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PUBMED FOR HANDHELDS

Journal Abstract Search


245 related items for PubMed ID: 23629055

  • 1. Porphyrin sensitizers with π-extended pull units for dye-sensitized solar cells.
    Reddy NM, Pan TY, Rajan YC, Guo BC, Lan CM, Diau EW, Yeh CY.
    Phys Chem Chem Phys; 2013 Jun 07; 15(21):8409-15. PubMed ID: 23629055
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  • 4. Influence of Phenylethynylene of Push-Pull Zinc Porphyrins on the Photovoltaic Performance.
    Chou HH, Reddy KS, Wu HP, Guo BC, Lee HW, Diau EW, Hsu CP, Yeh CY.
    ACS Appl Mater Interfaces; 2016 Feb 10; 8(5):3418-27. PubMed ID: 26752243
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  • 10. Effects of number and position of meta and para carboxyphenyl groups of zinc porphyrins in dye-sensitized solar cells: structure-performance relationship.
    Ambre RB, Mane SB, Chang GF, Hung CH.
    ACS Appl Mater Interfaces; 2015 Jan 28; 7(3):1879-91. PubMed ID: 25562465
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  • 11. Triarylamine-substituted imidazole- and quinoxaline-fused push-pull porphyrins for dye-sensitized solar cells.
    Hayashi H, Touchy AS, Kinjo Y, Kurotobi K, Toude Y, Ito S, Saarenpää H, Tkachenko NV, Lemmetyinen H, Imahori H.
    ChemSusChem; 2013 Mar 28; 6(3):508-17. PubMed ID: 23401121
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  • 13. A strategy to design highly efficient porphyrin sensitizers for dye-sensitized solar cells.
    Chang YC, Wang CL, Pan TY, Hong SH, Lan CM, Kuo HH, Lo CF, Hsu HY, Lin CY, Diau EW.
    Chem Commun (Camb); 2011 Aug 21; 47(31):8910-2. PubMed ID: 21677971
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  • 14. "Spider"-shaped porphyrins with conjugated pyridyl anchoring groups as efficient sensitizers for dye-sensitized solar cells.
    Stangel C, Bagaki A, Angaridis PA, Charalambidis G, Sharma GD, Coutsolelos AG.
    Inorg Chem; 2014 Nov 17; 53(22):11871-81. PubMed ID: 25365138
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  • 15. Systematic Investigations on the Roles of the Electron Acceptor and Neighboring Ethynylene Moiety in Porphyrins for Dye-Sensitized Solar Cells.
    Wei T, Sun X, Li X, Ågren H, Xie Y.
    ACS Appl Mater Interfaces; 2015 Oct 07; 7(39):21956-65. PubMed ID: 26355437
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  • 17. Saddle-shaped porphyrins for dye-sensitized solar cells: new insight into the relationship between nonplanarity and photovoltaic properties.
    Shahroosvand H, Zakavi S, Sousaraei A, Eskandari M.
    Phys Chem Chem Phys; 2015 Mar 07; 17(9):6347-58. PubMed ID: 25650290
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  • 18. New bithiazole-based sensitizers for efficient and stable dye-sensitized solar cells.
    He J, Guo F, Li X, Wu W, Yang J, Hua J.
    Chemistry; 2012 Jun 18; 18(25):7903-15. PubMed ID: 22573564
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  • 19. Donor-π-acceptors containing the 10-(1,3-dithiol-2-ylidene)anthracene unit for dye-sensitized solar cells.
    Bouit PA, Marszalek M, Humphry-Baker R, Viruela R, Ortí E, Zakeeruddin SM, Grätzel M, Delgado JL, Martín N.
    Chemistry; 2012 Sep 10; 18(37):11621-9. PubMed ID: 22865694
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  • 20. Highly asymmetrical porphyrins with enhanced push-pull character for dye-sensitized solar cells.
    Kurotobi K, Toude Y, Kawamoto K, Fujimori Y, Ito S, Chabera P, Sundström V, Imahori H.
    Chemistry; 2013 Dec 09; 19(50):17075-81. PubMed ID: 24227165
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