Search

Quantum control of solid-state spin qubits typically involves pulses in the microwave domain, drawing from the well-developed toolbox of magnetic resonance spectroscopy. Driving a solid-state spin by optical means offers a high-speed alternative, which in the presence of limited spin coherence makes it the preferred approach for high-fidelity quantum control. Bringing the full versatility of magnetic spin resonance to the optical domain requires full phase and amplitude control of the optical fields. Here, we imprint a programmable microwave sequence onto a laser field and perform electron spin resonance in a semiconductor quantum dot via a two-photon Raman process. We show that this approach yields full SU(2) spin control with over 98% pi-rotation fidelity. We then demonstrate its versatility by implementing a particular multi-axis control sequence, known as spin locking. Combined with electron-nuclear Hartmann-Hahn resonances which we also report in this work, this sequence will enable efficient coherent transfer of a quantum state from the electron spin to the mesoscopic nuclear ensemble., Comment: 11 pages, 10 figures

A heavy hole confined to an InGaAs quantum dot promises the union of a stable spin and optical coherence to form a near perfect, high-bandwidth spin-photon interface. Despite theoretical predictions and encouraging preliminary measurements, the dynamic processes determining the coherence of the hole spin are yet to be understood. Here, we establish the regimes that allow for a highly coherent hole spin in these systems, recovering a crossover from hyperfine to electrical-noise dominated decoherence with a few-Tesla external magnetic field. Dynamical decoupling allows us to reach the longest ground-state coherence time, T2, of 4.4 $\mu$s, observed in this system. The improvement of coherence we measure is quantitatively supported by an independent analysis of the local electrical environment., Comment: Supplemental material available upon request

A controlled quantum system can alter its environment by feedback, leading to reduced-entropy states of the environment and to improved system coherence. Here, using a quantum dot electron spin as control and probe, we prepare the quantum dot nuclei under the feedback of coherent population trapping and measure the evolution from a thermal to a reduced-entropy state, with the immediate consequence of extended qubit coherence. Via Ramsey interferometry on the electron spin, we directly access the nuclear distribution following its preparation, and measure the emergence and decay of correlations within the nuclear ensemble. Under optimal feedback, the inhomogeneous dephasing time of the electron, $T_2^*$, is extended by an order of magnitude to $39$~ns. Our results can be readily exploited in quantum information protocols utilizing spin-photon entanglement, and represent a step towards creating quantum many-body states in a mesoscopic nuclear spin ensemble., Comment: 6 pages, 3 figures

Quantum entanglement between distant qubits is an important feature of quantum networks. Distribution of entanglement over long distances can be enabled through coherently interfacing qubit pairs via photonic channels. Here, we report the realization of optically generated quantum entanglement between electron spin qubits confined in two distant semiconductor quantum dots. The protocol relies on spin-photon entanglement in the trionic $\Lambda$-system and quantum erasure of the Raman-photon path. The measurement of a single Raman photon is used to project the spin qubits into a joint quantum state with an interferometrically stabilized and tunable relative phase. We report an average Bell-state fidelity for $|\psi^{(+)}\rangle$ and $|\psi^{(-)}\rangle$ states of $61.6\pm2.3\%$ and a record-high entanglement generation rate of 7.3 kHz between distant qubits.

The Zeeman-split spin-states of a single electron confined in a self-assembled quantum dot provide an optically-accessible spin qubit. For III-V materials the nuclear spins of the solid-state host provide an intrinsic noise source, resulting in electron-spin dephasing times of few nanoseconds. While a comprehensive study of electron-spin dynamics at low magnetic field has recently been carried out, what limits the electron coherence in these systems remains unclear, in part due to the dominant effect of measurement-induced dynamic polarisation of the nuclear bath. We develop an all-optical method to access the quantum dot spin-state without perturbing the nuclear environment. We use this method to implement Hahn-echo decoupling and reach the intrinsic limit to coherence set by inhomogeneous strain fields coupling to quadrupolar moments of the nuclear bath. These results indicate that the extension of electron spin coherence beyond this few-microsecond limit necessitates the reduction of strain-induced quadrupolar broadening in these materials., Comment: Supplementary material can be found in the publications section of our website: http://www.amop.phy.cam.ac.uk/amop-ma

