Phthalocyanine-Pyrene Conjugates: A Powerful Approach toward Carbon Nanotube Solar Cells

被引:131
作者
Bartelmess, Juergen [3 ,4 ]
Ballesteros, Beatriz [5 ]
de la Torre, Gema [5 ]
Kiessling, Daniel [3 ,4 ]
Campidelli, Stephane [1 ,2 ]
Prato, Maurizio [1 ,2 ]
Torres, Tomas [5 ,6 ]
Guldi, Dirk M. [3 ,4 ]
机构
[1] Univ Trieste, Ctr Excellence Nanostruct & Mat, I-34127 Trieste, Italy
[2] Univ Trieste, INSTM, Unit Trieste, Dipartimento Sci Farmaceut, I-34127 Trieste, Italy
[3] Univ Erlangen Nurnberg, Dept Chem & Pharm, D-91058 Erlangen, Germany
[4] Univ Erlangen Nurnberg, Interdisciplinary Ctr Mol Mat, D-91058 Erlangen, Germany
[5] Univ Autonoma Madrid, Dept Quim Organ, E-28049 Madrid, Spain
[6] IMDEA Nanociencia, Fac Ciencias, Madrid 28049, Spain
关键词
PHOTOINDUCED ELECTRON-TRANSFER; NONCOVALENT FUNCTIONALIZATION; METAL-FREE; PORPHYRIN; COMPOSITES; FLUORESCENCE; CHEMISTRY; HETEROJUNCTION; SPECTROSCOPY; ATTACHMENT;
D O I
10.1021/ja107131r
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
In the present work, a new family of pyrene (Py)-substituted phthalocyanines (Pcs), i.e., ZnPc-Py and H2Pc-Py, were designed, synthesized, and probed in light of their spectroscopic properties as well as their interactions with single-wall carbon nanotubes (SWNTs). The pyrene units provide the means for non-covalent functionalization of SWNTs via pi-pi interactions. Such a versatile approach ensures that the electronic properties of SWNTs are not impacted by the chemical modification of the carbon skeleton. The characterization of ZnPc-Py/SWNT and H2Pc-Py/SWNT has been performed in suspension and in thin films by means of different spectroscopic and photoelectrochemical techniques. Transient absorption experiments reveal photoinduced electron transfer between the photoactive components. ZnPc-Py/SWNT and H2Pc-Py/SWNT have been integrated into photoactive electrodes, revealing stable and reproducible photocurrents with monochromatic internal photoconversion efficiency values for H2Pc-Py/SWNT as large as 15 and 23% without and with an applied bias of +0.1 V.
引用
收藏
页码:16202 / 16211
页数:10
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