共查询到14条相似文献,搜索用时 78 毫秒
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基于Re-BCP为缓冲层有机太阳能电池性能的研究 总被引:1,自引:1,他引:0
有机太阳能电池(OSCs)因成本低、质量轻、柔性 和可大面积制备等优点而被广泛关注。本文通过定向合成有机配合物Re-BCP,首次将其作 为阴极缓冲层引入到OSCs中。通过实验发现,OSCs效率与Re-BCP层厚度密切相关。在标准 太阳光照条件下,结构为ITO/CuPc(20nm)/C60(40nm)/Re-BCP(x nm)/Al(100nm)器件的效率随着Re-BCP厚度的增加先增大后变 小,当其厚为0nm时,效率为0.65%;厚为7nm时,效率为1.10%;而当厚为10nm时,效率降为0.50%。结合器件结构,探讨了器件性能提高的机理。 相似文献
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通过将聚乙二醇(PEG)掺入活性层制备聚合物太阳 能电池,利用PEG的迁移特性获得阴极修饰层,研 究PEG阴极修饰层对聚合物太阳能电池光电性能的影响。X射线光电子能谱(XPS)分 析表明,掺入活性层中的 PEG迁移到活性层与Al电极之间,形成了阴极缓冲层。吸收光谱、电流密度-电压 特性曲线和外量子 效率谱的分析表明,PEG阴极缓冲层的形成改善了活性层与阴极的界面接触特性, 降低了活性层与电 极之间的能级势垒,有利于载流子传输,因此显著地改善了聚合物太阳能电池的光电性能, 使得器件的开 路电压Voc、短路电流密度Jsc和填充因子(FF)都有明显提高。当P3HT:PCBM 活性层中掺入体积比为0.5%的PEG时,聚合物太阳能电池的能量转换 效率(P CE)最高,达到了3.07%,比未掺杂PEG的参考器件提 高了38.5%。 相似文献
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制备了有机紫外光探测器(OUV-PD),器件结构为I TO/m-MTDATA(30nm)/m-MTDATA:BAlq(40~60nm,1∶1)/BAlq(40nm)/LiF(1nm)/Al(100nm),并研究了施加Liq、TPBi、Bphen和Zn(4-MeBTZ)2为阴极缓冲层时对器件性 能的影响。实验结果表明,OUV-PD光响应与阴极缓冲层厚度和电子传输性能紧密相关,在 1.05mW/cm2的波长为365nm UV光照射下,响应度最大值分别达到218mA/W、247mA/W、305mA/W 和283mA/W。 相似文献
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制备了ITO/MoO3(6nm)/Rubrene(30nm)/C70(30nm)/BCP(6nm)/Al(150nm)的PN结构和ITO/MoO3(5nm)/Rubrene(25nm)/Rubrene:C70(5nm)/C70(25nm)/BCP(6nm)/Al(150nm)的PIN结构有机太阳能电池(OSCs)。通过对两种器件进行热处理,研究热处理对OSCs性能的影响。实验表明,在热处理后,PN结构和PIN结构器件的短路电流密度分别达到了3.526mA·cm-2和5.413mA·cm-2,功率转换效率分别达到了1.43%和2.09%。与未经过热处理的器件相比,PN结构和PIN结构器件的短路电流密度、填充因子、功率转换效率分别提高了19.0%、7.1%、28.3%和4.8%、20%、24.1%。可见,热处理可以提高Rubrene/C70OSCs的性能。 相似文献
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通过溶胶凝胶法(sol-gel)合成了TiO2纳米颗 粒(NPs),制备了结构为 ITO/PEDOT:PSS/P3HT:PCBM/TiO2/Al的有机太阳能电池(OSC)器件。通过优化阴极缓冲 层TiO2NPs的 热处理温度,考察了温度以及溶剂对TiO2NPs薄膜的光学性能、形貌结构和电学 性能的影响,并研究了其对OSC性能的影响及作用机理。实验发现,TiO2NPs处理温度 为80℃时,器件 的效率达到了2.52%。相对于参比器件,器件的光电转换效率(PCE) 、填充因子(FF)分别提高了60%、64.7%。 相似文献
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选用CuPc(酞菁酮)为供电子的材料,使用Bphen(4,7-二苯基-1,10-邻二氮杂菲)为缓冲层的材料,研究了结构为ITO/PEDOT:PSS/CuPc(20 nm)/C60(40 nm)/Bphen(x)/Ag(100 nm)的有机太阳能电池(OSC).考察OSC性能与缓冲层Bphen厚度之间的关系,优化器件的结构.在标准太阳光照条件下(AM1.5)测量器件的Ⅰ-Ⅴ特性,结果显示,太阳电池的能量转换效率与缓冲层厚度密切相关.采用高真空蒸发的方法,制作了结构为ITO/PEDOT:PSS/CuPc(20 nm)/C60(40 nm)/Bphen(x)/Ag(100 nm)的器件,器件效率随着Bphen厚度的增加先增大后变小,当厚度为0 nm时,效率为0.85%;当厚度为2.5 nm时,效率为1.22%;而当厚度为5 nm时,效率为1.69%;当厚度为7.5 nm时,效率则为0.79%,当厚度为10 nm时,效率则为0%. 相似文献
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采用NTCDA/PTCBI双阴极修饰层制备了结构为ITO /MoO3/Rubrene/C70/NTCDA/PTCBI/Al有机太阳能 电池(OSC),研究了双阴极修饰层对Rubrene/C70 OSC性能的影 响。实验结果表明,引入双阴极修饰层 后,器件的各性能参数有了显著提高。通过对PTCBI厚度优化发现,当PTCBI厚为5nm时器件 的各性 能参数最佳,器件的功率转换效率(PCE)=3.19%,电流密度Jsc=8.99mA·cm-2,开路电 压Voc=0.85V, 填充因子(FF)=41.58%,与未插入PTCBI 层相比器件的各性能分别提高了538%、338.5% 、13.3%和16.5%。 相似文献
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Cathode buffer layer (CBL) introduced between the active layer and cathode is crucial for selectively transporting electrons and blocking holes for polymer solar cells (PSCs). Calcium (Ca) is the most commonly used CBL in conventional-structure bulk heterojunction (BHJ) PSC devices, but is prone to oxidation due to its high reactivity, inhibiting its practical applications. Herein, we applied an alcohol-soluble fullerene aminoethanol derivative (C60-ETA) as an efficient CBL surpassing Ca in conventional-structure BHJ-PSC devices, leading to obvious efficiency enhancement with the best power conversion efficiency (PCE) reaching 9.66%. C60-ETA CBL was applied in PSC devices based on three different photoactive layer systems, including poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b′]dithiophene-co-3-fluorothieno[3,4-b]thiophene-2-carboxylate]:[6,6]-phenyl C71-butyric acid methyl ester (PTB7-Th:PC71BM), polythieno[3,4-b]thiophene-co-benzodithiophene (PTB7):PC71BM and poly(4,8-bis-alkyloxybenzo(l,2-b:4,5-b′)dithiophene-2,6-diylalt-(alkylthieno(3,4-b)thiophene-2-carboxylate)-2,6-diyl) (PBDTTT-C):PC71BM, affording the best PCE of 9.66%, 8.51% and 7.19%, respectively, which are all higher than those of the corresponding devices based on the commonly used Ca CBL. The mechanism of efficiency enhancement of C60-ETA CBL relative to Ca is studied, revealing that C60-ETA CBL may induce improvements on both the interfacial contact between the active layer/cathode and electron transport, facilitating electron extraction by the Al cathode, and consequently leading to the increase of short-circuit current density (Jsc), which contributes primarily to the PCE improvement. 相似文献
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阴极材料对有机太阳电池性能的影响 总被引:1,自引:1,他引:0
分别用Al、LiF/Al和Ca/Al制备了三种不同阴极材料的体相异质结有机太阳电池。对其光电特性进行了表征,分析了不同阴极材料对电池性能的影响机制。结果表明:所制备的有机太阳电池在10–1W/cm2辐照度的光照下,开路电压分别为0.419 3,0.565 0和0.591 1 V,能量转换效率分别为1.17%、2.06%和1.91%;采用LiF/Al层状阴极制备的有机太阳电池具有更高的能量转换效率;功函数愈低的材料做阴极,有机太阳电池的能量转换效率也愈高。 相似文献
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Nanocomposite buffer layer based on metal oxide and polymer is merging as a novel buffer layer for organic solar cells, which combines the high charge carrier mobility of metal oxide and good film formation properties of polymer. In this work, a nanocomposite of zinc oxide and a commercialized available polyethylenimine (PEI) was developed and used as the cathode buffer layer (CBL) for the inverted organic solar cells and p-i-n heterojunction perovskite solar cells. The cooperation of PEI in nano ZnO offers a good film forming ability of the composite material, which is an advantage in device fabrication. In addition, power conversion efficiency (PCE) of the ZnO:PEI CBL based device was also improved when compared to that of ZnO-only and PEI-only devices. The highest PCE of P3HT:PC61BM and PTB7-Th:PC61BM devices reached to 3.57% and 8.16%, respectively. More importantly, there is no obvious device performance loss with the increase of the layer thickness of ZnO:PEI CBL to 60 nm in organic solar cells, which is in contrast to the PEI based devices, whose device performance decreases dramatically when the PEI layer thickness is higher than 6 nm. Such a nano composite material is also applicable in inverted heterojunction perovskite solar cells. A PCE of 11.76% was achieved for the perovskite solar cell with a thick ZnO:PEI CBL (150 nm) CBL, which is around 1.71% higher than that of the reference cell without CBL, or with ZnO CBL. In addition, stability of the organic and perovskite solar cells having ZnO:PEI CBL was also found to be improved in comparison with that of PEI based device. 相似文献