石墨烯
材料科学
阳极
电解质
化学工程
纳米技术
电极
化学
工程类
物理化学
作者
Bochao Chen,Jiawei Ding,Xiangren Bai,Hanwen Zhang,Ming Liang,Shan Zhu,Chunsheng Shi,Liying Ma,Enzuo Liu,Naiqin Zhao,Fang He,Wei Zhou,Chunnian He
标识
DOI:10.1002/adfm.202109899
摘要
Abstract Resource‐rich FeS 2 is a promising anode for potassium‐ion batteries (PIBs). However, polysulfides emerge due to FeS 2 conversion during discharging, which dissolve into the ether‐based electrolyte and cause the continuous capacity degradation in PIBs. To address the polysulfides dissolution in PIBs, a graphene–shell‐encapsulated FeS 2 is fabricated and embedded in N/S codoped 3D hollow carbon spheres. As a protective pocket, the graphene–shell can effectively accommodate polysulfides inside the core–shell, inhibiting the polysulfides shuttle effect to enhance cycle stability of electrode. The density functional theory (DFT) calculations demonstrate that graphene–shells have a strong adsorption capacity for polysulfides, and the interfacial interaction between KFeS 2 and graphene–shell can boost the K ion mobility. As a result, the composite exhibits superior‐rate properties (524 and 224 mA h g −1 at 0.1 and 8 A g −1 , respectively) and long‐term cycle stability. This work demonstrates the promotion and protective effect of the graphene–shell for the FeS 2 to storage K from both experimental and computational perspectives. These research outputs can provide guidance for designing other metal‐based sulfide electrodes for PIBs.
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