Alexey Alfonsov
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The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
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Alexey Alfonsov has a total of 134 co-authors. Here are the top co-authors by number of shared publications:
- Vladislav Kataev
Leibniz Institute for Solid State and Materials Research
15 shared publications - Bernd Buchner
Leibniz Institute for Solid State and Materials Research
9 shared publications B. Büchner
Leibniz Institute for Solid State and Materials Research Dresden Dresden Germany
7 shared publicationsBernd Büchner
Leibniz Institute for Solid State and Materials Research Helmholtzstr. 20 D-01069 Dresden Germany
4 shared publications- Joyal John Abraham
Leibniz Institute for Solid State and Materials Research Helmholtzstr. 20 D‐01069 Dresden Germany
3 shared publications A. Isaeva
Leibniz Institute for Solid State and Materials Research, IFW Dresden, D-01069 Dresden, Germany
2 shared publications
Latest Publications
- Open Access
- 2 November 2026
- Published by Wiley in Advanced Physics Research
- Vol. 5 (11)
Signatures of Unconventional Magnetism in the Layered Metallic Ferromagnet LaCrSb 3 From Ferromagnetic Resonance Spectroscopy
Is a metallic ferromagnet with a layered crystal structure demonstrating intriguing electronic and magnetic properties, such as large anomalous Hall effect, strong canting of the spin lattice, and a peculiar spin‐reorientation transition. Here, we report the results of the temperature‐dependent X‐ray diffraction, static magnetization, and in particular electron spin resonance (ESR) and ferromagnetic resonance (FMR) experiments carried out over a wide range of frequencies, magnetic fields, and temperatures. Though X‐ray data reveals no structural transition down to 15 K, a strong magneto‐elastic coupling is detected across the ferromagnetic transition at K. ESR results indicate a presence of the quasi‐static short‐range correlations extending far above , which is a typical fingerprint of the low‐dimensional magnetism. The frequency‐field diagram of the FMR modes mapped below strongly suggests presence of two magnetic sublattices in . A quantitative understanding of the FMR excitations was achieved within a phenomenological model of interacting orthogonal ferro‐ and antiferromagnetic sublattices, which was earlier proposed to explain unusually strong spin canting observed by neutron diffraction [E. Granado et al., Phys. Rev.Lett. 89 , 107204 (2002)]. The FMR results corroborate this scenario and call for the development of the underlying microscopic model of unconventional magnetism in .
- 2 November 2026
- Published by Wiley in Advanced Physics Research
- Vol. 5 (11)
Open AccessSignatures of Unconventional Magnetism in the Layered Metallic Ferromagnet LaCrSb 3 From Ferromagnetic Resonance Spectroscopy
Is a metallic ferromagnet with a layered crystal structure demonstrating intriguing electronic and magnetic properties, such as large anomalous Hall effect, strong canting of the spin lattice, and a peculiar spin‐reorientation transition. Here, we report the results of the temperature‐dependent X‐ray diffraction, static magnetization, and in particular electron spin resonance (ESR) and ferromagnetic resonance (FMR) experiments carried out over a wide range of frequencies, magnetic fields, and temperatures. Though X‐ray data reveals no structural transition down to 15 K, a strong magneto‐elastic coupling is detected across the ferromagnetic transition at K. ESR results indicate a presence of the quasi‐static short‐range correlations extending far above , which is a typical fingerprint of the low‐dimensional magnetism. The frequency‐field diagram of the FMR modes mapped below strongly suggests presence of two magnetic sublattices in . A quantitative understanding of the FMR excitations was achieved within a phenomenological model of interacting orthogonal ferro‐ and antiferromagnetic sublattices, which was earlier proposed to explain unusually strong spin canting observed by neutron diffraction [E. Granado et al., Phys. Rev.Lett. 89 , 107204 (2002)]. The FMR results corroborate this scenario and call for the development of the underlying microscopic model of unconventional magnetism in .
