177 related articles for article (PubMed ID: 21428400)
1. Theoretical study of new ruthenium-based dyes for dye-sensitized solar cells.
Monari A; Assfeld X; Beley M; Gros PC
J Phys Chem A; 2011 Apr; 115(15):3596-603. PubMed ID: 21428400
[TBL] [Abstract][Full Text] [Related]
2. Theoretical study on the electronic absorption spectra and molecular orbitals of ten novel ruthenium sensitizers derived from N3 and K8.
Guo P; Ma R; Guo L; Yang L; Liu J; Zhang X; Pan X; Dai S
J Mol Graph Model; 2010 Nov; 29(3):498-505. PubMed ID: 21036083
[TBL] [Abstract][Full Text] [Related]
3. Measured binding coefficients for iodine and ruthenium dyes; implications for recombination in dye sensitised solar cells.
Li X; Reynal A; Barnes P; Humphry-Baker R; Zakeeruddin SM; De Angelis F; O'Regan BC
Phys Chem Chem Phys; 2012 Nov; 14(44):15421-8. PubMed ID: 23070136
[TBL] [Abstract][Full Text] [Related]
4. CdSe quantum dot (QD) and molecular dye hybrid sensitizers for TiO2 mesoporous solar cells: working together with a common hole carrier of cobalt complexes.
Lee HJ; Chang DW; Park SM; Zakeeruddin SM; Grätzel M; Nazeeruddin MK
Chem Commun (Camb); 2010 Dec; 46(46):8788-90. PubMed ID: 20957271
[TBL] [Abstract][Full Text] [Related]
5. Effects of dye-adsorption solvent on the performances of the dye-sensitized solar cells based on black dye.
Ozawa H; Awa M; Ono T; Arakawa H
Chem Asian J; 2012 Jan; 7(1):156-62. PubMed ID: 22114015
[TBL] [Abstract][Full Text] [Related]
6. Electronic structures and absorption properties of three kinds of ruthenium dye sensitizers containing bipyridine-pyrazolate for solar cells.
Zhang CR; Liu ZJ; Sun YT; Shen YL; Chen YH; Liu YJ; Wang W; Zhang HM
Spectrochim Acta A Mol Biomol Spectrosc; 2011 Sep; 79(5):1843-8. PubMed ID: 21684807
[TBL] [Abstract][Full Text] [Related]
7. Influence of molecular geometry, exchange-correlation functional, and solvent effects in the modeling of vertical excitation energies in phthalocyanines using time-dependent density functional theory (TDDFT) and polarized continuum model TDDFT methods: can modern computational chemistry methods explain experimental controversies?
Nemykin VN; Hadt RG; Belosludov RV; Mizuseki H; Kawazoe Y
J Phys Chem A; 2007 Dec; 111(50):12901-13. PubMed ID: 18004829
[TBL] [Abstract][Full Text] [Related]
8. A dendritic oligothiophene ruthenium sensitizer for stable dye-sensitized solar cells.
Sauvage F; Fischer MK; Mishra A; Zakeeruddin SM; Nazeeruddin MK; Bäuerle P; Grätzel M
ChemSusChem; 2009; 2(8):761-8. PubMed ID: 19569164
[TBL] [Abstract][Full Text] [Related]
9. Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers.
Nazeeruddin MK; De Angelis F; Fantacci S; Selloni A; Viscardi G; Liska P; Ito S; Takeru B; Grätzel M
J Am Chem Soc; 2005 Dec; 127(48):16835-47. PubMed ID: 16316230
[TBL] [Abstract][Full Text] [Related]
10. New ruthenium sensitizers featuring bulky ancillary ligands combined with a dual functioned coadsorbent for high efficiency dye-sensitized solar cells.
Shi Y; Liang M; Wang L; Han H; You L; Sun Z; Xue S
ACS Appl Mater Interfaces; 2013 Jan; 5(1):144-53. PubMed ID: 23234441
[TBL] [Abstract][Full Text] [Related]
11. The effect of conjugated spacer on novel carbazole derivatives for dye-sensitized solar cells: density functional theory/time-dependent density functional theory study.
Jungsuttiwong S; Yakhanthip T; Surakhot Y; Khunchalee J; Sudyoadsuk T; Promarak V; Kungwan N; Namuangruk S
J Comput Chem; 2012 Jun; 33(17):1517-23. PubMed ID: 22505327
[TBL] [Abstract][Full Text] [Related]
12. Substituent effect on the π linkers in triphenylamine dyes for sensitized solar cells: a DFT/TDDFT study.
Xu J; Zhu L; Fang D; Chen B; Liu L; Wang L; Xu W
Chemphyschem; 2012 Oct; 13(14):3320-9. PubMed ID: 22763917
[TBL] [Abstract][Full Text] [Related]
13. Heterogeneous electron transfer from dye-sensitized nanocrystalline TiO2 to [Co(bpy)3]3+: insights gained from impedance spectroscopy.
Liu Y; Jennings JR; Zakeeruddin SM; Grätzel M; Wang Q
J Am Chem Soc; 2013 Mar; 135(10):3939-52. PubMed ID: 23425317
[TBL] [Abstract][Full Text] [Related]
14. Molecular origins of optoelectronic properties in coumarin dyes: toward designer solar cell and laser applications.
Liu X; Cole JM; Waddell PG; Lin TC; Radia J; Zeidler A
J Phys Chem A; 2012 Jan; 116(1):727-37. PubMed ID: 22117623
[TBL] [Abstract][Full Text] [Related]
15. Large pi-aromatic molecules as potential sensitizers for highly efficient dye-sensitized solar cells.
Imahori H; Umeyama T; Ito S
Acc Chem Res; 2009 Nov; 42(11):1809-18. PubMed ID: 19408942
[TBL] [Abstract][Full Text] [Related]
16. Absorption and emission UV-Vis spectra of the TRITC fluorophore molecule in solution: a quantum mechanical study.
Pedone A; Bloino J; Monti S; Prampolini G; Barone V
Phys Chem Chem Phys; 2010 Jan; 12(4):1000-6. PubMed ID: 20066385
[TBL] [Abstract][Full Text] [Related]
17. Ruthenium phthalocyanine-bipyridyl dyads as sensitizers for dye-sensitized solar cells: dye coverage versus molecular efficiency.
Rawling T; Austin C; Buchholz F; Colbran SB; McDonagh AM
Inorg Chem; 2009 Apr; 48(7):3215-27. PubMed ID: 19278209
[TBL] [Abstract][Full Text] [Related]
18. Improvement of TiO2/dye/electrolyte interface conditions by positional change of alkyl chains in modified panchromatic Ru complex dyes.
Kimura M; Masuo J; Tohata Y; Obuchi K; Masaki N; Murakami TN; Koumura N; Hara K; Fukui A; Yamanaka R; Mori S
Chemistry; 2013 Jan; 19(3):1028-34. PubMed ID: 23197470
[TBL] [Abstract][Full Text] [Related]
19. Interfacial electron transfer in TiO(2) surfaces sensitized with Ru(II)-polypyridine complexes.
Jakubikova E; Snoeberger RC; Batista VS; Martin RL; Batista ER
J Phys Chem A; 2009 Nov; 113(45):12532-40. PubMed ID: 19594155
[TBL] [Abstract][Full Text] [Related]
20. Electronic structures and optical properties of organic dye sensitizer NKX derivatives for solar cells: a theoretical approach.
Zhang CR; Liu L; Liu ZJ; Shen YL; Sun YT; Wu YZ; Chen YH; Yuan LH; Wang W; Chen HS
J Mol Graph Model; 2012 Sep; 38():419-29. PubMed ID: 23117291
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
