Lu Yan, Wen Zhaoyin, Jin Jun, Rui Kun, Wu Xiangwei
CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, China.
Phys Chem Chem Phys. 2014 May 14;16(18):8556-62. doi: 10.1039/c4cp00568f.
Hierarchical mesoporous structured iron based fluorides (abbreviated as HMIFs) are successfully synthesized for the first time by a solvothermal method through self-assembly. The fluorides are built from a large amount of nanorods with a size more than a dozen nanometers and exhibit dual phases consisting of Fe1.9F4.75·0.95H2O and FeF3·H2O. A possible formation mechanism is proposed by systematically investigating the synthesis conditions including temperature, reaction time and the amount of the fluorides source. The electrochemical performance of HMIFs as cathodes for rechargeable lithium batteries is investigated. A large reversible capacity exceeding 200 mA h g(-1) without any conducting agent coating and excellent cyclic performance with a residual capacity of 148 mA h g(-1) after 100 cycles are obtained at 0.1 C. In addition, an outstanding rate performance exceeding 100 mA h g(-1) at 5 C highlights the advantages of HMIFs materials for energy storage applications in high-performance LIBs.
首次通过溶剂热法自组装成功合成了分级介孔结构的铁基氟化物(简称为HMIFs)。这些氟化物由大量尺寸超过十几纳米的纳米棒构成,并呈现出由Fe1.9F4.75·0.95H2O和FeF3·H2O组成的双相。通过系统研究包括温度、反应时间和氟化物源用量在内的合成条件,提出了一种可能的形成机制。研究了HMIFs作为可充电锂电池阴极的电化学性能。在0.1 C下,获得了超过200 mA h g(-1)的大可逆容量,且无需任何导电剂涂层,循环性能优异,100次循环后残余容量为148 mA h g(-1)。此外,在5 C下超过100 mA h g(-1)的出色倍率性能突出了HMIFs材料在高性能锂离子电池储能应用中的优势。