Relationship between Young's Modulus and Film Architecture in Cellulose Nanofibril-Based Multilayered Thin Films.

Young's moduli of cellulose nanofibril (CNF)-poly(allylamine hydrochloride) (PAH) multilayered thin films were measured using strain-induced elastic buckling instability for mechanical measurements (SIEBIMM) and the quantitative nanomechanical mapping technique (PF-QNM). To establish the relationship between structure and mechanical properties, three types of films with various architectures were built using the layer-by-layer method by changing the ionic strength of the dipping solution. Both methods demonstrate that the architecture of a film has a strong impact on its mechanical properties even though the film has similar cellulose content, emphasizing the role of the architecture. Films with lower porosity (Φair = 0.34) and a more intricate network display the highest Young's moduli (9.3 GPa), whereas others with higher and similar porosity (Φair = 0.46-0.48) present lower Young's moduli (4.0-5.0 GPa). PF-QNM measurements indicate a reverse ranking that is probably indicative of the surface composition of the films.

Cellulose nanocrystal-assisted dispersion of luminescent single-walled carbon nanotubes for layer-by-layer assembled hybrid thin films.

Highly stable single-walled carbon nanotube (SWNT) dispersions are obtained after ultrasonication in cellulose nanocrystal (CN) aqueous colloidal suspensions. Mild dispersion conditions were applied to preserve the SWNT length in order to facilitate the identification of hybrid objects. This led to a moderate dispersion of 24% of the SWNTs. Under these conditions, atomic force microscopy (AFM) and transmission electron microscopy (TEM) experiments succeeded in demonstrating the formation of hybrid particles in which CNs are aligned along the nanotube axis by a self-assembly process. These SWNT/CN dispersions are used to create multilayered thin films with the layer-by-layer method using polyallylamine hydrochloride as a polyelectrolyte. Homogeneous films from one to eight bilayers are obtained with an average bilayer thickness of 17 nm. The presence of SWNTs in each bilayer is attested to by characteristic Raman signals. It should be noted that these films exhibit a near-infrared luminescence signal due to isolated and well-separated nanotubes. Furthermore, scanning electron microscopy (SEM) suggests that the SWNT network is percolating through the film.

Macroporous hybrid Pickering foams based on carbon nanotubes and cellulose nanocrystals.

The association of nanoparticles with complementary properties to produce hybrids is an underestimated way to develop multifunctional original architectures. This strategy is used to prepare simple, low-cost, and environmentally friendly method to fabricate ultra-low density alveolar foam reinforced with carbon nanotubes (CNTs). This paper investigates the ability of cellulose nanocrystals (CNCs) to produce highly stable oil-in-water Pickering emulsions and to efficiently disperse carbon nanotubes in water to form three-dimensional macroporous conductive foam. It is shown that both single-walled carbon nanotubes (SWNTs) and multi-walled carbon nanotubes (MWNTs) are strongly linked to CNCs by non-covalent interactions, preserving the intrinsic properties of both nanoparticles. Homogeneous surfactant-free emulsions with a droplet diameter of 6 µm are produced. Once concentrated, they can form stable high internal phase emulsions. Incorporating CNTs into these CNC-based emulsions was shown to improve their rheological properties. Freeze-drying the concentrated emulsions produces ultra-low density solid foams (14 mg·cm-3) with several levels of porosity controlled by the emulsification step. Loading CNCs with only 2-4 wt% of CNTs, decreases the electrical resistivity of the foam to 104 Ω cm in high relative humidity. The mechanical and electrical properties are studied and discussed in light of the resulting specific foam structure.

Myomesin is a molecular spring with adaptable elasticity.

The M-band is a transverse structure in the center of the sarcomere, which is thought to stabilize the thick filament lattice. It was shown recently that the constitutive vertebrate M-band component myomesin can form antiparallel dimers, which might cross-link the neighboring thick filaments. Myomesin consists mainly of immunoglobulin-like (Ig) and fibronectin type III (Fn) domains, while several muscle types express the EH-myomesin splice isoform, generated by the inclusion of the unique EH-segment of about 100 amino acid residues (aa) in the center of the molecule. Here we use atomic force microscopy (AFM), transmission electron microscopy (TEM) and circular dichroism (CD) spectroscopy for the biophysical characterization of myomesin. The AFM identifies the "mechanical fingerprints" of the modules constituting the myomesin molecule. Stretching of homomeric polyproteins, constructed of Ig and Fn domains of human myomesin, produces a typical saw-tooth pattern in the force-extension curve. The domains readily refold after relaxation. In contrast, stretching of a heterogeneous polyprotein, containing several repeats of the My6-EH fragment reveals a long initial plateau corresponding to the sum of EH-segment contour lengths, followed by several My6 unfolding peaks. According to this, the EH-segment is characterized as an entropic chain with a persistence length of about 0.3nm. In TEM pictures, the EH-domain appears as a gap in the molecule, indicating a random coil conformation similar to the PEVK region of titin. CD spectroscopy measurements support this result, demonstrating a mostly non-folded conformation for the EH-segment. We suggest that similarly to titin, myomesin is a molecular spring, whose elasticity is modulated by alternative splicing. The Ig and Fn domains might function as reversible "shock absorbers" by sequential unfolding in the case of extremely high or long sustained stretching forces. These complex visco-elastic properties of myomesin might be crucial for the stability of the sarcomere.

