Literature DB >> 33423756

SABRE and PHIP pumped RASER and the route to chaos.

Stephan Appelt1, Sören Lehmkuhl2, Simon Fleischer3, Baptiste Joalland4, Nuwandi M Ariyasingha4, Eduard Y Chekmenev5, Thomas Theis6.   

Abstract

In a RASER (Radio-frequency Amplification by Stimulated Emission of Radiation), the fast relaxing electromagnetic modes of an LC resonator are enslaved by the slow nuclear spin motion, whose coherence decays with the transverse relaxation rate γm=1/T2∗. Such a system obeys the slaving principle, mathematically identical with the adiabatic elimination procedure, leading to multi-mode RASER equations. If the pumping rate of nuclear spin polarization Γ>>γm, a second adiabatic elimination process applies and the spectral properties of the RASER can be predicted. The resulting model is similar to the model of two non-linear coupled oscillators and predicts the observed RASER phenomena, including frequency combs and mode collapse. If the second adiabatic elimination is not applicable, mode collapse is completely absent and successive period doubling processes and chaos occur at very high population inversions. We compare these theoretical predictions with experimental results from a PHIP (Para-Hydrogen Induced Polarization) pumped 1H RASER. Moreover, in SABRE (Signal Amplification By Reversible Exchange) pumped 1H experiments, RASER revivals are observed long after the parahydrogen pumping source has been switched off. All these findings shed light onto the links between NMR spectroscopy, RASER physics, synergetics and chaos theory. Several new applications are envisioned in the fields of quantum sensor technology, structure investigation or magnetic resonance imaging (MRI).
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ALTADENA; Chaos; Hyperpolarization; Intermittence; MRI; Mode collapse; NMR spectroscopy; Non-linear coupled oscillators; PASADENA; PHIP; Parahydrogen; Period doubling; RASER; SABRE; Slaving principle; Synergetics

Year:  2020        PMID: 33423756      PMCID: PMC8026265          DOI: 10.1016/j.jmr.2020.106815

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  20 in total

1.  Transformation of symmetrization order to nuclear-spin magnetization by chemical reaction and nuclear magnetic resonance.

Authors: 
Journal:  Phys Rev Lett       Date:  1986-11-24       Impact factor: 9.161

2.  A theoretical basis for spontaneous polarization transfer in non-hydrogenative parahydrogen-induced polarization.

Authors:  Ralph W Adams; Simon B Duckett; Richard A Green; David C Williamson; Gary G R Green
Journal:  J Chem Phys       Date:  2009-11-21       Impact factor: 3.488

Review 3.  Quantum computing with NMR.

Authors:  Jonathan A Jones
Journal:  Prog Nucl Magn Reson Spectrosc       Date:  2010-11-08       Impact factor: 9.795

Review 4.  Paramagnetic NMR in solution and the solid state.

Authors:  Andrew J Pell; Guido Pintacuda; Clare P Grey
Journal:  Prog Nucl Magn Reson Spectrosc       Date:  2018-05-24       Impact factor: 9.795

Review 5.  The theory and practice of hyperpolarization in magnetic resonance using parahydrogen.

Authors:  Richard A Green; Ralph W Adams; Simon B Duckett; Ryan E Mewis; David C Williamson; Gary G R Green
Journal:  Prog Nucl Magn Reson Spectrosc       Date:  2012-03-15       Impact factor: 9.795

6.  Nanoscale nuclear magnetic resonance with a nitrogen-vacancy spin sensor.

Authors:  H J Mamin; M Kim; M H Sherwood; C T Rettner; K Ohno; D D Awschalom; D Rugar
Journal:  Science       Date:  2013-02-01       Impact factor: 47.728

7.  Nuclear magnetic resonance spectroscopy on a (5-nanometer)3 sample volume.

Authors:  T Staudacher; F Shi; S Pezzagna; J Meijer; J Du; C A Meriles; F Reinhard; J Wrachtrup
Journal:  Science       Date:  2013-02-01       Impact factor: 47.728

8.  15N Hyperpolarization by Reversible Exchange Using SABRE-SHEATH.

Authors:  Milton L Truong; Thomas Theis; Aaron M Coffey; Roman V Shchepin; Kevin W Waddell; Fan Shi; Boyd M Goodson; Warren S Warren; Eduard Y Chekmenev
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2015-03-30       Impact factor: 4.126

9.  Continuous Radio Amplification by Stimulated Emission of Radiation using Parahydrogen Induced Polarization (PHIP-RASER) at 14 Tesla.

Authors:  Andrey N Pravdivtsev; Frank D Sönnichsen; Jan-Bernd Hövener
Journal:  Chemphyschem       Date:  2020-02-11       Impact factor: 3.102

10.  Parahydrogen-Induced Radio Amplification by Stimulated Emission of Radiation.

Authors:  Baptiste Joalland; Nuwandi M Ariyasingha; Sören Lehmkuhl; Thomas Theis; Stephan Appelt; Eduard Y Chekmenev
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-24       Impact factor: 15.336

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  5 in total

1.  Background-Free Proton NMR Spectroscopy with Radiofrequency Amplification by Stimulated Emission Radiation.

Authors:  Baptiste Joalland; Thomas Theis; Stephan Appelt; Eduard Y Chekmenev
Journal:  Angew Chem Int Ed Engl       Date:  2021-10-01       Impact factor: 15.336

2.  RASER MRI: Magnetic resonance images formed spontaneously exploiting cooperative nonlinear interaction.

Authors:  Sören Lehmkuhl; Simon Fleischer; Lars Lohmann; Matthew S Rosen; Eduard Y Chekmenev; Alina Adams; Thomas Theis; Stephan Appelt
Journal:  Sci Adv       Date:  2022-07-13       Impact factor: 14.957

Review 3.  Advancing homogeneous catalysis for parahydrogen-derived hyperpolarisation and its NMR applications.

Authors:  Ben J Tickner; Vladimir V Zhivonitko
Journal:  Chem Sci       Date:  2022-03-22       Impact factor: 9.969

4.  Clinical-Scale Production of Nearly Pure (>98.5%) Parahydrogen and Quantification by Benchtop NMR Spectroscopy.

Authors:  Shiraz Nantogma; Baptiste Joalland; Ken Wilkens; Eduard Y Chekmenev
Journal:  Anal Chem       Date:  2021-02-04       Impact factor: 6.986

5.  A Versatile Compact Parahydrogen Membrane Reactor.

Authors:  Patrick M TomHon; Suyong Han; Sören Lehmkuhl; Stephan Appelt; Eduard Y Chekmenev; Milad Abolhasani; Thomas Theis
Journal:  Chemphyschem       Date:  2021-10-26       Impact factor: 3.102

  5 in total

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