Condensed Matter Physics (Experiment)
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Condensed Matter Physics (Experiment)

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Physics 70th anniversary of JINR
DOI: 10.54546/NaturalSciRev.200804

Radiation-induced surface smoothing and structural relaxation in electron-irradiated ZnS and ZnSe crystals

The evolution of surface morphology and structural parameters in ZnS and ZnSe crystals under highenergy electron irradiation was investigated using a phenomenological modeling approach based on experimentally obtained irradiation-dependent structural and morphological data. The analysis focused on the fluence dependence of the surface roughness parameters R a and R z , coherent-domain size, and lattice parameter in the electron fluence range of (0−2.5) · 10 17 electrons/cm 2 . It was found that the surface roughness parameters R a and R z decrease according to an exponential law, indicating the occurrence of radiation-induced surface smoothing. A phenomenological kinetic equation describing roughness relaxation as a function of electron fluence was proposed and solved analytically. The obtained model demonstrates that the smoothing rate is proportional to the excess surface roughness relative to the limiting relaxed state. In contrast, the coherent-domain size generally increases with increasing fluence, whereas the lattice parameter decreases nearly linearly, indicating radiation-induced structural relaxation, lattice compaction, and defect rearrangement processes. Comparative analysis of ZnS and ZnSe crystals revealed differences in the smoothing kinetics and structural evolution parameters, which may be associated with differences in defect mobility and irradiation-assisted relaxation processes. Correlations were observed between the fluence-dependent evolution of surface roughness and bulk structural parameters, indicating concurrent morphological and structural changes under electron irradiation. The proposed phenomenological description provides a framework for comparing these irradiation-induced responses in ZnS and ZnSe crystals.
M. Yu. Tashmetov, B. N. Madaminov
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Physics
DOI: 10.54546/NaturalSciRev.100704

Temperature-dependent conformational changes of amyloid-β42 in DPPC bilayers

The conformational behavior of the amyloid- β 42 (A β 42) peptide is strongly influenced by the physical state of its surrounding lipid environment. The effect of temperature on the A β 42 structure within dipalmitoylphosphatidylcholine (DPPC) bilayers was investigated using circular dichroism (CD), Raman spectroscopy, and molecular dynamics (MD) simulations. The study examined two thermal phases: room temperature (RT =∼ (25±2)◦C), corresponding to the gel phase of DPPC, and (48±2)◦C, representing the fluid phase above the lipid transition temperature . The CD spectroscopy measurements indicated a clear temperature-dependent structural transition of the peptide. At RT, A β 42 exhibited a conformation enriched in β structures, while at (48±2)◦C, the spectra revealed a notable increase in α -helical content, reflecting enhanced backbone organization under fluid-phase conditions. Raman spectral analysis supported this trend by demonstrating an increased contribution of α -helical components accompanied by a reduction in β -strand features upon heating. Minor variations in lipid vibrational markers further suggested greater acyl-chain flexibility and bilayer fluidity in the high-temperature state. Furthermore, MD simulations revealed enhanced α-helical content and deeper peptide insertion within the disordered bilayer compared with the ordered gel phase. The findings from experimental and computational investigations demonstrate that membrane fluidization above the DPPC phase transition favors α-helical stabilization of A β 42, emphasizing temperature as a key parameter governing peptide–lipid conformational equilibria. The results obtained provide a fundamental framework for understanding how thermal conditions modulate amyloid-membrane interactions, which is essential for elucidating the early molecular events associated with amyloid-related pathologies.
Khlood A. A. Abdeljawaad, Yersultan Arynbek , Kahramon Mamatkulov, Huy Le Duc, Grigory Arzumanyan
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Physics 70th anniversary of JINR
DOI: 10.54546/NaturalSciRev.200702

Structural, magnetic states and pressure-induced phenomena in complex nanosized magnetic oxides

The results of the recent investigations of the crystal and magnetic structure of complex nanosized manganese and iron oxides using neutron diffraction, X-ray diffraction and other techniques over a wide range of thermodynamic parameters (temperature and pressure) are considered. In the nanostructured manganites La 1-x Sr x MnO 3 ( x = 0.28−0.47), the coexistence of the ferromagnetic (FM) and A-type antiferromagnetic (AFM) states has been evidenced, implying the production of core-shell nanoparticles with distinctive structural and magnetic properties of ordering of internal and external components. Application of high pressure significantly modifies the ratio of FM and AFM components. For the nanostructured Zn 0.34 Fe 2.53 O 4 ferrite, a distribution of Zn and Fe atoms in the crystal structure, as well as the parameters of crystal and magnetic structures, have been estimated. The oxygen vacancies were detected and their amount was estimated. The gradual transition of the structural phase from the initial cubic spinel phase to the orthorhombic post spinel phase was observed at high pressures in this material, relevant to CoFe 2 O 4 ferrite. In the latter case, the phase transition is also accompanied by suppression of the ordered magnetic moments. Surprisingly, in the most cases, the properties of structural and magnetic states of the studied nanosized manganites and ferrites are notably different from those for the relevant bulk forms of these materials. The microscopic mechanisms responsible for this distinction have been discussed in detail. Corrected: 24 April 2026 (the incorrect order of the authors and the affiliation of one of them were corrected)
D. P. Kozlenko, N. M. Belozerova, S. E. Kichanov, E. V. Lukin, O. N. Lis, A. V. Rutkauskas, B. N. Savenko, Z. Jirák, G. S. Rymski, A. L. Zhaludkevich, N. T. Dang
Physics Life Sciences
DOI: 10.54546/NaturalSciRev.100202

Lipid membrane destabilization induced by amyloid-beta peptide in the systems mimicking preclinical Alzheimer’s disease

The amyloid-beta peptide (Aβ peptide) is proposed to play a central role in the onset of Alzheimer’s disease (AD). The pathology is associated with the fast accumulation of neurotoxic amyloid aggregates in brain tissues, though the fundamentals of the disease’s progression remain unsolved. It is noted that the preclinical stage of AD may play a crucial role in its further irreversible development. Namely, interactions between lipid membranes and Aβ-peptide molecules incorporated therein at relatively low concentrations should be under a close attention. In this review, we discuss recent works devoted to studying the lipid peptide interactions with a specific focus on the lipid membrane reorganizations caused by Aβ (25–35) peptide in the preclinical AD mimicking conditions. The interactions observed are believed to be important in understanding the mechanisms of the Aβ-peptide destructive effects on lipid membranes and the corresponding onset of the disease. The methods of applied nuclear physics have proven remarkably relevant in such research. The scattering methods provided instrumental information on a level of supramolecular assemblies, while spectrometry allowed obtaining information on the molecular level. Finally, molecular dynamics simulations provided details unachievable by experimental approaches, though the validation role of the latter cannot be undermined. Altogether, the recent advances in research results prove these complementary approaches the most appropriate for tackling the complex issues of biomembrane interactions.
Sergei A. Kurakin, Dr. Oleksandr I. Ivankov, Dr. Tatiana N. Murugova, Dina R. Badreeva, Dr. Ermuhammad B. Dushanov, Dr. Elena V. Ermakova, Dr. Alexander I. Kuklin, Dr. Norbert Kučerka