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Pecharsky, Vitalij K.ORCID iD iconorcid.org/0000-0001-9503-7567
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Publications (2 of 2) Show all publications
Alammar, T., Hlova, I. Z., Gupta, S., Biswas, A., Ma, T., Zhou, L., . . . Mudring, A.-V. (2020). Mechanochemical synthesis, luminescent and magnetic properties of lanthanide benzene-1,4-dicarboxylate coordination polymers (Ln(0.5)Gd(0.5))(2) (1,4-BDC)(3)(H2O)(4); Ln = Sm, Eu, Tb. New Journal of Chemistry, 44(3), 1054-1062
Open this publication in new window or tab >>Mechanochemical synthesis, luminescent and magnetic properties of lanthanide benzene-1,4-dicarboxylate coordination polymers (Ln(0.5)Gd(0.5))(2) (1,4-BDC)(3)(H2O)(4); Ln = Sm, Eu, Tb
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2020 (English)In: New Journal of Chemistry, ISSN 1144-0546, E-ISSN 1369-9261, Vol. 44, no 3, p. 1054-1062Article in journal (Refereed) Published
Abstract [en]

Mechanochemical reactions of benzene-1,4-dicarboxylate (BDC2-) and lanthanide carbonates, Ln(2)(CO3)(3)center dot xH(2)O (Ln = Sm, Eu, Gd, Tb) yield phase pure lanthanide coordination polymers, (Ln(0.5)Gd(0.5))(2)(1,4-BDC)(3)(H2O)(4) with Ln = Sm, Eu, Tb, which are isostructural with Tb-2(1,4-BDC)(3)(H2O)(4) as confirmed by powder X-ray diffraction and vibrational spectroscopy. Upon excitation with UV light all three compounds display strong emissions, characteristic for the respective optically active lanthanide ion, namely, red for Eu3+, green for Tb3+ and orange-red for Sm3+. In case of the Tb3+-containing compound, the energy difference between the triplet energy level of benzene-1,4-dicarboxylate ligand (BDC2-) allows for the most efficient BDC2--Tb3+ energy transfer. As a consequence, an intense green luminescence with rather long lifetime (0.81 ms) and high quantum yield (22%) is observed after allowed excitation of the BDC2- ligand. The compounds are paramagnetic with no onset of long range magnetic ordering down to liquid He temperatures.

National Category
Chemical Sciences
Identifiers
urn:nbn:se:su:diva-179621 (URN)10.1039/c9nj02583a (DOI)000509327200044 ()
Available from: 2020-03-16 Created: 2020-03-16 Last updated: 2022-11-29Bibliographically approved
Liu, J., Mudryk, Y., Smetana, V., Mudring, A.-V. & Pecharsky, V. K. (2019). Anomalous effects of Sc substitution and processing on magnetism and structure of (Gd1-xScx)(5)Ge-4. Journal of Magnetism and Magnetic Materials, 474, 482-492
Open this publication in new window or tab >>Anomalous effects of Sc substitution and processing on magnetism and structure of (Gd1-xScx)(5)Ge-4
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2019 (English)In: Journal of Magnetism and Magnetic Materials, ISSN 0304-8853, E-ISSN 1873-4766, Vol. 474, p. 482-492Article in journal (Refereed) Published
Abstract [en]

The kinetic arrest observed in the parent Gd5Ge4 gradually vanishes when a small fraction (x = 0.025, 0.05 and 0.10) of Gd is replaced by Sc in (Gd1-xScx)(5)Ge-4, and the magnetic ground state changes from antiferromagnetic (AFM) to ferromagnetic (FM). A first order phase transition coupled with the FM-AFM transition occurs at T-C = 41 K for x = 0.05 and at T-C = 53 K for x = 0.10 during heating in applied magnetic field of 1 kOe, and the thermal hysteresis is near 10 K. The first-order magnetic transition is coupled with the structural Sm5Ge4-type to Gd5Si4-type transformation. The magnetization measured as a function of applied magnetic field shows sharp metamagnetic-like behavior. At the same time, the AFM to paramagnetic transition in (Gd1-xScx)(5)Ge-4 with x = 0.10, is uncharacteristically broad indicating development of strong short-range AFM correlations above the Ned temperature. Comparison of the magnetization data of bulk, powdered, and metal-varnish composite samples of (Gd0.95Sc0.05)(5)Ge-4 shows that mechanical grinding and fabrication of a composite have little effect on the temperature of the first-order transformation, but short-range ordering and AFM/FM ratio below T-C are surprisingly strongly affected.

National Category
Materials Engineering Physical Sciences Chemical Sciences
Identifiers
urn:nbn:se:su:diva-167469 (URN)10.1016/j.jmmm.2018.11.004 (DOI)000459494600071 ()
Available from: 2019-04-03 Created: 2019-04-03 Last updated: 2022-02-26Bibliographically approved
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0001-9503-7567

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