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Non-resonant light scattering in dispersions of 2D nanosheets

Extinction spectra of nanomaterial suspensions can be dominated by light scattering, hampering quantitative spectral analysis. No simple models exist for the wavelength-dependence of the scattering coefficients in suspensions of arbitrary-sized, high-aspect-ratio nanoparticles. Here, suspensions of...

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Detalles Bibliográficos
Autores principales: Harvey, Andrew, Backes, Claudia, Boland, John B., He, Xiaoyun, Griffin, Aideen, Szydlowska, Beata, Gabbett, Cian, Donegan, John F., Coleman, Jonathan N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6212482/
https://www.ncbi.nlm.nih.gov/pubmed/30385771
http://dx.doi.org/10.1038/s41467-018-07005-3
Descripción
Sumario:Extinction spectra of nanomaterial suspensions can be dominated by light scattering, hampering quantitative spectral analysis. No simple models exist for the wavelength-dependence of the scattering coefficients in suspensions of arbitrary-sized, high-aspect-ratio nanoparticles. Here, suspensions of BN, talc, GaS, Ni(OH)(2), Mg(OH)(2) and Cu(OH)(2) nanosheets are used to explore non-resonant scattering in wide-bandgap 2D nanomaterials. Using an integrating sphere, scattering coefficient (σ) spectra were measured for a number of size-selected fractions for each nanosheet type. Generally, σ scales as a power-law with wavelength in the non-resonant regime: σ(λ)∝[λ/〈L〉](−m), where 〈L〉 is the mean nanosheet length. For all materials, the scattering exponent, m, forms a master-curve, transitioning from m = 4 to m = 2, as the characteristic nanosheet area increases, indicating a transition from Rayleigh to van der Hulst scattering. In addition, once material density and refractive index are factored out, the proportionality constant relating σ to [λ/〈L〉](−m), also forms a master-curve when plotted versus 〈L〉.