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Surface-Enhanced Raman scattering of methylene blue on titanium nitride nanoparticles synthesized by laser ablation in organic solvents.

Authors :
Esmaeilzadeh, Marzieh
Dizajghorbani-Aghdam, Hossein
Malekfar, Rasoul
Source :
Spectrochimica Acta Part A: Molecular & Biomolecular Spectroscopy. Aug2021, Vol. 257, pN.PAG-N.PAG. 1p.
Publication Year :
2021

Abstract

[Display omitted] • Synthesis of pure TiN NPs by pulsed laser ablation in N, N-Dimethylformamide liquid. • Synthesis of TiN NPs embedded in the graphitic carbon matrix by pulsed laser ablation. • Preparation of SERS substrates with all of the synthesized NPs by laser ablation. • The synthesized T-TiN, AN-TiN, and DMF-TiN NPs show good enhancement factors for MB. Suspensions of titanium nitride (TiN) nanoparticles (NPs) were prepared using nanosecond Ce:Nd:YAG pulsed laser ablation (λ = 1064 nm) of a TiN target immersed in various solvents such as Toluene (C 6 H 5 CH 3), Acetonitrile (CH 3 CN), and N, N-dimethylformamide (C 3 H 7 NO). The synthesized NPs were characterized by applying a range of spectroscopic, structural, and compositional analysis techniques. The obtained TiN NPs in N, N-dimethylformamide (DMF-TiN NPs) solvent showed strong optical absorption in the near-infrared (NIR) range; Whereas, the obtained TiN NPs in toluene (T-TiN NPs) and acetonitrile (AN-TiN NPs) solvents were covered with a carbon matrix layer that quenched their surface plasmon resonance (SPR). The carbon matrix on the NPs was removed by thermal oxidation to obtain carbon-free TiN NPs. All the prepared carbon-free TiN NPs were employed as substrates for the surface-enhanced Raman scattering (SERS) spectroscopy of methylene blue (MB) molecules as a probe molecule adsorbed on the surface. All substrates indicated nearly the same order of enhancement factors (EFs) (~103) for MB. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13861425
Volume :
257
Database :
Academic Search Index
Journal :
Spectrochimica Acta Part A: Molecular & Biomolecular Spectroscopy
Publication Type :
Academic Journal
Accession number :
150083551
Full Text :
https://doi.org/10.1016/j.saa.2021.119721