阳极
双金属片
纳米材料
材料科学
锂(药物)
纳米颗粒
电化学
化学工程
碳纤维
硫化物
热解
介电谱
复合数
纳米技术
化学
电极
金属
复合材料
冶金
内分泌学
工程类
物理化学
医学
作者
Feijiang Chen,Chengwei Deng,Yang Chen,Yaru Li,Dong Yan,Yu Su,Sailong Xu
标识
DOI:10.1007/s00339-021-05151-y
摘要
Long-cycling of anode nanomaterials is crucial for promoting lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) towards the further practical applications. Anode nanomaterials, such as transition-metal sulfides (TMSs), are conventionally prepared via sulfuration with additional conventional sulfur sources. Herein, we prepare bimetallic sulfide (Co0.83Fe0.17)9S8 nanoparticles confined within coral-like N,S co-doped carbon scaffolds ((Co0.83Fe0.17)9S8/N,S–C) as anode nanomaterials for LIBs and SIBs, without introducing additional sulfur source. The (Co0.83Fe0.17)9S8/N,S–C composite is eco-synthesized by direct pyrolysis of a mixture of metanilic acid intercalated CoFe-LDH and acid yellow 49 (AY49), thus endowed with the integrated advantageous features: bimetallic (Co0.83Fe0.17)9S8, N,S co-doped carbon scaffold (14.2 wt%), the appropriate specific surface area and mesoporous structure. The electrochemical testing demonstrates that the composite exhibits a reversible capacity of 948.8 mAh g–1 after 80 cycles at 0.1 A g–1 for LIBs, and a decent reversible capacity of 392.9 mAh g–1 after 50 cycles at 0.1 A g–1 for SIBs, which are both superior to those of the Co9S8/N,S–C counterpart. The enhancement is supported by the result of low charge resistance determined by electrochemical impedance spectroscopy. Our results may provide an eco-efficient synthetic method for the preparation of TMSs for energy storage.
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