Abstract
We report a facile nonaqueous emulsion synthesis of colloidal halide perovskite quantum dots by controlled addition of a demulsifier into an emulsion of precursors. The size of resulting CH3NH3PbBr3 quantum dots can be tuned from 2 to 8 nm by varying the amount of demulsifier. Moreover, this emulsion synthesis also allows the purification of these quantum dots by precipitation from the colloidal solution and obtains solid-state powder which can be redissolved for thin film coating and device fabrication. The photoluminescence quantum yields of the quantum dots is generally in the range of 80-92%, and can be well-preserved after purification (∼80%). Green light-emitting diodes fabricated comprising a spin-cast layer of the colloidal CH3NH3PbBr3 quantum dots exhibited maximum current efficiency of 4.5 cd/A, power efficiency of 3.5 lm/W, and external quantum efficiency of 1.1%. This provides an alternative route toward high efficient solution-processed perovskite-based light-emitting diodes. In addition, the emulsion synthesis is versatile and can be extended for the fabrication of inorganic halide perovskite colloidal CsPbBr3 nanocrystals.
| Original language | English |
|---|---|
| Pages (from-to) | 28128-28133 |
| Number of pages | 6 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 7 |
| Issue number | 51 |
| DOIs | |
| Publication status | Published - 30 Dec 2015 |
Keywords
- electroluminescence
- emulsion synthesis
- halide perovskite
- light-emitting diodes
- quantum dot
- semiconductor nanocrystals
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