vacancy become the most prevalent defects as the Fermi level approaches the valence band maximum. The divacancy complex, consisting of first nearest-neighboring zinc and selenium vacancies, is also found to have a favorable binding energy across the entire bandgap. Its formation energy is, however, always higher than either the isolated zinc or selenium vacancy, meaning it will never be the predominant defect in equilibrium. Finally, a point defect with extended spin coherence in Fluorine-implanted ZnSe was recently discovered, and it was found to exhibit a broad emission peak centered at 2.28 eV. The identity of this defect was determined to be either zinc vacancy or its associated complex according to the electron paramagnetic resonance measurements. Explicit simulations of the optical signatures of all zinc vacancy-related native defects were conducted here, showing that both zinc vacancy and divacancy are the most likely native defect contributors to that peak. [ABSTRACT FROM AUTHOR] |
