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Induced by an ultra-short laser pulse, the electronic structure of a material undergoes strong modifications leading to a fast demagnetization in magnetic materials. Induced spin-flip transitions are one of the reasons for demagnetization, that is associated in the literature with a Stoner-like mechanism. On the other hand, demagnetization due to transverse spin fluctuations is usually discussed on the basis of the Heisenberg Hamiltonian and hardly accounts for the modification of the electronic structure. In this work we demonstrate a strong impact of the laser-induced electron transitions, both spin-flip and spin-conserving, on the exchange coupling parameters. For this, a simple two-step scheme is suggested. As a first step, the electronic structure time evolution during the ultra-short laser pulse is described accurately within time-dependent density-functional theory calculations. As a next step, the information on the time-dependent electronic structure is used for calculations of the parameters of the Heisenberg Hamiltonian. A strong modification of the exchange coupling parameters is found on the femtosecond time scale as a consequence of the depopulation of the electronic states in response to the applied ultra-short laser pulse. Due to the relatively slow attenuation of these changes after the laser pulse, taking place on the subpicosecond/picosecond time scale, we expect an appreciable impact on the magnon energies and that way on the demagnetization/relaxation processes. The same concerns the spin-lattice interactions playing a central role for the relaxation process. A strong impact of the laser-induced modification of the electronic structure on the spin-lattice coupling parameters is also shown in this work.
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http://dx.doi.org/10.1088/1361-648X/adf1ce | DOI Listing |
J Phys Chem Lett
September 2025
Tianjin Key Laboratory of Film Electronic and Communication Devices, School of Integrated Circuit Science and Engineering, Tianjin University of Technology, Tianjin 300384, China.
Achieving UVA/B-selective, skin-inspired nociceptors with perception and blockade functions at the single-unit device level remains challenging. This is because the device necessitates distinct components for every performance metric, thereby leading to complex preparation processes and restricted performance, as well as the absence of deep UV (UVB and below)-selective semiconductors. Here, to address this, we develop a structure-simplification skin-inspired nociceptor using a reverse type-II CuAgSbI/MoS heterostructure.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
State Key Laboratory of Reliability and Intelligence of Electrical Equipment, Hebei University of Technology, Tianjin 300401, P. R. China.
Quantum dots (QDs) converted to micro light-emitting diodes (LEDs) have emerged as a promising technology for next-generation display devices. However, their commercial application has been hindered by the susceptibility of QDs to photodegradation when directly exposed to an open environment. Here, we develop functional ligand zinc bis[2-(methacryloyloxy)ethyl] phosphate (Zn(BMEP)) to passivate QD surface anions through a phosphine-mediated surface reaction.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry and Protein Research Center for Bio-Industry, Hankuk University of Foreign Studies, Yongin 17035, Republic of Korea.
The nanoscale environment within the void spaces of metal-organic frameworks (MOFs) can significantly influence the photoredox catalytic activity of encapsulated visible-light photoredox catalysts (PCs). To compare two isostructural PC@In-MOF systems, three cationic Ru(II) polypyridine complexes were successfully encapsulated within the mesoscale channels of the anionic framework of InTATB (HTATB = 4,4',4''--triazine-2,4,6-triyltribenzoic acid), which features a doubly interpenetrated framework structure. This encapsulation yielded three heterogenized visible-light PCs, RuL@InTATB, where L = 2,2'-bipyridine (bpy), 1,10-phenanthroline (phen), or 2,2'-bipyrazine (bpz).
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
Faculty of Chemistry, Wrocław University of Science and Technology, Wyb. Wyspiańskiego 27, PL-50370 Wrocław, Poland.
Computer simulations play an essential role in the interpretation of experimental multiphoton absorption spectra. In addition, models derived from theory allow for the establishment of "structure-property" relationships. This work contributes to these efforts and presents the results of an analysis of two- and three-photon absorptions for a set comprising 450 conjugated molecules performed at the CAM-B3LYP/aug-cc-pVDZ level.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
Perovskite materials have revolutionized optoelectronics by virtue of their tunable bandgaps, exceptional optoelectronic properties, and structural flexibility. Notably, the state-of-the-art performance of perovskite solar cells has reached 27%, making perovskite materials a promising candidate for next-generation photovoltaic technology. Although numerous reviews regarding perovskite materials have been published, the existing reviews generally focus on individual material systems (e.
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