Engineering clock transitions in molecular lanthanide complexes
Stewart, Robert and Canaj, Angelos B. and Liu, Shuanglong and Regincos Marti, Emma and Celmina, Anna and Nichol, Gary and Cheng, Hai-Ping and Murrie, Mark and Hill, Stephen (2024) Engineering clock transitions in molecular lanthanide complexes. Journal of the American Chemical Society, 146 (16). pp. 11083-11094. ISSN 1520-5126 (https://doi.org/10.1021/jacs.3c09353)
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Abstract
Molecular lanthanide (Ln) complexes are promising candidates for the development of next-generation quantum technologies. High-symmetry structures incorporating integer spin Ln ions can give rise to well-isolated crystal field quasi-doublet ground states, i.e., quantum two-level systems that may serve as the basis for magnetic qubits. Recent work has shown that symmetry lowering of the coordination environment around the Ln ion can produce an avoided crossing or clock transition within the ground doublet, leading to significantly enhanced coherence. Here, we employ single-crystal high-frequency electron paramagnetic resonance spectroscopy and high-level ab initio calculations to carry out a detailed investigation of the nine-coordinate complexes, [HoIIIL1L2], where L1 = 1,4,7,10-tetrakis(2-pyridylmethyl)-1,4,7,10-tetraaza-cyclododecane and L2 = F– (1) or [MeCN]0 (2). The pseudo-4-fold symmetry imposed by the neutral organic ligand scaffold (L1) and the apical anionic fluoride ion generates a strong axial anisotropy with an mJ = ±8 ground-state quasi-doublet in 1, where mJ denotes the projection of the J = 8 spin–orbital moment onto the ∼C4 axis. Meanwhile, off-diagonal crystal field interactions give rise to a giant 116.4 ± 1.0 GHz clock transition within this doublet. We then demonstrate targeted crystal field engineering of the clock transition by replacing F– with neutral MeCN (2), resulting in an increase in the clock transition frequency by a factor of 2.2. The experimental results are in broad agreement with quantum chemical calculations. This tunability is highly desirable because decoherence caused by second-order sensitivity to magnetic noise scales inversely with the clock transition frequency.
ORCID iDs
Stewart, Robert, Canaj, Angelos B., Liu, Shuanglong, Regincos Marti, Emma ORCID: https://orcid.org/0000-0002-5814-7596, Celmina, Anna, Nichol, Gary, Cheng, Hai-Ping, Murrie, Mark and Hill, Stephen;-
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Item type: Article ID code: 89751 Dates: DateEvent24 April 2024Published15 April 2024Published Online27 March 2024AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 27 Jun 2024 13:48 Last modified: 25 Sep 2024 14:52 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/89751