Optical Manipulation of Rashba Spin-Orbit Coupling at SrTiO3-Based Oxide Interfaces.

Spin-orbit coupling (SOC) plays a crucial role for spintronics applications. Here we present the first demonstration that the Rashba SOC at the SrTiO3-based interfaces is highly tunable by photoinduced charge doping, that is, optical gating. Such optical manipulation is nonvolatile after the removal of the illumination in contrast to conventional electrostatic gating and also erasable via a warming-cooling cycle. Moreover, the SOC evolutions tuned by illuminations with different wavelengths at various gate voltages coincide with each other in different doping regions and collectively form an upward-downward trend curve: In response to the increase of conductivity, the SOC strength first increases and then decreases, which can be attributed to the orbital hybridization of Ti 3d subbands. More strikingly, the optical manipulation is effective enough to tune the interferences of Bloch wave functions from constructive to destructive and therefore to realize a transition from weak localization to weak antilocalization. The present findings pave a way toward the exploration of photoinduced nontrivial quantum states and the design of optically controlled spintronic devices.

Giant photovoltaic effects driven by residual polar field within unit-cell-scale LaAlO3 films on SrTiO3.

For polar/nonpolar heterostructures, Maxwell's theory dictates that the electric potential in the polar components will increase divergently with the film thickness. For LaAlO3/SrTiO3, a conceptually intriguing route, termed charge reconstruction, has been proposed to avert such "polar catastrophe". The existence of a polar potential in LaAlO3 is a prerequisite for the validity of the charge reconstruction picture, yet to date, its direct measurement remains a major challenge. Here we establish unambiguously the existence of the residual polar potential in ultrathin LaAlO3 films on SrTiO3, using a novel photovoltaic device design as an effective probe. The measured lower bound of the residual polar potential is 1.0 V. Such a direct observation of the giant residual polar potential within the unit-cell-scale LaAlO3 films amounts to a definitive experimental evidence for the charge reconstruction picture, and also points to new technological significance of oxide heterostructures in photovoltaic and sensing devices with atomic-scale control.