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      產(chǎn)品詳情
      • 產(chǎn)品名稱:PDPP4T-2F

      • 產(chǎn)品型號:PDPP4T-2F
      • 產(chǎn)品廠商:Ossila
      • 產(chǎn)品價(jià)格:0
      • 折扣價(jià)格:0
      • 產(chǎn)品文檔:
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      簡單介紹:
      Applications Poly[2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione -3,6-diyl)-alt-(3'',4'-difluoro[2,2’;5’,2’’;5’’,2’’’-quaterthiophen]-5,5’’’-diyl)] (PDPP4T-2F) is the fluorinated version of PDPP4T with a device performance PCE of 7.59% [1].
      詳情介紹:

      General Information

      Full name Poly[2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione -3,6-diyl)-alt-(3'',4'-difluoro[2,2’;5’,2’’;5’’,2’’’-quaterthiophen]-5,5’’’-diyl)]
      Synonyms PFDPP4T, PDQT-2F
      CAS number n.a.
      Chemical formula (C62H88F2N2O2S4)n
      Molecular weight See Batch Details table above
      HOMO / LUMO HOMO = ~ 5.22 eV, LUMO = ~ 3.66 eV [3]
      Solubility Dichlorobenzene, chlorobenzene
      Classification / Family Quaterthiophene, Heterocyclic five-membered ring, Organic semiconducting materials, Low band gap polymers, Organic photovoltaics, Polymer solar cells, OFETs
      pdpp4t-2f chemical structure
      Chemical structure of PDPP4T-2F, Chemical formula (C62H88F2N2O2S4)n.

      Applications

      Poly[2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione -3,6-diyl)-alt-(3'',4'-difluoro[2,2’;5’,2’’;5’’,2’’’-quaterthiophen]-5,5’’’-diyl)] (PDPP4T-2F) is the fluorinated version of PDPP4T with a device performance PCE of 7.59% [1].

      In comparison to PDPP4T, PDPP4T-2F has a deeper highest-occupied molecular orbital (HOMO) level, due to the electron-withdrawing nature of the fluorine atoms on the thiophene units. It has also been reported that apart from being more favorable for realising higher Voc due to its deeper HOMO  energy level, PDPP4T-2F shows great potential in achieving a higher Jsc than PDPP4T in devices for its improved extinction coefficient.

      Literature and Reviews

      1. Sequential Deposition: Optimization of Solvent Swelling for High-Performance Polymer Solar Cells, Y. Liu et al., ACS Appl. Mater. Interfaces, 7, 653-661 (2015); DOI: 10.1021/am506868g.
      2. Effect of Fluorination on Molecular Orientation of Conjugated Polymers in High Performance Field-Effect Transistors, A. Zhang et al., Macromolecules, 49 (17), 6431–6438 (2016); DOI: 10.1021/acs.macromol.6b01446.
      3. Over 11% Efficiency in Tandem Polymer Solar Cells Featured by a Low-Band-Gap Polymer with Fine-Tuned Properties, Z. Zheng et al., Adv. Mater., 28, 5133–5138 (2016); DOI: 10.1002/adma.201600373.
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