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Appreciable progress of organometal halide perovskite materials has been achieved in recent years due to their controllable synthesis and excellent optoelectronic properties. And the potential uses of these perovskites in photovoltaics, light-emitting diodes (LEDs), photodetectors and lasers have been successfully demonstrated. Although organometal halide perovskites appear as emitters with extremely high color purity and low cost, the device performance is significantly limited by poor morphology of the perovskite layer. The addition of the polymer into the perovskite layer is a convenient and effective method to improve the homogeneity of the spin-coated perovskite film. In this work, we fabricate green perovskite light emitting diodes (PeLEDs) with poly(styrenesulfonate) (PSS)-modified poly(3,4-ethylenedioxythiophene):PSS (PEDOT:PSS) as the hole injection layer (HIL) and a single spin coating composite film consisting of methylammonium lead tribromide (MAPbBr3) and poly(ethylene oxide) (PEO) as the emissive layer. The PSS doping increases the work function of PEDOT:PSS and reduces the injection barrier between PEDOT:PSS HIL and MAPbBr3 perovskite, thus balancing the carriers within the PeLEDs. The PEO doping enables the MAPbBr3 to become a dense and uniform perovskite film with a ~100% coverage. With the above approaches, highly efficient PeLEDs with maximum luminance and current efficiency of 2476 cd·m–2 and 7.6 cd·A–1 are eventually acquired. This work provides a method of fabricating the high-coverage and high-efficiency PeLEDs.
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Keywords:
- perovskite /
- light emitting diode /
- composite film /
- charge injection
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图 1 (a) 掺杂和未掺杂PSS的PEDOT:PSS的UPS光谱; (b) PeLEDs能级示意图
Figure 1. (a) UPS spectra of PSS-doped and pristine PEDOT:PSS; (b) schematic energy-level of PeLEDs.
图 2 不同PSS与PEDOT:PSS体积比的PeLEDs的特性 (a)亮度-电压特性; (b) 电流密度-电压特性; (c) 电流效率-电压特性
Figure 2. The characteristics of PeLEDs with varying volume ratio of PSS and PEDOT:PSS: (a) Luminance-voltage; (b) current density-voltage; (c) current efficiency-voltage.
图 3 不同体积比的MAPbBr3:PEO薄膜的SEM形貌图 (a) 1∶0; (b) 1∶0.75; (c) 1∶1; (d) 1∶1.25
Figure 3. The SEM images of the MAPbBr3 films with different MAPbBr3:PEO volume ratio: (a) 1∶0; (b) 1∶0.75; (c) 1∶1; (d) 1∶1.25.
图 4 本征MAPbBr3钙钛矿和MAPbBr3:PEO(1∶1)钙钛矿薄膜的XRD. 图中Pe为MAPbBr3的简写
Figure 4. The XRD of the perovskite films of pristine MAPbBr3 and MAPbBr3:PEO (1∶1). Here, Pe is the abbreviation of MAPbBr3.
图 5 MAPbBr3和MAPbBr3:PEO (1∶1)复合薄膜的PL光谱
Figure 5. Photoluminescence spectra of the MAPbBr3 and MAPbBr3:PEO (1∶1) composite thin films.
图 6 (a) 使用了MAPbBr3:PEO的器件结构示意图; 不同MAPbBr3:PEO体积比钙钛矿所制备出发光器件的(b)亮度-电压, (c)电流密度-电压, (d)电流效率-电压和(e)电致发光光谱曲线
Figure 6. (a) PeLED structure using MAPbBr3:PEO, and the (b) luminance, (c) current density-voltage, (d) current efficiency-voltage and (e) electroluminant curves of PeLEDs with varying volume ratio of MAPbBr3:PEO.
