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Sensitivity optimization in pulse EPR experiments with photo-labels by multiple-echo-integrated dynamical decoupling. / Sannikova, Natalya E; Melnikov, Anatoly R; Veber, Sergey L et al.

In: Physical chemistry chemical physics : PCCP, Vol. 25, No. 17, 03.05.2023, p. 11971-11980.

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Sannikova NE, Melnikov AR, Veber SL, Krumkacheva OA, Fedin MV. Sensitivity optimization in pulse EPR experiments with photo-labels by multiple-echo-integrated dynamical decoupling. Physical chemistry chemical physics : PCCP. 2023 May 3;25(17):11971-11980. Epub 2023 Apr 18. doi: 10.1039/d3cp01056b

Author

Sannikova, Natalya E ; Melnikov, Anatoly R ; Veber, Sergey L et al. / Sensitivity optimization in pulse EPR experiments with photo-labels by multiple-echo-integrated dynamical decoupling. In: Physical chemistry chemical physics : PCCP. 2023 ; Vol. 25, No. 17. pp. 11971-11980.

BibTeX

@article{076b3b03f6784fe4a72ed59f9496a4d5,
title = "Sensitivity optimization in pulse EPR experiments with photo-labels by multiple-echo-integrated dynamical decoupling",
abstract = "Photo-excited triplet states represent a new class of spin labels in pulse electron paramagnetic resonance (EPR), attracting increasing attention because of their unique spectroscopic properties. Despite certain advantages, the use of photo-labels has also some challenges, e.g. low repetition rates due to technical laser-related limitations and intrinsic properties of the labels. The application of additional pulse trains for multiple refocusing of the electron spin echo and integration of all observed echoes can significantly enhance sensitivity at a given repetition rate. In this work, we demonstrate that the use of Carr-Parcel-Meiboom-Gill (CPMG) blocks followed by multiple echo integration is a promising route for sensitivity gain in pulsed EPR utilizing photo-excited triplet states, including light-induced pulsed dipolar spectroscopy (LiPDS). The reduction of accumulation time by a factor of 5.3 has been achieved using a commercial pulsed EPR spectrometer with the implementation of a CPMG block and an external digitizer. The methodology of using CPMG refocusing with multiple echo integration in light-induced pulsed EPR experiments is discussed, aiding future applications of this approach in LiPDS experiments.",
author = "Sannikova, {Natalya E} and Melnikov, {Anatoly R} and Veber, {Sergey L} and Krumkacheva, {Olesya A} and Fedin, {Matvey V}",
note = "This work was supported by the Russian Science Foundation (20-73-10239). The authors are grateful to L. Politanskaya, E. Tretyakov, and V. Tormyshev from the N. N. Vorozhtsov Institute of Organic Chemistry SB RAS for providing the C60TAM sample. The authors thank MSHE for access to the EPR equipment.",
year = "2023",
month = may,
day = "3",
doi = "10.1039/d3cp01056b",
language = "English",
volume = "25",
pages = "11971--11980",
journal = "Physical Chemistry Chemical Physics",
issn = "1463-9076",
publisher = "Royal Society of Chemistry",
number = "17",

}

RIS

TY - JOUR

T1 - Sensitivity optimization in pulse EPR experiments with photo-labels by multiple-echo-integrated dynamical decoupling

AU - Sannikova, Natalya E

AU - Melnikov, Anatoly R

AU - Veber, Sergey L

AU - Krumkacheva, Olesya A

AU - Fedin, Matvey V

N1 - This work was supported by the Russian Science Foundation (20-73-10239). The authors are grateful to L. Politanskaya, E. Tretyakov, and V. Tormyshev from the N. N. Vorozhtsov Institute of Organic Chemistry SB RAS for providing the C60TAM sample. The authors thank MSHE for access to the EPR equipment.

PY - 2023/5/3

Y1 - 2023/5/3

N2 - Photo-excited triplet states represent a new class of spin labels in pulse electron paramagnetic resonance (EPR), attracting increasing attention because of their unique spectroscopic properties. Despite certain advantages, the use of photo-labels has also some challenges, e.g. low repetition rates due to technical laser-related limitations and intrinsic properties of the labels. The application of additional pulse trains for multiple refocusing of the electron spin echo and integration of all observed echoes can significantly enhance sensitivity at a given repetition rate. In this work, we demonstrate that the use of Carr-Parcel-Meiboom-Gill (CPMG) blocks followed by multiple echo integration is a promising route for sensitivity gain in pulsed EPR utilizing photo-excited triplet states, including light-induced pulsed dipolar spectroscopy (LiPDS). The reduction of accumulation time by a factor of 5.3 has been achieved using a commercial pulsed EPR spectrometer with the implementation of a CPMG block and an external digitizer. The methodology of using CPMG refocusing with multiple echo integration in light-induced pulsed EPR experiments is discussed, aiding future applications of this approach in LiPDS experiments.

AB - Photo-excited triplet states represent a new class of spin labels in pulse electron paramagnetic resonance (EPR), attracting increasing attention because of their unique spectroscopic properties. Despite certain advantages, the use of photo-labels has also some challenges, e.g. low repetition rates due to technical laser-related limitations and intrinsic properties of the labels. The application of additional pulse trains for multiple refocusing of the electron spin echo and integration of all observed echoes can significantly enhance sensitivity at a given repetition rate. In this work, we demonstrate that the use of Carr-Parcel-Meiboom-Gill (CPMG) blocks followed by multiple echo integration is a promising route for sensitivity gain in pulsed EPR utilizing photo-excited triplet states, including light-induced pulsed dipolar spectroscopy (LiPDS). The reduction of accumulation time by a factor of 5.3 has been achieved using a commercial pulsed EPR spectrometer with the implementation of a CPMG block and an external digitizer. The methodology of using CPMG refocusing with multiple echo integration in light-induced pulsed EPR experiments is discussed, aiding future applications of this approach in LiPDS experiments.

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UR - https://www.mendeley.com/catalogue/e746088c-badb-3161-99ef-85a9c8905b9f/

U2 - 10.1039/d3cp01056b

DO - 10.1039/d3cp01056b

M3 - Article

C2 - 37070235

VL - 25

SP - 11971

EP - 11980

JO - Physical Chemistry Chemical Physics

JF - Physical Chemistry Chemical Physics

SN - 1463-9076

IS - 17

ER -

ID: 48455833