A universal strategy to prepare porous graphene films: binder-free anodes for high-rate lithium-ion and sodium-ion batteries

被引:61
作者
Zhang, Xiaoting [1 ]
Zhou, Jisheng [1 ]
Liu, Chengcheng [1 ]
Chen, Xiaohong [1 ]
Song, Huaihe [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Key Lab Electrochem Proc & Technol Mat, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-RATE PERFORMANCE; ENERGY-STORAGE; RATE CAPABILITY; ELECTRODES; OXIDE; INTERCALATION; CHALLENGES; CAPACITORS; NANOSHEETS; REDUCTION;
D O I
10.1039/c6ta01907b
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
Porous graphene films (PGFs) were developed by introducing defects and extra edges into graphene using GO and a metal salt (ferric nitrate) as sources via a facile filtration method together with a thermal reduction and subsequent removal of the metal. The pore size and density could be controlled by simply adjusting the amount of ferric nitrate. When used as an anode for lithium ion batteries, PGF-1 showed a high reversible capacity, improved cycling stability, and ultra-high rate performance (971, 298, and 163 mA h g(-1) at the rates of 10, 30, and 50 A g(-1) after 10 000 cycles). When used as an anode for sodium ion batteries, PGF-1 showed a reversible capacity of 195 mA h g(-1) at 50 mA g(-1) after 50 cycles. Even at a high rate of 1000 mA g(-1), the reversible capacity can still remain at 111 mA h g(-1) after 1000 cycles. The excellent performance should be attributed to the special porous structure of the PGF. On one hand, plenty of defects within the PGF provided extra reaction sites for lithium and sodium ion storage. On the other hand, the porous structure of the PGF resulted in fast diffusion and transfer of lithium/sodium ions and electrons throughout the electrodes.
引用
收藏
页码:8837 / 8843
页数:7
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