1 / 8

p -Conjugated Copolymers for Nanostructured Organic Photovoltaics

p -Conjugated Copolymers for Nanostructured Organic Photovoltaics. Rafael Verduzco Louis Owen Assistant Professor Department of Chemical and Biomolecular Engineering 6100 Main Street, MS-362 Houston, Texas 77005. Objectives.

kane
Download Presentation

p -Conjugated Copolymers for Nanostructured Organic Photovoltaics

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. p-Conjugated Copolymers for Nanostructured Organic Photovoltaics Rafael Verduzco Louis Owen Assistant Professor Department of Chemical and Biomolecular Engineering 6100 Main Street, MS-362 Houston, Texas 77005

  2. Objectives • Prepare Block Copolymers with n- and p-type polymers linked together covalently • Study the structure and self-assembly of the copolymers in the bulk, in solution, and in thin films • Investigate the potential improvement of polymeric OPV performance due to nanostructured active layer

  3. p-type block: Poly(3-hexylthiophene) HOMO/LUMO: -4.8/-2.6 eV Can be made with a variety of end groups and with a low (1.1-1.2) pdi. Polymers for Solar Energy • Desired properties: • pdi ~ 1.2 • low bandgap n-type block with good electron mobility • low bandgap p-type block with good hole mobility Scherf, Acc. Chem. Res., ASAP article 2008 Review of organic solar cells: Hoppe, H. et al. J. Mater. Res., 19, 1924 (2004)

  4. n-type block: Poly(benzothiadiazole-co-9,9-dioctyl-fluorene) HOMO/LUMO: -5.68/-3.67 eV (90 % fluorene groups) Lower bandgap, higher e- mobility than polyfluorene Herguth et al., Macromolecules, 35, 6094 (2002). Polymers for Solar Energy • Desired properties: • pdi ~ 1.2 • low bandgap n-type block with good electron mobility • low bandgap p-type block with good hole mobility Scherf, Acc. Chem. Res., ASAP article 2008 Review of organic solar cells: Hoppe, H. et al. J. Mater. Res., 19, 1924 (2004)

  5. Synthesis and Characterization Synthesis via Suzuki Polycondensation for n-type polymer MALDI-TOF MS SEC-RI AFM AFM shows the formation of a nanostructured polymer thin film after annealing at 150 oC

  6. Morphology of p3HT-pF copolymers Thin film morphology of all-conjugated block copolymers, SiO2 surface cast in dichlorobenzene

  7. Current Work • Fabrication of all-polymer OPVs • Synthesis of multi-grafted copolymers for broadband absorption in OPVs • Study of the self-assembly of side-chain conjugated copolymers

  8. Acknowledgments • Rice University School of Engineering Start-up Funding • Louis Owen Foundation • Welch Foundation for Chemical Research • Center for Nanophase Materials Sciences at Oak Ridge National Lab, a Department of Energy Facility

More Related