Research output: Contribution to journal › Article › peer-review
Temperature dynamics of magnetoactive compounds under terahertz irradiation: characterization by an EPR study. / Tumanov, S. V.; Melnikov, A. R.; Artiukhova, N. A. et al.
In: Russian Chemical Bulletin, Vol. 71, No. 7, 07.2022, p. 1378-1384.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Temperature dynamics of magnetoactive compounds under terahertz irradiation: characterization by an EPR study
AU - Tumanov, S. V.
AU - Melnikov, A. R.
AU - Artiukhova, N. A.
AU - Bogomyakov, A. S.
AU - Shevchenko, O. A.
AU - Getmanov, Ya V.
AU - Ovcharenko, V. I.
AU - Fedin, M. V.
AU - Veber, S. L.
N1 - Funding Information: This work was financially supported by the Russian Foundation for Basic Research (Project No. 20-33-90190). Publisher Copyright: © 2022, Springer Science+Business Media LLC.
PY - 2022/7
Y1 - 2022/7
N2 - A possibility of fast rapid temperature changing for the studied compound makes it possible to study related phenomena, such as thermally induced trapping of metastable states in magnetoactive compounds and thermally activated catalytic and biological processes. The Electron Paramagnetic Resonance (EPR) spectroscopy station at the Novosibirsk Free Electron Laser (NovoFEL) allows one to study effects of powerful terahertz (THz) radiation on the spin state of paramagnetic systems. A change in the sample temperature as a result of radiation absorption is an inevitable consequence of such an exposure. However, the sample heating at the NovoFEL EPR station itself is of interest due to the record power of THz radiation and small sizes of the samples used. A combination of these two factors can provide a significantly high heating rate. The magnetoactive complex [Cu(hfac)2LEt] was chosen as a model system for studying the heating process, since the complex has a magnetostructural transition at ∼125 K with substantially different spin states above and below the transition temperature. The heating processes with the amplitudes above 60 K were studied, the heating and cooling rates of the sample in similar experiments were estimated, and prospects for using the method to study various thermally induced effects are discussed.
AB - A possibility of fast rapid temperature changing for the studied compound makes it possible to study related phenomena, such as thermally induced trapping of metastable states in magnetoactive compounds and thermally activated catalytic and biological processes. The Electron Paramagnetic Resonance (EPR) spectroscopy station at the Novosibirsk Free Electron Laser (NovoFEL) allows one to study effects of powerful terahertz (THz) radiation on the spin state of paramagnetic systems. A change in the sample temperature as a result of radiation absorption is an inevitable consequence of such an exposure. However, the sample heating at the NovoFEL EPR station itself is of interest due to the record power of THz radiation and small sizes of the samples used. A combination of these two factors can provide a significantly high heating rate. The magnetoactive complex [Cu(hfac)2LEt] was chosen as a model system for studying the heating process, since the complex has a magnetostructural transition at ∼125 K with substantially different spin states above and below the transition temperature. The heating processes with the amplitudes above 60 K were studied, the heating and cooling rates of the sample in similar experiments were estimated, and prospects for using the method to study various thermally induced effects are discussed.
KW - EPR spectroscopy
KW - magnetoactive compound
KW - magnetostructural transition
KW - pulsed heating
KW - terahertz radiation
UR - http://www.scopus.com/inward/record.url?scp=85135613224&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/e38c3886-6308-3497-822a-5ead1faa782a/
U2 - 10.1007/s11172-022-3543-x
DO - 10.1007/s11172-022-3543-x
M3 - Article
AN - SCOPUS:85135613224
VL - 71
SP - 1378
EP - 1384
JO - Russian Chemical Bulletin
JF - Russian Chemical Bulletin
SN - 1066-5285
IS - 7
ER -
ID: 36821377