Metal Halide Passivation of Lead chalcogenide Quantum Dots Synthesized from Cation Exchange Reactions for Next Generation Photovoltaics
Joseph Luther a, Ryan Crisp, Ashley Marshall, Jianbing Zhang, Boris chernomordik, Sungwoo Kim, Matthew Beard
a NREL, 16253 Denver West Parkway, Golden, 80401, United States
Materials for Sustainable Development Conference (MATSUS)
Proceedings of nanoGe September Meeting 2015 (NFM15)
Santiago de Compostela, Spain, 2015 September 6th - 15th
Oral, Joseph Luther, presentation 045
Publication date: 8th June 2015

Quantum confined semiconductor nanocrystals called quantum dots (QDs), are promising materials for next-generation photovoltaic technologies and other various optoelectronic applications.  Even when the QDs are coupled in arrays through the utilization of recent developments in surface ligand modification, they still exhibit quantum confinement and possess intriguing ensemble properties. We will discuss new synthetic routes that employ cation-exchange reactions to produce well-controlled and stable lead chalcogenide materials. We will discuss treatments of PbSe QD solids with metal chloride salt solutions, with +1 to +3 metals, such as Na+, K+, Zn2+, Cd2+, Sn2+, Cu2+, and In3+. The QD films readily absorb the ions, which influence electronic properties of QD solids and the performance of devices. Furthermore, we will show that metal halide salts (PbI2, PbCl2, CdI2, or CdCl2) dissolved in dimethylformamide efficiently displace the native oleate surface ligands on the QDs, resulting in conductive QD solids. The resulting QD solids have a significant reduction in the carbon content compared to typical QD film treatments using thiols and organic halides. The PbI2 treatment is the most successful in removing alkyl surface ligands and also replaces most surface bound Cl- with I-. The treatment protocol results in PbS QD films exhibiting deeper work function and band positions than other ligand treatments reported previously. The method developed here produces QD solar cells that perform well even at film thicknesses approaching one micron, indicating improved carrier transport in the QD films. Furthermore, these QD synthesis and treatment methods lead to air-stable PbSe QD solar cells. We will present details on QD solids that have enabled the first high-efficiency certified PbSe solar cells and PbSe solar cells that are stable for over 250 days when stored in air as a result of these latest developments.



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