论文标题
从UV-VIS光谱法中快速确定单个替代氮N $ _s^0 $浓度
Rapid determination of single substitutional nitrogen N$_s^0$ concentration in diamond from UV-Vis spectroscopy
论文作者
论文摘要
单个替代氮原子n $ _s^0 $是在钻石中创建氮呈(NV)中心的先决条件。它们充当电子捐赠者,以创建所需的NV $^ - $中心,提供针对照片的电荷稳定性,但也是破坏的主要来源。因此,在材料改进和应用方面,精确而快速的n $ _s^0 $浓度是许多与NV相关的研究的关键优势。在这里,我们提出了一种基于紫外可见范围内的吸收光谱并拟合270 nm吸收带的n $ _s^0 $浓度的方法。紫外线可见光谱具有实验性的简单性和广泛的可用性,比建立的方法具有优势。它允许快速确定n $ _s^0 $密度,即使对于大量样品也是如此。我们的方法在确定低浓度以及局部测量的能力方面显示出进一步的优势,这与单个晶体中的N $ _S^0 $浓度大致相关。 A cross-check with electron paramagnetic resonance (EPR) shows high reliability of our method and yields the absorption cross section of the 270~nm absorption band, $σ=1.96\pm0.15$ cm$^{-1}\cdot$ppm$^{-1}$ (in common logarithm) or $σ_e=4.51\pm0.35$ cm $^{ - 1} \ cdot $ ppm $^{ - 1} $(在天然对数中),它是确定n $ _s^0 $浓度的参考,并使我们的方法适用于其他人,而无需使用已知的N $ _S^0 $ reference样品和校准。我们提供了一种快速,实用和可复制的途径,该途径独立于所使用的机器,可以广泛实施,作为确定N $ _S^0 $浓度的标准表征方法。
Single substitutional nitrogen atoms N$_s^0$ are the prerequisite to create nitrogen-vacancy (NV) centers in diamonds. They serve as the electron donors to create the desired NV$^-$ center, provide charge stability against photo-ionisation, but also are the main source of decoherence. Therefore, precise and quick determination of N$_s^0$ concentration is a key advantage to a multitude of NV-related research in terms of material improvement as well as applications. Here we present a method to determine the N$_s^0$ concentration based on absorption spectroscopy in the UV-Visible range and fitting the 270 nm absorption band. UV-Visible spectroscopy has experimental simplicity and widespread availability that bear advantages over established methods. It allows a rapid determination of N$_s^0$ densities, even for large numbers of samples. Our method shows further advantages in determining low concentrations as well as the ability to measure locally, which is highly relevant for diamonds with largely varying N$_s^0$ concentrations in a single crystal. A cross-check with electron paramagnetic resonance (EPR) shows high reliability of our method and yields the absorption cross section of the 270~nm absorption band, $σ=1.96\pm0.15$ cm$^{-1}\cdot$ppm$^{-1}$ (in common logarithm) or $σ_e=4.51\pm0.35$ cm$^{-1}\cdot$ppm$^{-1}$ (in natural logarithm), which serves as a reference to determine N$_s^0$ concentrations, and makes our method applicable for others without the need for a known N$_s^0$-reference sample and calibration. We provide a rapid, practical and replicable pathway that is independent of the machine used and can be widely implemented as a standard characterization method for the determination of N$_s^0$ concentrations.