Bismuth has emerged as a promising anode material for sodium‐ion batteries (SIBs), owing to its high capacity and suitable operating potential. However, large volume changes during alloying/dealloying processes lead to poor cycling performance. Herein, bismuth nanoparticle@carbon (Bi@C) composite is prepared via a facile annealing method using a commercial coordination compound precursor of bismuth citrate. The composite has a uniform structure with Bi nanoparticles embedded within a carbon framework. The nanosized structure ensures a fast kinetics and efficient alleviation of stress/strain caused by the volume change, and the resilient and conductive carbon matrix provides an interconnected electron transportation pathway. The Bi@C composite delivers outstanding sodium‐storage performance with an ultralong cycle life of 30 000 cycles at a high current density of 8 A g−1 and an excellent rate capability of 71% capacity retention at an ultrahigh current rate of 60 A g−1. Even at a high mass loading of 11.5 mg cm−2, a stable reversible capacity of 280 mA h g−1 can be obtained after 200 cycles. More importantly, full SIBs by pairing with a Na3V2(PO4)3 cathode demonstrates superior performance. Combining the facile synthesis and the commercial precursor, the exceptional performance makes the Bi@C composite very promising for practical large‐scale applications.

Lithium–sulfur batteries are regarded as one of the most promising candidates for next‐generation rechargeable batteries. However, the practical application of lithium–sulfur (Li–S) batteries is seriously impeded by the notorious shuttling of soluble polysulfide intermediates, inducing a low utilization of active materials, severe self‐discharge, and thus a poor cycling life, which is particularly severe in high‐sulfur‐loading cathodes. Herein, a polysulfide‐immobilizing polymer is reported to address the shuttling issues. A natural polymer of Gum Arabic (GA) with precise oxygen‐containing functional groups that can induce a strong binding interaction toward lithium polysulfides is deposited onto a conductive support of a carbon nanofiber (CNF) film as a polysulfide shielding interlayer. The as‐obtained CNF–GA composite interlayer can achieve an outstanding performance of a high specific capacity of 880 mA h g−1 and a maintained specific capacity of 827 mA h g−1 after 250 cycles under a sulfur loading of 1.1 mg cm−2. More importantly, high reversible areal capacities of 4.77 and 10.8 mA h cm−2 can be obtained at high sulfur loadings of 6 and even 12 mg cm−2, respectively. The results offer a facile and promising approach to develop viable lithium–sulfur batteries with high sulfur loading and high reversible capacities.

Red phosphorus (P) has been recognized as a promising storage material for Li and Na. However, it has not been reported for K storage and the reaction mechanism remains unknown. Herein, a novel nanocomposite anode material is designed and synthesized by anchoring red P nanoparticles on a 3D carbon nanosheet framework for K-ion batteries (KIBs). The red P@CN composite demonstrates a superior electrochemical performance with a high reversible capacity of 655 mA h g at 100 mA g and a good rate capability remaining 323.7 mA h g at 2000 mA g , which outperform reported anode materials for KIBs. The transmission electron microscopy and theoretical calculation results suggest a one-electron reaction mechanism ofP + K + e → KP, corresponding to a theoretical capacity of 843 mA h g ,which is the highest value for anode materials investigated for KIBs. The study not only sheds light on the rational design of high performance red P anodes for KIBs but also offers a fundamental understanding of the potassium storage mechanism of red P.

A SnO2-coated carbon fiber mat is fabricated and used to guide uniform K nucleation/deposition for dendrite free K metal anodes.

Organic electrode materials free of rare transition metal elements are promising for sustainable, cost‐effective, and environmentally benign battery chemistries. However, severe shuttling effect caused by the dissolution of active materials in liquid electrolytes results in fast capacity decay, limiting their practical applications. Here, using a gel polymer electrolyte (GPE) that is in situ formed on Nafion‐coated separators, the shuttle reaction of organic electrodes is eliminated while maintaining the electrochemical performance. The synergy of physical confinement by GPE with tunable polymer structure and charge repulsion of the Nafion‐coated separator substantially prevents the soluble organic electrode materials with different molecular sizes from shuttling. A soluble small‐molecule organic electrode material of 1,3,5‐tri(9,10‐anthraquinonyl)benzene demonstrates exceptional electrochemical performance with an ultra‐long cycle life of 10 000 cycles, excellent rate capability of 203 mAh g−1 at 100 C, and a wide working temperature range from −70 to 100 °C based on the solid–liquid conversion chemistry, which outperforms all previously reported organic cathode materials. The shielding capability of GPE can be designed and tailored toward organic electrodes with different molecular sizes, thus providing a universal resolution to the shuttling effect that all soluble electrode materials suffer.