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Chloride and Indium-Chloride-Complex Inorganic Ligands for Efficient Stabilization of Nanocrystals in Solution and Doping of Nanocrystal Solids

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Ruck,  Michael
Michael Ruck, Max Planck Fellow, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Citation

Sayevich, V., Guhrenz, C., Sin, M., Dzhagan, V. M., Weiz, A., Kasemann, D., et al. (2016). Chloride and Indium-Chloride-Complex Inorganic Ligands for Efficient Stabilization of Nanocrystals in Solution and Doping of Nanocrystal Solids. Advanced Functional Materials, 26(13), 2163-2175. doi:10.1002/adfm.201504767.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002A-5314-0
Abstract
Here, the surface functionalization of CdSe and CdSe/CdS core/shell nanocrystals (NCs) with compact chloride and indium-chloride-complex ligands is reported. The ligands provide not only short interparticle distances but additionally control doping and passivation of surface trap states, leading to enhanced electronic coupling in NC-based arrays. The solids based on these NCs show an excellent electronic transport behavior after heat treatment at the relatively low temperature of 190 degrees C. Indeed, the indium-chlorido-capped 4.5 nm CdSe NC based thin-film field-effect transistor reaches a saturation mobility of = 4.1 cm(2) (V s)(-1) accompanied by a low hysteresis, while retaining the typical features of strongly quantum confined semiconductor NCs. The capping with chloride ions preserves the high photoluminescence quantum yield (approximate to 66%) of CdSe/CdS core/shell NCs even when the CdS shell is relatively thin (six monolayers). The simplicity of the chemical incorporation of chlorine and indium species via solution ligand exchange, the efficient electronic passivation of the NC surface, as well as their high stability as dispersions make these materials especially attractive for wide-area solution-processable fabrication of NC-based devices.