journal article·2016-04-07

Electrodeposition of Polypyrenes with Tunable Hydrophobicity, Water Adhesion, and Fluorescence Properties

Gabriela Ramos Chagas, Xiao Xie, Thierry Darmanin, Karine Steenkeste, Anne Gaucher, Damien Prim, Rachel Méallet-Renault, Guilhem Godeau, Sonia Amigoni, Frédéric Guittard

The Journal of Physical Chemistry C· Volume 120· Issue 13
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Abstract

The control in surface hydrophobicity and water adhesion is extremely important for various applications in water harvesting, oil/water separation membrane, energy systems or biosensing, for example. Here, for the first time we show that the use of fluorescent monomers such as pyrene with various substituents differing by their hydrophobicity, size, or rigidity/flexibility can lead to surfaces with tunable hydrophobicity, water adhesion and fluorescence properties by a direct electropolymerization process. Seven original monomers with fluoroalkyl, alkyl, phenyl, adamantyl, and triethylene glycol substituents were synthesized and studied. The surface roughness is highly dependent on the substituent, and it seems that the fluorescence, although complex, correlates with the surface roughness. Superhydrophobic properties and highly oleophobic properties are obtained using fluoroalkyl chains due to the presence of nanostructured microparticles. In comparison to the structured absorption and emission bands of pyrene monomers, the pyrene polymers (oligomers) exhibit a broad structureless spectral shape both in absorption and in emission, which seems to be due to pyrene oligomerization and aggregation. This work is a first tentative attempt to combine superhydrophobic and fluorescent properties using an innovative strategy and opens new doors to explore in this domain.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Surface Modification and Superhydrophobicity · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Université Nice Sophia Antipolis, CNRS, LPMC, UMR 7336, 06100 Nice, France

ENS Cachan, Institut d’Alembert (FR3242), Laboratoire PPSM (UMR 8531), CNRS, Université Paris-Saclay, 61 av Président Wilson, 94230 Cachan, France

Institut des Sciences Moléculaires d’Orsay (ISMO), CNRS, Université Paris-Sud, Université Paris-Saclay, F-91405 Orsay, France

UMR CNRS 8180, Institut Lavoisier de Versailles, Université de Versailles St-Quentin, 45, avenue des Etats-Unis, 78035 Versailles Cedex, France

Funding

Agence Nationale de la Recherche · Conselho Nacional de Desenvolvimento Científico e Tecnológico

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