Phenyl-C61-butyric acid methyl ester

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For other uses, see PCBM (disambiguation).
Phenyl-C61-butyric acid methyl ester
Structural formula of phenyl-C61-butyric acid methyl ester
Names
Preferred IUPAC name
Phenyl-C61-butyric acid methyl ester
Identifiers
160848-21-5 N
ChemSpider 21170152 YesY
Jmol 3D model Interactive image
Properties
C72H14O2
Molar mass 910.90 g·mol−1
Structure
Monoclinic, Space group: P2(1)/n[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

PCBM is the common abbreviation for the fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester. It is being investigated in organic solar cells.[2]

PCBM is a fullerene derivative of the C60 buckyball that was first synthesized in the 1990s by Fred Wudl's group.[3] It is an electron acceptor material and is often used in plastic solar cells or flexible electronics in conjunction with electron donor materials such as P3HT or other polymers. It is a more practical choice for an electron acceptor when compared with fullerenes because of its solubility in chlorobenzene. This allows for solution processable donor/acceptor mixes, a necessary property for "printable" solar cells. However, considering the cost of fabricating fullerenes, it is not certain that this derivative can be synthesized on a large scale for commercial applications.

See also[edit]

References[edit]

  1. ^ G.M.Paternò, A.Warren; J.Spencer, G.Evans; J.Blumberger, V.Garcia Sakai; F.Cacialli (2013). "Micro-focused X-ray diffraction characterization of high-quality [6,6]-phenyl-C61-butyric acid methyl ester single crystals without solvent impurities". Journal of Materials Chemistry C. 1: 5619–5623. doi:10.1039/C3TC31075B. 
  2. ^ Björström, Cecilia; Bernasik, Andrzej; Rysz, Jakub; Budkowski, Andrzej; Nilsson, Svante; Svensson, Mattias; Andersson, Mats; Magnusson, Kjell; Moons, Ellen (December 21, 2005). "Multilayer formation in spin-coated thin films of low-bandgap polyfluorene: PCBM blends". Journal of Physics: Condensed Matter. 17 (50): L529–L534. doi:10.1088/0953-8984/17/50/L01. 
  3. ^ Hummelen, Jan C.; Knight, Brian W.; Lepeq, F.; Wudl, Fred; Yao, Jie; Wilkins, Charles L. (1995). "Preparation and Characterization of Fulleroid and Methanofullerene Derivatives". The Journal of Organic Chemistry. 60 (3): 532–538. doi:10.1021/jo00108a012.