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2-Methyl-butyric acid ester

Phenyl C60 butyric acid methyl ester (PCBM) derivative... [Pg.637]

Butyric acid, methyl ester 10 FALSE FALSE FALSE FALSE... [Pg.331]

One of the most promising uses of C60 involves its potential application, when mixed with 7r-conjligated polymers, in polymer solar cells. Most often the so-called bulk heterojunction configuration is used, in which the active layer consists of a blend of electron-donating materials, for example, p-type conjugated polymers, and an electron-accepting material (n-type), such as (6,6)-phenyl-Cgi -butyric acid methyl ester (PCBM, Scheme 9.6).38... [Pg.236]

In a bulk-heterojunction photovoltaic cell with methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM) as an electron acceptor, alternating copolymer 19 (Fig. 9), derived from 2,7-fluorene and 2,5-dithienylsilole, can show impressive performance as the electron donor.31 In a device configuration of ITO/PEDOT/active layer/Ba/Al, the dark current density—bias curve shows a small leakage current, suggesting a continuous, pinhole-free active layer in the device. Under illumination of an AM 1.5 solar simulator at 100 mW/cm2, a high short-circuit current of 5.4 mA/cm2, an open-circuit voltage of 0.7 V, and a fill factor of 31.5% are achieved. The calculated energy conversion efficiency is 2.01%. [Pg.199]

Nowadays the best performing organic photovoltaic cell is represented by a bulk heterojunction (BHJ) solar cell based on the polymer poly(3-hexylthiophene) (P3HT) and the fullerene derivative [6, 6]-phenyl-C61-butyric acid methyl ester (PCBM), with reproducible efficiencies approaching 5% [262,263], However, a serious drawback for the preparation of efficient organic photovoltaic cells is represented by the low optical absorbance in the red/near-infrared region of the lightharvesting component(s), as well as their low extinction coefflcient(s). [Pg.34]

In order to learn about the true quantum efficiency of photogeneration one therefore has to study the photoinduced charge generation mechanism at faster time scales. Pump probe spectroscopy utilising a few optical-cycle laser pulses (5-6 fs) in the visible spectral range with broadband frequency conversion techniques [89] now makes it possible to study extremely fast optically-initiated events with unprecedented time resolution. Such a setup was used to time-resolve the kinetics of the charge transfer process from a polymer chain to a fullerene moiety in thin films of poly[2-methoxy, 5-(3, 7 -dimethyl-octyloxy)]-p-phenylene vinylene (MDMO-PPV) and [6,6]-phenyl C6i butyric acid methyl ester (PCBM). Solutions prepared from 1 wt% solutions of toluene on thin quartz substrates were studied. [Pg.21]

Mihailetchi [134] investigated the open circuit voltage of the bulk heterojunction organic solar cells based on methanol-fullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM) as electron acceptor and poly[2-methoxy-5(3 ,7 -dimethyloctyloxy)-p-phenylene vinylene] (OC1C10-PPV) as an electron donor. It is known that a single layer device follows the MIM model [166] and the open circuit voltage V0c is equal to the difference in the work functions of the metal electrodes [134], If charges accumulate in the... [Pg.116]

PCBM [6,6]-Phenyl-C6i butyric acid methyl ester... [Pg.85]

Figure 7.1 Chemical stractures of some common organic photovoltaic materials poly(2-methoxy-5-(3,7-dimethyloctyloxy)-l,4 phenylenevinylene) (MDMO-PPV), poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl Cei-butyric acid methyl ester (PCBM). Figure 7.1 Chemical stractures of some common organic photovoltaic materials poly(2-methoxy-5-(3,7-dimethyloctyloxy)-l,4 phenylenevinylene) (MDMO-PPV), poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl Cei-butyric acid methyl ester (PCBM).
Pacios R., Chatten A. J., Kawano K., Durrant J. R., Bradley D. D. C. and Nelson J. (2006), Effects of photo-oxidation on the performance of poly 2-methoxy-5-(3, 7 -dimethyloctyloxy)-l,4-phenylenevinylene 6,6-phenyl Cei-butyric acid methyl ester solar cells , Adv. Eunct. Mat. 16, 2117-2126. [Pg.496]

Pacios R, Nelson J, Bradley DDC, Brabec CJ (2003) Composition dependence of electron and hole transport in polyfluorene [6,6]-phenyl C61-butyric acid methyl ester blend films. Appl Phys Lett 83 4764... [Pg.76]

Huang J, Li G, Yang Y (2005) Influence of composition and heat-treatment on the charge transport properties of poly(3-hexylthiophene) and [6,6]-phenyl C i-butyric acid methyl ester blends. Appl Phys Lett 87 112105... [Pg.78]

Another method of improving these solar cells is to dope the material with a fullerene derivative such as [6]-phenyl-C6]-butyric acid methyl ester (PCBM) 46,... [Pg.259]

The devices suffer from a relatively high threshold voltage > 25 V due to electron trapping, which might be related to the relatively low electron afhnity of fluoroalkyl substituted thiophene molecules [59]. -Type field-effect conduction has also been reported in methanofullerene phenyl Cg,-butyric acid methyl ester (PCBM) [60] and... [Pg.112]

BUTYRIC ACID, METHYL ESTER (623-42-7) Forms explosive mixture with air (flash point 57°F/14°C cc). Incompatible with strong acids, nitrates, oxidizers. [Pg.236]


See other pages where 2-Methyl-butyric acid ester is mentioned: [Pg.637]    [Pg.542]    [Pg.543]    [Pg.71]    [Pg.297]    [Pg.311]    [Pg.221]    [Pg.58]    [Pg.316]    [Pg.317]    [Pg.25]    [Pg.227]    [Pg.182]    [Pg.188]    [Pg.95]    [Pg.9]    [Pg.2]    [Pg.319]    [Pg.632]    [Pg.139]    [Pg.124]    [Pg.570]    [Pg.112]    [Pg.192]    [Pg.412]    [Pg.192]    [Pg.320]   
See also in sourсe #XX -- [ Pg.176 ]




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Methyl butyrate

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