With infrared (IR) ellipsometry and DC resistance measurements we investigated the photo-doping at the (001) and (110) surfaces of SrTiO 3 (STO) single crystals and at the corresponding interfaces of LaAlO 3 /SrTiO 3 (LAO/STO) heterostructures. In the bare STO crystals we find that the photo-generated charge carriers, which accumulate near the (001) surface, have a similar depth profile and sheet carrier concentration as the confined electrons that were previously observed in LAO/STO (001) heterostructures. A large fraction of these photo-generated charge carriers persist at low temperature at the STO (001) surface even after the UV light has been switched off again. These persistent charge carriers seem to originate from oxygen vacancies that are trapped at the structural domain boundaries which develop below the so-called antiferrodistortive transition at T* = 105 K. This is most evident from a corresponding photo-doping study of the DC transport in STO (110) crystals for which the concentration of these domain boundaries can be modified by applying a weak uniaxial stress. The oxygen vacancies and their trapping by defects are also the source of the electrons that are confined to the interface of LAO/STO (110) heterostructures which likely do not have a polar discontinuity as in LAO/STO (001). In the former, the trapping and clustering of the oxygen vacancies also has a strong influence on the anisotropy of the charge carrier mobility. We show that this anisotropy can be readily varied and even inverted by various means, such as a gentle thermal treatment, UV irradiation, or even a weak uniaxial stress. Our experiments suggest that extended defects, which develop over long time periods (of weeks to months), can strongly influence the response of the confined charge carriers at the LAO/STO (110) interface.
I) INTRODUCTIONThe discovery of a nearly two-dimensional electron gas (2DEG) with a high mobility at the interface of LAO/STO heterostructures [1], and the demonstration of subsequent electric-field-effect devices [2,3] have renewed the interest in the extraordinary structural and electronic properties of STO. At room temperature, it seems to be a rather ordinary material with a simple perovskite structure with cubic symmetry [4]. It is also a band-insulator with an indirect band-gap of 3.25 eV and a direct one of 3.75 eV [5]. Thanks to the flexible valence of the Ti ions, which can be varied continuously between 4+ and 3+, one can readily dope the conduction band of STO (it has mainly Ti-3d t 2g character) with electrons to make it metallic and even superconducting at very low temperature, for example by a partial replacement of Sr 2+ with La 3+ , Ti 4+ with Nb 5+ or by creating oxygen vacancies [6][7][8][9].STO undergoes several structural phase transitions as the temperature is lowered. The first one is the so-called antiferrodistortive (AFD) transition at T* = 105 K from the cubic to a tetragonal symmetry. It involves an antiphase rotation of the neighboring TiO 6 octahedra around the c-axis and leads to ...