ABSTRACT
g-C3N4 is introduced to the PEO electrolyte as a mediator to stabilize the interface to lithium metal anode. As a result, the interface resistance is stabilized after cycling and the symmetric cell exhibits a cycle life over 900 h, indicating that the interface stability is evidently promoted.
ABSTRACT
Metallic lithium is considered as the ultimate anode material for lithium-based batteries due to its highest energy density. However, as an anode, commercial Li metal foils are too thick, with a large amount of trouble to balance its exorbitant areal capacity with common cathodes in full cells. Here, a new chemical thinning strategy is proposed via a simple surface dissolving reaction between lithium and naphthalene, which enables scalable, continuous, and roll-to-roll preparation of ultrathin Li foil. A Li foil less than 15 µm with a clean surface can be successfully obtained within 20 min. The thinning rate and thickness of the lithium foil can be easily adjusted by changing the concentration, temperature, and operation mode. The produced Li-Naph solution after thinning can also be used as a multifunctional reagent of great value, and the Li ions in the final waste solution can be further extracted in the form of Li2CO3, showing superior lithium atom economy of our strategy.
ABSTRACT
The rational design and preparation of hierarchical hollow structures have promising potential in electrochemical energy storage systems. In this paper, double-shell hollow carbon fibers (DSHCFs) with tunable thickness and shell spacing are prepared using hollow electrospun polystyrene fibers as the hard template and in situ coated polypyrrole as the carbon source. The as-prepared DSHCFs with an optimized structure exhibit a submicrometer shell spacing and a nanoscaled shell thickness, which guarantees sufficient contact area with the electrolyte and provides abundant electrochemical active sites for Li+ storage. Owing to the unique structural advantages, a DSHCF-based anode shows favorable transport kinetics for both Li+ ions and electrons during the lithiation/delithiation process, and a high reversible capacity of 348 mAh g-1 at 5.0 A g-1 is well maintained even after 500 cycles with no obvious capacity attenuation. Particular emphasis is given to kinetic Li+ storage mechanisms in DSHCFs that are discussed in detail, providing a new avenue for developing high-performance carbon materials for the practical application of energy storage devices.
ABSTRACT
The emerging generation of flexible energy storage devices has accelerated the research pace in terms of new materials, new processing techniques, and new designs that can meet the demands of mechanical stability upon bending or stretching at an acceptable cost, without compromising their electrochemical performance. Among the materials currently explored, biomass-derived materials have received extensive attention, because they are renewable, low in cost, earth-abundant and structurally diverse. This review is focused on fundamentals and applications of the bio-derived material bacterial cellulose (BC) in flexible electrochemical energy storage systems. Specifically, recent advances are summarized in the utilization of BC in stretchable substrates, carbonaceous species, and scaffolds for flexible core component construction. Finally, several perspectives related to BC-based materials for flexible electrochemical energy storages are proposed, aiming to provide possible future research directions in these fields.
