Shimon Daphna, Cantwell Kelly A, Joseph Linta, Williams Ethan Q, Peng Zaili, Takahashi Susumu, Ramanathan Chandrasekhar
Institute of Chemistry, The Hebrew University of Jerusalem, Edmond J. Safra, Givat Ram, Jerusalem9190401, Israel.
Department of Physics and Astronomy, Dartmouth College, Hanover, New Hampshire03755, United States.
J Phys Chem C Nanomater Interfaces. 2022 Oct 20;126(41):17777-17787. doi: 10.1021/acs.jpcc.2c06145. Epub 2022 Oct 3.
We use microwave-induced dynamic nuclear polarization (DNP) of the substitutional nitrogen defects (P1 centers) in diamond to hyperpolarize bulk C nuclei in both single crystal and powder samples at room temperature at 3.34 T. The large (>100-fold) enhancements demonstrated correspond to a greater than 10 000-fold improvement in terms of signal averaging of the 1% abundant C spins. The DNP was performed using low-power solid state sources under static (nonspinning) conditions. The DNP spectrum (DNP enhancement as a function of microwave frequency) of diamond powder shows features that broadly correlate with the EPR spectrum. A well-defined negative Overhauser peak and two solid effect peaks are observed for the central ( = 0) manifold of the N spins. Previous low temperature measurements in diamond had measured a positive Overhauser enhancement in this manifold. Frequency-chirped millimeter-wave excitation of the electron spins is seen to significantly improve the enhancements for the two outer nuclear spin manifolds ( = ±1) and to blur some of the sharper features associated with the central manifold. The outer lines are best fit using a combination of the cross effect and the truncated cross effect, which is known to mimic features of an Overhauser effect. Similar features are also observed in experiments on single crystal samples. The observation of all of these mechanisms in a single material system under the same experimental conditions is likely due to the significant heterogeneity of the high pressure, high temperature (HPHT) type Ib diamond samples used. Large room temperature DNP enhancements at fields above a few tesla enable spectroscopic studies with better chemical shift resolution under ambient conditions.
我们利用金刚石中替代氮缺陷(P1中心)的微波诱导动态核极化(DNP),在3.34 T、室温下对单晶和粉末样品中的大量碳核进行超极化。所展示的大幅增强(>100倍)相当于在对1%丰度的碳自旋进行信号平均时提高了超过10000倍。DNP是在静态(非旋转)条件下使用低功率固态源进行的。金刚石粉末的DNP谱(DNP增强作为微波频率的函数)显示出与电子顺磁共振谱大致相关的特征。对于氮自旋的中心(m = 0)多重态,观察到一个明确的负奥弗豪泽峰和两个固体效应峰。此前在金刚石中的低温测量在该多重态中测得的是正奥弗豪泽增强。电子自旋的频率啁啾毫米波激发被发现可显著提高两个外层核自旋多重态(m = ±1)的增强,并模糊与中心多重态相关的一些更尖锐的特征。外层谱线使用交叉效应和截断交叉效应的组合进行最佳拟合,已知这种组合可模拟奥弗豪泽效应的特征。在单晶样品的实验中也观察到了类似特征。在相同实验条件下,在单一材料系统中观察到所有这些机制,可能是由于所使用的高压高温(HPHT)Ib型金刚石样品存在显著的不均匀性。在几特斯拉以上的磁场中实现的大室温DNP增强,使得在环境条件下能够进行具有更好化学位移分辨率的光谱研究。