- Open Access
- 4 October 2026
- Published by Wiley in Advanced Science
Cr 1/4 NbSe 2 ‐Single Crystal Growth and Evolution of Antiferromagnetic Correlated States
Transition‐metal dichalcogenides provide a versatile platform for the intercalation of magnetic ions in their van der Waals gaps, enabling tuning of correlated electronic and magnetic states. Despite extensive studies on sulfide‐based systems, Cr x NbSe 2 remains poorly understood due to scarcity of single‐crystals and uncertainties in structural analyses leading to contradictory reports on its magnetic behavior. Here, high‐quality single crystals of Cr 1/4 NbSe 2 via chemical vapor transport were synthesized, along with comprehensive investigation of chemical, structural, electronic, optical, electrical, and magnetic properties, supported by density‐functional theory calculations, presented for the first time. Single crystal x‐ray diffraction, scanning transmission electron microscopy, and selected area electron diffraction reveal ordered Cr intercalation forming a centrosymmetric 2 × 2 superlattice with hexagonal symmetry P 6 3 / mmc . Optical reflectivity indicates an enhanced electron scattering rate. DFT calculations predict antiferromagnetic ground state induced by Cr intercalation. Consistently, SQUID magnetometry and specific heat measurements hint a correlated antiferromagnetic state at T N ≈ 107 K, while resistivity measurements show metallic transport, with no signatures of superconductivity. Electron spin resonance suggests weak internal field which possibly arise from subtle magnetic anisotropy, undetectable in angle‐resolved magnetometry. These findings resolve longstanding inconsistencies and establish Cr 1/4 NbSe 2 as a benchmark vdW antiferromagnet for next‐generation spintronic and quantum materials.
- 4 October 2026
- Published by Wiley in Advanced Science
Open AccessCr 1/4 NbSe 2 ‐Single Crystal Growth and Evolution of Antiferromagnetic Correlated States
Transition‐metal dichalcogenides provide a versatile platform for the intercalation of magnetic ions in their van der Waals gaps, enabling tuning of correlated electronic and magnetic states. Despite extensive studies on sulfide‐based systems, Cr x NbSe 2 remains poorly understood due to scarcity of single‐crystals and uncertainties in structural analyses leading to contradictory reports on its magnetic behavior. Here, high‐quality single crystals of Cr 1/4 NbSe 2 via chemical vapor transport were synthesized, along with comprehensive investigation of chemical, structural, electronic, optical, electrical, and magnetic properties, supported by density‐functional theory calculations, presented for the first time. Single crystal x‐ray diffraction, scanning transmission electron microscopy, and selected area electron diffraction reveal ordered Cr intercalation forming a centrosymmetric 2 × 2 superlattice with hexagonal symmetry P 6 3 / mmc . Optical reflectivity indicates an enhanced electron scattering rate. DFT calculations predict antiferromagnetic ground state induced by Cr intercalation. Consistently, SQUID magnetometry and specific heat measurements hint a correlated antiferromagnetic state at T N ≈ 107 K, while resistivity measurements show metallic transport, with no signatures of superconductivity. Electron spin resonance suggests weak internal field which possibly arise from subtle magnetic anisotropy, undetectable in angle‐resolved magnetometry. These findings resolve longstanding inconsistencies and establish Cr 1/4 NbSe 2 as a benchmark vdW antiferromagnet for next‐generation spintronic and quantum materials.
