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Merck
모든 사진(1)

주요 문서

510823

Sigma-Aldrich

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

regiorandom

동의어(들):

P3HT

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About This Item

Linear Formula:
(C10H14S)n
CAS Number:
MDL number:
UNSPSC 코드:
12352103
NACRES:
NA.23

Quality Level

색상

red

mp

238 °C

solubility

chloroform, methylene chloride, toluene, and THF: soluble

형광

λex 420 nm; λem 551 nm in chloroform

OPV 기기 성능

ITO/NiO/P3HT/PC61BM/LiF/Al

  • Short-circuit current density (Jsc): 11.3 mA/cm2
  • Open-circuit voltage (Voc): 0.64 V
  • Fill Factor (FF): 0.69
  • Power Conversion Efficiency (PCE): 5.16 %

ITO/PEDOT:PSS/P3HT:PC61BM (1:08)/Al
  • Short-circuit current density (Jsc): 9.5 mA/cm2
  • Open-circuit voltage (Voc): 0.63 V
  • Fill Factor (FF): 0.68
  • Power Conversion Efficiency (PCE): 5 %

일반 설명

1:1 (head-to-head):(head-to-tail) linkages of regioisomers
Poly(3-hexylthiophene-2,5-diyl) (P3HT) is a poly(alkylthiophene) based semiconducting polymer that is hydrophobic at the neutral state and has π-π conjugation as a backbone. It′s hole mobility is in the range of 10-3-10-1cm2V-1s-1 and it can be mainly used in the development of organic electronic based devices.

애플리케이션

P3HT is a conducting polymer that can be used in the fabrication of a variety of devices which include solar cells, field effect transistors (FETs), light emitting diodes (LEDs) and photovoltaic cells.
This material has solid state properties.

포장

Packaged in glass bottles

법적 정보

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Effect of doping of zinc oxide on the hole mobility of poly (3-hexylthiophene) in hybrid transistors
Hammer MS, et al.
Organic Electronics, 11(9), 1569-1577 (2010)
Block copolymer containing poly (3-hexylthiophene) and poly (4-vinylpyridine): Synthesis and its interaction with CdSe quantum dots for hybrid organic applications
Palaniappan K, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 49(8), 1802-1808 (2011)
Effect of the end group of regioregular poly (3-hexylthiophene) polymers on the performance of polymer/fullerene solar cells
Kim Y, et al.
The Journal of Physical Chemistry C, 111(23), 8137-8141 (2007)
p-Type semiconducting nickel oxide as an efficiency-enhancing anode interfacial layer in polymer bulk-heterojunction solar cells
Irwin, M. D.; et al.
Proceedings of the National Academy of Sciences of the USA, 105, 2783-2787 (2008)
Morphological stabilization of polymer photovoltaic cells by using cross-linkable poly (3-(5-hexenyl) thiophene).
Miyanishi S, et al.
Macromolecules, 42(5), 1610-1618 (2009)

문서

The union of distinct scientific disciplines is revealing the leading edge of Nanotechnology.

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

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

While dye sensitization as the basis for color photography has been accepted for a very long time,1 attempts to use this principle for the conversion of solar light to electricity generally had resulted only in very low photocurrents, below 100 nA/cm2.2

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