期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 133, 期 13, 页码 4940-4947出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja1103734
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资金
- Initiative for Sustainability and Energy at Northwestern University (ISEN)
- National Science Foundation [DMR 0955612]
- Sony Corporation
- Northrop Grumman Corporation
- National Science Council (NSC), Taiwan [99-2221-E-001-012]
- Academia Sinica research program on nanoscience and nanotechnology
- U.S. Department of Energy, Office of Basic Energy Sciences [DE-FG02-00ER45810]
- NSF-NSEC
- NSF-MRSEC
- Keck Foundation
- State of Illinois
- Direct For Mathematical & Physical Scien
- Division Of Materials Research [0955612] Funding Source: National Science Foundation
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.
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