| Literature DB >> 35288686 |
Krishnendu Kundu1, Jessica R K White2, Samuel A Moehring2, Jason M Yu2, Joseph W Ziller2, Filipp Furche3, William J Evans4, Stephen Hill5,6.
Abstract
Spins in molecules are particularly attractive targets for next-generation quantum technologies, enabling chemically programmable qubits and potential for scale-up via self-assembly. Here we report the observation of one of the largest hyperfine interactions for a molecular system, Aiso = 3,467 ± 50 MHz, as well as a very large associated clock transition. This is achieved through chemical control of the degree of s-orbital mixing into the spin-bearing d orbital associated with a series of spin-½ La(II) and Lu(II) complexes. Increased s-orbital character reduces spin-orbit coupling and enhances the electron-nuclear Fermi contact interaction. Both outcomes are advantageous for quantum applications. The former reduces spin-lattice relaxation, and the latter maximizes the hyperfine interaction, which, in turn, generates a 9-GHz clock transition, leading to an increase in phase memory time from 1.0 ± 0.4 to 12 ± 1 μs for one of the Lu(II) complexes. These findings suggest strategies for the development of molecular quantum technologies, akin to trapped ion systems.Entities:
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Year: 2022 PMID: 35288686 DOI: 10.1038/s41557-022-00894-4
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274