Coupling individual quantum systems lies at the heart of building scalable quantum networks. Here, we report the first direct photonic coupling between a semiconductor quantum dot and a trapped ion and we demonstrate that single photons generated by a quantum dot controllably change the internal state of an $\textrm{Yb}^+$ ion. We ameliorate the effect of the sixty-fold mismatch of the radiative linewidths with coherent photon generation and a high-finesse fiber-based optical cavity enhancing the coupling between the single photon and the ion. The transfer of information presented here via the classical correlations between the $\sigma_z$-projection of the quantum-dot spin and the internal state of the ion provides a promising step towards quantum state-transfer in a hybrid photonic network.

We report on the dynamics of optically induced nuclear spin polarization in individual CdTe/ZnTe quantum dots loaded with one electron by modulation doping. The fine structure of the hot trion (charged exciton $X^-$ with an electron in the $P$-shell) is identified in photoluminescence excitation spectra. A negative polarisation rate of the photoluminescence, optical pumping of the resident electron and the built-up of dynamic nuclear spin polarisation (DNSP) are observed in time-resolved optical pumping experiments when the quantum dot is excited at higher energy than the hot trion triplet state. The time and magnetic field dependence of the polarisation rate of the $X^-$ emission allows to probe the dynamics of formation of the DNSP in the optical pumping regime. We demonstrate using time-resolved measurements that the creation of a DNSP at B=0T efficiently prevents longitudinal spin relaxation of the electron caused by fluctuations of the nuclear spin bath. The DNSP is built in the microsecond range at high excitation intensity. A relaxation time of the DNSP in about 10 microseconds is observed at $B=0T$ and significantly increases under a magnetic field of a few milli-Tesla. We discuss mechanisms responsible for the fast initialisation and relaxation of the diluted nuclear spins in this system.

We report on the observation of spin dependent optically dressed states and optical Stark effect on an individual Mn spin in a semiconductor quantum dot. The vacuum-to-exciton or the exciton-to-biexciton transitions in a Mn-doped quantum dot are optically dressed by a strong laser field and the resulting spectral signature is measured in photoluminescence. We demonstrate that the energy of any spin state of a Mn atom can be independently tuned using the optical Stark effect induced by a control laser. High resolution spectroscopy reveals a power, polarization and detuning dependent Autler-Townes splitting of each optical transition of the Mn-doped quantum dot. This experiment demonstrates a complete optical resonant control of the exciton-Mn system.

We have investigated the spin preparation efficiency by optical pumping of individual Mn atoms embedded in CdTe/ZnTe quantum dots. Monitoring the time dependence of the intensity of the fluorescence during the resonant optical pumping process in individual quantum dots allows to directly probe the dynamics of the initialization of the Mn spin. This technique presents the convenience of including preparation and read-out of the Mn spin in the same step. Our measurements demonstrate that Mn spin initialization, at zero magnetic field, can reach an efficiency of 75% and occurs in the tens of \emph{ns} range when a laser resonantly drives at saturation one of the quantum dot transition. We observe that the efficiency of optical pumping changes from dot to dot and is affected by a magnetic field of a few tens of mT applied in Voigt or Faraday configuration. This is attributed to the local strain distribution at the Mn location which predominantly determines the dynamics of the Mn spin under weak magnetic field. The spectral distribution of the spin-flip scattered photons from quantum dots presenting a weak optical pumping efficiency reveals a significant spin relaxation for the exciton split in the exchange field of the Mn spin., Comment: 10 pages, 8 figures

A hight degree of spin polarization is achieved for a Mn atom localized in a semiconductor quantum dot using quasi-resonant optical excitation at zero magnetic field. Optically created spin polarized carriers generate an energy splitting of the Mn spin and enable magnetic moment orientation controlled by the photon helicity and energy. The dynamics and the magnetic field dependence of the optical pumping mechanism shows that the spin lifetime of an isolated Mn atom at zero magnetic field is controlled by a magnetic anisotropy induced by the built-in strain in the quantum dots.