The band-edge emission of CsPb₂Br₅ was located at 385 nm, not in the visible range as reported in the literature.

The coupling between magnetic and electric subsystems in composites of ferromagnetic and ferroelectric phases is a product property that is facilitated by mechanical strain that arises due to magnetostriction and the piezoelectric effect in the constituent phases. Such multiferroic composites are of immense interests for studies on the physics of electromagnetic coupling and for use in a variety of applications. Here, we focus on magneto-electric (ME) coupling in nanocomposites. Particular emphasis is on core-shell particles and coaxial fibers, thin film heterostructures, and planar structures with a variety of mechanical connectivity. A brief review of models that predict strong ME effects in nanostructures is followed by synthesis and characterization. Core-shell particulate composites can be prepared by hydrothermal processes and chemical or deoxyribonucleic acid-assisted assembly. Electrospinning techniques have been utilized to prepare defect free core-shell nanofibers. Core-shell particles and fibers can be assembled into superstructures with the aid of magnetic and electric fields and characterized for possible use in advanced technologies. Chemical-vapor deposition techniques have been shown to be effective for the preparation of heterostructures of ferrites and ferroelectrics. Exotic planar multiferroic structures with potential for enhancing ME coupling strengths are also considered. Scanning probe microscopy techniques are ideal for probing the nature of direct- and converse-ME coupling in individual nanostructures. Magnetoelectric characterization of assemblies of nanocomposites can be done by ME voltage coefficient, magnetic field induced polarization, and magneto-dielectric effects. We conclude with a brief discussion on possible avenues for strengthening the product properties in the nanocomposites.

Perovskite solar cells have attracted great attention in recent years, due to their high conversion efficiency and solution-processable fabrication. However, most of the solar cells with high efficiency in the literature are prepared employing TiO₂ as electron transport material, which needs sintering at a temperature higher than 450 °C, and is not applicable to flexible device and low-cost fabrication. Herein, the MAPbI₃ perovskite solar cells are fabricated at a low temperature of 150 °C with SnO₂ as the electron transport layer. By dropping the antisolvent of ethyl acetate onto the perovskite precursor films during the spin coating process, compact MAPbI₃ films without pinholes are obtained. The addition of ethyl acetate is found to play an important role in regulating the nucleation, which subsequently improves the compactness of the film. The quality of MAPbI₃ films are further improved significantly through Ostwald recrystallization by optimizing the thermal treatment. The crystallinity is enhanced, the grain size is enlarged, and the defect density is reduced. Accordingly, the prepared MAPbI₃ perovskite solar cell exhibits a record-high conversion efficiency, outstanding reproducibility, and stability, owing to the reduced electron recombination. The average and best efficiency reaches 19.2% and 20.3%, respectively. The device without encapsulation maintains 94% of the original efficiency after storage in ambient air for 600 h.