Driven by electricity: multilayered GO-Fe3O4@PDA-PAM flake assembled micro flower-like anode for high-performance lithium ion batteries

被引:18
作者
Xiao, Zhi-Chao [1 ]
Li, Yan [1 ]
Liang, Cheng-Lu [2 ]
Bao, Rui-Ying [1 ]
Yang, Ming-Bo [1 ]
Yang, Wei [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Sichuan, Peoples R China
[2] Fujian Univ Technol, Dept Mat Sci & Engn, Fuzhou 350108, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Magnetite; Anode; Polydopamine; Flower-like; Multi-layer; ENHANCED ELECTROCHEMICAL PERFORMANCE; IN-SITU; SCALABLE SYNTHESIS; STABLE ANODE; FE3O4; CARBON; STORAGE; COMPOSITES; GRAPHENE; NANOSPHERES;
D O I
10.1016/j.apsusc.2019.143934
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Up to now, how to endow the electrode, composed of the high theoretical capacity materials, with high capacity and high capacity retention for lithium ion batteries (LIBs) is still a great challenge. Herein, for the anodes of LIBs, mull-layered GO-Fe3O4@PDA-PAM (graphene oxide-Fe3O4@polydopamine-polyacrylamide) composites, in which Fe3O4 nanoparticles (NPs) are confined by the polydopamine (PDA) shell and reduced graphene oxide (rGO) sheets, are fabricated through a green and scalable strategy. The mull-layered structure with confined Fe3O4 NPs endows the anodes with efficient cushion effect and good electrical conductivity, leading to a good lithium ion storage capacity. More interestingly, GO-Fe3O4@PDA-PAM flakes are generated driven by the electricity and grabbed by PAM linker to form the flower-like morphology and well-maintained during the following electrochemical process. The flower-like anode holds up the aggregation of active materials and provides abundant lithium ion diffusion pathway. Therefore, based on the entire composite mass, the flowerstructured GO-Fe3O4@PDA-PAM anode displays a high reversible capacity, a good cycle reversibility (1204 mAh g(-1) after the 100th cycle at 0.3A g(-1)) and an admirable rate performance (702 mAh g(-1) at 1A g(-1)).
引用
收藏
页数:8
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