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Spin-Lattice Relaxation and Spin-Phonon Coupling of ns1 Metal Ions at the Surface.
Bruzzese, Paolo Cleto; Liao, Yu-Kai; Donà, Lorenzo; Civalleri, Bartolomeo; Salvadori, Enrico; Chiesa, Mario.
Afiliación
  • Bruzzese PC; Max Planck Institute for Chemical Energy Conversion, Stiftstr. 34-36, 45470 Mülheim an der Ruhr, Germany.
  • Liao YK; Department of Chemistry and NIS Centre of Excellence, University of Turin, via Giuria 7, 10125 Torino, Italy.
  • Donà L; Department of Chemistry and NIS Centre of Excellence, University of Turin, via Giuria 7, 10125 Torino, Italy.
  • Civalleri B; Department of Chemistry and NIS Centre of Excellence, University of Turin, via Giuria 7, 10125 Torino, Italy.
  • Salvadori E; Department of Chemistry and NIS Centre of Excellence, University of Turin, via Giuria 7, 10125 Torino, Italy.
  • Chiesa M; Department of Chemistry and NIS Centre of Excellence, University of Turin, via Giuria 7, 10125 Torino, Italy.
J Phys Chem Lett ; 15(28): 7161-7167, 2024 Jul 18.
Article en En | MEDLINE | ID: mdl-38967545
ABSTRACT
To use transition metal ions for spin-based applications, it is essential to understand fundamental contributions to electron spin relaxation in different ligand environments. For example, to serve as building blocks for a device, transition metal ion-based molecular qubits must be organized on surfaces and preserve long electron spin relaxation times, up to room temperature. Here we propose monovalent group 12 ions (Zn+ and Cd+) as potential electronic metal qubits with an ns1 ground state. The relaxation properties of Zn+ and Cd+, stabilized at the interface of porous aluminosilicates, are investigated and benchmarked against vanadium (3d1) and copper (3d9) ions. The spin-phonon coupling has been evaluated through DFT modeling and found to be negligible for the ns1 states, explaining the long coherence time, up to 2 µs, at room temperature. These so far unexplored metal qubits may represent viable candidates for room temperature quantum operations and sensing.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Phys Chem Lett Año: 2024 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Phys Chem Lett Año: 2024 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos