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Items: 1 to 20 of 216

1.

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. doi: 10.1021/am302318z. Epub 2012 Dec 27.

PMID:
23234441
2.

Cyclometalated ruthenium sensitizers bearing a triphenylamino group for p-type NiO dye-sensitized solar cells.

Ji Z, Natu G, Wu Y.

ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8641-8. doi: 10.1021/am402263q. Epub 2013 Aug 22.

PMID:
23927567
3.

A highly conjugated benzimidazole carbene-based ruthenium sensitizer for dye-sensitized solar cells.

Ho SY, Su C, Li CY, Prabakaran K, Shen MT, Chen YF, Chang WC, Tingare YS, Akula S, Tsai SH, Li WR.

Chem Asian J. 2013 Sep;8(9):2196-203. doi: 10.1002/asia.201300447. Epub 2013 Jul 5.

PMID:
23832840
4.
5.

A simple synthetic route to obtain pure trans-ruthenium(II) complexes for dye-sensitized solar cell applications.

Barolo C, Yum JH, Artuso E, Barbero N, Di Censo D, Lobello MG, Fantacci S, De Angelis F, Grätzel M, Nazeeruddin MK, Viscardi G.

ChemSusChem. 2013 Nov;6(11):2170-80. doi: 10.1002/cssc.201200973. Epub 2013 Aug 7.

PMID:
23926052
6.

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 17;42(11):1809-18. doi: 10.1021/ar900034t.

PMID:
19408942
7.

A femtosecond study of the anomaly in electron injection for dye-sensitized solar cells: the influence of isomerization employing Ru(II) sensitizers with anthracene and phenanthrene ancillary ligands.

Cheema H, Younts R, Ogbose L, Gautam B, Gundogdu K, El-Shafei A.

Phys Chem Chem Phys. 2015 Jan 28;17(4):2750-6. doi: 10.1039/c4cp04741a. Epub 2014 Dec 15.

PMID:
25500934
8.

Thiocyanate-free ruthenium(II) sensitizers for dye-sensitized solar cells based on the cobalt redox couple.

Wu KL, Clifford JN, Wang SW, Aswani Y, Palomares E, Lobello MG, Mosconi E, De Angelis F, Ku WP, Chi Y, Nazeeruddin MK, Grätzel M.

ChemSusChem. 2014 Oct;7(10):2930-8. doi: 10.1002/cssc.201402030. Epub 2014 Aug 21.

PMID:
25146378
9.

Electron-rich heteroaromatic conjugated polypyridine ruthenium sensitizers for dye-sensitized solar cells.

Abbotto A, Manfredi N.

Dalton Trans. 2011 Dec 14;40(46):12421-38. doi: 10.1039/c1dt10832h. Epub 2011 Aug 11.

PMID:
21833401
10.

Superior Light-Harvesting Heteroleptic Ruthenium(II) Complexes with Electron-Donating Antennas for High Performance Dye-Sensitized Solar Cells.

Chen WC, Kong FT, Li ZQ, Pan JH, Liu XP, Guo FL, Zhou L, Huang Y, Yu T, Dai SY.

ACS Appl Mater Interfaces. 2016 Aug 3;8(30):19410-7. doi: 10.1021/acsami.6b04411. Epub 2016 Jul 22.

PMID:
27409513
11.

Effect of coadsorbent on the photovoltaic performance of zinc pthalocyanine-sensitized solar cells.

Yum JH, Jang SR, Humphry-Baker R, Grätzel M, Cid JJ, Torres T, Nazeeruddin MK.

Langmuir. 2008 May 20;24(10):5636-40. doi: 10.1021/la800087q. Epub 2008 Apr 25.

PMID:
18435553
12.

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 14;19(3):1028-34. doi: 10.1002/chem.201202709. Epub 2012 Nov 29.

PMID:
23197470
13.
14.

Electron transfer dynamics in dye-sensitized solar cells utilizing oligothienylvinylene derivates as organic sensitizers.

Clifford JN, Forneli A, López-Arroyo L, Caballero R, de la Cruz P, Langa F, Palomares E.

ChemSusChem. 2009;2(4):344-9. doi: 10.1002/cssc.200900043.

PMID:
19338013
15.

Exploring the heterogeneous interfaces in organic or ruthenium dye-sensitized liquid- and solid-state solar cells.

Kwon YS, Song I, Lim JC, Song IY, Siva A, Park T.

ACS Appl Mater Interfaces. 2012 Jun 27;4(6):3141-7. doi: 10.1021/am300480j. Epub 2012 Jun 11.

PMID:
22658859
16.

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. doi: 10.1016/j.saa.2011.05.070. Epub 2011 May 31.

PMID:
21684807
17.

D-π-A dye system containing cyano-benzoic acid as anchoring group for dye-sensitized solar cells.

Katono M, Bessho T, Meng S, Humphry-Baker R, Rothenberger G, Zakeeruddin SM, Kaxiras E, Grätzel M.

Langmuir. 2011 Dec 6;27(23):14248-52. doi: 10.1021/la203104v. Epub 2011 Oct 31.

PMID:
21999751
18.
19.

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 6;48(7):3215-27. doi: 10.1021/ic802087n.

PMID:
19278209
20.

Influence of polar solvents on photovoltaic performance of Monascusred dye-sensitized solar cell.

Lee JW, Kim TY, Ko HS, Han S, Lee SH, Park KH.

Spectrochim Acta A Mol Biomol Spectrosc. 2014 May 21;126:76-80. doi: 10.1016/j.saa.2014.01.122. Epub 2014 Feb 8.

PMID:
24589993

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