RESUMO
The photoluminescence (PL), color purity, and stability of lead halide perovskite nanocrystals depend critically on surface passivation. We present a study on the temperature-dependent PL and PL decay dynamics of lead bromide perovskite nanocrystals characterized by different types of A cations, surface ligands, and nanocrystal sizes. Throughout, we observe a single emission peak from cryogenic to ambient temperature. The PL decay dynamics are dominated by surface passivation, and a postsynthesis ligand exchange with a quaternary ammonium bromide (QAB) results in more stable passivation over a larger temperature range. The PL intensity is highest from 50 to 250 K, which indicates that ligand binding competes with the thermal energy at ambient temperature. Despite the favorable PL dynamics of nanocrystals passivated with QAB ligands (monoexponential PL decay over a large temperature range, increased PL intensity and stability), surface passivation still needs to be improved to achieve maximum emission intensity in nanocrystal films.
RESUMO
The structure and strain of ultrathin CoO films grown on a Pt(0 0 1) substrate and on a ferromagnetic FePt pseudomorphic layer on Pt(0 0 1) have been determined with in situ and real time surface x-ray diffraction. The films grow epitaxially on both surfaces with an in-plane hexagonal pattern that yields a pseudo-cubic CoO(1 1 1) surface. A refined x-ray diffraction analysis reveals a slight monoclinic distortion at RT induced by the anisotropic stress at the interface. The tetragonal contribution to the distortion results in a ratio [Formula: see text], opposite to that found in the low temperature bulk CoO phase. This distortion leads to a stable Co(2+) spin configuration within the plane of the film.