Centre de RMN a Tres Hauts Champs, Universite de Lyon (CNRS/ENS Lyon/UCB Lyon 1), 69100 Villeurbanne, France.
Acc Chem Res. 2013 Sep 17;46(9):1942-51. doi: 10.1021/ar300322x. Epub 2013 Mar 21.
Many of the functions and applications of advanced materials result from their interfacial structures and properties. However, the difficulty in characterizing the surface structure of these materials at an atomic level can often slow their further development. Solid-state NMR can probe surface structure and complement established surface science techniques, but its low sensitivity often limits its application. Many materials have low surface areas and/or low concentrations of active/surface sites. Dynamic nuclear polarization (DNP) is one intriguing method to enhance the sensitivity of solid-state NMR experiments by several orders of magnitude. In a DNP experiment, the large polarization of unpaired electrons is transferred to surrounding nuclei, which provides a maximum theoretical DNP enhancement of ∼658 for (1)H NMR. In this Account, we discuss the application of DNP to enhance surface NMR signals, an approach known as DNP surface enhanced NMR spectroscopy (DNP SENS). Enabling DNP for these systems requires bringing an exogeneous radical solution into contact with surfaces without diluting the sample. We proposed the incipient wetness impregnation technique (IWI), a well-known method in materials science, to impregnate porous and particulate materials with just enough radical containing solution to fill the porous volume. IWI offers several advantages: it is extremely simple, provides a uniform wetting of the surface, and does not increase the sample volume or substantially reduce the concentration of the sample. This Account describes the basic principles behind DNP SENS through results obtained for mesoporous and nanoparticulate samples impregnated with radical solutions. We also discuss the quantification of the overall sensitivity enhancements obtained with DNP SENS and compare that with ordinary room temperature NMR spectroscopy. We then review the development of radicals and solvents that give the best possible enhancements today. With the best polarizing mixtures, DNP SENS enhances sensitivity by a factor of up to 100, which decreases acquisition time by five orders of magnitude. Such enhancement enables the detailed and expedient atomic level characterization of the surfaces of complex materials at natural isotopic abundance and opens new avenues for NMR. To illustrate these improvements, we describe the successful application of DNP SENS to characterize hybrid materials, organometallic surface species, and metal-organic frameworks.
许多先进材料的功能和应用源于其界面结构和特性。然而,由于难以在原子水平上对这些材料的表面结构进行表征,因此往往会阻碍它们的进一步发展。固态 NMR 可以探测表面结构并补充已建立的表面科学技术,但它的低灵敏度通常限制了其应用。许多材料的表面积低,或活性/表面位点的浓度低。动态核极化 (DNP) 是一种通过几个数量级增强固态 NMR 实验灵敏度的诱人方法。在 DNP 实验中,未配对电子的大极化被转移到周围的核,这为 (1)H NMR 提供了最大的理论 DNP 增强约 658。在本报告中,我们讨论了 DNP 在增强表面 NMR 信号方面的应用,这种方法称为 DNP 表面增强 NMR 光谱学 (DNP SENS)。为了使这些系统能够实现 DNP,需要将外源自由基溶液与表面接触,而不会稀释样品。我们提出了初始湿浸渍技术 (IWI),这是材料科学中一种众所周知的方法,用于用足够的含自由基溶液浸渍多孔和颗粒状材料,以填充多孔体积。IWI 具有几个优点:它非常简单,均匀润湿表面,并且不会增加样品体积或大幅降低样品浓度。本报告通过对用自由基溶液浸渍的介孔和纳米颗粒样品获得的结果,描述了 DNP SENS 的基本原理。我们还讨论了用 DNP SENS 获得的整体灵敏度增强的定量,并将其与普通室温 NMR 光谱进行了比较。然后,我们回顾了当今提供最佳可能增强效果的自由基和溶剂的发展。使用最佳的极化混合物,DNP SENS 可将灵敏度提高 100 倍,从而将采集时间减少五个数量级。这种增强使得可以在自然同位素丰度下对复杂材料的表面进行详细和快速的原子级表征,并为 NMR 开辟了新的途径。为了说明这些改进,我们描述了 DNP SENS 在表征杂化材料、有机金属表面物种和金属有机骨架方面的成功应用。