“Medium-entropy” highly disordered amorphous Li garnets, with ≥4 unique local bonding units (LBUs), hold promise for use as solid-state electrolytes in hybrid or all-solid-state batteries owing to their grain-boundary-free nature and low-temperature synthesis requirement. Through this work, we resolved the local structure of amorphous Li garnet and understood their implication for Li dynamics. These medium-entropy amorphous structures possess unique characteristics with edge- and face-sharing LBUs, not conforming to the classic Zachariasen glass formation rules, and can be synthesized in a wide but processing-friendly temperature range (<680°C). Within these amorphous structures, Li and Zr are identified as the network formers and La as network modifier, with maxima in Li dynamics observed for smaller Li–O and Zr–O coordination; this structure understanding serves as a baseline for identifying additional network formers to further modulate Li transport. Our insight provides fundamental guidelines for the structure and phase design for amorphous Li garnets and paves the way for their integration in next-generation batteries.

This research investigates the feasibility of magnetic ion exchange (MIEX) resin as the adsorbent for the removal of chlorite through a laboratory study using batch adsorption experiments. The agitation speed of 100 rpm is the optimum agitation intensity. The removal efficiency of chlorite increases with increasing dosage of MIEX resin. The optimum pH is 5–7. The coexisting anions and natural organic matter reduce the removal efficiency of chlorite. The kinetic process at the low chlorite concentration (1.02 mg/L) is highly possible to be pseudo-first-order. However, the pseudo-second-order model can fit the kinetic data quite well at higher chlorite concentrations (2.28–5.57 mg/L). At the initial stage of adsorption, the intra-particle diffusion is the rate-limiting step, but the adsorption rate is controlled by the film diffusion and the intra-particle diffusion after 10 min. The adsorption equilibrium can be approximately attained within 40 min, and Redlich–Peterson isotherm model fits best to the equilibrium data. The adsorption is a thermodynamically feasible, spontaneous, and endothermic ion-exchange process. The removal of chloride on MIEX resin is an ion-exchange mechanism. Dissolved organic carbon can be removed effectively as well as chlorite and chlorate using MIEX resin in real water. Therefore, MIEX resin is a promising technology for the removal of chlorite from aqueous solution.