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81.
Silver nanoprisms (AgNPs) affect the performance of organic solar cells (OSCs) in different ways depending on their positions in the device. To investigate this issue, we incorporate AgNPs in different positions of OSCs and compare their performance. The power conversion efficiency (PCE) is improved by 23.60% to 3.98% when the AgNPs are in- corporated in front of the active layer. On the other hand, when AgNPs are incorporated in the back of the active layer, the short-circuit current density (Jsc) is improved by 17.44% to 10.84 mA/cm2. However, if AgNPs are incorporated in the active layer, both open-circuit voltage (Voc) and Jsc are decreased. We discuss the position effect on the device performance, clarify the absorption shadow and exciton recombination caused by AgNPs, and finally indicate that the optimal position ofplasmonic AgNPs is in front of the active layer. 相似文献
82.
Influence of Dopant Concentration on Electroluminescent Performance of Organic White-Light-Emitting Device with Double-Emissive-Layered Structure 下载免费PDF全文
A novel phosphorescent organic white-light-emitting device (WOLED) with contiguration of ITO/NPB/CBP: TBPe:rubrene/Zn(BTZ)2:Ir(piq)2(acac)/Zn(BTZ)2/Mg:Ag is fabricated successfully, where the phosphorescent dye bis (1-(phenyl)isoquinoline) iridium (Ⅲ) acetylanetonate (Ir(piq)2 (acac)) doped into bis-(2-(2-hydroxyphenyl) benzothiazole)zinc (Zn(BTZ)2) (greenish-blue emitting material with electron transport character) as the red emitting layer, and fluorescent dye 2,5,8,11-tetra-tertbutylperylene (TBPe) and 5,6,11,12-tetraphenyl-naphthacene (rubrene) together doped into 4,4'-N,N'-dicarbazole-biphenyl (CBP) (ambipolar conductivity material) as the blue-orange emitting layer, respectively. The two emitting layers are sandwiched between the hole-transport layer N ,N'-biphenyl-N , N'-bis (1-naph thyl)-(1,1'-biphenyl)-4, 4 Cdiamine (NP B) and electron-transport layer (Zn(BTZ)2 ) The optimum device turns on at the driving voltage of 4.5 V. A maximum external quantum efficiency of 1.53%. and brightness 15000 cd/m^2 are presented. The best point of the Commission Internationale de 1'Eclairage (CIE) coordinates locates at (0.335, 0.338) at about 13 V. Moreover, we also discuss how to achieve the bright pure white light through optimizing the doping concentration of each dye from the viewpoint of energy transfer process. 相似文献
83.
采用N,N'-二正辛烷基-3,4,9,10-苝四甲酰二亚胺(PTCDI-C8)对钙钛矿电池电子传输层(PCBM)进行界面修饰以减少PCBM与Al电极之间的漏电流,提高阴极的电子收集效率。通过调节PTCDI-C8薄膜的厚度优化界面接触和电子传输性能。实验结果表明:当PTCDI-C8薄膜的厚度为20 nm时得到的器件性能最优。光电转换效率(PCE)由5.26%提高到了8.65%,开路电压(Voc)为0.92 V,短路电流(Jsc)为15.68 mA/cm2,填充因子(FF)为60%。PTCDI-C8能够有效阻挡空穴向阴极传输,同时PTCDI-C8具有较高的电子迁移率以及较高的稳定性,在增加电子传输的同时,可减少环境对PCBM的侵蚀,提高了器件的稳定性。 相似文献
84.
采用N,N'-二正辛烷基-3,4,9,10-苝四甲酰二亚胺(PTCDI-C8)对钙钛矿电池电子传输层(PCBM)进行界面修饰以减少PCBM与Al电极之间的漏电流,提高阴极的电子收集效率。通过调节PTCDI-C8薄膜的厚度优化界面接触和电子传输性能。实验结果表明:当PTCDI-C8薄膜的厚度为20 nm时得到的器件性能最优。光电转换效率(PCE)由5.26%提高到了8.65%,开路电压(Voc)为0.92 V,短路电流(Jsc)为15.68 m A/cm2,填充因子(FF)为60%。PTCDI-C8能够有效阻挡空穴向阴极传输,同时PTCDI-C8具有较高的电子迁移率以及较高的稳定性,在增加电子传输的同时,可减少环境对PCBM的侵蚀,提高了器件的稳定性。 相似文献
85.
聚对二甲苯类薄膜用于有机电致发光器件的封装 总被引:1,自引:0,他引:1
采用热解化学气相沉积聚合(TCVDP)方法制备了聚对二甲苯(PPX)和聚一氯对二甲苯(PCPX)薄膜材料,利用其对有机电敛发光器件(OLED)进行了封装.利州紫外可见光谱、扫描电镜(SEM)对薄膜的相关性能进行了表征.比较了器件经过两种薄膜封装前后器件的工作寿命.实验结果表明:利用TCVDP方法,可以制备出透明的表面平整、结构致密的聚对二甲苯类薄膜材料;用于OLED)的封装能大幅度地提高器件的工作寿命,经过PPX封装后的寿命为1215 h,经过PCPX封装后的寿命为1 558 h,比未封装的器件寿命(197 h)提高了6~8倍. 相似文献
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选用一种新型高效的蓝光有机小分子荧光染料TBPe,首次制备了以PVK:TBPe为蓝光发光层和Alq3:rubrene为橙红光发光层的双层白光有机电致发光器件,器件结构为ITO/PVK:TBPe/Alq3:rubrene/Mg:Ag。通过适当调节各有机层的掺杂比例和厚度,得到了发光性能比较理想的白光器件。器件在7V左右启亮,而且随着外加电压的变化,色坐标基本保持不变,在外加驱动电压为16V时,器件的亮度为738cd/m2,外量子效率为0.2%。我们还尝试选用本身可以发绿白光,而且兼具电子传输特性的母体材料Zn(BTZ)2替代Alq3,器件的最大亮度提高到1300cd/m2,色坐标为(0.32,0.36),更加接近白色等能点,器件其他光电性能也得到了显著地提高。 相似文献
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制备了结构为ITO/NPB/CBP:TBPe:rubrene/BAlq:Ir(piq)2(acac)/BAlq/Alq3/Mg:Ag的白色磷光有机电致发光器件.利用两种不同的主体材料,即用双载流子传输型主体材料CBP掺杂荧光染料TBPe及rubrene作为蓝光和橙黄光发光层;用电子传输型主体材料BAlq掺杂磷光染料Ir(piq)2(acac)作为红色发光层.以上双发光层夹于空穴传输层NPB与具有电子传输性的阻挡层BALq之间.讨论了如何控制 相似文献