Extending The Calendar Life of Fiber Lithium-Ion Batteries to 200 Days with Ultra-High Barrier Polymer Tubes.

Scalable fiber lithium-ion batteries (FLIBs) have garnered significant attention due to huge potential applications in wearable technology. However, their widespread applications have been limited by inadequate cycle and calendar life, primarily due to the high permeability of the encapsulation layer to water vapor in ambient air. To address this challenge, an ultra-high barrier composite tube is developed by blending polytrifluorochloroethylene (PCTFE) with organically modified montmorillonite (OMMT) for the continuous packaging of FLIBs. Due to the high crystallinity (≈40.21%) and small free volume (103.443 Å3), the PCTFE tube exhibited a low water vapor transmission rate (WVTR) of 0.123 mg day-1 pkg-1. Furthermore, through the melt extrusion, OMMT with its plate-like morphology are fully exfoliated and dispersed within the PCTFE matrix. This created more complex pathways for water, increasing the diffusion path length and thereby reducing WVTR to 0.006 mg day-1 pkg-1. This innovation enabled an ultra-long calendar life of 200 days and cycle life of 870 cycles for FLIBs, with over 80% capacity retention in ambient air. Additionally, 2%OMMT-PCTFE-FLIBs exhibited excellent flexibility, retaining an impressive 85.31% capacity after 10 000 bending cycles. This research presents a simple yet effective approach to enhance the lifetime and practicality of FLIBs through building a high-performance polymer-based encapsulation layer.

High-performance fibre battery with polymer gel electrolyte.

Replacement of liquid electrolytes with polymer gel electrolytes is recognized as a general and effective way of solving safety problems and achieving high flexibility in wearable batteries1-6. However, the poor interface between polymer gel electrolyte and electrode, caused by insufficient wetting, produces much poorer electrochemical properties, especially during the deformation of the battery7-9. Here we report a strategy for designing channel structures in electrodes to incorporate polymer gel electrolytes and to form intimate and stable interfaces for high-performance wearable batteries. As a demonstration, multiple electrode fibres were rotated together to form aligned channels, while the surface of each electrode fibre was designed with networked channels. The monomer solution was effectively infiltrated first along the aligned channels and then into the networked channels. The monomers were then polymerized to produce a gel electrolyte and form intimate and stable interfaces with the electrodes. The resulting fibre lithium-ion battery (FLB) showed high electrochemical performances (for example, an energy density of about 128 Wh kg-1). This strategy also enabled the production of FLBs with a high rate of 3,600 m h-1 per winding unit. The continuous FLBs were woven into a 50 cm × 30 cm textile to provide an output capacity of 2,975 mAh. The FLB textiles worked safely under extreme conditions, such as temperatures of -40 °C and 80 °C and a vacuum of -0.08 MPa. The FLBs show promise for applications in firefighting and space exploration.

Sheet-Like Stacking SnS2/rGO Heterostructures as Ultrastable Anodes for Lithium-Ion Batteries.

SnS2-based materials have attracted considerable attention in energy storage and conversion owing to their high lithium activity and theoretical capacity. However, the practical application is severely limited by the low coulombic efficiency and short cycle life due to irreversible side reactions, low conductivity, and serious pulverization in the discharge/charge process. In this study, sheet-like stacking SnS2/reduced graphene oxide (rGO) heterostructures were developed using a facile solvothermal method. It was found that the composites between SnS2 nanoplates and rGO nanosheets are closely coupled through van der Waals interactions, providing efficient electron/ion paths to ensure high electrical conductivity and sufficient buffer space to alleviate volume expansion. Therefore, the SnS2/rGO heterostructure anode can obtain a high capacity of 840 mA h g-1 after 120 cycles at a current density of 200 mA g-1 and maintain a capacity of 450 mA h g-1 after 1000 cycles at 1000 mA g-1. In situ X-ray diffraction tests showed that SnS2/rGO undergoes typical initial intercalation, conversion, and subsequent alloying reactions during the first discharge, and most of the reactions are dealloying/alloying in the subsequent cycles. The galvanostatic intermittent titration technique showed that the diffusion of lithium ions in the SnS2/rGO heterostructures is faster in the intercalation and conversion reactions than in the alloying reactions. These observations help to clarify the reaction mechanism and ion diffusion behavior in the SnS2 anode materials, thus providing valuable insights for improving the energy efficiency of lithium-ion batteries.

Sandwich-like SnS2/graphene multilayers for efficient lithium/sodium storage.

2D materials have attracted extensive attention in energy storage and conversion due to their excellent electrochemical performances. Herein, we report utilization of monolayer SnS2 sheets within SnS2/graphene multilayers for efficient lithium and sodium storage. SnS2/graphene multilayers are synthesized through a solution-phase direct assembly method by electrostatic interaction between monolayer SnS2 and PDDA (polydimethyl diallyl ammonium chloride)-graphene nanosheets. It has been shown that the SnS2/graphene multilayer electrode has a large pseudocapacity contribution for enhanced lithium and sodium storage. Typical batteries deliver a stable reversible capacity of ∼160 mA h g-1 at 2 A g-1 after 2000 cycles for lithium and a stable reversible capacity of ∼142 mA h g-1 at 1 A g-1 after 1000 cycles for sodium. The excellent electrochemical performances of SnS2/graphene multilayers are attributed to the synergistic effect between the monolayer SnS2 sheets and the PDDA-graphene nanosheets. The multilayer structure assembled by different monolayer nanosheets is promising for the further development of 2D materials for energy storage and conversion.