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arXiv 1708.05906quant-phcond-mat.mes-hall
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分子核自旋的量子探针超极化

Quantum probe hyperpolarisation of molecular nuclear spins

David A. Broadway, Jean-Philippe Tetienne, Alastair Stacey, James D. A. Wood, David A. Simpson, Liam T. Hall, Lloyd C. L. Hollenberg

摘要:

在磁共振成像(MRI)和核磁共振(NMR)光谱学中,靶分子内核自旋的超极化是一个关键且复杂的挑战。超极化在信号和空间分辨率方面提供了巨大的增益,这可能最终导致分子MRI和NMR的发展。目前,用于极化核自旋的技术通常需要低温和/或高磁场、射频控制场或引入催化剂或自由基介质。室温固态自旋量子比特的出现开辟了令人兴奋的新途径,可以绕过这些要求,利用量子控制实现直接核自旋超极化。采用一种新的交叉弛豫诱导极化(CRIP)协议,使用一个单一的氮空位(NV)中心的金刚石,我们证明了第一个外部核自旋超极化实现的量子探针,在这种情况下的聚(甲基丙烯酸甲酯)中的$^1$ H分子自旋。在这样做的过程中,我们表明,一个单一的量子比特是能够增加的热极化的$\sim 10^6$核自旋的6个数量级,相当于一个外加磁场的$10^5$ \,T。该技术也可以调整到多个自旋物种,我们证明使用\C{13}和$^1$ H核自旋系综。我们的结果进行了分析和解释,通过一个详细的理论治疗,这也是用来描述该系统如何可以扩大到一个通用的量子超极化平台,用于生产宏观量的造影剂在高偏振水平的临床应用。这些结果代表了分子成像和光谱学的核自旋超极化的新范例,并超越了材料科学和量子信息处理等领域。

英文摘要:

The hyperpolarisation of nuclear spins within target molecules is a critical and complex challenge in magnetic resonance imaging (MRI) and nuclear magnetic resonance (NMR) spectroscopy. Hyperpolarisation offers enormous gains in signal and spatial resolution which may ultimately lead to the development of molecular MRI and NMR. At present, techniques used to polarise nuclear spins generally require low temperatures and/or high magnetic fields, radio-frequency control fields, or the introduction of catalysts or free-radical mediators. The emergence of room temperature solid-state spin qubits has opened exciting new pathways to circumvent these requirements to achieve direct nuclear spin hyperpolarisation using quantum control. Employing a novel cross-relaxation induced polarisation (CRIP) protocol using a single nitrogen-vacancy (NV) centre in diamond, we demonstrate the first external nuclear spin hyperpolarisation achieved by a quantum probe, in this case of $^1$H molecular spins in poly(methyl methacrylate). In doing so, we show that a single qubit is capable of increasing the thermal polarisation of $\sim 10^6$ nuclear spins by six orders of magnitude, equivalent to an applied magnetic field of $10^5$\,T. The technique can also be tuned to multiple spin species, which we demonstrate using both \C{13} and $^1$H nuclear spin ensembles. Our results are analysed and interpreted via a detailed theoretical treatment, which is also used to describe how the system can be scaled up to a universal quantum hyperpolarisation platform for the production of macroscopic quantities of contrast agents at high polarisation levels for clinical applications. These results represent a new paradigm for nuclear spin hyperpolarisation for molecular imaging and spectroscopy, and beyond into areas such as materials science and quantum information processing.

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