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Fabrication of CdS/SnS Heterojunction for Photovoltaic Application
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作者 Hongnan Li Shuying Cheng +3 位作者 Jie Zhang Weihui Huang Haifang Zhou Hongjie Jia 《World Journal of Condensed Matter Physics》 2015年第1期10-17,共8页
SnS/CdS heterojunction is a promising system for photovoltaic application. SnS thin films were thermally evaporated onto CdS/ITO coated glass substrates. The structure of the device was glass/ ITO/CdS/SnS/In/Ag and I-... SnS/CdS heterojunction is a promising system for photovoltaic application. SnS thin films were thermally evaporated onto CdS/ITO coated glass substrates. The structure of the device was glass/ ITO/CdS/SnS/In/Ag and I-V curves of the fabricated devices were measured under dark and illuminated conditions, respectively. We discussed the relationship of the thickness and annealing temperature of CdS buffer layers with the performance of SnS/CdS heterojunctions. The optimum thickness and annealing temperature of the CdS buffer layers were 50 nm and 350°C, respectively. The best device had a conversion efficiency of 0.0025%. 展开更多
关键词 SNS Films HETEROJUNCTION Thermally vacuum-evaporation I-V CURVES
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X-shape oligo(thiophene)s as donor materials for vacuum-deposited organic photovoltaic cells
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作者 王亚楠 周印华 +4 位作者 徐跃 孙晓波 吴伟才 田文晶 刘云圻 《Chinese Physics B》 SCIE EI CAS CSCD 2008年第4期1448-1453,共6页
The films of two x-shape oligo(thiophene)s, 3, 4-dibithienyl-2, 5-dithienylthiophene (7T) and 2, 5-dibithienyl-3, 4- ditrithienylthiophene (11T), which are prepared by vacuum evaporation, have been investigated ... The films of two x-shape oligo(thiophene)s, 3, 4-dibithienyl-2, 5-dithienylthiophene (7T) and 2, 5-dibithienyl-3, 4- ditrithienylthiophene (11T), which are prepared by vacuum evaporation, have been investigated as novel electron donor layers in two-layer photovoltaic cells. UV-Vis absorptions show red-shifted and broadened absorptions of the vacuumevaporated films as compared with those of the corresponding solutions and spin-coating films, which is beneficial for photovoltaic properties. X-ray diffraction (XRD) and differential scanning calorimetry (DSC) measurements show that the vacuum-evaporated films are almost amorphous. Two-layer photovoltaic cells have been realized by the thermal evaporation of 7T and llT as donors and N, N′-bis(1-ethylpropyl)-3, 4:9,10-perylene bis(tetracarboxyl diimide) (EP- PTC) as an acceptor. An energy conversion efficiency (ECE) of 0.18% of the cell based on 7T with an irradiation of white light at 100 mw/cm^2 has been demonstrated by the measurements of current (I)- voltage (V) curves of the cells to be higher than the ECE of the reference system based on donor dihexylterthienyl (H3T) that is linear and without α, β linkage. 展开更多
关键词 oligo(thiophene)s vacuum-evaporated film solar cell
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Fullerenes and derivatives as electron transport materials in perovskite solar cells 被引量:1
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作者 Kaicheng Zhang Hao Yu +6 位作者 Xiaodong Liu Qingqing Dong Zhaowei Wang Yaofeng Wang Ning Chen Yi Zhou Bo Song 《Science China Chemistry》 SCIE EI CAS CSCD 2017年第1期144-150,共7页
In this study,two fullerenes(C60,C70)and their methano-substitutions(PC61BM,PC71BM),as electron transport materials(ETMs)in perovskite solar cells(Pero-SCs),were systematically studied.As being used as ETMs,methanoful... In this study,two fullerenes(C60,C70)and their methano-substitutions(PC61BM,PC71BM),as electron transport materials(ETMs)in perovskite solar cells(Pero-SCs),were systematically studied.As being used as ETMs,methanofullerenes,though with lower electron mobility compared to the counterpart pristine fullerenes,lead to higher power conversion efficiencies(PCEs)of Pero-SCs.The difference is likely caused by the fill-out vacancies and smoother morphology of the interfaces between ETM and perovskite layers,as they were prepared by different methods.In addition,compared to C60 and PC61BM,C70 and PC71BM showed priority in terms of short-circuit current density,which should be attributed to fast free charge extraction abilities. 展开更多
关键词 perovskite solar cells pristine fullerenes methanofullerenes vacuum-evaporation solution-processed
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