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Items: 1 to 20 of 120

1.

Restricted rotation of σ-bonds through a rigidified donor structure to increase the ICT ability of platinum-acetylide-based DSSCs.

Li ZY, Wu W, Zhang Q, Jin B, Hua J, Yang HB, Tian H.

Chem Asian J. 2013 Nov;8(11):2660-9. doi: 10.1002/asia.201300578. Epub 2013 Jul 4.

PMID:
23828774
2.

Organic dyes containing carbazole as donor and π-linker: optical, electrochemical, and photovoltaic properties.

Venkateswararao A, Thomas KR, Lee CP, Li CT, Ho KC.

ACS Appl Mater Interfaces. 2014 Feb 26;6(4):2528-39. doi: 10.1021/am404948w. Epub 2014 Feb 5.

PMID:
24456063
3.

New dual donor-acceptor (2D-π-2A) porphyrin sensitizers for stable and cost-effective dye-sensitized solar cells.

Ambre RB, Chang GF, Zanwar MR, Yao CF, Diau EW, Hung CH.

Chem Asian J. 2013 Sep;8(9):2144-53. doi: 10.1002/asia.201300328. Epub 2013 Jul 3.

PMID:
23825005
4.

Organic dyes containing fluorene decorated with imidazole units for dye-sensitized solar cells.

Kumar D, Thomas KR, Lee CP, Ho KC.

J Org Chem. 2014 Apr 4;79(7):3159-72. doi: 10.1021/jo500330r. Epub 2014 Mar 24.

PMID:
24628443
5.

Unsymmetric platinum(II) bis(aryleneethynylene) complexes as photosensitizers for dye-sensitized solar cells.

Dai FR, Chen YC, Lai LF, Wu WJ, Cui CH, Tan GP, Wang XZ, Lin JT, Tian H, Wong WY.

Chem Asian J. 2012 Jun;7(6):1426-34. doi: 10.1002/asia.201200027. Epub 2012 Apr 11.

PMID:
22492546
6.

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. doi: 10.1002/asia.201100967. Epub 2012 Feb 10.

PMID:
22328182
7.

Enhanced performance of quasi-solid-state dye-sensitized solar cells by branching the linear substituent in sensitizers based on thieno[3,4-c]pyrrole-4,6-dione.

Feng Q, Zhang W, Zhou G, Wang ZS.

Chem Asian J. 2013 Jan;8(1):168-77. doi: 10.1002/asia.201200720. Epub 2012 Oct 18.

PMID:
23081835
8.

Theoretical studies on organic D-π-A sensitizers with planar triphenylamine donor and different π-linkers for dyes-sensitized solar cells.

Li HB, Zhang JZ, Zhang J, Wu Y, Duan YA, Su ZM, Geng Y.

J Mol Model. 2014 Jul;20(7):2309. doi: 10.1007/s00894-014-2309-2. Epub 2014 Jun 25.

PMID:
24961897
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 16;73(10):3791-7. doi: 10.1021/jo800159t. Epub 2008 Apr 15.

PMID:
18412319
10.

Carbazole-dendrimer-based donor-π-acceptor type organic dyes for dye-sensitized solar cells: effect of the size of the carbazole dendritic donor.

Thongkasee P, Thangthong A, Janthasing N, Sudyoadsuk T, Namuangruk S, Keawin T, Jungsuttiwong S, Promarak V.

ACS Appl Mater Interfaces. 2014 Jun 11;6(11):8212-22. doi: 10.1021/am500947k. Epub 2014 May 30.

PMID:
24878449
11.

D-A-π-A featured sensitizers bearing phthalimide and benzotriazole as auxiliary acceptor: effect on absorption and charge recombination dynamics in dye-sensitized solar cells.

Li W, Wu Y, Zhang Q, Tian H, Zhu W.

ACS Appl Mater Interfaces. 2012 Mar;4(3):1822-30. doi: 10.1021/am3001049. Epub 2012 Mar 12.

PMID:
22387485
12.

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. doi: 10.1002/chem.201103702. Epub 2012 May 9.

PMID:
22573564
13.

Constructing organic D-A-π-A-featured sensitizers with a quinoxaline unit for high-efficiency solar cells: the effect of an auxiliary acceptor on the absorption and the energy level alignment.

Pei K, Wu Y, Wu W, Zhang Q, Chen B, Tian H, Zhu W.

Chemistry. 2012 Jun 25;18(26):8190-200. doi: 10.1002/chem.201103542. Epub 2012 May 21.

PMID:
22615266
14.

Dye-sensitized solar cells based on (donor-π-acceptor)2 dyes with dithiafulvalene as the donor.

Lee TH, Hsu CY, Liao YY, Chou HH, Hughes H, Lin JT.

Chem Asian J. 2014 Jul;9(7):1933-42. doi: 10.1002/asia.201402232. Epub 2014 May 27.

PMID:
24867366
15.

Organic sensitizers containing julolidine moiety for dye-sensitized solar cells.

Kim DW, Choi JJ, Kang MK, Kang Y, Lee C.

J Nanosci Nanotechnol. 2008 Sep;8(9):4761-6.

PMID:
19049103
16.

Molecular design and performance of hydroxylpyridium sensitizers for dye-sensitized solar cells.

Zhao J, Yang X, Cheng M, Li S, Sun L.

ACS Appl Mater Interfaces. 2013 Jun 12;5(11):5227-31. doi: 10.1021/am4010545. Epub 2013 May 31.

PMID:
23692189
17.

Effects of bis-carbazole based D-π-A sensitizers on solar energy capture in DSSCs.

Kim BH, Freeman HS.

Photochem Photobiol Sci. 2013 Mar;12(3):421-31. doi: 10.1039/c2pp25262g.

PMID:
23149843
18.

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 25;16(40):12244-54. doi: 10.1002/chem.201001424.

PMID:
20842671
19.

Series of new D-A-π-A organic broadly absorbing sensitizers containing isoindigo unit for highly efficient dye-sensitized solar cells.

Ying W, Guo F, Li J, Zhang Q, Wu W, Tian H, Hua J.

ACS Appl Mater Interfaces. 2012 Aug;4(8):4215-24. doi: 10.1021/am300925e. Epub 2012 Aug 2.

PMID:
22817332
20.

Fine tuning the performance of DSSCs by variation of the π-spacers in organic dyes that contain a 2,7-diaminofluorene donor.

Baheti A, Thomas KR, Lee CP, Ho KC.

Chem Asian J. 2012 Dec;7(12):2942-54. doi: 10.1002/asia.201200752. Epub 2012 Sep 28.

PMID:
23023960
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