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Merck
모든 사진(1)

주요 문서

682799

Sigma-Aldrich

P3OT

regioregular, electronic grade, 99.995% trace metals basis, average Mn ~25,000

동의어(들):

Poly(3-octylthiophene-2,5-diyl)

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About This Item

Linear Formula:
(C12H18S)n
CAS Number:
MDL number:
UNSPSC 코드:
12352103
NACRES:
NA.23

material

black

Grade

electronic grade

설명

Band gap: 1.7 eV

분석

99.995% trace metals basis

양식

solid

분자량

average Mn ~25,000

mp

198-211 °C

오비탈 에너지

HOMO -5.25 eV 
LUMO -3.55 eV 

OPV 기기 성능

ITO/PEDOT:PSS/P3OT:PC61BM (1:2)/LiF/Al

  • Short-circuit current density (Jsc): 5.55 mA/cm2
  • Open-circuit voltage (Voc): 0.5 V
  • Fill Factor (FF): 0.33
  • Power Conversion Efficiency (PCE): 0.91 %

반도체 특성

P-type (mobility=10−4 - 10−1 cm2/V·s)

SMILES string

[s]1cc(cc1)CCCCCCCC

InChI

1S/C12H20S/c1-2-3-4-5-6-7-8-12-9-10-13-11-12/h9-11H,2-8H2,1H3

InChI key

WQYWXQCOYRZFAV-UHFFFAOYSA-N

일반 설명

Poly(3-octylthiophene-2,5-diyl) (P3OT) is a conducting polymer that is a class of polyalkylthiophene with intrinsic photoluminescence and good electrochemical properties. It can be prepared by oxidative polymerization of 3-octylthiophene (3OT).

애플리케이션

Conducting polymer.
Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials.
Used in organic field-effect transistors and in polymer-based solar cells.
P3OT can be used as a conjugating polymer for the fabrication of organic electronic based devices which include photovoltaic cells, flexible electronics, light emitting electrochemical cells and solar cell based applications.
p-type polymer semiconductor.

특징 및 장점

Good processability, environmental stability and electroactivity.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Side chain length affects backbone dynamics in poly (3-alkylthiophene) s
Zhan P, et al.
Journal of Polymer Science. Part B, Polymer Physics, 56(17), 1193-1202 (2018)
Deep eutectic solvent systems for FeCl 3-catalyzed oxidative polymerization of 3-octylthiophene
Park T and Lee SH
Green Chemistry, 19(4), 910-913 (2017)
Organic photovoltaic devices based on a novel acceptor material: graphene
Liu Z, et al.
Advanced Materials, 20(20), 3924-3930 (2008)
Single-wall carbon nanotube/conjugated polymer photovoltaic devices
Kymakis E and Amaratunga G
Applied Physics Letters, 80(1), 112-114 (2002)
Fabrication of a poly (3-octylthiophene-2, 5-diyl) electrochemiluminescence device assisted by perylene
Daimon T and Nihei E
Materials, 6(5), 1704-1717 (2013)

문서

The application of conducting polymers at the interface with biology is an exciting new trend in organic electronics research.

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

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

Novel Graphene‑Based Nanostructures Production, Functionalization, and Engineering

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