Search

Author(s): David A. Muller (corresponding author) [1, 2]; Naoyuki Nakagawa [1, 3]; Akira Ohtomo [1, 4]; John L. Grazul [1, 2]; Harold Y. Hwang [1, 3, 5] At the heart [...]

Highly transparent Cu2O thin films on transparent conducting oxide on a glass substrate were fabricated using reactive sputtering by carefully controlling the O2 flow. The impurity dependence of transmittance was thoroughly investigated, and the transmittance was found heavily depending on impurities in Cu2O thin films as confirmed by x-ray diffraction analysis. A highly transparent Cu2O thin film was fabricated using precisely impurity-controlled Cu2O thin films. The effects of impurities in a Cu2O thin film on photovoltaic properties were studied. A maximum efficiency of 8.4% was observed in the lowest-impurity Cu2O thin film. [ABSTRACT FROM AUTHOR]

A central goal of modern materials physics and nanoscience is the control of materials and their interfaces to atomic dimensions. For interfaces between polar and nonpolar layers, this goal is thwarted by a polar catastrophe that forces an interfacial reconstruction. In traditional semiconductors, this reconstruction is achieved by an atomic disordering and stoichiometry change at the interface, but a new option is available in multivalent oxides: if the electrons can move, the atoms do not have to. Using atomic-scale electron energy loss spectroscopy, we have examined the microscopic distribution of charge and ions across the (001) LaAlO3/SrTiO3 interface. We find that there is a fundamental asymmetry between the ionically compensated AlO2/SrO/TiO2 interface, and the electronically compensated AlO2/LaO/TiO2 interface, both in interfacial sharpness and charge density. This suggests a general strategy to design sharp interfaces, remove interfacial screening charges, control the band offset and, hence, markedly improve the performance of oxide devices. [ABSTRACT FROM AUTHOR]

At the heart of modern oxide chemistry lies the recognition that beneficial (as well as deleterious) materials properties can be obtained by deliberate deviations of oxygen atom occupancy from the ideal stoichiometry. Conversely, the capability to control and confine oxygen vacancies will be important to realize the full potential of perovskite ferroelectric materials, varistors and field-effect devices. In transition metal oxides, oxygen vacancies are generally electron donors, and in strontium titanate (SrTiO3) thin films, oxygen vacancies (unlike impurity dopants) are particularly important because they tend to retain high carrier mobilities, even at high carrier densities. Here we report the successful fabrication, using a pulsed laser deposition technique, of SrTiO3 superlattice films with oxygen doping profiles that exhibit subnanometre abruptness. We profile the vacancy concentrations on an atomic scale using annular-dark-field electron microscopy and core-level spectroscopy, and demonstrate absolute detection sensitivities of one to four oxygen vacancies. Our findings open a pathway to the microscopic study of individual vacancies and their clustering, not only in oxides, but in crystalline materials more generally. [ABSTRACT FROM AUTHOR]

At the heart of modern oxide chemistry lies the recognition that beneficial (as well as deleterious) materials properties can be obtained by deliberate deviations of oxygen atom occupancy from the ideal stoichiometry. Conversely, the capability to control and confine oxygen vacancies will be important to realize the full potential of perovskite ferroelectric materials, varistors and field-effect devices. In transition metal oxides, oxygen vacancies are generally electron donors, and in strontium titanate (SrTiO3) thin films, oxygen vacancies (unlike impurity dopants) are particularly important because they tend to retain high carrier mobilities, even at high carrier densities. Here we report the successful fabrication, using a pulsed laser deposition technique, of SrTiO3 superlattice films with oxygen doping profiles that exhibit subnanometre abruptness. We profile the vacancy concentrations on an atomic scale using annular-dark-field electron microscopy and core-level spectroscopy, and demonstrate absolute detection sensitivities of one to four oxygen vacancies. Our findings open a pathway to the microscopic study of individual vacancies and their clustering, not only in oxides, but in crystalline materials more generally. [ABSTRACT FROM AUTHOR]