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Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM
The development of quantum technologies requires a thorough understanding of systems possessing quantum effects that can ultimately be manipulated. In the field of molecular magnetism, one of the main challenges is to measure high-order ligand field parameters, which play an essential role in the re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250539/ https://www.ncbi.nlm.nih.gov/pubmed/37291099 http://dx.doi.org/10.1038/s41467-023-39003-5 |
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author | Taran, Gheorghe Moreno-Pineda, Eufemio Schulze, Michael Bonet, Edgar Ruben, Mario Wernsdorfer, Wolfgang |
author_facet | Taran, Gheorghe Moreno-Pineda, Eufemio Schulze, Michael Bonet, Edgar Ruben, Mario Wernsdorfer, Wolfgang |
author_sort | Taran, Gheorghe |
collection | PubMed |
description | The development of quantum technologies requires a thorough understanding of systems possessing quantum effects that can ultimately be manipulated. In the field of molecular magnetism, one of the main challenges is to measure high-order ligand field parameters, which play an essential role in the relaxation properties of SMMs. The development of highly advanced theoretical calculations has allowed the ab-initio determination of such parameters; however, currently, there is a lack of quantitative assessment of how good the ab-initio parameters are. In our quest for technologies that can allow the extraction of such elusive parameters, we develop an experimental technique that combines the EPR spectroscopy and µSQUID magnetometry. We demonstrate the power of the technique by performing EPR-µSQUID measurement of a magnetically diluted single crystal of Et(4)N[GdPc(2)], by sweeping the magnetic field and applying a range of multifrequency microwave pulses. As a result, we were able to directly determine the high-order ligand field parameters of the system, enabling us to test theoretical predictions made by state-of-the-art ab-initio methods. |
format | Online Article Text |
id | pubmed-10250539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102505392023-06-10 Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM Taran, Gheorghe Moreno-Pineda, Eufemio Schulze, Michael Bonet, Edgar Ruben, Mario Wernsdorfer, Wolfgang Nat Commun Article The development of quantum technologies requires a thorough understanding of systems possessing quantum effects that can ultimately be manipulated. In the field of molecular magnetism, one of the main challenges is to measure high-order ligand field parameters, which play an essential role in the relaxation properties of SMMs. The development of highly advanced theoretical calculations has allowed the ab-initio determination of such parameters; however, currently, there is a lack of quantitative assessment of how good the ab-initio parameters are. In our quest for technologies that can allow the extraction of such elusive parameters, we develop an experimental technique that combines the EPR spectroscopy and µSQUID magnetometry. We demonstrate the power of the technique by performing EPR-µSQUID measurement of a magnetically diluted single crystal of Et(4)N[GdPc(2)], by sweeping the magnetic field and applying a range of multifrequency microwave pulses. As a result, we were able to directly determine the high-order ligand field parameters of the system, enabling us to test theoretical predictions made by state-of-the-art ab-initio methods. Nature Publishing Group UK 2023-06-08 /pmc/articles/PMC10250539/ /pubmed/37291099 http://dx.doi.org/10.1038/s41467-023-39003-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Taran, Gheorghe Moreno-Pineda, Eufemio Schulze, Michael Bonet, Edgar Ruben, Mario Wernsdorfer, Wolfgang Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM |
title | Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM |
title_full | Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM |
title_fullStr | Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM |
title_full_unstemmed | Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM |
title_short | Direct determination of high-order transverse ligand field parameters via µSQUID-EPR in a Et(4)N[(160)GdPc(2)] SMM |
title_sort | direct determination of high-order transverse ligand field parameters via µsquid-epr in a et(4)n[(160)gdpc(2)] smm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250539/ https://www.ncbi.nlm.nih.gov/pubmed/37291099 http://dx.doi.org/10.1038/s41467-023-39003-5 |
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