Understanding polycarbazole-based polymer: CdSe hybrid solar cells

被引:23
作者
Lek, Jun Yan [1 ]
Lam, Yeng Ming [1 ,3 ]
Niziol, Jacek [2 ]
Marzec, Mateusz [2 ]
机构
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[2] AGH Univ Sci & Technol, Fac Phys & Appl Comp Sci, PL-30059 Krakow, Poland
[3] Rhein Westfal TH Aachen, Inst Werkstoffe Elektrotech 2, D-52074 Aachen, Germany
关键词
OPEN-CIRCUIT VOLTAGE; PHOTOVOLTAIC DEVICES; EFFICIENCY; NANOCRYSTALS; NANOPARTICLES; ENHANCEMENT; CONVERSION; NETWORK; BLENDS;
D O I
10.1088/0957-4484/23/31/315401
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report for the first time the fabrication and characterization of organic-inorganic bulk heterojunction (BHJ) hybrid solar cells made of poly[N-9 ''-hepta-decanyl-2,7-carbazole-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (PCDTBT) and pyridine-capped CdSe nanorods. By optimizing both CdSe loading and active layer film thickness, the power conversion efficiencies (PCEs) of PCDTBT: CdSe hybrid solar cells were able to reach 2%, with PCDTBT: CdSe devices displaying an open-circuit voltage (V-OC) that is 35% higher than P3HT:CdSe devices due to the deeper HOMO level of PCDTBT polymer. The performance of PCDTBT:CdSe devices is limited by its morphology and also its lower LUMO energy offset compared to P3HT:CdSe devices. Hence, the performance of PCDTBT:CdSe solar cells could be further improved by modifying the morphology of the films and also by including an interlayer to generate a built-in voltage to encourage exciton dissociation. Our results suggest that PCDTBT could be a viable alternative to P3HT as an electron donor in hybrid BHJ solar cells for high photovoltage application.
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页数:9
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