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Marcos Rubín-Osanz

Publications and source records attributed to Marcos Rubín-Osanz.

5 recordsLinked to original sources

Polariton-polariton coherent coupling in a molecular spin-superconductor chip

The ability to establish coherent communication channels is key for scaling up quantum devices. Here, we engineer interactions between distant polaritons, hybrid spin-photon excitations formed at different lumped-element superconducting resonators within a chip. The chip consists of several resonator pairs, slightly detuned in frequency to make them addressable, capacitively coupled within each pair and inductively coupled to a common readout line. They interact locally with samples of PTMr and Tripak$^{-}$ organic free radicals, deposited onto their inductors, which provide model $S = 1/2$, $g \simeq 2$ spin ensembles. Frequency-dependent microwave transmission experiments, performed at very low temperatures, measure polariton frequencies as a function of magnetic field in different scenarios. When only one resonator within a pair hosts a molecular sample, the results evidence that spins couple remotely to the empty LER as well as to the local cavity mode. If both resonators interact with a spin ensemble, the magnetic field tunes the polariton frequencies relative to each other, on account of the different spin-photon interactions at each LER. When polaritons are brought into mutual resonance, an avoided level crossing emerges that gives direct spectroscopic evidence for a coherent polariton-polariton interaction mediated by the circuit. Pump-probe experiments reveal that the excitation of a polariton within a connected pair is felt, thus it can be read out, by the other one. These observations, backed by model calculations, illustrate the control and detection of distant photon-photon and spin-spin correlations and entanglement in a scalable modular chip.

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Optimizing magnetic coupling in lumped element superconducting resonators for molecular spin qubits

We engineer lumped-element superconducting resonators that maximize magnetic coupling to molecular spin qubits, achieving record single-spin couplings up to $100$ kHz and collective couplings exceeding $10$ MHz. The resonators interact with PTMr organic free radicals, model spin systems with $S=1/2$ and a quasi-isotropic $g \simeq 2$, dispersed in polymer matrices. The highest collective spin-photon coupling strengths are attained with resonators having large inductors, which therefore interact with most spins in the molecular ensemble. By contrast, the coupling of each individual spin $G_{1}$ is maximized in resonators having a minimum size inductor, made of a single wire. The same platform has been used to study spin relaxation and spin coherent dynamics in the dispersive regime, when spins are energetically detuned from the resonator. We find evidences for the Purcell effect, i.e. the photon induced relaxation of those spins that are most strongly coupled to the circuit. The rate of this process gives access to the distribution of single spin photon couplings in a given device. For resonators with a $50$ nm wide constriction at the inductor center, single maximum $G_{1}$ values reach $\sim 100$ kHz. Pumping the spins with strong pulses fed through an independent transmission line induces coherent Rabi oscillations. The spin excitation then proceeds via either direct resonant processes induced by the main pulse frequency or, in the case of square-shaped pulses, via the excitation of the cavity by sideband frequency components. The latter process measures the cavity mode hybridization with the spins and can be eliminated by using Gaussian shaped pulses. These results establish a scalable route toward integrated molecular-spin quantum processors.

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Implementation of the Quantum Fourier Transform on a molecular qudit with full refocusing and state tomography

Molecular spin qudits based on lanthanide complexes offer a promising platform for quantum technologies, combining chemical tunability with multi-level encoding. However, experimental demonstrations of their envisaged capabilities remain scarce, posing the difficulty of achieving precise control over coherences between qudit states in long pulse sequences. Here, we implement in 173Yb(trensal) qudit the Quantum Fourier Transform (QFT), a core component of numerous quantum algorithms, storing quantum information in the phases of coherences. QFT provides an ideal benchmark for coherence manipulation and an unprecedented challenge for molecular spin qudits. We address this challenge by embedding a full-refocusing protocol for spin qudits in our algorithm, mitigating inhomogeneous broadening and enabling a high-fidelity recovery of the state. Complete state tomography demostrates the performance of the algorithm, while simulations provide insight into the physical mechanisms behind inhomogeneous broadening. This work shows the feasibility of quantum logic on molecular spin qudits and highlights their potential.

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Waveguide quantum electrodynamics at the onset of spin-spin correlations

We explore the competition between light-mediated and intrinsic matter-matter interactions in waveguide quantum electrodynamics. For this, we couple a superconducting transmission line to a model magnetic material, made of organic free radical molecules with a spin $S=1/2$ and a $g_{S}$ factor very close to that of a free electron. The microwave transmission has been measured in a wide range of temperatures ($0.013$ K $\leq T \leq 2$ K), magnetic fields ($0\leq B \leq 0.5$ T) and frequencies ($0 \leq ω/2 π\leq 14$ GHz). We find that molecules belonging to one of the two crystal sublattices form one-dimensional spin chains. Temperature then controls the intrinsic correlations along these chains in a continuous and monotonic way. In the paramagnetic region ($T > 0.7$ K), the microwave transmission shows evidences for the collective coupling of quasi-identical spins to the propagating photons, with coupling strengths that reach values close to the dissipation rates. As $T$ decreases, the growth of spin correlations, combined with the anisotropy in the spin-spin exchange constants, tend to suppress the collective spin-photon coupling. In this regime, the spin visibility in transmission reflects also a gradual change in the nature of the dominant spin excitations, from single spin flips to bosonic magnons.

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Chemical tuning of spin clock transitions in molecular monomers based on nuclear spin-free Ni(II)

We report the existence of a sizeable quantum tunnelling splitting between the two lowest electronic spin levels of mononuclear Ni complexes. The level anti-crossing, or magnetic clock transition, associated with this gap has been directly monitored by heat capacity experiments. The comparison of these results with those obtained for a Co derivative, for which tunnelling is forbidden by symmetry, shows that the clock transition leads to an effective suppression of intermolecular spin-spin interactions. In addition, we show that the quantum tunnelling splitting admits a chemical tuning via the modification of the ligand shell that determines the crystal field and the magnetic anisotropy. These properties are crucial to realize model spin qubits that combine the necessary resilience against decoherence, a proper interfacing with other qubits and with the control circuitry and the ability to initialize them by cooling.

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