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Imma Ratera

Publications and source records attributed to Imma Ratera.

2 recordsLinked to original sources

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.

quant-ph

Luminescent Trityl-based Diradicaloids: A Theoretical and Experimental Assessment of Charge-Resonance in Low-Lying Excited States

The tris(2,4,6-trichlorophenyl)methyl radical (TTM) has inspired the synthesis of several luminescent diradicals and diradicaloids, providing an extraordinary opportunity to control the nature of the low-lying excited states by fine-tuning the diradical character. However, the photophysical properties of TTM-derived diradicals remain not fully understood yet. Here we present a combined theoretical and experimental investigation on TTM-derived diradicals to elucidate the origin of their luminescence. The theoretical analysis focuses on a series of symmetric TTM-derived diradicals with singlet ground state, featuring radical moieties linked by pi-conjugated spacers of different length. The nature of the lowest excited electronic states that control their photophysical behaviour is discussed in detail. The study is complemented by a complete spectroscopic characterization of the TTM-TTM diradical, synthesized using a novel, simpler and more efficient procedure exploiting the unique reactivity of TTM. The lowest excited states of the diradicals differ qualitatively from those of TTM: two novel low-lying states emerge in the diradical, due to charge resonance (CR) between the two radical units. The lowest CR state is a dark state for symmetric diradicals. The CR nature explains the blue-shifted emission observed by increasing the distance between the radical centres as seen in TTM-ph-TTM. This insight suggests different design strategies to improve the luminescence properties of TTM-derived diradicals

physics.chem-ph