高(12-20 T)磁场下 P1 中心的特殊 EPR 光谱。

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Orit Nir-Arad, Eyal Laster, Mais Daksi, Nurit Manukovsky and Ilia Kaminker
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引用次数: 0

摘要

高压高温(HPHT)金刚石中最常见的晶格缺陷是氮置换(P1)中心。这是一种顺磁缺陷,其单个未配对电子自旋与 14N 核自旋耦合,形成一个 S = 1/2、I = 1 的自旋系统。通过电子顺磁共振(EPR)光谱研究 P1 中心已有几十年的历史,但直到最近,人们才开始关注它们在超高(大于 12 T)磁场中的行为。这是因为最近发现 P1 中心是动态核极化(DNP)实验中非常有效的极化剂,而动态核极化实验通常是在高磁场下进行的。P1 超高磁场 EPR 光谱显示多个峰值,而低磁场光谱则没有。在本文中,我们介绍了 P1 中心在超高磁场下的 EPR 光谱,并表明在 12-20 T 时更为复杂的光谱是 mS = +1/2 电子自旋流形中显著的状态混合的结果。状态混合是满足抵消条件的结果,即 e-14N 超精细相互作用等于 14N 核自旋拉莫尔频率的两倍。我们通过比较在 6.9 和 13.8 T 下获得的 EPR 光谱来说明抵消条件对 EPR 光谱的影响。前者与在较低场强下观察到的共识光谱相似,而后者则截然不同。最后,我们利用电子双共振(ELDOR)测量结果表明,抵消条件导致 13.8 T 光谱的光谱扩散增加。这项研究揭示了 P1 中心在 DNP 特性条件下的自旋特性,这将有利于它们在 DNP 中的有效利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

On the peculiar EPR spectra of P1 centers at high (12–20 T) magnetic fields†

On the peculiar EPR spectra of P1 centers at high (12–20 T) magnetic fields†

On the peculiar EPR spectra of P1 centers at high (12–20 T) magnetic fields†

The most common lattice defect in high-pressure high-temperature (HPHT) diamonds is the nitrogen substitution (P1) center. This is a paramagnetic defect with a single unpaired electron spin coupled to a 14N nuclear spin forming an S = 1/2, I = 1 spin system. While P1 centers have been studied by electron paramagnetic resonance (EPR) spectroscopy for decades, only recently did their behavior at ultra-high (>12 T) magnetic fields become of interest. This is because P1 centers were recently found to be very efficient polarizing agents in dynamic nuclear polarization (DNP) experiments, which are typically carried out at high magnetic fields. The P1 ultra-high field EPR spectra show multiple peaks which the lower fields spectra do not. In this paper, we present an account of the EPR spectra of P1 centers at ultra-high fields and show that the more complex spectra at 12–20 T are the result of significant state mixing in the mS = +1/2 electron spin manifold. The state mixing is a result of fulfilling the cancellation condition, meaning the e–14N hyperfine interaction equals twice the Larmor frequency of the 14N nuclear spin. We illustrate the influence of the cancellation condition on the EPR spectra by comparing EPR spectra acquired at 6.9 and 13.8 T. While the former are similar to the consensus spectra observed at lower fields, the latter are very different. We present numerical simulations that quantitatively account for the experimental spectra at both 6.9 and 13.8 T. Finally, we use electron electron double resonance (ELDOR) measurements to show that the cancellation condition results in increased spectral diffusion in the 13.8 T spectrum. This work sheds light on the spin properties of P1 centers under DNP-characteristic conditions, which will be conducive to their efficient utilization in DNP.

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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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