Surfactant-Free Water-Processable Photoconductive All-Carbon Composite

被引:180
作者
Tung, Vincent C. [1 ]
Huang, Jen-Hsien [1 ,3 ]
Tevis, Ian [2 ]
Kim, Franklin [1 ]
Kim, Jaemyung [1 ]
Chu, Chih-Wei [1 ,3 ]
Stupp, Samuel I. [1 ,2 ,4 ]
Huang, Jiaxing [1 ]
机构
[1] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Acad Sinica, Res Ctr Appl Sci, Taipei 11529, Taiwan
[4] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
基金
美国国家科学基金会;
关键词
GRAPHENE OXIDE; GRAPHITE OXIDE; COAXIAL NANOTUBES; SOLAR-CELLS; DISPERSIONS; POLYMER; FULLERENES; ENERGY; LAYERS; C-60;
D O I
10.1021/ja1103734
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterojunctions between different graphitic nanostructures, including fullerenes, carbon nanotubes and graphene-based sheets, have attracted significant interest for light to electrical energy conversion. Because of their poor solubility, fabrication of such all-carbon nanocomposites typically involves covalently linking the individual constituents or the extensive surface functionalization to improve their solvent processability for mixing. However, such strategies often deteriorate or contaminate the functional carbon surfaces. Here we report that fullerenes, pristine single walled carbon nanotubes, and graphene oxide sheets can be conveniently coassembled in water to yield a stable colloidal dispersion for thin film processing. After thermal reduction of graphene oxide, a solvent-resistant photoconductive hybrid of fullerene nanotube graphene was obtained with on off ratio of nearly 6 orders of magnitude. Photovoltaic devices made with the all-carbon hybrid as the active layer and an additional fullerene block layer showed unprecedented photovoltaic responses among all known all-carbon-based materials with an open circuit voltage of 0.59 V and a power conversion efficiency of 0.21%. The ease of making such surfactant-free, water-processed, carbon thin films could lead to their wide applications in organic optoelectronic devices.
引用
收藏
页码:4940 / 4947
页数:8
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