Quaternized Pyridyloxy Phthalocyanines Render Aqueous Electron-Donor Carbon Nanotubes as Unprecedented Supramolecular Materials for Energy Conversion

被引:15
作者
Anaya-Plaza, Eduardo [1 ]
Oliva, Maria Moreno [2 ,3 ]
Kunzmann, Andreas [2 ,3 ]
Romero-Nieto, Carlos [2 ,3 ]
Costa, Ruben D. [2 ,3 ]
de la Escosura, Andres [1 ]
Guldi, Dirk M. [2 ,3 ]
Torres, Tomas [1 ]
机构
[1] Univ Autonoma Madrid, IMDEA Nanociencia TT, Dept Quim Organ C 1, E-28049 Madrid, Spain
[2] Univ Erlangen Nurnberg, Dept Chem & Pharm, D-91058 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Interdisciplinary Ctr Mol Mat, D-91058 Erlangen, Germany
关键词
carbon nanotubes; phthalocyanines; supramolecular aqueous photovoltaics; SOLAR-CELLS; RAMAN-SPECTROSCOPY; CHEMISTRY; NANOCARBONS; HYBRIDS; SERIES;
D O I
10.1002/adfm.201503002
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Exploring new properties in known materials, sometimes even achieving behaviors opposite to those traditionally encountered, is a fundamental aspect of innovation in materials science. In the field of energy conversion, for example, the development of water-processed organic solar cells provides environmentally friendlier materials, which contribute to reduce health risks. Herein, a novel approach is described to produce water-soluble electron-donor single wall carbon nanotube (SWCNT) hybrids based on the noncovalent immobilization of quaternized pyridyloxy zinc phthalocyanines (ZnPc) with a varying number of pyridyl substituents. Moreover, the excellent electron-accepting ability of the latter ZnPcs is reported. The introduction of tert-butylphenyl groups at the pyridines enables for the first time a complete characterization. The electron-acceptor nature of the ZnPcs enables switching the role of SWCNTs within the resulting supramolecular hybrids. Finally, a proof-of-concept demonstration of the SWCNT/ZnPc hybrids' capacity for energy conversion is presented, paving their way to possible use as active layer material in solar cells processed entirely from aqueous solutions.
引用
收藏
页码:7418 / 7427
页数:10
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