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[1] Yang W S, Park BW, Jung E H, Jeon N J, Kim Y C, Lee D U, Shin S S, Seo J, Kim E K, Noh J H, Seok S I 2017 Science 356 1376
Google Scholar
[2] Stranks S D, Snaith H J 2015 Nat. Nanotechnol. 10 391
Google Scholar
[3] Adjokatse S, Fang H H, Loi M A 2017 Mater. Today 20 413
Google Scholar
[4] Kim Y H, Cho H, Heo J H, Kim T S, Myoung N S, Lee L C, Im S H, Lee T W 2015 Adv. Mater. 27 1248
Google Scholar
[5] Yu J C, Kim D W, Kim D B, Jung E D, Park J H, Lee A Y, Lee B R, Nuzzo D D, Friend R H, Song M H 2016 Adv. Mater. 28 6906
Google Scholar
[6] Huang C F, Keshtov M L, Chen F C 2016 ACS Appl. Mater. Interfaces 8 27006
Google Scholar
[7] Era M, Morimoto S, Tsutsui T, Saito S 1994 Appl. Phys. Lett. 65 676
Google Scholar
[8] Tan Z K, Moghaddam R S, Lai M L, Docampo P, Higler R, Deschler F, Price M, Sadhanala A, Pazos L M, Credgington D, Hanusch F, Bein T, Snaith H J, Friend R H 2014 Nat. Nanotechnol. 9 687
Google Scholar
[9] Sessolo M, Gil E L, Longo G, Bolink H J 2016 Top. Curr. Chem. 374 1
Google Scholar
[10] Naphade R, Zhao B, Richter J M, Booker E, Krishnamurthy S, Friend I H, Sadhanala A, Ogale S 2017 Adv. Mater. Interfaces. 4 1700562
Google Scholar
[11] Zhang X L, Wang W G, Xu B, Liu S, Dai H T, Bian D, Chen S M, Wang K, Sun X W 2017 Nano Energy 37 40
Google Scholar
[12] Yu J C, Kim D B, Jung E D, Lee B R, Song M H 2016 Nanoscale 8 7036
Google Scholar
[13] Wang Z, Cheng T, Wang F, Dai S, Tan Z 2016 Small 12 4412
Google Scholar
[14] Yantara N, Bhaumik S, Yan F, Sabba D, Dewi H A, Mathews N A, Boix P P, Demir H V, Mhaisalkar S 2015 J. Phys. Chem. Lett. 6 4360
Google Scholar
[15] Li G, Tan Z K, Di D, Lai M L, Jiang L, Lim J H, Friend R H, Greenham N C 2015 Nano Lett. 15 2640
Google Scholar
[16] Ji X, Peng X, Lei Y, Liu Z, Yang X 2017 Org. Electron. 43 167
Google Scholar
[17] Chen P, Xiong Z, Wu X, Shao M, Ma X, Xiong ZH, Gao C 2017 J. Phys. Chem. Lett. 8 1810
Google Scholar
[18] Cho H, Jeong S H, Park M H, Kim Y H, Wolf C, Lee C L, Heo J H, Sadhanala A, Myoung N, Yoo S, Im S H, Friend R H, Lee T W 2015 Science 350 1222
Google Scholar
[19] Masi S, Rizzo A, Aiello F, Balzano F, Uccello-Barretta G, Listorti A, Gigli G, Colella S 2015 Nanoscale 7 18956
Google Scholar
[20] Ng Y F, Kulkarni S A, Parida S, Jamaludin N F, Yantara N, Bruno A, Soci C, Mhaisalkar S, Mathews N 2017 Chem. Commun. 53 12004
Google Scholar
[21] Peng X F, Wu X Y, Ji X X, Ren J, Wang Q, Li G Q, Yang X H 2017 J. Phys. Chem. Lett. 8 4691
Google Scholar
[22] Groenendaal L, Jonas F, Freitag D, Pielartzik H, Reynolds J R 2000 Adv. Mater. 12 481
Google Scholar
[23] Chan W C, Maxwel D J, Gao X, Bailey R E, Han M, Nie S 2002 Curr. Opin. Biotechnol. 13 1340
[24] Vengrenovich R D, Gudyma Y V, Yarema S V 2001 Semiconductors 35 1378
Google Scholar
[25] Noh J H, Im S H, Heo J H, Mandal T N, Seok S I 2013 Nano Lett. 13 1764
Google Scholar
[26] Zhang X Y, Lin H, Huang H, Reckmeier C, Zhang Y, Choy W C H, Rogach A L 2016 Nano Lett. 16 1415
Google Scholar
[27] Yu H T, Lu Y, Feng Z Q, Wu Y N, Liu Z W, Xia P F, Qian J, Chen Y F, Liu L H, Cao K, Chen S F, Huang W 2019 Nanoscale 11 9103
Google Scholar
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