Highly flexible metal/metal oxide embedded carbon nanofiber membranes as binder-free materials for Lithium-ion batteries

被引:6
|
作者
Divya, Ponnusamy [1 ]
Vadivel, Subramaniam [2 ]
Prakash, Nunna Guru [3 ]
Ko, Tae Jo [3 ]
Rosaiah, Pitcheri [1 ,3 ]
机构
[1] Paavai Engn Coll, Dept Phys, Namakkal, India
[2] Saveetha Inst Med & Tech Sci SIMATS, Saveetha Sch Engn, Dept Phys, Chennai, Tamil Nadu, India
[3] Yeungnam Univ, Sch Mech Engn, 280 Daehak Ro, Gyoungsan Si 38541, Gyeongsangbuk D, South Korea
基金
新加坡国家研究基金会;
关键词
electrochemistry; electrospinning; flexible electrodes; Li-ion batteries; MnO; ENHANCED ELECTROCHEMICAL PERFORMANCE; ADVANCED ANODE MATERIAL; FACILE SYNTHESIS; STORAGE PROPERTIES; MNO; GRAPHENE; COMPOSITE; NANOWIRES; DESIGN; NANOCOMPOSITE;
D O I
10.1002/er.8672
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Free-standing materials with good flexibility is of great interest for energy storage applications. Herein, N-MnO carbon nanofibers (N-MnC) composite is synthesized by introducing one dimensional MnO2 nanowires (1D MnO2 NWs) into PAN and PVB composite solution through electrospinning. The synthesized membranes are directly used as freestanding electrodes for lithium-ion battery (LIB) applications. During synthesis, MnO2 NWs transformed into MnO spherical nanoparticles (NPs) and embedded on carbon nanofibers (CNFs), resulting in an N-MnC composite. N-MnC composite exhibited a discharge/charge capacity of 1405/1114 mAhg(-1) at a current density of 0.1 Ag-1 as an anode for LIBs which is much better than that of pure MnO, MnO2 electrodes. The outstanding performance of N-MnC composite may be credited to its good electrical conductivity, structural integrity, low dimension CNFs (high surface area), and good contact between CNFs and MnO NPs. Hence, the simple and cost-effective strategy of fabricating freestanding electrodes with high flexibility and good conductivity is the most promising approach for addressing practical concerns at the device level, especially for lightweight and flexible electronics.
引用
收藏
页码:23746 / 23756
页数:11
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