4.7 Article

High Mobility Thiazole-Diketopyrrolopyrrole Copolymer Semiconductors for High Performance Field-Effect Transistors and Photovoltaic Devices

Journal

MACROMOLECULES
Volume 45, Issue 22, Pages 9029-9037

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma301660j

Keywords

-

Funding

  1. NSF [DMR-0805259]
  2. Solvay S. A.
  3. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Material Sciences [DE-FG02-07ER46467]
  4. Direct For Mathematical & Physical Scien
  5. Division Of Materials Research [805259] Funding Source: National Science Foundation

Ask authors/readers for more resources

New donor-acceptor copolymers incorporating both a strong electron accepting diketopyrrolopyrrole unit and a weak electron deficient thiazolothiazole or benzobisthiazole moiety were synthesized, characterized, and found to exhibit very high charge carrier mobility. Stille coupling copolymerization gave copolymers having moderate number-average molecular weights of 17.0-18.5 kDa with polydispersities of 3.3-4.0 and optical band gaps of 1.22-1.38 eV. High performance p-channel field-effect transistors were obtained using the thizolothiazole-linked copolymers, PDPTT and PDPTTOx, giving hole mobilities of 0.5 and 1.2 cm(2)/(V s), respectively, with on/off current ratios of 10(5) to 10(6). In contrast, the benzobisthiazole-linked copolymer PDPBT had a substantially lower field-effect mobility of holes (0.005 cm(2)/(V s)) due to its amorphous solid state morphology. Bulk heterojunction solar cells fabricated by using one of the thiazolothiazole-linked copolymer, PDPTT, as electron donor and PC71BM acceptor show a power conversion efficiency of 3.4% under 100 mW/cm(2) AM1.5 irradiation in air.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available