Shahal Ilani

A universal critical density underlying the physics of electrons at the LaAlO3/SrTiO3 interface

The two-dimensional electron system at the interface between the insulating oxides LaAlO(3) and SrTiO(3) exhibits ferromagnetism, superconductivity and a range of unique magnetotransport properties. An open experimental challenge is to identify, out of the multitudinous energy bands predicted to exist at the interface, the key ingredients underlying its emergent transport phenomena. Here we show, using magnetotransport measurements, that a universal Lifshitz transition between d orbitals of different symmetries lies at the core of the observed phenomena. We find that LaAlO(3)/SrTiO(3) systems generically switch from one- to two-carrier transport at a universal carrier density, which is independent of the LaAlO(3) thickness and electron mobility. Interestingly, the maximum superconducting critical temperature occurs also at the Lifshitz density, indicating a possible connection between the two phenomena. A simple band model, allowing for spin-orbit coupling at the atomic level, connects the observed transition to a variety of previously reported properties. Our results demonstrate that the fascinating behaviour observed so far in these oxides follows from a small but fundamental set of bands.

Ab initio study of the alternating current impedance of a molecular junction

The small-bias conductance of the C6 molecule, stretched between two metallic leads, is studied using time-dependent density functional theory within the adiabatic local density approximation. The leads are modeled by jellium slabs, the electronic density and the current density are described on a grid, whereas the core electrons and the highly oscillating valence orbitals are approximated using standard norm-conserving pseudopotentials. The jellium leads are supplemented by a complex absorbing potential that serves to absorb charge reaching the edge of the electrodes and hence mimic irreversible flow into the macroscopic metal. The system is rapidly exposed to a ramp potential directed along the C6 axis, which gives rise to the onset of charge and current oscillations. As time progresses, a fast redistribution of the molecular charge is observed, which translates into a direct current response. Accompanying the dc signal, alternating current fluctuations of charge and currents within the molecule and the metallic leads are observed. These form the complex impedance of the molecule and are especially strong at the plasmon frequency of the leads and the lowest excitation peak of C6. We study the molecular conductance in two limits: the strong coupling limit, where the edge atoms of the chain are submerged in the jellium and the weak coupling case, where the carbon atoms and the leads do not overlap spatially.

Local electrostatic imaging of striped domain order in LaAlO3/SrTiO3

The emerging field of complex oxide interfaces is generically built on one of the most celebrated substrates--strontium titanate (SrTiO3). This material hosts a range of phenomena, including ferroelasticity, incipient ferroelectricity, and most puzzlingly, contested giant piezoelectricity. Although these properties may markedly influence the oxide interfaces, especially on microscopic length scales, the lack of local probes capable of studying such buried systems has left their effects largely unexplored. Here we use a scanning charge detector--a nanotube single-electron transistor--to non-invasively image the electrostatic landscape and local mechanical response in the prototypical LaAlO3/SrTiO3 system with unprecedented sensitivity. Our measurements reveal that on microscopic scales SrTiO3 exhibits large anomalous piezoelectricity with curious spatial dependence. Through electrostatic imaging we unravel the microscopic origin for this extrinsic piezoelectricity, demonstrating its direct, quantitative connection to the motion of locally ordered tetragonal domains under applied gate voltage. These domains create striped potential modulations that can markedly influence the two-dimensional electron system at the conducting interface. Our results have broad implications to all complex oxide interfaces built on SrTiO3 and demonstrate the importance of microscopic structure to the physics of electrons at the LaAlO3/SrTiO3 interface.

Nanoscale Phenomena in Oxide Heterostructures

Recent advances in creating complex oxide heterostructures, interfaces formed between two different transition-metal oxides, have heralded a new era of materials and physics research, enabling a uniquely diverse set of coexisting physical properties to be combined with an ever-increasing degree of experimental control. These systems have exhibited varied phenomena such as superconductivity, magnetism, and ferroelasticity, all of which are gate tunable, demonstrating their promise for fundamental discovery and technological innovation. To fully exploit this richness, it is necessary to understand and control the physics on the smallest scales, making the use of nanoscale probes essential. Using the prototypical LaAlO3/SrTiO3 interface as a guide, we explore the exciting developments in the physics of oxide-based heterostructures, with a focus on nanostructures and the nanoscale probes employed to unravel their complex behavior.

