Tunable Microwave Dielectric Properties in Rare-Earth Niobates via a High-Entropy Configuration Strategy To Induce Ferroelastic Phase Transition

In this study, (La0.2Nd0.2Sm0.2Ho0.2Y0.2)­(Nb1–xVx)­O4 (0.1 ≤ x ≤ 0.4) ceramics were prepared using a high-entropy strategy via the solid-phase method. The crystal structure, microstructure, vibration modes, and phase transition were studied by X-ray diffraction, scanning electron microscopy/transmission electron microscopy (SEM/TEM), and Raman spectroscopy techniques. The phase of ceramics was confirmed to be a monoclinic fergusonite in the range of x ≤ 0.28, a tetragonal scheelite was in the range of 0.3 ≤ x ≤ 0.32, a complex phase of tetragonal scheelite, and zircon was observed in the ceramics when x ≥ 0.35. A zircon phase was also detected by TEM at x = 0.4. The ceramic at x = 0.25 exhibited outstanding temperature stabilization with εr = 18.06, Q × f = 56,300 GHz, and τf = −1.52 ppm/°C, while the x = 0.2 ceramic exhibited a low dielectric loss with εr = 18.14, Q × f = 65,200 GHz, and τf = −7.96 ppm/°C. Moreover, the permittivity, quality factor, and the temperature coefficient of resonance frequency were related to the polarizability, packing fraction, density, and the temperature coefficient of permittivity caused by phase transition. This is an effective method to regulate near-zero τf by the synergism of the high-entropy strategy and substituting Nb with V in LnNbO4 ceramics

An anti-aging polymer electrolyte for flexible rechargeable zinc-ion batteries

Polymer electrolytes have been extensively applied in zinc-ion batteries, especially those based on hydrogels; however, the densification of the hydrogel electrolytes during cycling affects the durability, resulting in capacity attenuation. It is revealed in this work that the surface electrical resistance of hydrogels is particularly affected by the aging effect. Hence, an adhesive bonding solid polymer electrolyte (ABSPE) for zinc-ion batteries was developed exhibiting significantly enhanced anti-aging properties, where the surface resistance remains constant for over 200 hours, twice that of conventional hydrogel electrolytes. For the hydrogel electrolyte, the surface resistance only remains constant for less than 100 hours which is half of the time achieved by the ABSPE. The ionic conductivity increases with plasticizer loading, reaching 3.77 × 10?4 S cm?1. The kinetic mechanism probed in this work revealed a diffusion-controlled mechanism for Zn/ABSPE/?-MnO2 instead of a capacitive dominated process in the hydrogel electrolyte. In addition, a flexible device was fabricated using a carbon fibre-reinforced polymer composite; this device showed superior power supply performance even under twisting, cutting and bending conditions.</p