نتایج جستجو برای: PC71BM
تعداد نتایج: 134 فیلتر نتایج به سال:
Control over the ratio of two blocks in a new class of all-conjugated diblock copolymers, poly(3-butylthiophene)-b-poly(3-hexylthiophene) (P3BHT), provides a facile approach to precisely tune the molecular organization and nanoscale morphology in polymer bulk heterojunction (BHJ) solar cells. In stark contrast to the power conversion efficiency, PCE, of 1.08% in poly(3-butylthiophene) (P3BT)/ [...
The energy level alignments at donor/acceptor interfaces in organic photovoltaics (OPVs) play a decisive role in device performance. However, little is known about the interfacial energetics in polymer OPVs due to technical issues of the solution process. Here, the frontier ortbial line-ups at the donor/acceptor interface in high performance polymer OPVs, PTB7/PC71BM, were investigated using in...
We report a trap-assisted photomultiplication (PM) phenomenon in solution-processed polymer photodetectors (PPDs) based on P3HT:PC71BM as the active layer, the maximum EQE of 16,700% is obtained for the PPDs with PC71BM doping weight ratio of 1%. The PM phenomenon is attributed to the enhanced hole tunneling injection assisted by trapped electrons in PC71BM near Al cathode, which can be demonst...
Polymer:fullerene blends have been widely studied as an inexpensive alternative to traditional silicon solar cells. Some polymer:fullerene blends, such as blends of poly(2,5bis(3-tetradecylthiophen-2-yl)thieno[3,2-b]thiophene (pBTTT) with phenyl-c71-butyric acid methyl ester (PC71BM), form bimolecular crystals due to fullerene intercalation between the polymer side chains. Here we present the d...
In the current work, a series of bithiopheneimide (BTI)-based D-A copolymers were investigated based on the reported PDTSBTI (1) to screen excellent molecules toward organic photovoltaic (OPV) donor materials. It is found that the PCE based on the proposed derivative 4, where the silicon atom is replaced with vinyl and cyano groups on the DTS unit, shows a 70 percent improvement by Scharber dia...
In this paper the three new narrow bandgap D–A conjugated copolymers P1, P2 and P3 based on different weak donor fused thiophene-imidazole containing derivatives and the same benzothiadiazole acceptor unit were synthesized by Stille cross-coupling polymerization and characterized by 1H NMR, elemental analysis, GPC, TGA, DSC. These copolymers exhibit intensive absorbance in the range 350–900 nm ...
We report an indium tin oxide (ITO) free inverted organic solar cell with alternate aluminium doped zinc (AZO) front cathode layer based on the consideration of blocking harmful ultraviolet (UV) rays, which is one prominent reasons for degradation cells. To further enhance power conversion efficiency AZO/ZnO/PTB7:PC71BM/MoO3/Ag cell, plasmonic gold nanoflowers were embedded inside active layer....
The use of templating method to synthesize the vanadyl 2,9,16,23-tetraphenoxy-29H,31H-phthalocyanine (VOPcPhO):[6,6]-phenyl C71 butyric acid methyl ester (PC71BM) composite nanotubes is presented here. VOPcPhO is a p-type material and PC71BM is an n-type material which acts as an electron donor and electron acceptor, respectively. Both materials have been studied due to their potential applicat...
The light absorption ability and morphology of the active components are two of the key factors that determine the energy conversion efficiency in organic solar cells (OSCs). Determining the relative importance of each of these aspects is decisive for the construction of more efficient OSCs. Here we introduce two p-extended derivatives of tetrathiafulvalene as electron donors for solution-proce...
A strategy for increasing the conversion efficiency of organic photovoltaics has been to increase the VOC by tuning the energy levels of donor and acceptor components. However, this opens up a new loss pathway from an interfacial charge transfer state to a triplet exciton (TE) state called electron back transfer (EBT), which is detrimental to device performance. To test this hypothesis, we stud...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید