145 related articles for article (PubMed ID: 22744408)
1. Origins of device performance in dicarboxyterpyridine Ru(II) dye-sensitized solar cells.
Lin HW; Wang YS; Huang ZY; Lin YM; Chen CW; Yang SH; Wu KL; Chi Y; Liu SH; Chou PT
Phys Chem Chem Phys; 2012 Nov; 14(41):14190-5. PubMed ID: 22744408
[TBL] [Abstract][Full Text] [Related]
2. Oligothiophene-containing coumarin dyes for efficient dye-sensitized solar cells.
Hara K; Wang ZS; Sato T; Furube A; Katoh R; Sugihara H; Dan-Oh Y; Kasada C; Shinpo A; Suga S
J Phys Chem B; 2005 Aug; 109(32):15476-82. PubMed ID: 16852963
[TBL] [Abstract][Full Text] [Related]
3. Dye molecular structure device open-circuit voltage correlation in Ru(II) sensitizers with heteroleptic tridentate chelates for dye-sensitized solar cells.
Wu KL; Li CH; Chi Y; Clifford JN; Cabau L; Palomares E; Cheng YM; Pan HA; Chou PT
J Am Chem Soc; 2012 May; 134(17):7488-96. PubMed ID: 22506606
[TBL] [Abstract][Full Text] [Related]
4. Benzotriazole-bridged sensitizers containing a furan moiety for dye-sensitized solar cells with high open-circuit voltage performance.
Mao J; Guo F; Ying W; Wu W; Li J; Hua J
Chem Asian J; 2012 May; 7(5):982-91. PubMed ID: 22328182
[TBL] [Abstract][Full Text] [Related]
5. 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(25):7903-15. PubMed ID: 22573564
[TBL] [Abstract][Full Text] [Related]
6. Co-sensitization of organic dyes for efficient dye-sensitized solar cells.
Cheng M; Yang X; Li J; Zhang F; Sun L
ChemSusChem; 2013 Jan; 6(1):70-7. PubMed ID: 23193040
[TBL] [Abstract][Full Text] [Related]
7. Dyes and Redox Couples with Matched Energy Levels: Elimination of the Dye-Regeneration Energy Loss in Dye-Sensitized Solar Cells.
Jiang D; Darabedian N; Ghazarian S; Hao Y; Zhgamadze M; Majaryan N; Shen R; Zhou F
Chemphyschem; 2015 Nov; 16(16):3385-8. PubMed ID: 26314383
[TBL] [Abstract][Full Text] [Related]
8. A selective co-sensitization approach to increase photon conversion efficiency and electron lifetime in dye-sensitized solar cells.
Nguyen LH; Mulmudi HK; Sabba D; Kulkarni SA; Batabyal SK; Nonomura K; Grätzel M; Mhaisalkar SG
Phys Chem Chem Phys; 2012 Dec; 14(47):16182-6. PubMed ID: 23090062
[TBL] [Abstract][Full Text] [Related]
9. Starburst triarylamine based dyes for efficient dye-sensitized solar cells.
Ning Z; Zhang Q; Wu W; Pei H; Liu B; Tian H
J Org Chem; 2008 May; 73(10):3791-7. PubMed ID: 18412319
[TBL] [Abstract][Full Text] [Related]
10. High-performance organic materials for dye-sensitized solar cells: triarylene-linked dyads with a 4-tert-butylphenylamine donor.
Chang YJ; Chou PT; Lin SY; Watanabe M; Liu ZQ; Lin JL; Chen KY; Sun SS; Liu CY; Chow TJ
Chem Asian J; 2012 Mar; 7(3):572-81. PubMed ID: 22213741
[TBL] [Abstract][Full Text] [Related]
11. Kinetics of electron recombination of dye-sensitized solar cells based on TiO2 nanorod arrays sensitized with different dyes.
Wang H; Liu M; Zhang M; Wang P; Miura H; Cheng Y; Bell J
Phys Chem Chem Phys; 2011 Oct; 13(38):17359-66. PubMed ID: 21881630
[TBL] [Abstract][Full Text] [Related]
12. Influence of solvent and bridge structure in alkylthio-substituted triphenylamine dyes on the photovoltaic properties of dye-sensitized solar cells.
Sakong C; Kim SH; Yuk SB; Namgoong JW; Park SW; Ko MJ; Kim DH; Hong KS; Kim JP
Chem Asian J; 2012 Aug; 7(8):1817-26. PubMed ID: 22623408
[TBL] [Abstract][Full Text] [Related]
13. Charge transport versus recombination in dye-sensitized solar cells employing nanocrystalline TiO2 and SnO2 films.
Green AN; Palomares E; Haque SA; Kroon JM; Durrant JR
J Phys Chem B; 2005 Jun; 109(25):12525-33. PubMed ID: 16852549
[TBL] [Abstract][Full Text] [Related]
14. Electronic optimization of heteroleptic Ru(II) bipyridine complexes by remote substituents: synthesis, characterization, and application to dye-sensitized solar cells.
Han WS; Han JK; Kim HY; Choi MJ; Kang YS; Pac C; Kang SO
Inorg Chem; 2011 Apr; 50(8):3271-80. PubMed ID: 21417428
[TBL] [Abstract][Full Text] [Related]
15. Synthetic analogues of anthocyanins as sensitizers for dye-sensitized solar cells.
Calogero G; Sinopoli A; Citro I; Di Marco G; Petrov V; Diniz AM; Parola AJ; Pina F
Photochem Photobiol Sci; 2013 May; 12(5):883-94. PubMed ID: 23467482
[TBL] [Abstract][Full Text] [Related]
16. Functionalized alkynylplatinum(II) polypyridyl complexes for use as sensitizers in dye-sensitized solar cells.
Kwok EC; Chan MY; Wong KM; Lam WH; Yam VW
Chemistry; 2010 Oct; 16(40):12244-54. PubMed ID: 20842671
[TBL] [Abstract][Full Text] [Related]
17. Red electroluminescence of ruthenium sensitizer functionalized by sulfonate anchoring groups.
Shahroosvand H; Abbasi P; Mohajerani E; Janghouri M
Dalton Trans; 2014 Jun; 43(24):9202-15. PubMed ID: 24818219
[TBL] [Abstract][Full Text] [Related]
18. The origin of higher open-circuit voltage in Zn-doped TiO2 nanoparticle-based dye-sensitized solar cells.
Zhu F; Zhang P; Wu X; Fu L; Zhang J; Xu D
Chemphyschem; 2012 Nov; 13(16):3731-7. PubMed ID: 22899421
[TBL] [Abstract][Full Text] [Related]
19. Application of the tris(acetylacetonato)iron(III)/(II) redox couple in p-type dye-sensitized solar cells.
Perera IR; Daeneke T; Makuta S; Yu Z; Tachibana Y; Mishra A; Bäuerle P; Ohlin CA; Bach U; Spiccia L
Angew Chem Int Ed Engl; 2015 Mar; 54(12):3758-62. PubMed ID: 25631105
[TBL] [Abstract][Full Text] [Related]
20. Dye-sensitized solar cells based on a donor-acceptor system with a pyridine cation as an electron-withdrawing anchoring group.
Cheng M; Yang X; Li J; Chen C; Zhao J; Wang Y; Sun L
Chemistry; 2012 Dec; 18(50):16196-202. PubMed ID: 23081757
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