Unexpected behavior of the local compressibility near the B = 0 metal-insulator transition

We have measured the local electronic compressibility of a two-dimensional hole gas as it crosses the B = 0 metal-insulator transition. In the metallic phase, the compressibility follows the mean-field Hartree-Fock (HF) theory and is found to be spatially homogeneous. In the insulating phase it deviates by more than an order of magnitude from the HF predictions and is spatially inhomogeneous. The crossover density between the two types of behavior agrees quantitatively with the transport critical density, suggesting that the system undergoes a thermodynamic change at the transition.

Gate-tunable polarized phase of two-dimensional electrons at the LaAlO3/SrTiO3 interface

Controlling the coupling between localized spins and itinerant electrons can lead to exotic magnetic states. A novel system featuring local magnetic moments and extended 2D electrons is the interface between LaAlO3 and SrTiO3. The magnetism of the interface, however, was observed to be insensitive to the presence of these electrons and is believed to arise solely from extrinsic sources like oxygen vacancies and strain. Here we show the existence of unconventional electronic phases in the LaAlO3/SrTiO3 system pointing to an underlying tunable coupling between itinerant electrons and localized moments. Using anisotropic magnetoresistance and anomalous Hall effect measurements in a unique in-plane configuration, we identify two distinct phases in the space of carrier density and magnetic field. At high densities and fields, the electronic system is strongly polarized and shows a response, which is highly anisotropic along the crystalline directions. Surprisingly, below a density-dependent critical field, the polarization and anisotropy vanish whereas the resistivity sharply rises. The unprecedented vanishing of the easy axes below a critical field is in sharp contrast with other coupled magnetic systems and indicates strong coupling with the moments that depends on the symmetry of the itinerant electrons. The observed interplay between the two phases indicates the nature of magnetism at the LaAlO3/SrTiO3 interface as both having an intrinsic origin and being tunable.

Real-space tailoring of the electron–phonon coupling in ultraclean nanotube mechanical resonators

A mechanism for coupling the electrons and vibrational motion of a suspended carbon nanotube is now demonstrated. Tailoring the coupling between specific electronic and phononic modes by controlling the position of quantum dots along the resonating tube enables spatial imaging of the mode shape.

Realization of pristine and locally tunable one-dimensional electron systems in carbon nanotubes

The ability to tune local parameters of quantum Hamiltonians has been demonstrated in experimental systems including ultracold atoms, trapped ions, superconducting circuits and photonic crystals. Such systems possess negligible disorder, enabling local tunability. Conversely, in condensed-matter systems, electrons are subject to disorder, which often destroys delicate correlated phases and precludes local tunability. The realization of a disorder-free and locally-tunable condensed-matter system thus remains an outstanding challenge. Here, we demonstrate a new technique for deterministic creation of locally-tunable, ultralow-disorder electron systems in carbon nanotubes suspended over complex electronic circuits. Using transport experiments we show that electrons can be localized at any position along the nanotube and that the confinement potential can be smoothly moved from location to location. The high mirror symmetry of transport characteristics about the nanotube centre establishes the negligible effects of electronic disorder, thus allowing experiments in precision-engineered one-dimensional potentials. We further demonstrate the ability to position multiple nanotubes at chosen separations, generalizing these devices to coupled one-dimensional systems. These capabilities could enable many novel experiments on electronics, mechanics and spins in one dimension.

Electron attraction mediated by Coulomb repulsion

One of the defining properties of electrons is their mutual Coulomb repulsion. However, in solids this basic property may change; for example, in superconductors, the coupling of electrons to lattice vibrations makes the electrons attract one another, leading to the formation of bound pairs. Fifty years ago it was proposed that electrons can be made attractive even when all of the degrees of freedom in the solid are electronic, by exploiting their repulsion from other electrons. This attraction mechanism, termed ‘excitonic’, promised to achieve stronger and more exotic superconductivity. Yet, despite an extensive search, experimental evidence for excitonic attraction has yet to be found. Here we demonstrate this attraction by constructing, from the bottom up, the fundamental building block of the excitonic mechanism. Our experiments are based on quantum devices made from pristine carbon nanotubes, combined with cryogenic precision manipulation. Using this platform, we demonstrate that two electrons can be made to attract each other using an independent electronic system as the ‘glue’ that mediates attraction. Owing to its tunability, our system offers insights into the underlying physics, such as the dependence of the emergent attraction on the underlying repulsion, and the origin of the pairing energy. We also demonstrate transport signatures of excitonic pairing. This experimental demonstration of excitonic pairing paves the way for the design of exotic states of matter.

Competition between Kondo screening and Magnetism in the LaAlO3/SrTiO3 Interface

We present a theory of magnetic and magnetotransport phenomena at