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Spectroscopic and Hydrodynamic Characterisation of DNA‐Linked Gold Nanoparticle Dimers in Solution using Two‐Photon Photoluminescence
Author(s) -
Midelet Johanna,
ElSagheer Afaf H.,
Brown Tom,
Kanaras Antonios G.,
Débarre Anne,
Werts Martinus H. V.
Publication year - 2018
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201701228
Subject(s) - photoluminescence , dynamic light scattering , spectroscopy , nanoparticle , materials science , molecular physics , plasmon , particle (ecology) , microsecond , scattering , monomer , chemistry , analytical chemistry (journal) , photochemistry , chemical physics , optoelectronics , nanotechnology , optics , physics , polymer , composite material , oceanography , chromatography , quantum mechanics , geology
Two‐photon photoluminescence (TPPL) emission spectra of DNA–gold nanoparticle (AuNP) monoconjugates and the corresponding DNA‐linked AuNP dimers are obtained by photon time‐of‐flight spectroscopy. This technique is combined with two‐photon photoluminescence fluctuation correlation spectroscopy (TPPL–FCS) to simultaneously monitor the optical and hydrodynamic behaviour of these nano‐assemblies in solution, with single‐particle sensitivity and microsecond temporal resolution. In this study, the AuNPs have an average core diameter of 12 nm, which renders their dark‐field plasmonic light scattering too weak for single‐particle imaging. Moreover, as a result of the lack of plasmonic coupling in the dimers, the optical extinction, scattering and photoluminescence spectra of the DNA–AuNP complexes are not sufficiently different to distinguish between monomers and dimers. The use of TPPL–FCS successfully addresses these bottlenecks and enables the distinction between AuNP monomers and AuNP dimers in solution by measurement of their hydrodynamic rotational and translational diffusion.