• Tabachnyk, M.
• De, La Peña Fj
• Wisnivesky, Rocca Rivarola F.
• Davis, Njlk
• Greenham, Neil
• Lamboll, Robin
• Booker, Ep
• Griffiths, James
• Deschler, F.
• Richter, Jm
• Menke, Stephen Matthew
• Ducati, Caterina

Abstract

Cesium lead halide nanocrystals, CsPbX$_{3}$ (X = Cl, Br, I), exhibit photoluminescence quantum efficiencies approaching 100% without the core-shell structures usually used in conventional semiconductor nanocrystals. These high photoluminescence efficiencies make these crystals ideal candidates for light-emitting diodes (LEDs). However, because of the large surface area to volume ratio, halogen exchange between perovskite nanocrystals of different compositions occurs rapidly, which is one of the limiting factors for white-light applications requiring a mixture of different crystal compositions to achieve a broad emission spectrum. Here, we use mixtures of chloride and iodide CsPbX$_{3}$ (X = Cl, I) perovskite nanocrystals where anion exchange is significantly reduced. We investigate samples containing mixtures of perovskite nanocrystals with different compositions and study the resulting optical and electrical interactions. We report excitation transfer from CsPbCl$_{3}$ to CsPbI$_{3}$ in solution and within a poly(methyl methacrylate) matrix via photon reabsorption, which also occurs in electrically excited crystals in bulk heterojunction LEDs.

Topics

• perovskite
• impedance spectroscopy
• surface
• photoluminescence
• semiconductor