pH-Sensitive photoinduced energy transfer from bacteriorhodopsin to single-walled carbon nanotubes in SWNT-bR hybrids.

Energy transfer mechanisms in noncovalently bound bacteriorhodopsin/single-walled carbon nanotube (SWNT) hybrids are investigated using optical absorption and photoluminescence excitation measurements. The morphology of the hybrids was investigated by atomic force microscopy. In this study, proteins are immobilized onto the sidewall of the carbon nanotubes using a sodium cholate suspension-dialysis method that maintains the intrinsic optical and fluorescence properties of both molecules. The hybrids are stable in aqueous solutions for pH ranging from 4.2 to 9 and exhibit photoluminescence properties that are pH-dependent. The study reveals that energy transfer from bacteriorhodopsin to carbon nanotubes takes place. So, at pH higher than 5 and up to 9, the SWNTs absorb the photons emitted by the aromatic residues of the protein, inducing a strong increase in intensity of the E11 emissions of SWNTs through their E33 and E44 excitations. From pH = 4.2 to pH = 5, the protein fluorescence is strongly quenched whatever the emission wavelengths, while additional fluorescence features appear at excitation wavelengths ranging from 660 to 680 nm and at 330 nm. The presence of these features is attributed to a resonance energy transfer mechanism that has an efficiency of 0.94 ± 0.02. More, by increasing the pH of the dispersion, the fluorescence characteristics become those observed at higher pH values and vice versa.

Color control in coaxial two-luminophore nanowires.

We report a general and simple approach to take control of the color of light-emitting two-luminophore hybrid nanowires (NWs). Our strategy is based on the spatial control at the nanoscale (coaxial geometry) and the spectral selection of the two kinds of luminophores in order to restrict complex charge and energy transfers. Thus, it is possible to control the color of the photoluminescence (PL) as an interpolation of the CIE (Commission Internationale de l'Eclairage) coordinates of each luminophore. For this purpose, we selected a green-emitting semiconducting polymer and a red-emitting hexanuclear metal cluster compound, (n-Bu4N)2Mo6Br8F6, dispersed in a poly(methyl-methacrylate) (PMMA) matrix. The great potential and the versatility of this strategy have been demonstrated for two configurations. First, a yellow PL with a continuous change along the nanowire has been evidenced when the proportion of the PPV shell versus the nanocomposite core, that is, the green/red volumic ratio, progressively shifts from 1:2 to 1:5. Second, an extremely abrupt change in the PL color with red-green-yellow segments has been achieved. A simple model corroborates the effectiveness of this strategy. PL excitation and time-resolved experiments also confirm that no significant charge and energy transfers are involved. The two-luminophore hybrid nanowires may find widespread nanophotonic applications in multicolor emitting sources, lasers and chemical and biological sensors.

Conformational structural changes of bacteriorhodopsin adsorbed onto single-walled carbon nanotubes.

The interaction between purple membranes, composed of proteins of bacteriorhodopsin (bR) and their native surrounding lipids, and single-walled carbon nanotubes (SWNT) has been investigated. In this work, sonication has been used to debundle SWNT in buffer solution without surfactant before the addition of native purple membranes. The sample was then sonicated in a bath for a short time, followed by a centrifugation. The supernatants contain proteins in excess and SWNT as individual and small bundles covered by a bR layer with an average thickness of 1.5 nm. TEM and AFM observations support the idea that only a protein monolayer surrounds the tubes. Optical absorption and infrared spectroscopy measurements provide evidence that the proteins adsorbed onto the SWNT undergo orientational changes of the helical segments in bR and helix conformational changes. We ascribe the main driving force to the hydrophobic interactions between the sidewall of the SWNT and the hydrophobic residues of the alpha-helices of bR.

Temperature dependence of unbinding forces between complementary DNA strands.

Force probe techniques such as atomic force microscopy can directly measure the force required to rupture single biological ligand receptor bonds. Such forces are related to the energy landscape of these weak, noncovalent biological interactions. We report unbinding force measurements between complementary strands of DNA as a function of temperature. Our measurements emphasize the entropic contributions to the energy landscape of the bond.