0000000001309638

AUTHOR

Cheng-yong Su

showing 8 related works from this author

Performance of dye-sensitized solar cells based on novel sensitizers bearing asymmetric double D−π−A chains with arylamines as donors

2012

Abstract Three novel, metal-free organic sensitizers bearing two asymmetric double donor-π-acceptor (D-π-A) chains ( DC1 - 3 ), each, and a reference dye containing single D-π-A chain ( SC ) with cyanoacrylic acid as electron acceptor are synthesized. Their photophysical, electrochemical properties and the performances of the corresponding dye-sensitized solar cells (DSSCs) are further investigated. The dyes, DC1, DC2 and DC3 contain one chain with diphenylamine and another chain with carbazole or phenothiazine as electron donor, while diphenylamine is only employed as electron donor in SC . Compared to the inferior solar energy to electricity conversion efficiency ( η ) of 2.82%, 4.66% and…

chemistry.chemical_classificationCarbazoleProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy conversion efficiencyDiphenylamineElectron donorElectron acceptorPhotochemistryElectrochemistrychemistry.chemical_compoundDye-sensitized solar cellchemistryPhenothiazineDyes and Pigments
researchProduct

Organic Dye Bearing Asymmetric Double Donor-π-Acceptor Chains for Dye-Sensitized Solar Cells

2011

A novel efficient metal free sensitizer containing asymmetric double donor-π-acceptor chains (DC) was synthesized for dye-sensitized solar cells (DSSCs). Comparing to 3.80%, 4.40% and 4.64% for the DSSCs based on the dyes with single chain (SC1, SC2) and cosensitizers (SC1 + SC2), the overall conversion efficiency reaches 6.06% for DC-sensitized solar cells as a result of its longer electron lifetime and higher incident monochromatic photon-to-current conversion efficiency.

Dye-sensitized solar cellBearing (mechanical)Metal freeChemistrylawOrganic ChemistryOrganic dyeEnergy conversion efficiencySingle chainMonochromatic colorPhotochemistryAcceptorlaw.inventionThe Journal of Organic Chemistry
researchProduct

2-Organoselenomethyl-1H-benzimidazole Complexes of Copper(II) and Copper(I)

2009

Structurally characterized 2-methylselenomethyl-1H-benzimidazole (msbi) is shown to form complexes in 2:1 ratio with copper(II). Whereas the central cation [Cu(msbi)2Cl]+ = 1+ in [Cu(msbi)2Cl]Cl·2MeOH crystallizes in an approximately mixed square-pyramidal/trigonal-bipyramidal structure (τ = 0.52) with the second and third row atoms chlorine and selenium in the equatorial plane, the related [Cu(msbi)2(MeOH)](BF4)2 = [2](BF4)2 exhibits a closer to square-pyramidal arrangement with τ = 0.36 for that complex dication 22+. In both cases, the Cu–N bonds are short at about 1.94 A, whereas the Cu–Se distances vary between 2.62 A for 1+ and ca. 2.54 A for 22+. Slight differences between the Jahn–Te…

Ligandchemistry.chemical_elementCrystal structureCopperDicationlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographyThioetherchemistrylawX-ray crystallographyElectron paramagnetic resonanceAcetonitrileZeitschrift für anorganische und allgemeine Chemie
researchProduct

CCDC 722408: Experimental Crystal Structure Determination

2010

Related Article: M.Leboschka, M.Sieger, B.Sarkar, J.Heck, M.Niemeyer, D.Bubrin, F.Lissner, T.Schleid, S.Zalis, Cheng-Yong Su, W.Kaim|2009|Z.Anorg.Allg.Chem.|635|2177|doi:10.1002/zaac.200900265

Space GroupCrystallographyChloro-bis(2-((methylselanyl)methyl)-1H-benzimidazole)-copper(ii) chloride methanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 722407: Experimental Crystal Structure Determination

2010

Related Article: M.Leboschka, M.Sieger, B.Sarkar, J.Heck, M.Niemeyer, D.Bubrin, F.Lissner, T.Schleid, S.Zalis, Cheng-Yong Su, W.Kaim|2009|Z.Anorg.Allg.Chem.|635|2177|doi:10.1002/zaac.200900265

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2-((Methylselanyl)methyl)-1H-benzimidazoleExperimental 3D Coordinates
researchProduct

CCDC 722406: Experimental Crystal Structure Determination

2010

Related Article: M.Leboschka, M.Sieger, B.Sarkar, J.Heck, M.Niemeyer, D.Bubrin, F.Lissner, T.Schleid, S.Zalis, Cheng-Yong Su, W.Kaim|2009|Z.Anorg.Allg.Chem.|635|2177|doi:10.1002/zaac.200900265

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(1-methyl-2-((phenylselanyl)methyl)-1H-benzimidazole)-copper(i) tetrafluoroborateExperimental 3D Coordinates
researchProduct

CCDC 722404: Experimental Crystal Structure Determination

2010

Related Article: M.Leboschka, M.Sieger, B.Sarkar, J.Heck, M.Niemeyer, D.Bubrin, F.Lissner, T.Schleid, S.Zalis, Cheng-Yong Su, W.Kaim|2009|Z.Anorg.Allg.Chem.|635|2177|doi:10.1002/zaac.200900265

(Methanol)-bis(2-((methylselanyl)methyl)-1H-benzimidazole)-copper(ii) bis(tetrafluoroborate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 722405: Experimental Crystal Structure Determination

2010

Related Article: M.Leboschka, M.Sieger, B.Sarkar, J.Heck, M.Niemeyer, D.Bubrin, F.Lissner, T.Schleid, S.Zalis, Cheng-Yong Su, W.Kaim|2009|Z.Anorg.Allg.Chem.|635|2177|doi:10.1002/zaac.200900265

Space GroupCrystallographyCrystal Systembis(2-((phenylselanyl)methyl)-1H-benzimidazole)-copper(i) (2-((phenylselanyl)methyl)-1H-benzimidazole)-(2-((phenylselanyl)methyl)-1H-benzimidazolide)-copper(i) hexafluorophosphate acetonitrile solvateCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct