Item

Abstract

Shallow donors in semiconductors are known to form impurity bands that induce metallic conduction at sufficient doping densities. The perhaps most direct analogy to such doping in optically excited semiconductors is the photoexcitation of deep electronic defect or dopant levels creating defect excitons (DX) which may act like shallow donors. In this work, we use time- and angle-resolved photoelectron spectroscopy to observe and characterize DX at the surface of ZnO. The DX are created on a femtosecond timescale upon photoexcitation and have a spatial extend of few nanometers that is confined to the ZnO surface. The localized electronic levels lie at 150 meV below the Fermi energy, very similar to the shallow donor states induced by hydrogen doping [Deinert et al, Phys. Rev. B, 91, 235313 (2015)]. The transient dopants exhibit a multi-step decay ranging from hundred’s of picoseconds to 77 μs and even longer. By enhancing the DX density, a Mott transition occurs, enabling the ultrafast metallization of the ZnO surface, which we described previously [Gierster et al. Nat. Commun. 12, 978 (2021)]. Depending on the defect density, the duration of the photoinduced metallization ranges from picoseconds to μs and longer, corresponding to the decay dynamics of the DX. The metastable lifetime of the DX is consistent with the observation of persistent photoconductivity (PPC) in ZnO reported in literature [Madel et al., J. Appl. Phys. 121, 124301 (2017)]. In agreement with theory on PPC [Lany and Zunger, Phys. Rev. B 72, 035215 (2005)], the deep defects are attributed to oxygen vacancies due to their energetic position in the band gap and their formation by surface photolysis upon UV illumination. We show that the photoexcitation of these defects is analogous to chemical doping and enables the transient control of material properties such as the electrical conductivity from ultrafast to metastable timescales. The same mechanism should be at play in other semiconductor compounds with deep defects.