Confining single Er<sup>3+</sup> ions in sub-3 nm NaYF<sub>4</sub> nanoparticles to induce slow relaxation of the magnetisation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38664382.
- Also identified by DOI 10.1038/s41467-024-47682-x and PMC identifier 11045814.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Molecular systems known as single-molecule magnets (SMMs) exhibit magnet-like behaviour of slow relaxation of the magnetisation and magnetic hysteresis and have potential application in high-density memory storage or quantum computing. Often, their intrinsic magnetic properties are plagued by low-energy molecular vibrations that lead to phonon-induced relaxation processes, however, there is no straightforward synthetic approach for molecular systems that would lead to a small amount of low-energy vibrations and low phonon density of states at the spin-resonance energies. In this work, we apply knowledge accumulated over the last decade in molecular magnetism to nanoparticles, incorporating Er<sup>3+</sup> ions in an ultrasmall sub-3 nm diamagnetic NaYF<sub>4</sub> nanoparticle (NP) and probing the slow relaxation dynamics intrinsic to the Er<sup>3+</sup> ion. Furthermore, by increasing the doping concentration, we also investigate the role of intraparticle interactions within the NP. The knowledge gained from this study is anticipated to enable better design of magnetically high-performance molecular and bulk magnets for a wide variety of applications, such as molecular electronics.