- Open Access
Disentangling the unusual magnetic anisotropy of the near-room-temperature ferromagnet Fe$_{4}$GeTe$_{2}$
In the quest for two-dimensional conducting materials with high ferromagnetic ordering temperature the new family of the layered Fe$_{n}$GeTe$_{2}$ compounds, especially the near-room-temperature ferromagnet Fe$_{4}$GeTe$_{2}$, receives a significant attention. Fe$_{4}$GeTe$_{2}$ features a peculiar spin reorientation transition at $T_\mathrm{SR} \sim 110$ K suggesting a non-trivial temperature evolution of the magnetic anisotropy (MA) - one of the main contributors to the stabilization of the magnetic order in the low-D systems. An electron spin resonance (ESR) spectroscopic study reported here provides quantitative insights into the unusual magnetic anisotropy of Fe$_{4}$GeTe$_{2}$. At high temperatures the total MA is mostly given by the demagnetization effect with a small contribution of the counteracting intrinsic magnetic anisotropy of an easy-axis type, whose growth below a characteristic temperature $T_{\rm shape} \sim 150$ K renders the sample seemingly isotropic at $T_\mathrm{SR}$. Below one further temperature $T_{\rm d} \sim 50$ K the intrinsic MA becomes even more complex. Importantly, all the characteristic temperatures found in the ESR experiment match those observed in transport measurements, suggesting an inherent coupling between magnetic and electronic degrees of freedom in Fe$_{4}$GeTe$_{2}$. This finding together with the observed signatures of the intrinsic two-dimensionality should facilitate optimization routes for the use of Fe$_{4}$GeTe$_{2}$ in the magneto-electronic devices, potentially even in the monolayer limit.Open AccessDisentangling the unusual magnetic anisotropy of the near-room-temperature ferromagnet Fe$_{4}$GeTe$_{2}$
In the quest for two-dimensional conducting materials with high ferromagnetic ordering temperature the new family of the layered Fe$_{n}$GeTe$_{2}$ compounds, especially the near-room-temperature ferromagnet Fe$_{4}$GeTe$_{2}$, receives a significant attention. Fe$_{4}$GeTe$_{2}$ features a peculiar spin reorientation transition at $T_\mathrm{SR} \sim 110$ K suggesting a non-trivial temperature evolution of the magnetic anisotropy (MA) - one of the main contributors to the stabilization of the magnetic order in the low-D systems. An electron spin resonance (ESR) spectroscopic study reported here provides quantitative insights into the unusual magnetic anisotropy of Fe$_{4}$GeTe$_{2}$. At high temperatures the total MA is mostly given by the demagnetization effect with a small contribution of the counteracting intrinsic magnetic anisotropy of an easy-axis type, whose growth below a characteristic temperature $T_{\rm shape} \sim 150$ K renders the sample seemingly isotropic at $T_\mathrm{SR}$. Below one further temperature $T_{\rm d} \sim 50$ K the intrinsic MA becomes even more complex. Importantly, all the characteristic temperatures found in the ESR experiment match those observed in transport measurements, suggesting an inherent coupling between magnetic and electronic degrees of freedom in Fe$_{4}$GeTe$_{2}$. This finding together with the observed signatures of the intrinsic two-dimensionality should facilitate optimization routes for the use of Fe$_{4}$GeTe$_{2}$ in the magneto-electronic devices, potentially even in the monolayer limit. - Open Access
- 11 October 2025
- Published by Springer Nature in Applied Magnetic Resonance
- Vol. 56 (11) , 1507-1521
Ferromagnetic Resonance Spectroscopy on the Kagome Magnet MgMn$_{6}$Sn$_{6}$MgMn $$_{6}$$ Sn $$_{6}$$ is the itinerant ferromagnet on the kagome lattice with high ordering temperature featuring complex electronic properties due to the nontrivial topological electronic band structure where the spin–orbit coupling (SOC) plays a crucial role. Here, we report a detailed ferromagnetic resonance (FMR) spectroscopic study of MgMn $$_{6}$$ Sn $$_{6}$$ aimed to elucidate and quantify the intrinsic magnetocrystalline anisotropy that is responsible for the alignment of the Mn magnetic moments in the kagome plane. By analyzing the frequency, magnetic field, and temperature dependences of the FMR modes, we have quantified the magnetocrystalline anisotropy energy density that reaches the value of approximately $$3.5\cdot 10^{6}$$ erg/cm $$^{3}$$ at $$T = 3$$ K and reduces to about $$1\cdot 10^{6}$$ erg/cm $$^{3}$$ at $$T = 300$$ K. The revealed significantly strong magnetic anisotropy suggests a sizable contribution of the orbital magnetic moment to the spin magnetic moment of Mn, supporting the scenario of the essential role of SOC for the nontrivial electronic properties of MgMn $$_{6}$$ Sn $$_{6}$$ .- 11 October 2025
