Encapsulation Enhances the Quantum Coherence of a Solid‐State Molecular Spin Qubit

A Abinash Swain (Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain) L Leoní A. Barrios (Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain) Y Yulia Nelyubina (Nesmeyanov Institute of Organoelement Compounds Russian Academy of Sciences Moscow 119334 Russia) S Simon J. Teat (Advanced Light Source) O Olivier Roubeau (Instituto de Nanociencia y Materiales de Aragón (INMA) CSIC and Universidad de Zaragoza Plaza San Francisco s/n Zaragoza 50009 Spain) V Valentin Novikov (Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain) G Guillem Aromí (Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain)

Abstract

Abstract Spins within molecules benefit from the atomistic control of synthetic chemistry for the realization of qubits. One advantage is that the quantum superpositions of the spin states encoding the qubit can be coherently manipulated using electromagnetic radiation. The main challenge is the fragility of these superpositions when qubits are to partake of solid‐state devices. We address this issue with a supramolecular approach for protecting molecular spin qubits against decoherence. The molecular qubit [Cr(ox) 3 ] 3− has been encapsulated inside the diamagnetic triple‐stranded helicate [Zn 2 L 3 ] 4+ (L is a bis ‐pyrazolylpyridine ligand). The quantum coherence of the protected qubit is then analyzed with pulsed EPR spectroscopy and compared with the unprotected qubit, both in solution and in the solid state. Crucially, the spin–spin relaxation in the solid state has been examined within diamagnetic crystal lattices of the isostructural ([Al(ox) 3 ]@[Zn 2 L 3 ]) + or [Al(ox) 3 ] 3‐ assemblies, respectively, doped with the Cr 3+ qubit in two different (<10%) concentrations. The study unveils a surprising increase of the phase memory time of the qubit upon encapsulation only in the solid. Spin‐lattice relaxation times also exhibit a significant enhancement, as established from inversion recovery pulse sequences and from slow relaxation of the magnetization of the protected qubit, not featured by the free qubit.

Article Details

Volume / Issue Vol. 64, Issue 42
Published October 13, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

A

Abinash Swain

Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain

L

Leoní A. Barrios

Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain

Y

Yulia Nelyubina

Nesmeyanov Institute of Organoelement Compounds Russian Academy of Sciences Moscow 119334 Russia

S

Simon J. Teat

Advanced Light Source

O

Olivier Roubeau

Instituto de Nanociencia y Materiales de Aragón (INMA) CSIC and Universidad de Zaragoza Plaza San Francisco s/n Zaragoza 50009 Spain

V

Valentin Novikov

Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain

G

Guillem Aromí

Departament de Química Inorgànica i Orgànica Universitat de Barcelona Diagonal 645 Barcelona 08028 Spain