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Xiong, Peixun; Bai, Panxing; Li, Ang; Li, Benfang; Cheng, Mingren; Chen, Yiping; Huang, Shuping; Jiang, Qiang; Bu, Xian‐He; Xu, Yunhua
Advanced materials (Weinheim), 11/2019, Letnik: 31, Številka: 48Journal Article
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. A Bi nanoparticle@carbon composite is synthesized by a facile heating method from a commercial product of bismuth citrate. Superior sodium storage performance with ultralong cycle life of 30 000 cycles at 8 A g−1 and ultrahigh rate capability of 71% capacity retention at 60 A g−1 are obtained. Full cells by coupling with a well‐developed cathode also deliver impressive capacity and cyclability.
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