- Published by Springer Nature in Applied Magnetic Resonance
- Vol. 56 (11) , 1507-1521
Open AccessFerromagnetic Resonance Spectroscopy on the Kagome Magnet MgMn$_{6}$Sn$_{6}$MgMn $$_{6}$$ Sn $$_{6}$$ is the itinerant ferromagnet on the kagome lattice with high ordering temperature featuring complex electronic properties due to the nontrivial topological electronic band structure where the spin–orbit coupling (SOC) plays a crucial role. Here, we report a detailed ferromagnetic resonance (FMR) spectroscopic study of MgMn $$_{6}$$ Sn $$_{6}$$ aimed to elucidate and quantify the intrinsic magnetocrystalline anisotropy that is responsible for the alignment of the Mn magnetic moments in the kagome plane. By analyzing the frequency, magnetic field, and temperature dependences of the FMR modes, we have quantified the magnetocrystalline anisotropy energy density that reaches the value of approximately $$3.5\cdot 10^{6}$$ erg/cm $$^{3}$$ at $$T = 3$$ K and reduces to about $$1\cdot 10^{6}$$ erg/cm $$^{3}$$ at $$T = 300$$ K. The revealed significantly strong magnetic anisotropy suggests a sizable contribution of the orbital magnetic moment to the spin magnetic moment of Mn, supporting the scenario of the essential role of SOC for the nontrivial electronic properties of MgMn $$_{6}$$ Sn $$_{6}$$ . - Open Access
- 26 August 2025
- Published by Wiley in Advanced Functional Materials
- Vol. 36 (5)
Magnetic‐Field Tuning of the Spin Dynamics in the Quasi‐2D Van der Waals Antiferromagnet CuCrP 2 S 6
The use of antiferromagnets in magnetoelectronic devices as counterparts of ferromagnets is a new, rapidly developing trend in spintronics that leverages antiferromagnetic (AFM) magnons for transmitting of spin currents. Van der Waals (vdW) antiferromagnets are particularly attractive in this respect as they possess tunable magnetic properties and can be easily integrated into spintronic devices. In this work, electron spin resonance (ESR) spectroscopy is used to assess the potential of the vdW AFM compound CuCrP 2 S 6 for magnonic applications by exploring the magnetic field ( H ) dependence of the spectrum of magnon excitations below its AFM ordering temperature T N ≈ 30 K and the correlated spin dynamics above T N . ESR reveals prominent ferromagnetic (FM) spin correlations that persist far above T N suggesting an intrinsically 2D character of the spin dynamics in CuCrP 2 S 6 . Most interestingly, at T < T N , CuCrP 2 S 6 features two non‐degenerate, i.e., distinct in energy AFM magnon modes at H = 0 which can be tuned to the FM type of collective spin excitations with increasing H . These remarkable properties are favorable for the induction and control of unidirectional spin current in CuCrP 2 S 6 and suggest it as a new functional material for magnetoelectronics.
- 26 August 2025
- Published by Wiley in Advanced Functional Materials
- Vol. 36 (5)
Open AccessMagnetic‐Field Tuning of the Spin Dynamics in the Quasi‐2D Van der Waals Antiferromagnet CuCrP 2 S 6
The use of antiferromagnets in magnetoelectronic devices as counterparts of ferromagnets is a new, rapidly developing trend in spintronics that leverages antiferromagnetic (AFM) magnons for transmitting of spin currents. Van der Waals (vdW) antiferromagnets are particularly attractive in this respect as they possess tunable magnetic properties and can be easily integrated into spintronic devices. In this work, electron spin resonance (ESR) spectroscopy is used to assess the potential of the vdW AFM compound CuCrP 2 S 6 for magnonic applications by exploring the magnetic field ( H ) dependence of the spectrum of magnon excitations below its AFM ordering temperature T N ≈ 30 K and the correlated spin dynamics above T N . ESR reveals prominent ferromagnetic (FM) spin correlations that persist far above T N suggesting an intrinsically 2D character of the spin dynamics in CuCrP 2 S 6 . Most interestingly, at T < T N , CuCrP 2 S 6 features two non‐degenerate, i.e., distinct in energy AFM magnon modes at H = 0 which can be tuned to the FM type of collective spin excitations with increasing H . These remarkable properties are favorable for the induction and control of unidirectional spin current in CuCrP 2 S 6 and suggest it as a new functional material for magnetoelectronics.
