Design of high-temperature f -block molecular nanomagnets through the control of vibration-induced spin relaxation

One of the main roadblocks that still hamper the practical use of molecular nanomagnets is their cryogenic working temperature. In the pursuit of rational strategies to design new molecular nanomagnets with increasing blocking temperature, ab initio methodologies play an important role by guiding sy...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemical science (Cambridge) Jg. 11; H. 6; S. 1593 - 1598
Hauptverfasser: Escalera-Moreno, Luis, Baldoví, José J., Gaita-Ariño, Alejandro, Coronado, Eugenio
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England Royal Society of Chemistry 14.02.2020
Schlagworte:
Blocking
Chemistry
Cryogenic temperature
Electron spin
First principles
High temperature
Magnets
Organic chemistry
Uranium
Vibration control
ISSN:2041-6520, 2041-6539
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:One of the main roadblocks that still hamper the practical use of molecular nanomagnets is their cryogenic working temperature. In the pursuit of rational strategies to design new molecular nanomagnets with increasing blocking temperature, ab initio methodologies play an important role by guiding synthetic efforts at the lab stage. Nevertheless, when evaluating vibration-induced spin relaxation, these methodologies are still far from being computationally fast enough to provide a useful predictive framework. Herein, we present an inexpensive first-principles method devoted to evaluating vibration-induced spin relaxation in molecular f -block single-ion magnets, with the important advantage of requiring only one CASSCF calculation. The method is illustrated using two case studies based on uranium as the magnetic centre. Finally, we propose chemical modifications in the ligand environment with the aim of suppressing spin relaxation.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:2041-6520
2041-6539
DOI:10.1039/C9SC03133B