Bacterial Cellulose Applications in Electrochemical Energy Storage Devices.

Bacterial cellulose (BC) is produced via the fermentation of various microorganisms. It has an interconnected 3D porous network structure, strong water-locking ability, high mechanical strength, chemical stability, anti-shrinkage properties, renewability, biodegradability, and a low cost. BC-based materials and their derivatives have been utilized to fabricate advanced functional materials for electrochemical energy storage devices and flexible electronics.

Work-Function-Induced Interfacial Electron/Ion Transport in Carbon Hosts toward Dendrite-Free Lithium Metal Anodes.

Coupled electron/ion transport is a decisive feature of Li plating/stripping, wherein the compatibility of electron/ion transport rates determines the morphology of deposited Li. Local Li hotspots form due to inhomogeneous interfacial charge transfer and lead to uncontrolled Li deposition, which decreases the Li utilization rate and safety of Li metal anodes. Herein, we report a method to obtain dendrite-free Li metal anodes by driving electron pumping and accumulating and boosting Li ion diffusion by tuning the work function of a carbon host using cobalt-containing catalysts.

Reshaping Zinc Plating/Stripping Behavior by Interfacial Water Bonding for High-Utilization-Rate Zinc Batteries.

Aqueous zinc batteries have emerged as promising energy storage devices; however, severe parasitic reactions lead to the exacerbated production of Zn dendrites that decrease the utilization rate of Zn anodes. Decreasing the electrolyte content and regulating the water activity are efficient means to address these issues. Herein, this work shows that limiting the aqueous electrolyte and bonding water to bacterial cellulose (BC) can suppress side reactions and regulate stable Zn plating/stripping.

Fatigue-Resistant Interfacial Layer for Safe Lithium Metal Batteries.

The plating/stripping of Li dendrites can fracture the static solid electrolyte interphase (SEI) and cause significant dynamic volume variations in the Li anode, which give rise to poor cyclability and severe safety hazards. Herein, a tough polymer with a slide-ring structure was designed as a self-adaptive interfacial layer for Li anodes. The slide-ring polymer with a dynamically crosslinked network moves freely while maintaining its toughness and fracture resistance, which allows it can to dissipate the tension induced by Li dendrites on the interphase layer.

Recent Progress in Designing Stable Composite Lithium Anodes with Improved Wettability.

Lithium (Li) is a promising battery anode because of its high theoretical capacity and low reduction potential, but safety hazards that arise from its continuous dendrite growth and huge volume changes limit its practical applications. Li can be hosted in a framework material to address these key issues, but methods to encage Li inside scaffolds remain challenging. The melt infusion of molten Li into substrates has attracted enormous attention in both academia and industry because it provides an industrially adoptable technology capable of fabricating composite Li anodes.

A Fe/Fe3O4/N-carbon composite with hierarchical porous structure and in situ formed N-doped graphene-like layers for high-performance lithium ion batteries.

A Fe/Fe3O4/N-carbon composite consisting of a porous carbon matrix containing a highly conductive N-doped graphene-like network and Fe/Fe3O4 nanoparticles was prepared. The porous carbon has a hierarchical structure which is inherited from rice husk and the N-doped graphene-like network formed in situ. When used as an anode material for lithium batteries, the composite delivered a reversible capacity of approximately 610 mA h g(-1) at a current density of 200 mA g(-1) even after 100 cycles, due to the synergism between the unique hierarchical porous structures, highly electrically conductive N-doped graphene-like networks and nanosized particles of Fe/Fe3O4.

Catalytic role of Ge in highly reversible GeO2/Ge/C nanocomposite anode material for lithium batteries.

GeO2/Ge/C anode material synthesized using a simple method involving simultaneous carbon coating and reduction by acetylene gas is composed of nanosized GeO2/Ge particles coated by a thin layer of carbon, which is also interconnected between neighboring particles to form clusters of up to 30 μm. The GeO2/Ge/C composite shows a high capacity of up to 1860 mAh/g and 1680 mAh/g at 1 C (2.1 A/g) and 10 C rates, respectively.

Diffusion and kinetics of solvent-free reaction between molecular crystals by time-resolved powder UV-Vis reflection spectrum.

Traditionally, chemical reaction between solids has been considered to typically occur on a geological time scale without the benefit of high temperature, due to diffusion block in the solids. However, recent advancements have revealed that many solvent-free reactions between molecular crystals can quickly occur at room or near-room temperature. These reactions have raised a novel scientific question as to how the reactive species can overcome the diffusion-controlled kinetic limitations under such moderate conditions.