Ion transport in crystalline fast ionic conductors is a complex physical phenomenon. Certain ionic species (e.g., Ag+, Cu+, Li+, F–, O2–, H+) in a solid crystalline framework can move as fast as in liquids. This property, although only observed in a limited number of materials, is a key enabler for a broad range of technologies, including batteries, fuel cells, and sensors. However, the mechanisms of ion transport in the crystal lattice of fast ionic conductors are still not fully understood despite the substantial progress achieved in the last 40 years, partly because of the wide range of length and time scales involved in the complex migration processes of ions in solids. Without a comprehensive understanding of these ion transport mechanisms, the rational design of new fast ionic conductors is not possible. In this review, we cover classical and emerging characterization techniques (both experimental and computational) that can be used to investigate ion transport processes in bulk crystalline inorganic materials which exhibit predominant ion conduction (i.e., negligible electronic conductivity) with a primary focus on literature published after 2000 and critically assess their strengths and limitations. Together with an overview of recent understanding, we highlight the need for a combined experimental and computational approach to study ion transport in solids of desired time and length scales and for precise measurements of physical parameters related to ion transport.

This work demonstrates a simple‐structured, low‐cost magnetically modulated micromotor of MnFe2O4 pot‐like hollow microparticles as well as its facile, versatile, and large‐scale growing‐bubble‐templated nanoparticle (NP) assembly fabrication approach. In this approach, the hydrophobic MnFe2O4@oleic acid NPs in an oil droplet of chloroform and hexane assembled into a dense NP shell layer due to the hydrophobic interactions between the NP surfaces. With the encapsulated oil continuously vaporizing into high‐pressured gas bubbles, the dense MnFe2O4 NP shell layer then bursts, forming an asymmetric pot‐like MnFe2O4 micromotor by creating a single hole in it. For the as‐developed simple pot‐like MnFe2O4 micromotor, the catalytically generated O2 molecules nucleate and grow into bubbles preferentially on the inner concave surface rather than on the outer convex surface, resulting in continuous ejection of O2 bubbles from the open hole to propel it. Dexterously integrating the high catalytic activity for H2O2 decomposition to produce O2 bubbles, excellent magnetic property with the instinctive surface hydrophobicity, the MnFe2O4 pot‐like micromotor not only can autonomously move in water media with both velocity and direction modulated by external magnetic field but also can directly serve for environmental oil removal without any further surface modification. The results here may inspire novel practical micromotors.

As economically viable alternatives to lithium-ion batteries, magnesium-ion-based all-solid-state batteries have been researched to meet the criteria for an ideal energy storage device.

In this work, we propose and demonstrate a dynamic colloidal molecule that is capable of moving autonomously and performing swift, reversible, and in-place assembly dissociation in a high accuracy by manipulating a TiO/Pt Janus micromotor with light irradiation. Due to the efficient motion of the TiO/Pt Janus motor and the light-switchable electrostatic interactions between the micromotor and colloidal particles, the colloidal particles can be captured and assembled one by one on the fly, subsequently forming into swimming colloidal molecules by mimicking space-filling models of simple molecules with central atoms. The as-demonstrated dynamic colloidal molecules have a configuration accurately controlled and stabilized by regulating the time-dependent intensity of UV light, which controls the stop-and-go motion of the colloidal molecules. The dynamic colloidal molecules are dissociated when the light irradiation is turned off due to the disappearance of light-switchable electrostatic interaction between the motor and the colloidal particles. The strategy for the assembly of dynamic colloidal molecules is applicable to various charged colloidal particles. The simulated optical properties of a dynamic colloidal molecule imply that the results here may provide a novel approach for in-place building functional microdevices, such as microlens arrays, in a swift and reversible manner.

From the discovery of the first fast ionic conductor silver iodide in the early 20th century to the recent discovery of lithium fast ionic conductors with ionic conductivities surpassing those of liquid electrolytes, high ionic conductivity σ has often been associated with low activation energy Ea following the Arrhenius equation. However, the Meyer–Neldel rule (MNR) indicates that the Ea and prefactor σ0 are correlated, suggesting the relation between the Ea and σ is, in fact, complex. In this perspective, the use of the Meyer–Neldel–conductivity plot and a critical descriptor, Meyer–Neldel energy Δ0, to guide the search for fast ionic conductors is proposed. Reported lithium, sodium, and magnesium ionic conductors are categorized into three types, depending on the relative magnitude between the Δ0 and thermal energy (kBT) at the application temperature. The process by which σ can be optimized by tuning Ea for these types of ionic conductors is elaborated. This principle can be widely applied to all ionic conductors that obey the MNR at any application temperature. Furthermore, a pressure‐tuning approach to measure the Δ0 rapidly is developed. These findings establish a previously missing step for designing new ionic conductors with improved ionic conductivity.