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本文引用的文献

1
Dynamics of frequency-swept nuclear spin optical pumping in powdered diamond at low magnetic fields.低磁场下粉末金刚石中扫频核自旋光泵浦的动力学
Proc Natl Acad Sci U S A. 2019 Feb 12;116(7):2512-2520. doi: 10.1073/pnas.1811994116. Epub 2019 Jan 24.
2
Orientation-independent room temperature optical C hyperpolarization in powdered diamond.粉末金刚石中与取向无关的室温光学碳超极化
Sci Adv. 2018 May 18;4(5):eaar5492. doi: 10.1126/sciadv.aar5492. eCollection 2018 May.
3
Thermal annihilation of photo-induced radicals following dynamic nuclear polarization to produce transportable frozen hyperpolarized C-substrates.通过动态核极化产生可传输的冷冻高极化 C 底物,实现光诱导自由基的热消除。
Nat Commun. 2017 Jun 1;8:15757. doi: 10.1038/ncomms15757.
4
Frequency-Swept Integrated Solid Effect.扫频集成固效。
Angew Chem Int Ed Engl. 2017 Jun 6;56(24):6744-6748. doi: 10.1002/anie.201700032. Epub 2017 May 12.
5
Arbitrary waveform modulated pulse EPR at 200GHz.200吉赫兹的任意波形调制脉冲电子顺磁共振。
J Magn Reson. 2017 Jun;279:81-90. doi: 10.1016/j.jmr.2017.04.016. Epub 2017 Apr 27.
6
Electron Decoupling with Dynamic Nuclear Polarization in Rotating Solids.固态中通过动态核极化实现电子去耦。
J Am Chem Soc. 2017 May 10;139(18):6310-6313. doi: 10.1021/jacs.7b02714. Epub 2017 Apr 27.
7
Hyperpolarized Nanodiamond Surfaces.超极化纳米金刚石表面。
J Am Chem Soc. 2017 Jan 11;139(1):193-199. doi: 10.1021/jacs.6b09293. Epub 2016 Dec 23.
8
Dynamic nuclear polarization by frequency modulation of a tunable gyrotron of 260GHz.通过260GHz可调谐回旋管的频率调制实现动态核极化
J Magn Reson. 2016 Jan;262:62-67. doi: 10.1016/j.jmr.2015.11.008. Epub 2015 Dec 18.
9
Design and characterization of a W-band system for modulated DNP experiments.用于调制动态核极化实验的W波段系统的设计与特性分析
J Magn Reson. 2015 Dec;261:11-8. doi: 10.1016/j.jmr.2015.09.011. Epub 2015 Oct 14.
10
Frequency swept microwaves for hyperfine decoupling and time domain dynamic nuclear polarization.用于超精细去耦和时域动态核极化的扫频微波。
Solid State Nucl Magn Reson. 2015 Nov;72:79-89. doi: 10.1016/j.ssnmr.2015.10.001. Epub 2015 Oct 9.

通过扫频微波梳实现增强的动态核极化。

Enhanced dynamic nuclear polarization via swept microwave frequency combs.

机构信息

Department of Chemistry, University of California, Berkeley, CA 94720;

Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720.

出版信息

Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):10576-10581. doi: 10.1073/pnas.1807125115. Epub 2018 Oct 2.

DOI:10.1073/pnas.1807125115
PMID:30279178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6196520/
Abstract

Dynamic nuclear polarization (DNP) has enabled enormous gains in magnetic resonance signals and led to vastly accelerated NMR/MRI imaging and spectroscopy. Unlike conventional -techniques, DNP methods that exploit the full electron spectrum are appealing since they allow direct participation of all electrons in the hyperpolarization process. Such methods typically entail sweeps of microwave radiation over the broad electron linewidth to excite DNP but are often inefficient because the sweeps, constrained by adiabaticity requirements, are slow. In this paper, we develop a technique to overcome the DNP bottlenecks set by the slow sweeps, using a swept microwave frequency comb that increases the effective number of polarization transfer events while respecting adiabaticity constraints. This allows a multiplicative gain in DNP enhancement, scaling with the number of comb frequencies and limited only by the hyperfine-mediated electron linewidth. We demonstrate the technique for the optical hyperpolarization of C nuclei in powdered microdiamonds at low fields, increasing the DNP enhancement from 30 to 100 measured with respect to the thermal signal at 7T. For low concentrations of broad linewidth electron radicals [e.g., TEMPO ((2,2,6,6-tetramethylpiperidin-1-yl)oxyl)], these multiplicative gains could exceed an order of magnitude.

摘要

动态核极化(DNP)极大地提高了磁共振信号,从而大大加快了 NMR/MRI 成像和光谱学的速度。与传统技术不同,利用全电子谱的 DNP 方法很有吸引力,因为它们允许所有电子直接参与超极化过程。此类方法通常需要在宽电子线宽上扫过微波辐射以激发 DNP,但通常效率不高,因为扫频受到绝热性要求的限制,速度较慢。在本文中,我们开发了一种克服慢扫频带来的 DNP 瓶颈的技术,使用扫频微波频梳来增加极化转移事件的有效数量,同时尊重绝热性限制。这允许 DNP 增强的乘法增益,与频梳频率的数量成比例,并且仅受超精细介导的电子线宽限制。我们在低场下对粉末微金刚石中的 C 核进行了光学超极化实验,相对于 7T 下的热信号,DNP 增强从 30 提高到 100。对于宽线宽电子自由基的低浓度[例如,TEMPO((2,2,6,6-四甲基哌啶-1-基)氧自由基)],这些乘法增益可能超过一个数量级。