In this work, we develop a novel, in situ characterization method to measure the orientation order parameter and investigate the reorientation and reshaping dynamics of polymer grafted gold nanorods (AuNRs)… Click to show full abstract
In this work, we develop a novel, in situ characterization method to measure the orientation order parameter and investigate the reorientation and reshaping dynamics of polymer grafted gold nanorods (AuNRs) in polymer nanocomposite (PNC) thin films. The long aspect-ratio of AuNRs results in two well-defined plasmon resonance modes, allowing the optical properties of the PNC to be tuned over a wide spectral range. The alignment of the AuNRs in a particular direction can also be used to further tune these optical properties. We utilize variable angle spectroscopic ellipsometry as a unique technique to measure the optical properties of PNC films containing AuNRs at various angles of incidence, and use effective index of refraction analysis of the PNC to relate the birefringence in the film due to changes of the plasmon coupling to the orientation order parameter of AuNRs. Polymer thin films (ca. 70 nm) of either polystyrene (PS) or poly(methyl methacrylate) (PMMA) containing PS grafted AuNRs are probed with ellipsometry, and the resulting extinction coefficient spectra compare favorably with more traditional analytical techniques, electron microscopy (EM) and optical absorbance (vis-NIR) spectroscopy. Furthermore, variable angle spectroscopic ellipsometry measures optical birefringence, which allows us to determine the in- and out-of plane order of the AuNRs, a property that is not easily accessible using other measurement techniques. Additionally, this technique is applied in situ to demonstrate that AuNRs undergo a rapid (ca. 1-5 hours) reorientation before undergoing a slower (ca. 24 hours) rod to sphere shape transition. The reorientation behavior is different depending on the polymer matrix used. In the athermal case (i.e. PS matrix), the AuNRs reorient isotropically, while in PMMA the AuNRs do not become isotropic, which we hypothesize is due to PMMA preferentially wetting the silica substrate, leaving less vertical space for the AuNRs to reorient.
               
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