- 1 August 2025
- Published by AIP Publishing in Review of Scientific Instruments
- Vol. 96 (8)
Cryogenic continuous-wave optical spectrometer for sub-THz frequencies
We present the design of a continuous-wave, highly sensitive optical spectrometer for millimeter-wave frequencies between 50 and 1000 GHz, with optimal performance at cryogenic temperatures. The spectrometer uses photomixing of near-infrared light to generate radiation over a wide frequency range, and the optical power absorbed by the sample is determined directly by measuring the sample temperature. This enables a dynamic range of up to 106 for the absorption coefficient below liquid-helium temperatures, making it suitable for measurements on highly reflective samples. The instrument can also be used in combination with high magnetic fields. In order to validate its performance, we measure the ferromagnetic resonance in the Mott insulator YTiO3, the electron spin resonance in a standard free-radical reference compound, and the antiferromagnetic resonance in a van der Waals magnetic material.
- 1 August 2025
- Published by AIP Publishing in Review of Scientific Instruments
- Vol. 96 (8)
Cryogenic continuous-wave optical spectrometer for sub-THz frequencies
We present the design of a continuous-wave, highly sensitive optical spectrometer for millimeter-wave frequencies between 50 and 1000 GHz, with optimal performance at cryogenic temperatures. The spectrometer uses photomixing of near-infrared light to generate radiation over a wide frequency range, and the optical power absorbed by the sample is determined directly by measuring the sample temperature. This enables a dynamic range of up to 106 for the absorption coefficient below liquid-helium temperatures, making it suitable for measurements on highly reflective samples. The instrument can also be used in combination with high magnetic fields. In order to validate its performance, we measure the ferromagnetic resonance in the Mott insulator YTiO3, the electron spin resonance in a standard free-radical reference compound, and the antiferromagnetic resonance in a van der Waals magnetic material.
- Open Access
- 2 September 2024
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 146 (36) , 25328-25342
Thirty Years of Hide-and-Seek: Capturing Abundant but Elusive MIII@C3v(8)-C82 Isomer, and the Study of Magnetic Anisotropy Induced in Dy3+ Ion by the Fullerene π-Ligand
Our knowledge about endohedral metallofullerenes (EMFs) is restricted to the structures with sufficient kinetic stability to be extracted from the arc-discharge soot and processed by chromatographic and structural techniques. For the most abundant rare-earth monometallofullerene MIII@C82, experimental studies repeatedly demonstrated C2v(9) and Cs(6) carbon cage isomers, while computations predicted equal stability of the "missing" C3v(8) isomer. Here we report that this isomer is indeed formed but has not been recovered from soot using standard protocols. Using a combination of redox extraction and subsequent benzylation and trifluoromethylation with single-crystal XRD analysis of CF3 adduct, we prove that Dy@C3v(8)-C82 is one of the most abundantly produced metallofullerenes, which was not identified in earlier studies because of the low kinetic stability. Further, using the Dy@C3v(8)-C82(CF3) and Dy@C3v(8)-C82(CH2Ph) monoadducts for the case study, we analyzed the role of metal-fullerene bonding on the single-ion magnetic anisotropy of Dy in EMFs. The multitechnique approach, combining ab initio calculations, EPR spectroscopy, and SQUID magnetometry, demonstrated that coordination of the Dy ion to the fullerene cage induces moderate, nonaxial, and very fluid magnetic anisotropy, which strongly varies with small alterations in the Dy-fullerene coordination geometry. As a result, Dy@C3v(8)-C82(CH2Ph) is a weak field-induced single-molecule magnet (SMM), whose signatures of magnetic relaxation are detectable only below 3 K. Our results demonstrate that metal-cage interactions should have a detrimental effect on the SMM performance of EMFs. At the same time, the strong variability of the magnetic anisotropy with metal position suggests tunability and offers strategies for future progress.
