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Study of structural, optical, and thermal properties in MoS2-based nanocomposites: iron and gold
Recently, molybdenum disulfide (MoS 2 ), as one of the most stable layered transitional metal dichalcogenides, has attracted lots of attention because it shows high absorbance in the near-infrared (NIR) region, high surface area, good photothermal properties, and good biosafety. So it has been exten...
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Published in: | European physical journal plus 2022-11, Vol.137 (11), p.1284, Article 1284 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Recently, molybdenum disulfide (MoS
2
), as one of the most stable layered transitional metal dichalcogenides, has attracted lots of attention because it shows high absorbance in the near-infrared (NIR) region, high surface area, good photothermal properties, and good biosafety. So it has been extensively applied as a novel photothermal agent in biomedical applications. Here, we examine two nanocomposites comprised of molybdenum disulfide-gold nanorod (MoS
2
–Au) and molybdenum disulfide-iron oxide magnetic nanoparticle (MoS
2
-Fe
3
O
4
) having unique structural features. These nanocomposites were developed by using facile preparation strategies; then, all samples (MoS
2
nanoflakes, MoS
2
–Au, and MoS
2
–Fe
3
O
4
) were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Raman, Fourier transform infrared (FTIR), and ultraviolet–visible (UV–Vis) spectroscopies. These characterizations confirm that gold nanorods (AuNRs) and Fe
3
O
4
nanoparticles have been incorporated between MoS
2
nanoflakes separately. Finally, photothermal results of samples indicate that MoS
2
–Au nanocomposite produced higher photothermal heat than two other samples after 10-min laser irradiation. So, MoS
2
–Au nanocomposite can be a suitable photothermal agent for further biological applications such as photothermal therapy and drug delivery. |
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ISSN: | 2190-5444 2190-5444 |
DOI: | 10.1140/epjp/s13360-022-03502-z |