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Register a new userOrientational tuning of the 2D-superconductivity in LaAlO3/SrTiO3 interfaces
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The discovery of a two-dimensional (2D) electron gas at the (110)-oriented LaAlO3/SrTiO3 in- terface provided us with the opportunity to probe the effect of crystallographic orientation and the ensuing electronic reconstructions on interface properties beyond the conventional (001)-orientation. At temperatures below 200 mK, we have measured 2D superconductivity with a spatial extension significantly larger (d approx. 24 - 30 nm) than previously reported for (001)-oriented LaAlO3/SrTiO3 interfaces (d approx. 10 nm). The more extended superconductivity brings about the absence of violation of the Pauli paramagnetic limit for the upper critical fields, signaling the distinctive nature of the electronic structure of the (110)-oriented interface with respect to their (001)-counterparts
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We formulate a model for magnetic and superconducting ordering at LaAlO3/SrTiO3 interfaces containing both localized magnetic moments and itinerant electrons. Though these both originate in Ti 3d orbitals, the former may be due to electrons more tightly-bound to the interface while the latter are extended over several layers. Only the latter contribute significantly to metallic conduction and superconductivity. In our model, the interplay between the two types of electrons, which is argued to be ferromagnetic, combined with strong spin-orbit coupling of the itinerant electrons, leads to magnetic ordering. Furthermore, we propose a model for interfacial superconductivity, consisting of random superconducting grains in the bulk STO driven, via coupling to the interface conduction band, towards long-ranged or quasi-long-ranged order. Most interestingly, the magnetic order and strong spin orbit coupling can lead in this manner to unconventional interfacial superconductivity, yielding a possible realization of Majorana physics.
A large variety of transport properties have been observed at the interface between the insulating oxides SrTiO3 and LaAlO3 such as insulation, 2D interface metallicity, 3D bulk metallicity, Kondo scattering, magnetism and superconductivity. The relation between the structure and the properties of the SrTiO3-LaAlO3 interface can be explained in a meaningful way by taking into account the relative contribution of three structural aspects: oxygen vacancies, structural deformations (including cation disorder) and electronic interface reconstruction. The emerging phase diagram is much richer than for related bulk oxides due to the occurrence of interface electronic reconstruction. The observation of this interface phenomenon is a display of recent advances in thin film deposition and characterization techniques, and provides an extension to the range of exceptional electronic properties of complex oxides.
The two-dimensional electron system formed at the interface between the insulating oxides LaAlO3 and SrTiO3 exhibits ferromagnetism, superconductivity, and a wide range of unique magnetotransport properties. A key challenge is to find a unified microscopic mechanism that underlies these emergent phenomena. Here we show that a universal Lifshitz transition between d-orbitals lies at the core of the observed transport phenomena in this system. Our measurements find a critical electronic density at which the transport switches from single to multiple carriers. This density has a universal value, independent of the LaAlO3 thickness and electron mobility. The characteristics of the transition, its universality, and its compatibility with spectroscopic measurements establish it as a transition between d-orbitals of different symmetries. A simple band model, allowing for spin-orbit coupling at the atomic level, connects the observed universal transition to a range of reported magnetotransport properties. Interestingly, we also find that the maximum of the superconducting transition temperature occurs at the same critical transition, indicating a possible connection between the two phenomena. Our observations demonstrate that orbital degeneracies play an important role in the fascinating behavior observed so far in these oxides.
To form a conducting layer at the interface between the oxide insulators LaAlO3 and SrTiO3, the LaAlO3 layer on the SrTiO3 substrate must be at least four unit-cells-thick. The LaAlO3 SrTiO3 heterointerface thus formed exhibits various intriguing phenomena such as ferromagnetism and superconductivity. It has been widely studied for being a low-dimensional ferromagnetic oxide superconducting system with a strong gate-tunable spin-orbit interaction. However, its lack of stability and environmental susceptiveness have been an obstacle to its further experimental investigations and applications. Here, we demonstrate that capping the bilayer with SrTiO3 relieves this thickness limit, while enhancing the stability and controllability of the interface. In addition, the SrTiO3-capped LaAlO3 exhibits unconventional superconductivity; the critical current dramatically increases under a parallel magnetic field, and shows a reversed hysteresis contrary to the conventional hysteresis of magnetoresistance. Its superconducting energy gap of $Delta sim 1.31k_BT_c$ also deviates from conventional BCS-type superconductivity. The oxide trilayer could be a robust platform for studying the extraordinary interplay of superconductivity and ferromagnetism at the interface electron system between LaAlO3 and SrTiO3.
The relative significance of quantum conductivity correction and magnetic nature of electrons in understanding the intriguing low-temperature resistivity minimum and negative magnetoresistance of the two-dimensional electron gas at LaAlO3/SrTiO3 interfaces has been a long outstanding issue since its discovery. Here we report a comparative magnetotransport study on amorphous and oxygen-annealed crystalline LaAlO3/SrTiO3 heterostructures at a relatively high-temperature range, where the orbital scattering is largely suppressed by thermal fluctuations. Despite of a predominantly negative out-of-plane magnetoresistance effect for both, the magnetotransport is isotropic for amorphous LaAlO3/SrTiO3 while strongly anisotropic and well falls into a two-dimensional quantum correction frame for annealed crystalline LaAlO3/SrTiO3. These results clearly indicate that a large portion of electrons from oxygen vacancies are localized at low temperatures, serving as magnetic centers, while the electrons from the polar field are only weakly localized due to constructive interference between time-reversed electron paths in the clean limit and no signature of magnetic nature is visible.
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