Aqueous sodium‐ion battery of low cost, inherent safety, and environmental benignity holds substantial promise for new‐generation energy storage applications. However, the narrow potential window of water and the enlarged ionic radius because of hydration restrict the selection of electrode materials used in the aqueous electrolyte. Here, inspired by the efficient redox reaction of biomolecules during cellular energy metabolism, a proof of concept is proposed that the redox‐active biomolecule alizarin can act as a novel electrode material for the aqueous sodium‐ion battery. It is demonstrated that the specific capacity of the self‐assembled alizarin nanowires can reach as high as 233.1 mA h g−1, surpassing the majority of anodes ever utilized in the aqueous sodium‐ion batteries. Paired with biocompatible and biodegradable polypyrrole, this full battery system shows excellent sodium storage ability and flexibility, indicating its potential applications in wearable electronics and biointegrated devices. It is also shown that the electrochemical properties of electrodes can be tailored by manipulating naturally occurring 9,10‐anthroquinones with various substituent groups, which broadens application prospect of biomolecules in aqueous sodium‐ion batteries.
Elemental 2D materials with fascinating characteristics are regarded as an influential portion of the 2D family. Iodine is as a typical monoelemental molecular crystal and exhibits great prospects of applications. To realize 2D iodine, not only is it required to separate the weak interlayer van der Waals interactions, but also to reserve the weak intramolecular halogen bonds; thus, 2D iodine is still unexploited until now. Herein, atomically thin iodine nanosheets (termed “iodinene”) with the thickness around 1.0 nm and lateral sizes up to hundreds of nanometers are successfully fabricated by a liquid‐phase exfoliation strategy. When used for the cathode of rechargeable sodium‐ion batteries, the ultrathin iodinene exhibits superb rate properties with a high specific capacity of 109.5 mA h g−1 at the high rate of 10 A g−1 owing to its unique 2D ultrathin architecture with remarkably enhanced pseudocapacitive behavior. First‐principles calculations reveal that the diffusion of sodium ions in few‐layered iodinene changes from the original horizontal direction in bulk to the vertical with a small energy barrier of 0.07 eV because of the size effect. The successful preparation and intensive structural investigation of iodinene paves the way for the development of novel iodine‐based science and technologies.
Uncontrollable growth of lithium (Li) dendrite has severely hindered the development of Li metal anodes, while separator modification is regarded as a simple and effective way to mitigate the growth of Li dendrite. However, the "drop-dregs" phenomenon of coating layer desquamated from polyolefin separator due to their different Young's modulus would induce a nonuniform Li ionic flux, finally resulting in deteriorative electrochemical performance and even thermal runaway of the battery. Herein, we introduce a novel nanopile mechanical interlocking strategy to create delamination-free separator modification, which could stably generate a homogeneous Li ionic flux to guide long-term uniform Li deposition. Both experimental and simulation results demonstrate a strong bonding strength between the coating layer and membrane matrix based on this physical interlocking mechanism. Consequently, with a nearly dendrite-free Li deposition and a largely reduced interface impedance, 1000 h stable cycling of Li/Li half cells enrolled this modified separator is successfully achieved. Also, a significant improvement in Li/LiFePO 4 full cells in long-term cycling stability to 500 cycles further indicates its promising practical potential. Moreover, this presented approach without any binding agents or surface activation procedures could be facilely scaled up, providing an applicable and durable separator modification solution toward stable Li metal anodes.
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