天堂国产午夜亚洲专区-少妇人妻综合久久蜜臀-国产成人户外露出视频在线-国产91传媒一区二区三区

當前位置:主頁 > 科技論文 > 電子信息論文 >

有機藍色熒光和磷光主體材料的制備及電致發(fā)光性能研究

發(fā)布時間:2018-11-05 15:00
【摘要】:有機光電材料是有機電致發(fā)光二極管(OLED)的關鍵,其自身結構在很大程度上決定了器件的發(fā)光性能和操作穩(wěn)定性。因此,如何設計、開發(fā)與制備性能優(yōu)異的發(fā)光材料是實現(xiàn)高性能OLED器件的關鍵科學問題。在此背景下,本文設計、制備了扭轉型蒽類衍生物、新型D-A-D-A-D型化合物兩組有機藍色熒光材料以及硅烷衍生物磷光主體材料,并對其電致發(fā)光性能進行了研究,具體工作如下: (1)以蒽為中心,,菲并咪唑、菲為功能活性單元,制備扭轉型藍光材料:p-PABPI和m-PABPI,對其光物理、光化學性能及電致發(fā)光性能進行了研究。p-PABPI基非摻雜器件展示了強的藍光,最大的亮度為18980cd/m2,最大電流效率為3.98cd/A,最大功率效率為2.80lm/W,色坐標為(0.15,0.13),該效率為m-PABPI基非摻雜器件的3倍,這為我們提供了一種新的高性能藍光分子的設計方法。p-PABPI基摻雜電致發(fā)光器件p1和p2展示了色坐標CIE(x, y)分別為(0.15,0.08)和(0.15,0.09),非常接近標準藍光色坐標(0.14,0.08),而m-PABPI基摻雜OLED展示了一種罕見的色坐標為(0.15,0.04)的藍紫光,且不隨摻雜濃度的變化而變化。 (2)基于菲并咪唑缺電子基團和三苯胺、咔唑富電子基團合成D-A-D-A-D型藍色熒光材料:“N”型和“H”型分子,對其光物理、光化學和電致發(fā)光性能(旋涂法)進行了研究!癗”型分子基器件和“H”型分子基器件的最大發(fā)光效率(CEmax)分別為1.51cd/A和1.14cd/A,最大功率效率(PEmax)分別為0.56lm/W和0.38lm/W,最大外量子效率(EQEmax)分別為1.04%和0.80%,為適合濕法加工小分子的結構設計提供了新的思路。 (3)設計并合成了以四苯基硅為中心,咔唑、苯并咪唑為取代基的化合物TCzPSi和DCzIPSi,對其光物理、光化學性能進行了研究。它們的三線態(tài)能級高于FIrpic的三線態(tài)能級,且相應的單/三線態(tài)交換能ΔEST小,為理想的藍色磷光主體材料。
[Abstract]:Organic optoelectronic material is the key of electromechanical light-emitting diode (OLED). Its structure determines the luminescence performance and operation stability of the device to a great extent. Therefore, how to design, develop and fabricate luminescent materials with excellent performance is a key scientific problem in the realization of high performance OLED devices. In this context, torsional anthracene derivatives, two groups of organic blue fluorescent materials of novel D-A-D compounds and phosphorescent host materials of silane derivatives were designed and prepared, and their electroluminescent properties were studied. The main works are as follows: (1) taking anthracene as the center, phenanthrene imidazole and phenanthrene as functional active units, the torsional blue light materials, p-PABPI and m-PABPI, were prepared, and their photophysical properties were analyzed. The photochemical and electroluminescent properties of p-PABPI based non-doped devices are studied. The maximum luminance is 18980cd / m ~ 2, the maximum current efficiency is 3.98cdr / A, the maximum power efficiency is 2.80lm / r / W, the maximum luminance is 18980cd / m ~ 2, the maximum current efficiency is 3.98cdr / A, the maximum power efficiency is 2.80lmW, The color coordinate is (0.15 ~ 0.13), and the efficiency is three times that of the m-PABPI based undoped device. This provides us with a new design method for blue light molecules with high performance. P-PABPI doped electroluminescent devices p1 and p2 show that the color coordinate CIE (x, y) is (0.15 ~ 0.08) and (0.15 ~ 0.09), respectively. It is very close to the standard blue color coordinate (0. 14 ~ 0. 08), while m-PABPI based doped OLED shows a rare blue violet light with a color coordinate of (0. 15 ~ 0. 04) and does not vary with the concentration of doping. (2) based on the electron-deficient group and trianiline, carbazole-rich groups were used to synthesize D-A-D type blue fluorescent materials: "N" and "H" molecules. The photochemical and electroluminescent properties (spin-coating method) were studied. The maximum luminescence efficiency (CEmax) of "N" type molecular based devices and "H" type molecular based devices were 1.51cd/A and 1.14 CD / A, respectively. The maximum power efficiency (PEmax) is 0.56lm/W and 0.38lm / W, and the maximum external quantum efficiency (EQEmax) is 1.04% and 0.80, respectively, which provides a new idea for the structural design of small molecules in wet processing. (3) the photophysical and photochemical properties of TCzPSi and DCzIPSi, compounds with tetraphenylsilicon as the center and carbazole and benzimidazole as substituents were studied. Their three-wire energy levels are higher than those of FIrpic's, and the exchange energy 螖 EST of the corresponding single / three-wire states is small, which is an ideal blue phosphorescence host material.
【學位授予單位】:中北大學
【學位級別】:碩士
【學位授予年份】:2015
【分類號】:TN383.1

【參考文獻】

相關博士學位論文 前1條

1 胡德華;含硅類寬禁帶母體材料的設計合成與光電性質研究[D];吉林大學;2011年



本文編號:2312433

資料下載
論文發(fā)表

本文鏈接:http://www.sikaile.net/kejilunwen/dianzigongchenglunwen/2312433.html


Copyright(c)文論論文網All Rights Reserved | 網站地圖 |

版權申明:資料由用戶c8442***提供,本站僅收錄摘要或目錄,作者需要刪除請E-mail郵箱bigeng88@qq.com