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Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces
The success of the emerging field of solid-state optical quantum information processing (QIP) critically depends on the access to resonant optical materials. Rare-earth ion (REI)-based molecular systems, whose quantum properties could be tuned taking advantage of molecular engineering strategies, ar...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042120/ https://www.ncbi.nlm.nih.gov/pubmed/33846323 http://dx.doi.org/10.1038/s41467-021-22383-x |
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author | Kumar, Kuppusamy Senthil Serrano, Diana Nonat, Aline M. Heinrich, Benoît Karmazin, Lydia Charbonnière, Loïc J. Goldner, Philippe Ruben, Mario |
author_facet | Kumar, Kuppusamy Senthil Serrano, Diana Nonat, Aline M. Heinrich, Benoît Karmazin, Lydia Charbonnière, Loïc J. Goldner, Philippe Ruben, Mario |
author_sort | Kumar, Kuppusamy Senthil |
collection | PubMed |
description | The success of the emerging field of solid-state optical quantum information processing (QIP) critically depends on the access to resonant optical materials. Rare-earth ion (REI)-based molecular systems, whose quantum properties could be tuned taking advantage of molecular engineering strategies, are one of the systems actively pursued for the implementation of QIP schemes. Herein, we demonstrate the efficient polarization of ground-state nuclear spins—a fundamental requirement for all-optical spin initialization and addressing—in a binuclear Eu(III) complex, featuring inhomogeneously broadened (5)D(0) →( 7)F(0) optical transition. At 1.4 K, long-lived spectral holes have been burnt in the transition: homogeneous linewidth (Γ(h)) = 22 ± 1 MHz, which translates as optical coherence lifetime (T(2opt)) = 14.5 ± 0.7 ns, and ground-state spin population lifetime (T(1spin)) = 1.6 ± 0.4 s have been obtained. The results presented in this study could be a progressive step towards the realization of molecule-based coherent light-spin QIP interfaces. |
format | Online Article Text |
id | pubmed-8042120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80421202021-04-30 Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces Kumar, Kuppusamy Senthil Serrano, Diana Nonat, Aline M. Heinrich, Benoît Karmazin, Lydia Charbonnière, Loïc J. Goldner, Philippe Ruben, Mario Nat Commun Article The success of the emerging field of solid-state optical quantum information processing (QIP) critically depends on the access to resonant optical materials. Rare-earth ion (REI)-based molecular systems, whose quantum properties could be tuned taking advantage of molecular engineering strategies, are one of the systems actively pursued for the implementation of QIP schemes. Herein, we demonstrate the efficient polarization of ground-state nuclear spins—a fundamental requirement for all-optical spin initialization and addressing—in a binuclear Eu(III) complex, featuring inhomogeneously broadened (5)D(0) →( 7)F(0) optical transition. At 1.4 K, long-lived spectral holes have been burnt in the transition: homogeneous linewidth (Γ(h)) = 22 ± 1 MHz, which translates as optical coherence lifetime (T(2opt)) = 14.5 ± 0.7 ns, and ground-state spin population lifetime (T(1spin)) = 1.6 ± 0.4 s have been obtained. The results presented in this study could be a progressive step towards the realization of molecule-based coherent light-spin QIP interfaces. Nature Publishing Group UK 2021-04-12 /pmc/articles/PMC8042120/ /pubmed/33846323 http://dx.doi.org/10.1038/s41467-021-22383-x Text en © The Author(s) 2021 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 Kumar, Kuppusamy Senthil Serrano, Diana Nonat, Aline M. Heinrich, Benoît Karmazin, Lydia Charbonnière, Loïc J. Goldner, Philippe Ruben, Mario Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
title | Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
title_full | Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
title_fullStr | Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
title_full_unstemmed | Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
title_short | Optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
title_sort | optical spin-state polarization in a binuclear europium complex towards molecule-based coherent light-spin interfaces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042120/ https://www.ncbi.nlm.nih.gov/pubmed/33846323 http://dx.doi.org/10.1038/s41467-021-22383-x |
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