Triggering hollow carbon nanotubes via dual doping for fast pseudocapacitive potassium-ion storage

被引:8
|
作者
Cao, Min [1 ]
Jin, Xin [1 ]
Zhao, Jingwen [2 ]
Wang, Xianfen [1 ,3 ]
机构
[1] Qingdao Univ, Inst Mat Energy & Environm, Coll Mat Sci & Engn, Qingdao 266071, Peoples R China
[2] Chinese Acad Sci, Qingdao Ind Energy Storage Res Inst, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China
[3] Nankai Univ, Coll Chem, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
关键词
HCNT; Potassium ion battery; In situ Raman; Heteroatom doping; PERFORMANCE; ENERGY; NITROGEN; ANODE;
D O I
10.1016/j.apmt.2022.101694
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Heteroatom doping is effective to adjust the active site, ion transportation and electronic transfer in carbonaceous materials for electrochemical energy storage. Herein, we report hollow carbon nanotubes (HCNT) co-doped with boron and nitrogen for fast potassium-ion storage. With the doping level of (B = 13.4 at.%, N = 14.3 at.%), HCNT anodes display unique performance merits: large specific capacity (383 mA h g(-1) at 0.02 A g(-1)), enhanced rate capability (189 mA h g(-1) even at 1.0 A g(-1)) and improved cycling stability (capacity remaining 70% after 500 cycles at 1.0 A g(-1)). In-situ Raman and ex-situ morphology investigations demonstrate a highly reversible evolution in G and D bands of HCNT and confirm the sturdy structure for highly reversible potassium ion storage. Further electrochemical kinetics analyses reveal the dominated capacitive potassium-storage process with a high average K+ diffusion coefficient. These findings enrich the understanding of the heteroatom doping engineering in carbons for potassium-ion batteries.
引用
收藏
页数:9
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