Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 8, Pages 10508-10516Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c18791
Keywords
perovskite nanocrystals; light-emitting diodes; methylammonium lead bromide; complementary ligands; surface passivation
Funding
- National Key Research and Development Plan of China [2019YFE0111900]
- National Natural Science Foundation of China [12004298, 61875161, 62174128]
- China Postdoctoral Science Foundation [2020M673399]
- Fundamental Research Funds for the Central Universities [xzy012020077]
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This study presents a complementary ligand synthesis method to improve the emissive features of MAPbBr(3) NCs and achieve high-efficiency green LEDs. The complementary ligand strategy enhances charge transport and modifies interfacial energy-level alignment in the NCs, leading to improved performance. This finding could open up new avenues for the development and commercial application of LEDs.
Conjugated and short-molecule capping ligands have been demonstrated as a valid strategy for achieving high-efficiency perovskite nanocrystal (NCs) light-emitting diodes (LEDs) owing to their advantage of allowing efficient carrier transport between NCs. However, monotonously utilizing conjugated ligands cannot achieve sufficient surface modification/passivation for perovskite NCs, leading to their poor photoluminescence quantum yield (PLQY) and dispersibility. This work designs a complementary ligand synthesis method to obtain high-quality methylamine lead bromide (MAPbBr(3)) NCs and then leverage them into efficient LEDs. The complementary ligand system combines a conjugated ligand 3-phenyl-2-propen-1-amine (PPA) and a long-chain ligand didodecyldimethylammonium bromide (DDAB) together with a well-known inductive inorganic ligand ZnBr2. With such complementary ligand engineering, we significantly improve the emissive features of MAPbBr(3) NCs (PLQY: 99% +/- 0.7%). Simultaneously, the complementary ligand strategy facilitated the adequate charge transportation in related NCs films and modified the interfacial energy-level alignment when the NCs assemble as an emitting layer into LEDs. Finally, based on this NCs synthesis method, high-efficiency green LEDs were achieved, exhibiting the maximum luminance of 1.59 X 10(4) cd m(-2), a current efficiency of 23.7 cd A(-1), and an external quantum efficiency of 7.8%. Our finding could provide a new avenue for further development of LEDs and their commercial application.
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