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753955

Sigma-Aldrich

ICBA

99% (HPLC)

Synonyme(s) :

1′,1′′,4′,4′′-Tetrahydro-di[1,4]methanonaphthaleno[1,2:2′,3′,56,60:2′′,3′′][5,6]fullerene-C60, C60 derivative, indene-C60 bisadduct

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About This Item

Formule empirique (notation de Hill):
C78H16
Numéro CAS:
1207461-57-1
Poids moléculaire :
952.96
Code UNSPSC :
12352103
Nomenclature NACRES :
NA.23

Pureté

99% (HPLC)

Forme

solid

Perte

0.5 wt. % TGA, 235 °C

Pf

253-260 °C

Énergie orbitale

LUMO 3.67 eV (CV)

Performance des dispositifs OPV

ITO/PEDOT:PSS/P3HT: ICBA (1:1)/Al

  • Short-circuit current density (Jsc): 10.82 mA/cm2
  • Open-circuit voltage (Voc): 0.78 V
  • Fill Factor (FF): 0.56
  • Power Conversion Efficiency (PCE): 4.65 %

ITO/PEDOT:PSS/P3HT:ICBA(1.5:1)/LiF/Al
  • Short-circuit current density (Jsc): 10.53 mA/cm2
  • Open-circuit voltage (Voc): 0.83 V
  • Fill Factor (FF): 0.60
  • Power Conversion Efficiency (PCE): 5.26 %

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Description générale

ICBA is a C60 derivative that can be synthesized from C60 and indene. It is an acceptor material with shallow lowest occupied molecular orbital(LUMO) which can be used to enhance the performance of polymeric solar cells(PSCs).
The performance of indene-C60 bisadduct (ICBA) as organic solar cell (OSC) has been described in a study. Simple preparation and high solubility inorganic solvents renders ICBA as an efficient substitute to [6,6]-phenyl-C61 butyric acid methyl ester (PCBM).

Application

A ternary bulk heterojunction system (BHJ) may be fabricated with ICBA low band gap polymer, for IR sensitized organic solar cells. 1-3ICBA/thiazolo-thiazolo donor polymer blend may be used to enhance the charge generation in BHJ solar cells.
ICBA can be used with poly(3-hexylthiophene)(P3HT) as an active layer which can be used in the fabrication of organic solar cells(OSCs).ICBA in combination with thiazolo-thiazolo can be used as a donor. It can be blended with PCBM for photovoltaic based application.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Photo-physics of PTB7, PCBM and ICBA based ternary solar cells.
Sharma R, et al.
Organic Electronics, 34(4), 111-117 (2016)
Optimization of the structural configuration of ICBA/P3HT photovoltaic cells.
Nemnes GA, et al.
Applied Surface Science, 424(4), 264-268 (2017)
Temperature dependence of P3HT: ICBA polymer solar cells.
2017 International Conference on Numerical Simulation of Optoelectronic Devices, 133-134 (2017)
Charge Photogeneration for a Series of Thiazolo-Thiazole Donor Polymers Blended with the Fullerene Electron Acceptors PCBM and ICBA.
Shoaee S, et al.
Advances in Functional Materials, 23(26), 3286-3298 (2013)
Hyunbum Kang et al.
ACS applied materials & interfaces, 4(1), 110-116 (2011-12-14)
The ability to tune the lowest unoccupied molecular orbital (LUMO)/highest occupied molecular orbital (HOMO) levels of fullerene derivatives used as electron acceptors is crucial in controlling the optical/electrochemical properties of these materials and the open circuit voltage (V(oc)) of solar
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