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Room-temperature quantum sensing with photoexcited triplet electrons in organic crystals

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arxiv 2402.13898 v2 pith:5B64G5F3 submitted 2024-02-21 quant-ph cond-mat.mes-hallphysics.chem-ph

classification quant-phcond-mat.mes-hallphysics.chem-ph
keywords quantumsensingtripletorganicstatesapproxcontrastcrystals
verification ladder T0 review T1 audit T2 compute T3 formal
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abstract

Quantum sensors have notably advanced high-sensitivity magnetic field detection. Here, we report quantum sensors constructed from polarized spin-triplet electrons in photoexcited organic chromophores, specifically focusing on pentacene-doped para-terphenyl (${\approx}$0.1%). We demonstrate essential quantum sensing properties at room temperature: electronic optical polarization and state-dependent fluorescence contrast, by leveraging differential pumping and relaxation rates between triplet and ground states. We measure high optically detected magnetic resonance (ODMR) contrast ${\approx}16.8\%$ of the triplet states at room temperature, along with long coherence times under spin echo and CPMG sequences, $T_2{=}2.7\mu$s and $T_2^{DD}{=}18.4\mu$s respectively, limited only by the triplet lifetimes. The material offers several advantages for quantum sensing, including the ability to grow large ($cm$-scale) crystals at low cost, the absence of paramagnetic impurities, and the diamagnetism of electronic states used for sensing when not optically illuminated. Utilizing pentacene as a representative of a broader class of spin triplet-polarizable organic molecules, this study highlights new potential for quantum sensing in chemical systems.

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Forward citations

Cited by 2 Pith papers

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    quant-ph 2024-11 conditional novelty 8.0 of 10

    EYFP, a standard fluorescent protein, is shown to be an optically addressable spin qubit with coherent microwave control and optically detected magnetic resonance.

  2. Cryogenic field-cycling instrument for optical NMR hyperpolarization studies

    quant-ph 2024-12 conditional novelty 7.0 of 10

    A cryogenic field-cycling instrument enables optical dynamic nuclear polarization studies from 10 mT to 9.4 T and 10 K to 300 K, demonstrated on 13C nuclei in diamond.

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