Electrochromic windows with fast response and wide dynamic range for visible-light modulation without traditional electrodes.

Electrochromic (EC) devices represent an emerging energy-saving technology, exhibiting the capability to dynamically modulate light and heat transmittance. Despite their promising potential, the commercialization of EC devices faces substantial impediments such as high cost, intricate fabrication process, and low optical contrast inherent in conventional EC materials relying on the ion insertion/extraction mechanism. In this study, we introduce an innovative "electrode-free" electrochromic (EC) device, termed the EECD, which lacks an EC-layer on the electrodes during device assembling and in the bleached state.

Heterointerfaces: Unlocking Superior Capacity and Rapid Mass Transfer Dynamics in Energy Storage Electrodes.

Heterogeneous electrode materials possess abundant heterointerfaces with a localized "space charge effect", which enhances capacity output and accelerates mass/charge transfer dynamics in energy storage devices (ESDs). These promising features open new possibilities for demanding applications such as electric vehicles, grid energy storage, and portable electronics. However, the fundamental principles and working mechanisms that govern heterointerfaces are not yet fully understood, impeding the rational design of electrode materials.

The Influence of Ions on the Electrochemical Stability of Aqueous Electrolytes.

The electrochemical stability window of water is known to vary with the type and concentration of dissolved salts. However, the underlying influence of ions on the thermodynamic stability of aqueous solutions has not been fully understood. Here, we investigated the electrolytic behaviors of aqueous electrolytes as a function of different ions.

Reversible Cl/Cl redox in a spinel MnO electrode.

A unique prospect of using halides as charge carriers is the possibility of the halides undergoing anodic redox behaviors when serving as charge carriers for the charge-neutrality compensation of electrodes. However, the anodic conversion of halides to neutral halogen species has often been irreversible at room temperature due to the emergence of diatomic halogen gaseous products. Here, we report that chloride ions can be reversibly converted to near-neutral atomic chlorine species in the MnO electrode at room temperature in a highly concentrated chloride-based aqueous electrolyte.

Electrolyte Interphases in Aqueous Batteries.

The narrow electrochemical stability window of water poses a challenge to the development of aqueous electrolytes. In contrast to non-aqueous electrolytes, the products of water electrolysis do not contribute to the formation of a passivation layer on electrodes. As a result, aqueous electrolytes require the reactions of additional components, such as additives and co-solvents, to facilitate the formation of the desired solid electrolyte interphase (SEI) on the anode and cathode electrolyte interphase (CEI) on the cathode.

Dynamically Adaptive Bubbling for Upgrading Oxygen Evolution Reaction Using Lamellar Fern-Like Alloy Aerogel Self-Standing Electrodes.

Adopting renewable electricity to produce "green" hydrogen has been a critical challenge because at a high current density the mass transfer capability of most catalytic electrodes deteriorates significantly. Herein, a unique lamellar fern-like alloy aerogel (LFA) electrode, showing a unique dynamically adaptive bubbling capability and can effectively avoid stress concentration caused by bubble aggregation is reported. The LFA electrode is intrinsically highly catalytic-active and shows a highly porous, resilient, hierarchically ordered, and well-percolated conductive network.

Li MnO : A Catalyst for a Liquid Cl Electrode in Low-Temperature Aqueous Batteries.

Li MnO has been contemplated as a high-capacity cathode candidate for Li-ion batteries; however, it evolves oxygen during battery charging under ambient conditions, which hinders a reversible reaction. However, it is unclear if this irreversible process still holds under subambient conditions. Here, the low-temperature electrochemical properties of Li MnO in an aqueous LiCl electrolyte are evaluated and a reversible discharge capacity of 302 mAh g at a potential of 1.

Strengthening Aqueous Electrolytes without Strengthening Water.

Aqueous electrolytes typically suffer from poor electrochemical stability; however, eutectic aqueous solutions-25 wt.% LiCl and 62 wt.% H PO -cooled to -78 °C exhibit a significantly widened stability window.

Microbial inactivation of milk by low intensity direct current electric field: Inactivation kinetics model and milk characterization.

Microbial inactivation by pulsed electric field (PEF) has been studied widely although with high operational risk, while few studies on the potential of low intensity electric fields for microbial inactivation have been reported. In this study, the feasibility of inactivating microorganisms in milk by low intensity direct current (DC) electric field was investigated. Then a kinetics model was proposed based on the inactivation curves.

Reversible Copper Cathode for Nonaqueous Dual-Ion Batteries.

Most reported cathodes of nonaqueous dual-ion batteries (DIBs) host anions via insertion reactions. It is necessary to explore new cathode chemistry to increase the battery energy density. To date, transition metals have yet to be investigated for nonaqueous DIBs, albeit they may offer high capacity in anodic conversion reactions.

Anticatalytic Strategies to Suppress Water Electrolysis in Aqueous Batteries.

Aqueous electrolytes are the leading candidate to meet the surging demand for safe and low-cost storage batteries. Aqueous electrolytes facilitate more sustainable battery technologies due to the attributes of being nonflammable, environmentally benign, and cost effective. Yet, water's narrow electrochemical stability window remains the primary bottleneck for the development of high-energy aqueous batteries with long cycle life and infallible safety.

Polymorph Evolution Mechanisms and Regulation Strategies of Lithium Metal Anode under Multiphysical Fields.

Lithium (Li) metal, a typical alkaline metal, has been hailed as the "holy grail" anode material for next generation batteries owing to its high theoretical capacity and low redox reaction potential. However, the uncontrolled Li plating/stripping issue of Li metal anodes, associated with polymorphous Li formation, "dead Li" accumulation, poor Coulombic efficiency, inferior cyclic stability, and hazardous safety risks (such as explosion), remains as one major roadblock for their practical applications. In principle, polymorphous Li deposits on Li metal anodes includes smooth Li (film-like Li) and a group of irregularly patterned Li (, whisker-like Li (Li whiskers), moss-like Li (Li mosses), tree-like Li (Li dendrites), and their combinations).

Exploration of the form factors of turbulence kinetic energy transfer for shear exfoliation of graphene.

Mass production of defect-free and large-lateral-size 2D materials via cost-effective methods is very important. Recently, shear exfoliation has shown great promise for large-scale production due to its simple operation, environmental-benignity and wide adaptability. However, a long-standing challenge is that with the production of more nanosheets, a ceiling yield and shattered products are encountered, which significantly limits their wider application.

Polypyrrole coated δ-MnO nanosheet arrays as a highly stable lithium-ion-storage anode.

Manganese dioxide (MnO) with a conversion mechanism is regarded as a promising anode material for lithium-ion batteries (LIBs) owing to its high theoretical capacity (∼1223 mA h g) and environmental benignity as well as low cost. However, it suffers from insufficient rate capability and poor cyclic stability. To circumvent this obstacle, semiconducting polypyrrole coated-δ-MnO nanosheet arrays on nickel foam (denoted as MnO@PPy/NF) are prepared via hydrothermal growth of MnO followed by the electrodeposition of PPy on the anode in LIBs.