2001
DOI: 10.1016/s0379-6779(00)00440-9
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Electrostatic self-assembly as a means to create organic photovoltaic devices

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Cited by 42 publications
(28 citation statements)
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“…While not a CPE, it is worth noting that there is a body of related work where polycationic PPV precursors and a host of different donors are used to fabricated LBL solar cells and photodetectors. [156][157][158][159][160][161][162] As reported by Yoshino and coworkers in 1996, solutions of poly(3-a-carboxylmethylthiophene) (P32) (Scheme 9) at pH ¼ 4.5 and poly(dihexyldipropargyl ammonium bromide) (P33) (Scheme 9) were used to fabricate by a LBL processes an ITO/ P32:P33/Al device containing 11-13 bilayers. [21] This group similarly prepared devices with P32 and poly(N-methyl-2,5-pyridinium vinylene) (P34) (Scheme 9), [163][164][165] as well as REVIEW the same P32:P34 devices doped with C 60 or a porphyrin derivative by using a mixed solution of P32 with an adduct of fullerene and 8-(9-anthryl)-7-oxaoctanoic acid [163] or a mixed solution of P34 with a porphyrin derivative.…”
Section: Solar Cells and Photodetectorsmentioning
confidence: 96%
“…While not a CPE, it is worth noting that there is a body of related work where polycationic PPV precursors and a host of different donors are used to fabricated LBL solar cells and photodetectors. [156][157][158][159][160][161][162] As reported by Yoshino and coworkers in 1996, solutions of poly(3-a-carboxylmethylthiophene) (P32) (Scheme 9) at pH ¼ 4.5 and poly(dihexyldipropargyl ammonium bromide) (P33) (Scheme 9) were used to fabricate by a LBL processes an ITO/ P32:P33/Al device containing 11-13 bilayers. [21] This group similarly prepared devices with P32 and poly(N-methyl-2,5-pyridinium vinylene) (P34) (Scheme 9), [163][164][165] as well as REVIEW the same P32:P34 devices doped with C 60 or a porphyrin derivative by using a mixed solution of P32 with an adduct of fullerene and 8-(9-anthryl)-7-oxaoctanoic acid [163] or a mixed solution of P34 with a porphyrin derivative.…”
Section: Solar Cells and Photodetectorsmentioning
confidence: 96%
“…With this technique it is possible to tune the composition of the layers at molecular scale, fabricate interesting composite materials in a simple and inexpensive way onto substrates composed by almost any material and with almost any size or shape. This technique has been successfully demonstrated in many applications such as conductive coatings [7], antireflective coatings [8], sensitive coatings [9][10][11][12][13][14], organic light emitting diodes [15], photovoltaic cells [16], and so forth.…”
Section: Introductionmentioning
confidence: 99%
“…More recently, this approach was used in the fabrication of polymer thin films for optoelectronic devices, such as field-effect transistors, [9] lightemitting devices, [10][11][12][13][14][15] and photovoltaic cells. [16][17][18][19] A relatively low turn-on voltage was observed in the light-emitting diodes fabricated by multilayer deposition, which was attributed to the defect-free films obtained. [10] Although the performances of these devices were not satisfactory compared to those of the extensively studied multilayer organic devices, the LBL deposition method provides an alternative approach to fabricate multilayer thin films.…”
Section: Introductionmentioning
confidence: 99%