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Merck

906921

Sigma-Aldrich

PQT-12

Synonym(e):

Poly(3,3′′′-didodecyl[2,2′:5′,2′′:5′′,2′′′-quaterthiophene]-5,5′′′-diyl), Poly(4,4′′-didodecyl[2,2′:5′,2′′:5′′,2′′′-quaterthiophene]-5,5′′′-diyl)

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About This Item

Lineare Formel:
(C40H56S4)n
CAS-Nummer:
UNSPSC-Code:
12162002
NACRES:
NA.23

Beschreibung

Band gap: 2.27 eV
Eox = 0.45 V
Solution processable (chloroform, chlorobenzene, etc)
LIFT transferable

Form

solid

Mol-Gew.

Mw 10,000-25,000 by GPC

Farbe

brown

Löslichkeit

>5 mg/mL (in CHCl3)

λmax

473 nm in toluene

Energie der Orbitale

HOMO -5.24 eV 
LUMO -2.97 eV 

Lagertemp.

15-25°C

Verwandte Kategorien

Anwendung

PQT-12 can be employed as the semiconductor material in organic field-effect transistors(OFETs). Its high charge carrier mobility, good film-forming properties, and stability make it useful for the channel layer, enabling efficient electronic device performance. The conjugated polymer structure and charge storage capability of PQT-12 make it potentially useful for energy storage applications such as super capacitors and batteries.
PQT-12 exhibits strong absorption in the visible and near-infrared regions of the spectrum. This property enables effective utilization of a broad range of solar radiation, enhancing the light-harvesting capability and efficiency of OPV devices. PQT-12 can serve as the donor material in the active layer of OPV devices. PQT-12′s unique properties and charge transport characteristics contribute to the development of low voltage and low-power OFET devices. Its high charge carrier mobility allows for better device performance with lower operational voltages.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

20 megahertz operation of organic nanodiodes.
Majewski L A, et al.
Physica Status Solidi B, 253(8), 1507-1510 (2016)
Modification of the Poly(bisdodecylquaterthiophene) Structure for High and Predominantly Nonionic Conductivity with Matched Dopants
Hui Li, et al.
Journal of the American Chemical Society, 139,, 11149- 11157 (2017)
Highly Flexible Organic Nanofiber Phototransistors Fabricated on a Textile Composite for Wearable Photosensors
Lee M Y, et al.
Advances in Functional Materials, (2016), 1445-1445 (2016)
Self-assembly of regioregular poly (3,3'''-didodecylquarterthiophene) in chloroform and study of its junction properties
Singh M K, et al.
Journal of Chemical and Pharmaceutical Sciences , 217, 12-17 (2017)
Electrical and ammonia gas sensing properties of PQT-12/CdSe quantum dots composite-based organic thin film transistors
Kumar C, et al.
IEEE Sensors Journal, 18(15), 6805-6805 (2018)

Artikel

Small molecular weight organic semiconductors are promising for flexible transistor applications in next-gen soft electronics.

Professors Tokito and Takeda share design principles and optimization protocols for organic electronic devices, focusing on flexibility and low cost.

Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

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