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Merck
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Documentos

753947

Sigma-Aldrich

ICMA

97% (HPLC)

Sinónimos:

1′,4′-Dihydro-naphtho[2′,3′:1,2][5,6]fullerene-C60, C60 derivative, indene-C60 monoadduct

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About This Item

Fórmula empírica (notación de Hill):
C69H8
Número de CAS:
186682-36-0
Peso molecular:
836.80
UNSPSC Code:
12352103
NACRES:
NA.23

assay

97% (HPLC)

form

solid

loss

0.5 wt. %, 390 °C

mp

320-340 °C

orbital energy

LUMO 3.84 eV (CV)

OPV device performance

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

  • Short-circuit current density (Jsc): 10.56 mA/cm2
  • Open-circuit voltage (Voc): 0.69 V
  • Fill Factor (FF): 0.54
  • Power Conversion Efficiency (PCE): 3.92 %

ITO/PEDOT:PSS/P3HT:ICMA(1:1)/LiF/Al
  • Short-circuit current density (Jsc): 9.66 mA/cm2
  • Open-circuit voltage (Voc): 0.65 eV
  • Fill Factor (FF): 0.59
  • Power Conversion Efficiency (PCE): 3.65 %

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General description

Dipole moment of indene-C60 monoadduct (ICMA) was estimated to be 2.34 debye. Film formation of ICMA under optimum conditions was studied.1 As a potential candidate for field effect transistors (FETs), ICMA exhibits unipolar n-channel characteristics and high electron mobility.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Polarity and Air-Stability Transitions in Field-Effect Transistors Based on Fullerenes with Different Solubilizing Groups.
Yu H, et al.
ACS Applied Materials & Interfaces, 5(11), 4865-4871 (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
Beyond PCBM: Understanding the Photovoltaic Performance of Blends of Indene-C60 Multiadducts with Poly(3-hexylthiophene)
Nardes, A. M.; et al.
Advances in Functional Materials, 22, 4115-4127 (2012)

Artículos

Optoelectronic Devices with DPP-containing Molecules

Organic materials in optoelectronic devices like LEDs and solar cells are of significant academic and commercial interest.

Polymer-Sorted Carbon Nanotubes

SWCNTs show promise in FETs, solar cells, and photodetectors due to their ultrafast charge transport mobility.

Soluble Pentacene Precursors

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

Development of Small Molecule Donors for Solution-Processed Organic Solar Cells

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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