Whilst quantum computing has recently taken great leaps ahead, the development of quantum memories has decidedly lagged behind. Quantum memories are essential devices in the quantum technology palette and are needed for intermediate storage of quantum bit states and as quantum repeaters in long-distance quantum communication. Current quantum memories operate at cryogenic, mostly sub-Kelvin temperatures and require extensive and costly peripheral hardware. It is demonstrated that ensembles of weakly coupled molecular spins show long coherence times and can be used to store microwave pulses of arbitrary phase. These studies exploit strong coupling of the spin ensemble to special 3D microwave resonators. Most importantly, these systems operate at room temperature.
Abstract The strong coupling regime is essential for efficient transfer of excitations between states in different quantum systems on timescales shorter than their lifetimes. The coupling of single spins to microwave photons is very weak but can be enhanced by increasing the local density of states by reducing the magnetic mode volume of the cavity. In practice, it is difficult to achieve both small cavity mode volume and low cavity decay rate, so superconducting metals are often employed at cryogenic temperatures. For an ensembles of N spins, the spin–photon coupling can be enhanced by N N through collective spin excitations known as Dicke states. For sufficiently large N the collective spin–photon coupling can exceed both the spin decoherence and cavity decay rates, making the strong-coupling regime accessible. Here we demonstrate strong coupling and cavity quantum electrodynamics in a solid-state system at room-temperature. We generate an inverted spin-ensemble with N ~ 1015 by photo-exciting pentacene molecules into spin-triplet states with spin dephasing time T2∗∼3 T 2 * ~ 3 μs. When coupled to a 1.45 GHz TE01δ mode supported by a high Purcell factor strontium titanate dielectric cavity ( Vm∼0.25 V m ~ 0.25 cm3, Q ~ 8,500), we observe Rabi oscillations in the microwave emission from collective Dicke states and a 1.8 MHz normal-mode splitting of the resultant collective spin–photon polariton. We also observe a cavity protection effect at the onset of the strong-coupling regime which decreases the polariton decay rate as the collective coupling increases.
We propose a method to create a room-temperature maser operating at approximately 2.9~GHz frequency using an ensemble of negatively charged nitrogen-vacancy electronic spins (NV) in diamond, without requiring population inversion. Our method considers a DC magnetic field of a few milli-Tesla (mT) applied along the perpendicular direction of an ensemble of NV spins aligned along a common axis. This perpendicular magnetic-field creates superposition states of ∣ms=−1⟩ and ∣ms=+1⟩ of the NV spin's ground state triplet levels and thereby makes it possible to drive all three transitions in the NV spin ground state. We model the system by including optical pumping of the NV spins, near-resonant driving of two transitions, and coupling the third transition to a near-resonant microwave resonator. Numerical estimates using experimentally realizable parameters show that inversionless masing can be achieved inside the microwave resonator using our method. As an application, we show that the output intensity of an inversionless maser (1.1×1014 spins) can be used for magnetic field sensing with a DC sensitivity on the order of a hundred pT/Hz. Our study opens a new direction in room-temperature diamond NV maser devices for quantum technological applications without the requirement of a strong bias magnetic field, as in conventional NV diamond masers.