- 2 September 2024
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 146 (36) , 25328-25342
Open AccessThirty Years of Hide-and-Seek: Capturing Abundant but Elusive MIII@C3v(8)-C82 Isomer, and the Study of Magnetic Anisotropy Induced in Dy3+ Ion by the Fullerene π-Ligand
Our knowledge about endohedral metallofullerenes (EMFs) is restricted to the structures with sufficient kinetic stability to be extracted from the arc-discharge soot and processed by chromatographic and structural techniques. For the most abundant rare-earth monometallofullerene MIII@C82, experimental studies repeatedly demonstrated C2v(9) and Cs(6) carbon cage isomers, while computations predicted equal stability of the "missing" C3v(8) isomer. Here we report that this isomer is indeed formed but has not been recovered from soot using standard protocols. Using a combination of redox extraction and subsequent benzylation and trifluoromethylation with single-crystal XRD analysis of CF3 adduct, we prove that Dy@C3v(8)-C82 is one of the most abundantly produced metallofullerenes, which was not identified in earlier studies because of the low kinetic stability. Further, using the Dy@C3v(8)-C82(CF3) and Dy@C3v(8)-C82(CH2Ph) monoadducts for the case study, we analyzed the role of metal-fullerene bonding on the single-ion magnetic anisotropy of Dy in EMFs. The multitechnique approach, combining ab initio calculations, EPR spectroscopy, and SQUID magnetometry, demonstrated that coordination of the Dy ion to the fullerene cage induces moderate, nonaxial, and very fluid magnetic anisotropy, which strongly varies with small alterations in the Dy-fullerene coordination geometry. As a result, Dy@C3v(8)-C82(CH2Ph) is a weak field-induced single-molecule magnet (SMM), whose signatures of magnetic relaxation are detectable only below 3 K. Our results demonstrate that metal-cage interactions should have a detrimental effect on the SMM performance of EMFs. At the same time, the strong variability of the magnetic anisotropy with metal position suggests tunability and offers strategies for future progress.
- Open Access
Electron Spin Resonance Spectroscopy on Magnetic Van der Waals Compounds
The field of research on magnetic van der Waals compounds -- a special subclass of quasi-two-dimensional materials -- is currently rapidly expanding due to the relevance of these compounds to fundamental research where they serve as a playground for the investigation of different models of quantum magnetism and also in view of their unique magneto-electronic and magneto-optical properties pertinent to novel technological applications. The Electron Spin Resonance (ESR) spectroscopy plays an important role in the exploration of the rich magnetic behavior of van der Waals compounds due to its high sensitivity to magnetic anisotropies and unprecedentedly high energy resolution that altogether enable one to obtain thorough insights into the details of the spin structure in the magnetically ordered state and the low-energy spin dynamics in the ordered and paramagnetic phases. This article provides an overview of the recent achievements in this field made by the ESR spectroscopic techniques encompassing representatives of antiferro- and ferromagnetic van der Waals compounds of different crystal structures and chemical composition as well as of a special category of these materials termed magnetic topological insulators.
Open AccessElectron Spin Resonance Spectroscopy on Magnetic Van der Waals Compounds
The field of research on magnetic van der Waals compounds -- a special subclass of quasi-two-dimensional materials -- is currently rapidly expanding due to the relevance of these compounds to fundamental research where they serve as a playground for the investigation of different models of quantum magnetism and also in view of their unique magneto-electronic and magneto-optical properties pertinent to novel technological applications. The Electron Spin Resonance (ESR) spectroscopy plays an important role in the exploration of the rich magnetic behavior of van der Waals compounds due to its high sensitivity to magnetic anisotropies and unprecedentedly high energy resolution that altogether enable one to obtain thorough insights into the details of the spin structure in the magnetically ordered state and the low-energy spin dynamics in the ordered and paramagnetic phases. This article provides an overview of the recent achievements in this field made by the ESR spectroscopic techniques encompassing representatives of antiferro- and ferromagnetic van der Waals compounds of different crystal structures and chemical composition as well as of a special category of these materials termed magnetic topological insulators.