We report the experimental realization of coherent electron spin flip in a modulation-doped CdTe quantum well. Coherent spin rotation is realized with an off-resonant laser pulse, which induces a polarization-dependent optical Stark shift in the trion resonance. Complete electron spin flip is made possible by a laser pulse designed to avoid excessive excitations of nearby exciton resonances and minimizes detrimental many-body effects. These results demonstrate an effective approach for ultrafast optical spin control in a complex spin system.
Nuclear spins in certain solids couple weakly to their environment, making them attractive candidates for quantum information processing and inertial sensing. When coupled to the spin of an optically active electron, nuclear spins can be rapidly polarized, controlled, and read via lasers and radio-frequency (rf) fields. Possessing typical coherence times of several milliseconds at room temperature, nuclear spins hosted by a nitrogen-vacancy center in diamond are thus intriguing systems to observe how classical physical rotation at quantum timescales affects a quantum system. In this work, we demonstrate optical nuclear-spin polarization and rapid quantum control of nuclear spins in a diamond physically rotating at
1kHz, faster than the nuclear-spin coherence time. Free from the need to maintain strict field alignment, we are able to measure and control nuclear spins in the presence of a large, time-varying magnetic field that makes an angle of more than ${100}^{\ensuremath{\circ}}$ to the nitrogen-lattice vacancy axis. The field induces spin mixing between the electron and nuclear states of the qubits, decoupling them from oscillating rf fields. We are able to demonstrate that coherent spin state control is possible at any point of the rotation. We combine continuous dynamical decoupling with feed-forward control to eliminate decoherence induced by imperfect mechanical rotation. Our work liberates a previously inaccessible degree of freedom of the NV nuclear spin, unlocking new approaches to quantum control and rotation sensing.
Optically addressable shallow donors in ZnO combine efficient spin-selective optical transitions with the potential for long spin coherence in an isotopically purifiable host lattice, making them an attractive platform for spin-photon quantum technologies. A key missing capability, however, has been coherent control beyond the small-angle rotations accessible with ultrafast optical pulses. Here we demonstrate coherent microwave control of implanted
115In donors in ZnO. Resonant optical pumping initializes and reads out the donor electron spin. Pulsed optically-detected magnetic resonance resolves the ten hyperfine transitions associated with the coupled
115In nuclear spin (I = 9/2) and reveals optical-pumping-induced nuclear spin polarization. We observe coherent Rabi oscillations with a maximum Rabi frequency of
Ω/2π=36.2±0.7\;MHz, corresponding to a
π-pulse time of 13.8$\pm$0.3\;ns, and characterize the spin coherence using Ramsey, Hahn echo and dynamical-decoupling measurements. Unexpectedly, the measured coherence is substantially shorter than reported in previous optical studies of donor spins in ZnO at high magnetic field. Control experiments rule out several simple explanations including microwave heating and instantaneous diffusion from the driven donor ensemble, leaving an open question regarding the origin of decoherence at low magnetic field in microwave-controlled ZnO donors. These results establish microwave control of ZnO donor qubits with resonant optical access to specific donor species. More broadly, they demonstrate that coherent microwave control can be achieved in optically addressable spin systems with nanosecond-scale inhomogeneous dephasing, enabling field-, temperature-, and materials-dependent studies of coherence-limiting mechanisms and the development of optically interfaced electron-nuclear spin registers.
We investigate an all-optical, pump-probe scheme for the polarization rotation of linearly polarized light in an atomic medium. A circularly polarized control light is shown to play the role of a static magnetic field via a Zeeman-like ac Stark interaction and to induce the optical Faraday rotation (OFR) of the probe light. As a model system, we consider a stationary atom with $nS\text{\ensuremath{-}}nP\text{\ensuremath{-}}nD$ level scheme without electronic or nuclear spin. In addition to OFR, we find that electromagnetically induced transparency for the three-level atom and circular dichroism also contribute to the polarization change. We characterize these three effects over different frequency ranges through an explicit calculation of the fractional transmission and the output polarization of the probe light. Our results are compared with the $nS\text{\ensuremath{-}}nP\text{\ensuremath{-}}(n+1)S$ scheme, which has been previously studied both theoretically and experimentally. We also compare the optically induced Faraday effect with the Faraday effect from a static magnetic field. We propose an experimental situation to test the theory and address the possibility of producing an atomic medium that is both optically active and transparent.