Revealing the nanogeometry of WS2 nanoflowersby polarization-resolved Raman spectroscopy

Journal Article (2022)
Author(s)

I. Komen (Kavli institute of nanoscience Delft, TU Delft - QN/Kuipers Lab)

S.E. Van Heijst (Kavli institute of nanoscience Delft, TU Delft - QN/Conesa-Boj Lab)

M. Caldarola (TU Delft - QN/Kuipers Lab, Kavli institute of nanoscience Delft)

Sonia Conesa Conesa Boj (TU Delft - QN/Conesa-Boj Lab, Kavli institute of nanoscience Delft)

Kobus Kuipers (TU Delft - QN/Quantum Nanoscience, Kavli institute of nanoscience Delft)

Research Group
QN/Kuipers Lab
Copyright
© 2022 I. Komen, S.E. van Heijst, M. Caldarola, S. Conesa Boj, L. Kuipers
DOI related publication
https://doi.org/10.1063/5.0102381
More Info
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Publication Year
2022
Language
English
Copyright
© 2022 I. Komen, S.E. van Heijst, M. Caldarola, S. Conesa Boj, L. Kuipers
Research Group
QN/Kuipers Lab
Issue number
17
Volume number
132
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Abstract

Recent studies of transition metal dichalcogenides (TMDs) have revealed exciting optical properties, such as stable excitons and chiral light–matter interactions. Chemical vapor deposition techniques provide a platform for the fabrication of nanostructures with diverse geometries, ranging from horizontal flakes to flower-like structures. Raman spectroscopy is commonly used to characterize TMDs and their properties. Here, we use polarization-resolved Raman spectroscopy to probe the nanogeometry and orientation of WS 2 nanoflower petals.Exciting the nanoflowers with linearly polarized light, we observe an enhanced Raman response from flower petals oriented along the excitation polarization direction. Furthermore, the helicity-resolved Raman response of vertically oriented wall-like flower petals exhibits clear differences with horizontally oriented flakes. Although the photoluminescence from the nanoflowers is strongly reduced, the Raman response upon excitation in resonance with the WS 2 excitonic transition does reveal the presence of the exciton, which results in a distinct temperature dependence of the Raman response.

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