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Lead halide perovskites are promising for spintronics due to their strong spin-orbit coupling (SOC). Experiments show asymmetric, temperature-dependent spin relaxation in γ-CsPbI, with electrons relaxing faster than holes via the Elliott-Yafet carrier-phonon mechanism. non-adiabatic molecular dynamics with SOC and half-electron correction reproduce this asymmetry. The difference arises from band-edge orbital character: the conduction band minimum (CBM) is Pb-p-dominated and spin-mixed under SOC, while the valence band maximum remains spin-pure due to s-type Pb and I p orbitals. Spin mixing in the CBM leads to a smaller spin mismatch and stronger non-adiabatic couplings, accelerating electron spin relaxation. Lower temperatures extend spin lifetimes by reducing carrier-phonon interactions. In contrast, elevated temperatures enhance lattice disorder and spin state mixing, increasing wave function overlap and non-adiabatic couplings, thereby speeding up spin relaxation. This work offers atomistic insight into asymmetric and temperature-dependent spin dynamics, influencing spintronic device design through thermal and structural control.
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http://dx.doi.org/10.1021/acs.jpclett.5c01534 | DOI Listing |
Magn Reson Chem
September 2025
Institute of Scientific and Industrial Research, Osaka University, Osaka, Japan.
We reveal contrasting behaviors in molecular motion between the two materials, including the identification of resonance-enhanced dynamic features in elastomers. We present a depth-resolved analysis of molecular dynamics in semicrystalline polytetrafluoroethylene (PTFE) and fully amorphous fluorinated elastomer (SIFEL) films using static-gradient solid-state F NMR imaging. By measuring spin-lattice relaxation rates ( ) at multiple frequencies and evaluating the corresponding spectral density functions, we reveal distinct dynamic behaviors between the two materials.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Masaryk University, Faculty of Science, Department of Chemistry, Kotlářská 2, Brno, 611 37, Czech Republic.
Structural and magnetic properties of ultra-small tetrahedron-shaped iron oxide nanoparticles were investigated using density functional theory. Tetrahedral and truncated tetrahedral models were considered in both non-functionalized form and with surfaces passivated by pseudo-hydrogen atoms. The focus on these two morphologies reflects their experimental relevance at this size scale and the feasibility of performing fully relaxed, atomistically resolved first-principles simulations.
View Article and Find Full Text PDFMagn Reson Lett
November 2024
Sorbonne Université, CNRS, Laboratoire de Chimie de la Matière Condensée de Paris, LCMCP, UMR 7574, 75005 Paris, France.
Elastomer blends, among which natural rubber (NR) and butadiene rubber (BR), are involved in many components of the automotive/tire industry. A comprehensive understanding of their mechanical behavior requires, among other features, a detailed description of the cross-link density in these mixtures. In the case of vulcanized immiscible blends, the distribution of the cross-link density within each of the NR- and BR-rich domains is key information, but difficult to determine using the conventional approaches used for one-component cross-linked elastomers.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemical Sciences, Tezpur University, Napaam 784028, Sonitpur, Assam, India.
Reaction of [Mn(salophen)Cl] {salophen = -phenylenediamine bis(salicylidenaminato)} with a tricyano Fe(III) precursor complex, [Fe(bbp)(CN)] {Hbbp = bis(2-benzimidazolyl)pyridine}, affords a dinuclear cyano-bridged heterometallic Mn-(μ-NC)-Fe fragment in the complex salt [Mn(salophen)(HO)][Mn(salophen)(HO)(μ-NC)Fe(bbp)(CN)]·4HO (1). The title compound shows field-induced slow relaxation of magnetization below 2.8 K.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Chemistry and Biochemistry, School of Materials Science and Engineering, Center for Organic Photonics and Electronics, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Molecular spin systems that can be chemically tuned, coherently controlled, and readily integrated within devices remain central to the realization of emerging quantum technologies. Organic high-spin materials are prime candidates owing to their similarity in electronic structure to leading solid-state defect-based systems, light element composition, and the potential for entanglement and qubit operations mediated through spin-spin exchange. However, the inherent instability of these species precludes their rational design, development, and application.
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