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Epitaxial Growth of PbSe Quantum Dots on MoS2 Nanosheets and their Near-Infrared Photoresponse
A facile one‐pot synthesis of hybrid materials consisting of PbSe quantum dots (QDs) that grow epitaxially on MoS2 nanoflakes resulting in three equivalent orientation variants of the PbSe QDs with respect to the MoS2 lattice is demonstrated. The epitaxial growth and cross‐sectional high‐resolution...
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Published in: | Advanced functional materials 2014-10, Vol.24 (37), p.5798-5806 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | A facile one‐pot synthesis of hybrid materials consisting of PbSe quantum dots (QDs) that grow epitaxially on MoS2 nanoflakes resulting in three equivalent orientation variants of the PbSe QDs with respect to the MoS2 lattice is demonstrated. The epitaxial growth and cross‐sectional high‐resolution transmission electron microscopy (HRTEM) investigations verify a direct and linker‐free contact between the quantum dots and the transition metal dichalcogenide (TMD) nanoflakes, while maintaining surface passivation of the PbSe with oleic acid ligands on the outside. Solution‐processed photodetectors based on PbSe‐MoS2 hybrids exhibit stable photoconduction when illuminated with near‐IR light (wavelength > 1200 nm) without any laborious ligand‐exchange steps. Flexible devices fabricated on polyethylene terephthalate (PET) substrates show excellent stability upon repeated bending. These hybrid materials are air‐stable and solution‐processable at low temperatures and thus promising for low‐cost flexible near‐IR photodetectors.
A simple wet‐chemical synthesis
of hybrid materials consisting of PbSe quantum dots (QDs) and MoS2 nanoflakes is demonstrated. PbSe QDs grow epitaxially on MoS2 resulting in a direct and linker‐free contact between the two components. Solution‐processed, flexible, and air‐stable photodetectors based on PbSe‐MoS2 hybrids exhibit clear photoswitching when illuminated with near‐infrared light. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.201400330 |