journal article·2016-02-23

Fully Printed Halide Perovskite Light-Emitting Diodes with Silver Nanowire Electrodes

Sri Ganesh R. Bade, Junqiang Li, Xin Shan, Yichuan Ling, Yu Tian, Tristan Dilbeck, Tiglet Besara, Thomas Geske, Hanwei Gao, Biwu Ma, Kenneth Hanson, Theo Siegrist, Chengying Xu, Zhibin Yu

ACS Nano· Volume 10· Issue 2
Publisher page

Abstract

Printed organometal halide perovskite light-emitting diodes (LEDs) are reported that have indium tin oxide (ITO) or carbon nanotubes (CNTs) as the transparent anode, a printed composite film consisting of methylammonium lead tribromide (Br-Pero) and poly(ethylene oxide) (PEO) as the emissive layer, and printed silver nanowires as the cathode. The fabrication can be carried out in ambient air without humidity control. The devices on ITO/glass have a low turn-on voltage of 2.6 V, a maximum luminance intensity of 21014 cd m(-2), and a maximum external quantum efficiency (EQE) of 1.1%, surpassing previous reported perovskite LEDs. The devices on CNTs/polymer were able to be strained to 5 mm radius of curvature without affecting device properties.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Perovskite Materials and Applications · Organic Light-Emitting Diodes Research · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Industrial and Manufacturing Engineering, High Performance Materials Institute, §Department of Chemical and Biomedical Engineering, #National High Magnetic Field Laboratory, and ⊗Department of Mechanical Engineering, Florida State University, Tallahassee Florida 32310, United States

Department of Physics, ∥Department of Chemistry and Biochemistry, and ⊥Materials Science and Engineering, Florida State University, Tallahassee Florida 32306, United States

Funding

National Science Foundation

References (31)

Show source-provided references
1. 10.1038/nnano.2015.9010.1038/nnano.2015.90 ↗
2. 10.1126/science.122860410.1126/science.1228604 ↗
3. 10.1038/nnano.2014.14910.1038/nnano.2014.149 ↗
4. 10.1038/nature1413310.1038/nature14133 ↗
5. 10.1126/science.125405010.1126/science.1254050 ↗
6. 10.1021/acs.jpclett.5b0073210.1021/acs.jpclett.5b00732 ↗
7. 10.1021/acs.nanolett.5b0236910.1021/acs.nanolett.5b02369 ↗
8. 10.1002/adma.20140521710.1002/adma.201405217 ↗
9. 10.1039/C4CC07518H10.1039/C4CC07518H ↗
10. 10.1002/anie.20150303810.1002/anie.201503038 ↗
11. 10.1021/acsnano.5b0115410.1021/acsnano.5b01154 ↗
12. 10.1021/jz502703p10.1021/jz502703p ↗
13. 10.1557/mrs.2015.16710.1557/mrs.2015.167 ↗
14. 10.1039/C5EE00645G10.1039/C5EE00645G ↗
15. 10.1021/acsami.5b0449010.1021/acsami.5b04490 ↗
16. 10.1002/adma.20140459810.1002/adma.201404598 ↗
17. 10.1126/science.125476310.1126/science.1254763 ↗
18. 10.1002/aenm.20150056910.1002/aenm.201500569 ↗
19. 10.1002/aenm.20150032810.1002/aenm.201500328 ↗
20. 10.1002/adma.20150249010.1002/adma.201502490 ↗
21. 10.1002/adma.20140375110.1002/adma.201403751 ↗
22. 10.1021/acs.nanolett.5b0023510.1021/acs.nanolett.5b00235 ↗
23. 10.1063/1.490151010.1063/1.4901510 ↗
24. 10.1021/acsnano.5b0362610.1021/acsnano.5b03626 ↗
25. 10.1039/C4CC05231E10.1039/C4CC05231E ↗
26. 10.1126/science.aaa272510.1126/science.aaa2725 ↗
27. 10.1021/ja511132a10.1021/ja511132a ↗
28. 10.1002/adma.20140504410.1002/adma.201405044 ↗
29. 10.1021/acs.jpcc.5b0295910.1021/acs.jpcc.5b02959 ↗
30. 10.1002/adma.20150046510.1002/adma.201500465 ↗
31. 10.1002/adma.20110198610.1002/adma.201101986 ↗