Phase Stability and Mechanical Properties of the Monoclinic, Monoclinic-Prime and Tetragonal REMO4 (M = Ta, Nb) from First-Principles Calculations

YTaO4 and the relevant modification are considered to be a promising new thermal barrier coating. In this article, phase stability and mechanical properties of the monoclinic (M), monoclinic-prime (M′), and tetragonal (T) REMO4 (M = Ta, Nb) are systematically investigated from first-principles calculations method based on density functional theory (DFT). Our calculations show that M′-RETaO4 is the thermodynamically stable phase at low temperatures, but the stable phase is a monoclinic structure for RENbO4. Moreover, the calculated relative energies between M (or M′) and T phases are inversely proportional to the ionic radius of rare earth elements. It means that the phase transformation temperature of M′→T or M→T could decrease along with the increasing ionic radius of RE3+, which is consistent with the experimental results. Besides, our calculations exhibit that adding Nb into the M′-RETaO4 phase could induce phase transformation temperature of M′→M. Elastic coefficient is attained by means of the strain-energy method. According to the Voigt–Reuss–Hill approximation method, bulk modulus, shear modulus, Young’s modulus, and Poisson’s ratio of T, M, and M’ phases are obtained. The B/G criterion proposed by Pugh theory exhibits that T, M, and M’ phases are all ductile. The hardness of REMO4 (M = Ta, Nb) phases are predicted based on semi-empirical equations, which is consistent with the experimental data. Finally, the anisotropic mechanical properties of the REMO4 materials have been analyzed. The emerging understanding provides theoretical guidance for the related materials development.

Sequential Cesium Incorporation for Highly Efficient Formamidinium-Cesium Perovskite Solar Cells

Although pure formamidinium iodide perovskite (FAPbI3) possesses an optimal gap for photovoltaics, their poor phase stability limits the long-term operational stability of the devices. A promising approach to enhance their phase stability is to incorporate cesium into FAPbI3. However, state-of-the-art formamidinium-cesium (FA-Cs) iodide perovskites demonstrate much worse efficiency compared with FAPbI3, limited by different crystallization dynamics of formamidinium and cesium, which result in poor composition homogeneity and high trap densities. We develop a novel strategy of crystallization decoupling processes of formamidinium and cesium via a sequential cesium incorporation approach. As such, we obtain highly reproducible and highly efficient solar cells based on FA1-xCsxPbI3 films, with uniform composition distribution and low defect densities. In addition, our cesium-incorporated perovskites demonstrate much enhanced stability compared with FAPbI3, as a result of suppressed ionic migration due to reduced electron-phonon coupling.