Additive Engineering Enables Ionic-Liquid Electrolyte-Based Supercapacitors To Deliver Simultaneously High Energy and Power Density

被引:20
|
作者
Jiang, Xinglin [1 ]
Wu, Xinzheng [2 ]
Xie, Yanting [1 ]
Wang, Zixing [3 ]
Huang, Junfeng [1 ]
Qu, Yuanxiao [1 ]
Mu, Dali [1 ]
Zhang, Xiong [4 ]
Yang, Weiqing [1 ]
Zhang, Haitao [1 ]
机构
[1] Southwest Jiaotong Univ, Sch Mat Sci & Engn, Key Lab Adv Technol Mat, Minist Educ, Chengdu 610031, Peoples R China
[2] Shanghai Suyu New Energy Co Ltd, Shanghai 201611, Peoples R China
[3] Hunan Univ, Coll Mat Sci & Engn, Hunan Joint Int Lab Adv Mat & Technol Clean Energy, Hunan Prov Key Lab Adv Carbon Mat & Appl Technol, Changsha 410082, Peoples R China
[4] Chinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
additive engineering; supercapacitors; ionic liquid; MXene; power density; energy density; SOLID-STATE; CARBON NANOTUBE; PERFORMANCE; TEMPERATURE; DYNAMICS; BEHAVIOR; STORAGE; RAMAN;
D O I
10.1021/acssuschemeng.3c00213
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ionic liquid (IL) electrolytes with a high potential window are promising candidates to high-energy-density supercapacitors; however, they commonly suffer from serious kinetic barriers that lead to poor power density. In this work, we propose an additive engineering method to promote rapid dynamics of ILbased supercapacitors. Additive engineering is based on adding cetyltrimethylammonium bromide-grafted Ti3C2 MXene (Ti3C2CTAB) into 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF4), a typical IL electrolyte for supercapacitors. Remarkably, IL electrolytes show a considerable increase by 38% in ionic conductivity and great reduction in solid-liquid surface energy from 18.03 to 12.37 mN m-1. We prove that electrostatic force and hydrogen bonds generated from the interaction between Ti3C2-CTAB and EMIMBF4 facilitate considerable dissociation of electrolyte ion pairs and ion-transfer capability. Consequently, additive engineering-designed IL-based supercapacitors deliver simultaneously a high energy density of 28.3 Wh kg-1 and power density of 18.3 kW kg-1. The increased high-power characteristics are supported by a faster ion diffusion coefficient (1.50 x 10-12 vs 4.04 x 10-13 cm2 s-1) and shorter relaxation time (3.83 vs 6.81 s). In addition, additive engineering guarantees a stable cycling life of 83.6% capacitance retention after 9000 cycles at the depth potential window from 0 to 3.0 V.
引用
收藏
页码:5685 / 5695
页数:11
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