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Abstract Topological spin textures (e.g., skyrmions) can be stabilized by interfacial Dzyaloshinskii‐Moriya interaction (DMI) in the magnetic multilayer, which has been intensively studied. Recently, Bloch‐type magnetic skyrmions stabilized by composition gradient‐induced DMI (g‐DMI) have been observed in 10‐nm thick CoPt single layer. However, magnetic anisotropy in gradient‐composition engineered CoPt (g‐CoPt) films is highly sensitive to both the relative Co/Pt composition and the film thickness, leading to a complex interplay with g‐DMI. The stability of skyrmions under the combined influence of magnetic anisotropy and g‐DMI is crucial yet remains poorly understood. Here, we condcut a systematic study on the characteristics of magnetic skyrmions as a function of gradient polarity and effective gradient (defined as gradient/thickness) in g‐CoPt single layers (thickness of 10–30 nm) using magnetic force microscopy (MFM), bulk magnetometry, and topological Hall effect measurements. Brillouin light scattering spectroscopy confirms that both the sign and magnitude of g‐DMI depend on the polarity and amplitude of the composition gradient in g‐CoPt films. MFM reveals that skyrmion size and density vary with g‐CoPt film thickness, gradient polarity, and applied magnetic field. An increased skyrmion density is observed in samples exhibiting higher magnetic anisotropy, in agreement with micromagnetic simulations and energy barrier calculations. 

The widespread utilization of perovskite-based photovoltaics requires probing both the structural and optical properties under extreme operating conditions to gain a holistic understanding of the material behavior under stressors. Here, we investigate the temperature-dependent behavior of mixed A-site cation lead triiodide perovskite thin films (85% methylammonium and 15% formamidinium) in the range from 300 to 20 K. Through a combination of optical and structural techniques, we find that the tetragonal-to-orthorhombic phase transition occurs at ∼110 K for this perovskite composition, as indicated by the change in the diffraction pattern. With decreasing temperature, the quantum yield increases with a concurrent elongation of the carrier lifetimes, indicating suppression of nonradiative recombination pathways. Interestingly, in contrast to single A-site cation perovskites, an additional optical transition appears in the absorption spectrum when the phase transition is approached, which is also reflected in the emission spectrum. We propose that the splitting of the optical absorption and emission is due to local segregation of the mixed cation perovskite during the phase transition. 

Temperatures below ambient room temperature (298 K) are ideal for perovskite-sensitized upconversion devices where maximum efficiency is reached at 170 K. Here, the underlying triplet diffusion rate governs the overall upconversion dynamics.