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تسجيل مستخدم جديدNeutron Scattering Signature of Phonon Renormalization in Nickel (II) Oxide
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The physics of mutual interaction of phonon quasiparticles with electronic spin degrees of freedom, leading to unusual transport phenomena of spin and heat, has been a subject of continuing interests for decades. Understanding phonon properties in the context of spin-phonon coupling is essential for engineering functional phononic and spintronic devices. By means of inelastic neutron scattering and first-principle calculations, anomalous scattering spectral intensity from acoustic phonon was identified in the exemplary collinear antiferromagnetic nickel (II) oxide, unveiling strong correlations between spin and lattice degrees of freedom that renormalize the polarization of acoustic phonon. Anomalously large spectral intensity from acoustic phonons observed at small momentum transfer decays with increasing temperature and is successfully modeled with a modified magneto-vibrational scattering cross section, suggesting the presence of phonon driven of spin precession. On the other hand, TA phonon intensity that are forbidden by the scattering geometry is observed at a wide span of momentum transfer, suggesting a renormalization of phonon eigenvector.
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Nickel oxide (NiO) has been studied extensively for various applications ranging from electrochemistry to solar cells [1,2]. In recent years, NiO attracted much attention as an antiferromagnetic (AF) insulator material for spintronic devices [3-10].
Understanding the spin - phonon coupling in NiO is a key to its functionalization, and enabling AF spintronics promise of ultra-high-speed and low-power dissipation [11,12]. However, despite its status as an exemplary AF insulator and a benchmark material for the study of correlated electron systems, little is known about the spin - phonon interaction, and the associated energy dissipation channel, in NiO. In addition, there is a long-standing controversy over the large discrepancies between the experimental and theoretical values for the electron, phonon, and magnon energies in NiO [13-23]. This gap in knowledge is explained by NiO optical selection rules, high Neel temperature and dominance of the magnon band in the visible Raman spectrum, which precludes a conventional approach for investigating such interaction. Here we show that by using ultraviolet (UV) Raman spectroscopy one can extract the spin - phonon coupling coefficients in NiO. We established that unlike in other materials, the spins of Ni atoms interact more strongly with the longitudinal optical (LO) phonons than with the transverse optical (TO) phonons, and produce opposite effects on the phonon energies. The peculiarities of the spin - phonon coupling are consistent with the trends given by density functional theory calculations. The obtained results shed light on the nature of the spin - phonon coupling in AF insulators and may help in developing innovative spintronic devices.
We report results of an investigation of the temperature dependence of the magnon and phonon frequencies in NiO. A combination of Brillouin - Mandelstam and Raman spectroscopies allowed us to elucidate the evolution of the phonon and magnon spectral
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Sodium niobate (NaNbO3) exhibits most complex sequence of structural phase transitions in perovskite family and therefore provides as excellent model system for understanding the mechanism of structural phase transitions. We report temperature depend
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The development of new electrochromic materials and devices, like smart windows, has an enormous impact on the energy efficiency of modern society. One of the crucial materials in this technology is nickel-oxide. Ni-deficient NiO shows anodic electro
chromism whose mechanism is still under debate. Using DFT+U calculations, we show that Ni vacancy generation results in the formation of hole polarons localised at the two oxygens next to the vacancy. Upon Li insertion or injection of an extra electron into Ni-deficient NiO, one hole gets filled, and the hole bipolaron is converted into a hole polaron well-localized at one O atom. Furthermore, the calculated absorption coefficients demonstrate that Li insertion/extraction or rather the addition/removal of an extra electron into Ni-deficient NiO can lead to switching between the oxidized (colored) and the reduced (bleached) states. Hence, our results suggest a new mechanism of Ni-deficient NiO electrochromism not related to the Ni2+/Ni3+ transition but based on the formation and annihilation of hole polarons in oxygen p-states.
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