AVS 61st International Symposium & Exhibition | |
Thin Film | Thursday Sessions |
Session TF-ThP |
Session: | Thin Films Poster Session |
Presenter: | Judith Reynolds, North Carolina State University |
Authors: | J. Reynolds, North Carolina State University J.E. Rowe, North Carolina State University L. Reynolds, North Carolina State University D.E. Aspnes, North Carolina State University |
Correspondent: | Click to Email |
We report the MOCVD growth of doped thin 2-D MgZnO films on c-plane sapphire substrates for solar-blind detector applications. Spectroscopic ellipsometry (SE), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) are used to determine the composition. The carrier gas is N2. For pure ZnO, the precursors are diethylzinc (DEZ) and nitrous oxide (N2O). When growing p-type material, 3% nitric oxide (NO) in N2 provides N ions in the +2 oxidation state needed for doping, and growth occurs as a two-step process monitored in real time by the SE. In the first step, we use a low Zn partial pressure to induce VZn formation. Because VZn energies are low for Fermi levels from mid-gap to the conduction band edge, and because the absorption energy for NZn is 0.08 eV for the hexagonal close packed site of the Zn-polar surface, this allows the N to incorporate at Zn sites as NZn. In the second step, we use a high Zn partial pressure to drive the formation of oxygen vacancies (VO). Growth is then followed by an appropriate annealing sequence. While substitutional N on the O sublattice is a deep acceptor, we find that acceptor complexes involving N, H and VZn can provide p-type ZnO films with a hole concentration of ~1018 cm-3 at room temperature. For MgZnO growth, we use bis-cyclopentadienyl magnesium (BcMg) in addition to DEZ, N2O, and NO. Although we deposit MgZnO, films of a quality that we consider acceptable have not yet been produced owing to the large parameter space of temperature, precursor flows, and gas pressure.