Cardenas Lopez P, Yarawsky AE, Berthold M, Bleyer G, Su TL, Paul LN, Vogel N, Walter J (2026)
Publication Type: Journal article
Publication year: 2026
Book Volume: 42
Pages Range: 5823-5839
Journal Issue: 7
DOI: 10.1021/acs.langmuir.5c06504
Polystyrene–polydopamine (PS@PDA) core–shell particles are widely used as building blocks to form colloidal photonic crystals with tunable light absorption. Increasing the PDA shell thickness typically leads to more saturated colors but also diminishes the structural order of the resulting assemblies. To understand this phenomenon, we correlate particle properties in solution with the structural properties of the formed colloidal crystals. In particular, we focus on correlating the water swellability of the PDA shell with the agglomeration behavior upon drying. To this end, we combine density variation sedimentation velocity (SV) and buoyant density gradient equilibrium (DGE) experiments in analytical ultracentrifugation (AUC) to quantify the hydration of the PDA shell. Density variation SV-AUC in H
APA:
Cardenas Lopez, P., Yarawsky, A.E., Berthold, M., Bleyer, G., Su, T.-L., Paul, L.N.,... Walter, J. (2026). Quantifying Polydopamine Shell Hydration in Core–Shell Colloids by Analytical Ultracentrifugation: Implications for Self-Assembly and Structural Color of Photonic Crystals. Langmuir, 42(7), 5823-5839. https://doi.org/10.1021/acs.langmuir.5c06504
MLA:
Cardenas Lopez, Paola, et al. "Quantifying Polydopamine Shell Hydration in Core–Shell Colloids by Analytical Ultracentrifugation: Implications for Self-Assembly and Structural Color of Photonic Crystals." Langmuir 42.7 (2026): 5823-5839.
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