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Merck

684465

Sigma-Aldrich

[6,6]-Phenyl C71 butyric acid methyl ester

99%

Sinónimos:

3′H-Cyclopropa[8,25] [5,6]fullerene-C70-D5h(6)-3′butanoic acid, 3′Phenyl-3′H-cyclopropa[8,25] [5,6]fullerene-C70-D5h(6)-3′butanoic acid, methyl ester, [70]PCBM

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About This Item

Fórmula empírica (notación de Hill):
C82H14O2
Número de CAS:
Peso molecular:
1030.99
UNSPSC Code:
12352103
NACRES:
NA.23

assay

99%

form

powder

solubility

chlorobenzene: soluble
organic solvents: soluble
toluene: soluble

orbital energy

HOMO 6 eV 
LUMO 3.9 eV 

semiconductor properties

N-type (mobility=0.1 cm2/V·s)

SMILES string

COC(=O)CCCC2(c1ccccc1)C34c5c6ccc7c8cc9Cc%10cc%11cc%12Cc%13cc%14c%15ccc6c3c%15c%16c%17c%18c%19c(c(c57)c8c%20c9c%10c%21c%11c%22c%12c%13c(c%14%16)c%18c%22c%21c%19%20)C24%17

General description

[6,6]-Phenyl C71 butyric acid methyl ester, mixture of isomers ([70]PCBM), is a high fullerene analog to [60]PCBM, which has an enhanced absorption of light in the visible region. It can be used in the development of electrochemical devices with a high current density.

Application

[70]PCBM and PCDTBT can be used as an acceptor and donor based fullerene derivative, which can be used in the fabrication of organic photovoltaics. It may be used with P3HT as an electron transporting material for the fabrication of solar cells with higher power efficiency.
[70]PCBM can be blended with a variety of electron donors, which include P3HT and MDMO-PPV, for the fabrication of polymeric solar cells with a high power conversion efficiency (PCE). It can also be used in the organic field effect transistor (OFET) based applications.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Regioisomer effects of (70) PCBM on film structures and photovoltaic properties of composite films with a crystalline conjugated polymer P3HT.
Umeyama T, et al.
Royal Society of Chemistry Advances, 7(72), 45697-45704 (2017)
Analysis and modification of defective surface aggregates on PCDTBT: PCBM solar cell blends using combined Kelvin probe, conductive and bimodal atomic force microscopy.
Noh H, et al.
Beilstein Journal of Nanotechnology, 8(72), 579-579 (2017)
A planar copolymer for high efficiency polymer solar cells
Qin R, et al.
Journal of the American Chemical Society, 131(41), 14612-14613 (2009)
Low-bandgap poly (thiophene-phenylene-thiophene) derivatives with broaden absorption spectra for use in high-performance bulk-heterojunction polymer solar cells
Chen C, et al.
Journal of the American Chemical Society, 130(38), 12828-12833 (2008)
Highly efficient organic thin-film solar cells based on poly (3-hexylthiophene) and soluble C70 fullerene derivative
Yamanari T, et al.
Japanese Journal of Applied Physics, 47(2S), 1230-1230 (2008)

Artículos

Progress in bulk heterojunction photodiodes since 1995 has improved device performance and widened research scope.

Progress in bulk heterojunction photodiodes since 1995 has improved device performance and widened research scope.

Progress in bulk heterojunction photodiodes since 1995 has improved device performance and widened research scope.

Progress in bulk heterojunction photodiodes since 1995 has improved device performance and widened research scope.

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