MXene/Organics Heterostructures Enable Ultrastable and High-Rate Lithium/Sodium Batteries

被引:62
|
作者
Wei, Chuanliang [1 ]
Tan, Liwen [1 ]
Zhang, Yuchan [1 ]
Xi, Baojuan [2 ]
Xiong, Shenglin [2 ]
Feng, Jinkui [1 ]
机构
[1] Shandong Univ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Res Ctr Carbon Nanomat,Sch Mat Sci & Engn, Jinan 250061, Peoples R China
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
MXene; PTCDA cathode; electrostatic self-assembly; organic battery; lithium-ion battery; sodium-ion battery; ORGANIC ELECTRODE MATERIALS; DENDRITE-FREE; ENERGY-STORAGE; METAL; NUCLEATION; ANODES;
D O I
10.1021/acsami.1c22787
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Organic electrode materials have shown potential for rechargeable batteries because they are environmentally friendly, earth-abundant sources, recyclable, high sustainable, designable, flexible, and lightweight. However, low electrical conductivity and dissolution in organic liquid electrolytes hinder their further development. Herein, MXene/organics heterostructures are designed to address the problems of organic electrodes via a scalable and simple electrostatic self-assembly strategy. Under the effect of the electrostatic interaction, organic cathode material, 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), is tightly attached to MXene nanosheets. Owing to the high electronic conductivity and special two-dimensional (2D) structure of MXene nanosheets, the issues of PTCDA cathode are effectively relieved. When applied in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs), the MXene@ PTCDA heterostructure exhibits significantly enhanced rate capability and cycling performance than bare PTCDA. The heterostructures proposed here can be applied to other (K, Zn, Al, Mg, Ca, etc.) battery systems. In addition to energy storage and conversion, the heterostructures can be also extended to many fields such as catalysis, sensors, electronics, optics, membranes, semiconductors, biomedicines, etc.
引用
收藏
页码:2979 / 2988
页数:10
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