Ultrasmall antimony nanodots embedded in carbon nanowires with three-dimensional porous structure for high-performance potassium dual-ion batteries

被引:54
作者
Gong, Decai [1 ]
Wei, Chenyang [1 ]
Xie, Donghao [1 ]
Tang, Yongbing [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, Adv Energy Storage Technol Res Ctr, Shenzhen 518055, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[3] Zhengzhou Univ, Minist Educ, Key Lab Adv Mat Proc & Mold, Zhengzhou 450002, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
K+-based dual-ion batteries; In-situ nitrogen doping; Three-dimensional carbon matrix; Electrochemical working mechanism; ANODE; NANOPARTICLES; ELECTROLYTES; NANOFIBERS; CAPACITY; STORAGE;
D O I
10.1016/j.cej.2021.133444
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Recently, potassium dual-ion batteries (PDIBs) have attracted considerable attention owing to the advantages of low cost, environmental friendliness, and high working voltage. However, the lack of suitable anode materials to adapt the slow diffusion of K(+ )ions leads to the low capacity and poor cycling stability of PDIBs, which seriously impedes their further development. Herein, a simple strategy is proposed to in-situ encapsulate ultrasmall Sb nanodots into N-doped carbon nanowires (Sb@NCNWs) with a three-dimensional (3D) porous structure, yielding high-performance anodes for PDIBs. The nitrogen doping and 3D porous structure can facilitate the transport of electrons and K+ ions, while the carbon matrix can effectively buffer the volumetric change of Sb nanodots during the charge/discharge process. Combining this Sb@NCNWs anode with expanded graphite cathode, we construct a novel PDIB with the alloying and intercalation mechanism in the anode and cathode, respectively. The PDIB displays a high capacity of 218 mAh g(-1) at 0.2 A g(-1) (based on anodes) and capacity retention of 92.5% after 400 cycles at 0.4 A g(-1), which is the best performance among the previously reported PDIBs.
引用
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页数:8
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