Two title compounds, 4,4?diformyl-diphenoxyethane (compound 1, C16H14O4) and 4,4?4创-triformyl-triphenoxytriethylamine (compound 2, C27H27NO6), were synthesized by condensation of 4-hydroxybenzaldehyde with 1,2-dichlo...Two title compounds, 4,4?diformyl-diphenoxyethane (compound 1, C16H14O4) and 4,4?4创-triformyl-triphenoxytriethylamine (compound 2, C27H27NO6), were synthesized by condensation of 4-hydroxybenzaldehyde with 1,2-dichloroethane and tris(2-chloroethyl)amine, respectively in dimethyl formamide in the presence of anhydrous potassium carbonate. The crystal data are: monoclinic, P21/c, a = 7.571(2), b = 12.608(3), c = 7.357(2) ? b = 105.823(6)? V = 675.7(2) 3, Mr = 270.3, Z = 2, Dc = 1.328 g/cm3, F(000) = 284, m(MoKa) = 0.096 mm-1, R = 0.0537 and wR = 0.2189 for compound 1; and monoclinic, P21/n, a = 11.7162(6), b = 9.0042(6), c = 22.908(2) ? b = 99.505(1)? V = 2383.5(3) ?, Mr = 461.50, Z = 4, Dc = 1.286 g/cm3, F(000)= 976, m(MoKa) = 0.091 mm-1, R = 0.0464 and wR = 0.1462 for compound 2. The molecule of compound 1 (dialdehyde) is located at the crystallographic inversion center nearby the midpoint of C(8)C(8A) single bond. The three chains in the molecule of compound 2 (trialdehyde) are of non-crystallographic pseudo-C3 symmetry, and each of them is quite planar.展开更多
Photovoltaic performance of the organic solar cells （OSCs） based on 2-（（5＇-（4-（（4-（（E）-2-（5＇-（2,2-dicyanovinyl）-3＇,4-dihexyl- 2,2＇-bithiophen-5-yl）vinyl） phenyl）（phenyl）amino）styryl）-4~4＇-dihe...Photovoltaic performance of the organic solar cells （OSCs） based on 2-（（5＇-（4-（（4-（（E）-2-（5＇-（2,2-dicyanovinyl）-3＇,4-dihexyl- 2,2＇-bithiophen-5-yl）vinyl） phenyl）（phenyl）amino）styryl）-4~4＇-dihexyl-2,2＇-bithiophen-5-yl）methylene）malononitrile （L（TPA- bTV-DCN）） as donor and PC70BM as acceptor was optimized using 0.25 vol% high boiling point solvent additive of 1-chloronaphthalene （CN）, 1,6-hexanedithiol （HDT）, or 1,8-diodooctane （DIO）. The optimized OSC based on L（TPA-bTV- DCN）-PC70BM （1：2, w/w） with 0.25 vol% CN exhibits an enhanced power conversion efficiency （PCE） of 2.61%, with Voc of 0.87 V, Jsc of 6.95 mA/cm2, and FF of 43.2%, under the illumination of 100 mW/cm2 AM 1.5 G simulated solar light, whereas the PCE of the OSC based on the same active layer without additive is only 1.79%. The effect of the additive on absorption spectra and the atomic force microscopy images of L（TPA-bTV-DCN）-PCv0BM blend films were further investigated. The improved efficiency of the device could be ascribed to the enhanced absorption and optimized domain size in the L（TPA-bTV-DCN）-PC70BM blend film.展开更多
基金The authors thank the financial support of the Natural Science Foundation of Fujian Province (No. E0110010)
文摘Two title compounds, 4,4?diformyl-diphenoxyethane (compound 1, C16H14O4) and 4,4?4创-triformyl-triphenoxytriethylamine (compound 2, C27H27NO6), were synthesized by condensation of 4-hydroxybenzaldehyde with 1,2-dichloroethane and tris(2-chloroethyl)amine, respectively in dimethyl formamide in the presence of anhydrous potassium carbonate. The crystal data are: monoclinic, P21/c, a = 7.571(2), b = 12.608(3), c = 7.357(2) ? b = 105.823(6)? V = 675.7(2) 3, Mr = 270.3, Z = 2, Dc = 1.328 g/cm3, F(000) = 284, m(MoKa) = 0.096 mm-1, R = 0.0537 and wR = 0.2189 for compound 1; and monoclinic, P21/n, a = 11.7162(6), b = 9.0042(6), c = 22.908(2) ? b = 99.505(1)? V = 2383.5(3) ?, Mr = 461.50, Z = 4, Dc = 1.286 g/cm3, F(000)= 976, m(MoKa) = 0.091 mm-1, R = 0.0464 and wR = 0.1462 for compound 2. The molecule of compound 1 (dialdehyde) is located at the crystallographic inversion center nearby the midpoint of C(8)C(8A) single bond. The three chains in the molecule of compound 2 (trialdehyde) are of non-crystallographic pseudo-C3 symmetry, and each of them is quite planar.
基金supported by the National Basic Research Program of China(2014CB643501)the National Natural Science Foundation of China(91333204)the support from Ministry of Education and Jiangsu Province(20100092120037,XNY-48-037)
文摘Photovoltaic performance of the organic solar cells （OSCs） based on 2-（（5＇-（4-（（4-（（E）-2-（5＇-（2,2-dicyanovinyl）-3＇,4-dihexyl- 2,2＇-bithiophen-5-yl）vinyl） phenyl）（phenyl）amino）styryl）-4~4＇-dihexyl-2,2＇-bithiophen-5-yl）methylene）malononitrile （L（TPA- bTV-DCN）） as donor and PC70BM as acceptor was optimized using 0.25 vol% high boiling point solvent additive of 1-chloronaphthalene （CN）, 1,6-hexanedithiol （HDT）, or 1,8-diodooctane （DIO）. The optimized OSC based on L（TPA-bTV- DCN）-PC70BM （1：2, w/w） with 0.25 vol% CN exhibits an enhanced power conversion efficiency （PCE） of 2.61%, with Voc of 0.87 V, Jsc of 6.95 mA/cm2, and FF of 43.2%, under the illumination of 100 mW/cm2 AM 1.5 G simulated solar light, whereas the PCE of the OSC based on the same active layer without additive is only 1.79%. The effect of the additive on absorption spectra and the atomic force microscopy images of L（TPA-bTV-DCN）-PCv0BM blend films were further investigated. The improved efficiency of the device could be ascribed to the enhanced absorption and optimized domain size in the L（TPA-bTV-DCN）-PC70BM blend film.
