High-performance, low-voltage organic field-effect transistors using thieno[3, 2-b]thiophene and benzothiadiazole co-polymers. Issue 21 (16th May 2022)
- Record Type:
- Journal Article
- Title:
- High-performance, low-voltage organic field-effect transistors using thieno[3, 2-b]thiophene and benzothiadiazole co-polymers. Issue 21 (16th May 2022)
- Main Title:
- High-performance, low-voltage organic field-effect transistors using thieno[3, 2-b]thiophene and benzothiadiazole co-polymers
- Authors:
- Amna, Bibi
Isci, Recep
Siddiqi, Humaira M.
Majewski, Leszek A.
Faraji, Sheida
Ozturk, Turan - Abstract:
- Abstract : A series of new linear conjugated polymers incorporating different substituted thieno[3, 2- b ]thiophenes as donor, acetylene as π-bridge and benzothiadiazole as acceptor units were synthesized via Pd-catalyzed Sonogashira cross-coupling polymerization. Abstract : A series of new linear conjugated co-polymers, incorporating different substituted thieno[3, 2- b ]thiophenes (TTs) as the donor, acetylene as the π-bridge and benzothiadiazole (BT) as the acceptor units, were synthesized via palladium-catalyzed Sonogashira cross-coupling polymerization. The optical, electrochemical, and thermal properties of these conjugated polymers were evaluated via UV-vis, fluorescence, cyclic voltammetry, and thermogravimetric analysis. These readily soluble TT–BT co-polymers were employed as the semiconducting channel materials in bottom-gate, top-contact (BGTC) organic field-effect transistors (OFETs). The OFET devices showed p-channel field-effect behavior and successfully operated below −3 V in high yield. The polymeric materials comprising TTs with aliphatic side chains exhibited a better OFET performance compared with those with aromatic side chains. The OFETs using TT–BT with thienothiophene bearing a nonyl (C9 H19 ) side chain showed the highest hole average carrier mobility in the saturation regime, μ sat = 0.1 cm −2 V −1 s −1, on/off current ratio, I ON / I OFF = 3.5 × 10 3, and the smallest subthreshold swing, SS < 200 mV dec −1 . The observed differentiation in deviceAbstract : A series of new linear conjugated polymers incorporating different substituted thieno[3, 2- b ]thiophenes as donor, acetylene as π-bridge and benzothiadiazole as acceptor units were synthesized via Pd-catalyzed Sonogashira cross-coupling polymerization. Abstract : A series of new linear conjugated co-polymers, incorporating different substituted thieno[3, 2- b ]thiophenes (TTs) as the donor, acetylene as the π-bridge and benzothiadiazole (BT) as the acceptor units, were synthesized via palladium-catalyzed Sonogashira cross-coupling polymerization. The optical, electrochemical, and thermal properties of these conjugated polymers were evaluated via UV-vis, fluorescence, cyclic voltammetry, and thermogravimetric analysis. These readily soluble TT–BT co-polymers were employed as the semiconducting channel materials in bottom-gate, top-contact (BGTC) organic field-effect transistors (OFETs). The OFET devices showed p-channel field-effect behavior and successfully operated below −3 V in high yield. The polymeric materials comprising TTs with aliphatic side chains exhibited a better OFET performance compared with those with aromatic side chains. The OFETs using TT–BT with thienothiophene bearing a nonyl (C9 H19 ) side chain showed the highest hole average carrier mobility in the saturation regime, μ sat = 0.1 cm −2 V −1 s −1, on/off current ratio, I ON / I OFF = 3.5 × 10 3, and the smallest subthreshold swing, SS < 200 mV dec −1 . The observed differentiation in device characteristics can be beneficial in applications where selectivity is as essential as the field-effect behavior. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 10:Issue 21(2022)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 10:Issue 21(2022)
- Issue Display:
- Volume 10, Issue 21 (2022)
- Year:
- 2022
- Volume:
- 10
- Issue:
- 21
- Issue Sort Value:
- 2022-0010-0021-0000
- Page Start:
- 8254
- Page End:
- 8265
- Publication Date:
- 2022-05-16
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2tc01222g ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21768.xml