A facile soft-template synthesis of mesoporous polymeric and carbonaceous nanospheres

被引:548
作者
Liu, Jian [1 ,2 ]
Yang, Tianyu [2 ]
Wang, Da-Wei [2 ]
Lu, Gao Qing [2 ]
Zhao, Dongyuan [3 ]
Qiao, Shi Zhang [2 ,4 ]
机构
[1] Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia
[2] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Queensland 4072, Australia
[3] Fudan Univ, Dept Chem, Adv Mat Lab, Shanghai 200433, Peoples R China
[4] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
来源
NATURE COMMUNICATIONS | 2013年 / 4卷
基金
澳大利亚研究理事会;
关键词
NANOPARTICLES; FRAMEWORKS; ROUTE;
D O I
10.1038/ncomms3798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Owing to the weak self-assembly ability of precursor components and the serious cross-linking of neighbouring nanospheres during a hydrothermal process, the synthesis of monodisperse mesoporous polymer nanospheres with diameters below 500 nm remains a great challenge. Here we extend the synthesis method of mesoporous silica nanospheres to enable the preparation of ordered mesoporous resorcinol formaldehyde nanospheres with particle size from 80 to 400 nm and mesopores of similar to 3.5 nm in diameter. By finely tuning the synthesis parameters, multi-layered mesoporous resorcinol formaldehyde hollow nanospheres can be successfully synthesized. Mesoporous carbon nanospheres and hollow nanospheres with high surface area are further obtained through carbonization of the polymer spheres. The resulting mesoporous carbon nanospheres are demonstrated as the host cathode material for lithium-sulphur batteries. The synthesis strategy provides a benchmark for fabricating well-defined porous carbonaceous nanospheres with potential for energy storage and conversion applications.
引用
收藏
页数:7
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