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Merck
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Key Documents

753955

Sigma-Aldrich

ICBA

99% (HPLC)

동의어(들):

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

실험식(Hill 표기법):
C78H16
CAS Number:
Molecular Weight:
952.96
UNSPSC 코드:
12352103
NACRES:
NA.23

분석

99% (HPLC)

형태

solid

손실

0.5 wt. % TGA, 235 °C

mp

253-260 °C

오비탈 에너지

LUMO 3.67 eV (CV)

OPV 기기 성능

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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일반 설명

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).

애플리케이션

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.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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)
Photo-physics of PTB7, PCBM and ICBA based ternary solar cells.
Sharma R, et al.
Organic Electronics, 34(4), 111-117 (2016)
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
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)

문서

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Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

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