Unified understanding of the breakdown of thermal mixing dynamic nuclear polarization: The role of temperature and radical concentration

IF 2 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
Ludovica M. Epasto , Thibaud Maimbourg , Alberto Rosso , Dennis Kurzbach
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引用次数: 0

Abstract

We reveal an interplay between temperature and radical concentration necessary to establish thermal mixing (TM) as an efficient dynamic nuclear polarization (DNP) mechanism. We conducted DNP experiments by hyperpolarizing widely used DNP samples, i.e., sodium pyruvate-1-13C in water/glycerol mixtures at varying nitroxide radical (TEMPOL) concentrations and microwave irradiation frequencies, measuring proton and carbon-13 spin temperatures. Using a cryogen consumption-free prototype-DNP apparatus, we could probe cryogenic temperatures between 1.5 and 6.5 K, i.e., below and above the boiling point of liquid helium. We identify two mechanisms for the breakdown of TM: (i) Anderson type of quantum localization for low radical concentration, or (ii) quantum Zeno localization occurring at high temperature. This observation allowed us to reconcile the recent diverging observations regarding the relevance of TM as a DNP mechanism by proposing a unifying picture and, consequently, to find a trade-off between radical concentration and electron relaxation times, which offers a pathway to improve experimental DNP performance based on TM.

统一理解热混合动态核极化的分解:温度和自由基浓度的作用
我们揭示了温度与自由基浓度之间的相互作用,这种相互作用是将热混合(TM)作为一种有效的动态核极化(DNP)机制所必需的。我们对广泛使用的 DNP 样品,即水/甘油混合物中的丙酮酸钠-1-13C,在不同的亚硝基自由基(TEMPOL)浓度和微波辐照频率下进行了超极化,测量质子和碳-13 的自旋温度,从而开展了 DNP 实验。利用无低温消耗原型-DNP 仪器,我们可以探测 1.5 至 6.5 K 之间的低温,即低于和高于液氦沸点的温度。我们确定了 TM 破裂的两种机制:(i) 低自由基浓度下的安德森量子定位,或 (ii) 高温下发生的量子芝诺定位。这一观察结果使我们能够调和最近关于 TM 作为 DNP 机制的相关性的不同观察结果,提出一个统一的图景,从而找到自由基浓度和电子弛豫时间之间的权衡,这为提高基于 TM 的 DNP 实验性能提供了一条途径。
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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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