| Literature DB >> 33445737 |
Francesco Milano1, Maria Rachele Guascito2,3, Paola Semeraro2,3, Shadi Sawalha4,5, Tatiana Da Ros6, Alessandra Operamolla7, Livia Giotta2,3, Maurizio Prato6,8,9, Ludovico Valli2,3.
Abstract
Cellulose nanomaterials have been widely investigated in the last decade, unveiling attractive properties for emerging applications. The ability of sulfated cellulose nanocrystals (CNCs) to guide the supramolecular organization of amphiphilic fullerene derivatives at the air/water interface has been recently highlighted. Here, we further investigated the assembly of Langmuir hybrid films that are based on the electrostatic interaction between cationic fulleropyrrolidines deposited at the air/water interface and anionic CNCs dispersed in the subphase, assessing the influence of additional negatively charged species that are dissolved in the water phase. By means of isotherm acquisition and spectroscopic measurements, we demonstrated that a tetra-sulfonated porphyrin, which was introduced in the subphase as anionic competitor, strongly inhibited the binding of CNCs to the floating fullerene layer. Nevertheless, despite the strong inhibition by anionic molecules, the mutual interaction between fulleropyrrolidines at the interface and the CNCs led to the assembly of robust hybrid films, which could be efficiently transferred onto solid substrates. Interestingly, ITO-electrodes that were modified with five-layer hybrid films exhibited enhanced electrical capacitance and produced anodic photocurrents at 0.4 V vs Ag/AgCl, whose intensity (230 nA/cm2) proved to be four times higher than the one that was observed with the sole fullerene derivative (60 nA/cm2).Entities:
Keywords: Langmuir-Schäfer deposition; cellulose nanocrystals; fullerene; fulleropyrrolidine; photocatalysis; photocurrent; voltammetry
Year: 2021 PMID: 33445737 PMCID: PMC7828161 DOI: 10.3390/polym13020243
Source DB: PubMed Journal: Polymers (Basel) ISSN: 2073-4360 Impact factor: 4.329