Ref HAL: hal-04414670_v1
DOI: 10.1039/d3cp05143a
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The formation and properties of smart (stimuli-responsive) membranes are reviewed, with a special focus on temperature and pH triggering of gating to water, ions, polymers, nanoparticles, or other molecules of interest. The review is organized in two parts, starting with all-smart membranes based on intrinsically smart materials, in particular of the poly(N-isopropylacrylamide) family and similar polymers.The key steps of membrane fabrication are discussed, namely the deposition into thin films, functionalization of pores, and the secondary crosslinking of pre-existing microgel particles into membranes. The latter may be free-standing and do not necessitate the presence of a porous support layer. The temperature-dependent swelling properties of polymers provide a means of controlling the size of pores, and thus size-sensitive gating. Throughout the review, we highlight ‘‘positive’’ (gates open) or ‘‘negative’’ (closed) gating effects with respect to increasing temperature. In the second part, the functionalization of porous organic or inorganic membranes of various origins by either microgel particles or linear polymer brushes is discussed. In this case, the key steps are the adsorption or grafting mechanisms. Finally, whenever provided by the authors, the suitability of smart gating membranes for specific applications is highlighted.

Ref HAL: hal-04398741_v1
DOI: 10.1039/D3TC03211F
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Carbon-based dots (CDs) are a novel class of luminescent carbon nanomaterials that have attracted much attention as promising alternatives for cadmium-based quantum dots and fluorescent organic dyes. Although different strategies have been proposed to produce CDs with intense and tuneable one-photon excited fluorescence (OPEF), the case of analogous two-photon excited fluorescence (TPEF) has not been fully explored yet. By varying the synthesis conditions, we produced three types of phloroglucinol-based carbon nanodots (PG CNDs). Their remarkable OPEF and TPEF properties can be tuned by (Ia) the conjugated aromatic domains and (Ib) the content of oxygenous moieties. In addition, the emission colour of the PG CNDs is strongly responsive to (II) the hydrogen-bonding network, enabling colour-switching while maintaining excellent fluorescence yields (both OPEF and TPEF). These three factors were evaluated for their suitability for the tuning of the emission colour. Our studies point out the advantages of the tuneable PG CNDs to be used in optoelectronics and biological application domains.

DOI: 10.1088/1361-6463/ad18f6
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In recent years, the excitation of surface phonon polaritons (SPhPs) in van der Waals materials received wide attention from the nanophotonics community. Alpha-phase Molybdenum trioxide (α-MoO3), a naturally occurring biaxial hyperbolic crystal, emerged as a promising polaritonic material due to its ability to support SPhPs for three orthogonal directions at different wavelength bands (range 10–20 μm). Here, we report on the fabrication, structural, morphological, and optical IR characterization of large-area (over 1 cm2 size) α-MoO3 polycrystalline film deposited on fused silica substrates by pulsed laser deposition. Due to the random grain distribution, the thin film does not display any optical anisotropy at normal incidence. However, the proposed fabrication method allows us to achieve a single α-phase, preserving the typical strong dispersion related to the phononic response of α-MoO3 flakes. Remarkable spectral properties of interest for IR photonics applications are reported. For instance, a polarization-tunable reflection peak at 1006 cm−1 with a dynamic range of ΔR = 0.3 and a resonance Q-factor as high as 53 is observed at 45° angle of incidence. Additionally, we report the fulfillment of an impedance matching condition with the SiO2 substrate leading to a polarization-independent almost perfect absorption condition (R < 0.01) at 972 cm−1 which is maintained for a broad angle of incidence. In this framework our findings appear extremely promising for the further development of mid-IR lithography-free, scalable films, for efficient and large-scale sensors, filters, thermal emitters, and label-free biochemical sensing devices operating in the free space, using far-field detection setups.

Ref HAL: hal-04399066_v1
Ref Arxiv: 2307.04162
DOI: 10.1016/j.marpolbul.2023.116012
Ref. & Cit.: NASA ADS
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Plastic pollution in the aquatic environment has been assessed for many years by ocean waste collection expeditions around the globe or by river sampling. While the total amount of plastic produced worldwide is well documented, the amount of plastic found in the ocean, the distribution of particles on its surface and its evolution over time are still the subject of much debate. In this article, we propose a general fragmentation model, postulating the existence of a critical size below which particle fragmentation becomes extremely unlikely. In the frame of this model, an abundance peak appears for sizes around 1mm, in agreement with real environmental data. Using, in addition, a realistic exponential waste feed to the ocean, we discuss the relative impact of fragmentation and feed rates, and the temporal evolution of microplastics (MP) distribution. New conclusions on the temporal trend of MP pollution are drawn.

Ref HAL: hal-04366049_v1
Ref Arxiv: 2310.18121
DOI: 10.1021/acsphotonics.3c01561
Ref. & Cit.: NASA ADS
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Ref HAL: hal-04324164_v1
Ref Arxiv: 2311.05001
Ref INSPIRE: 2720608
DOI: 10.1103/PhysRevB.109.035422
Ref. & Cit.: NASA ADS
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The Casimir interaction and torque are related phenomena originating from the exchange of electromagnetic excitations between objects. While the Casimir force exists between any types of objects, the materials or geometrical anisotropy drives the emergence of the Casimir torque. Here both phenomena are studied theoretically between dielectric films with immersed parallel single wall carbon nanotubes in the dilute limit with their chirality and collective electronic and optical response properties taken into account. It is found that the Casimir interaction is dominated by thermal fluctuations at sub-micron separations, while the torque is primarily determined by quantum mechanical effects. This peculiar quantum vs. thermal separation is attributed to the strong influence of reduced dimensionality and inherent anisotropy of the materials. Our study suggests that nanostructured anisotropic materials can serve as novel platforms to uncover new functionalities in ubiquitous Casimir phenomena.

Ref HAL: hal-04274983_v1
DOI: 10.1016/j.ijhydene.2023.10.244
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We investigate anatase TiO 2 doping with Au to determine the change in the band gap energy and optoelectronic properties using experimental and theoretical analysis. The structural analysis using XRD patterns revealed that the synthesized materials primarily exhibited an anatase phase of TiO 2 , with no impurity peaks observed. However, as the concentration of Au increased, additional diffraction peaks corresponding to Au crystalline phases were detected, indicating successful doping. Furthermore, the crystallite size was found to decrease with increasing Au concentration. We observe that the band gap reduces through substitution of Au into the TiO 2 lattice from 3.09 eV to 2.78 eV, demonstrating the feasibility of bandgap tuning of the TiO 2 system. A redshift for Au doped TiO 2 is observed from absorption spectroscopy and optical absorption intensity using hybrid density functional theory, facilitating visible light absorption, although with potential electron-hole recombination limitations. To enhance a visible light photocatalytic activity for water splitting, we extend our work to explore the impact of N and Au codoping into TiO 2 lattice. It reveals that the combination between N and Au leads to a suitable reduction in the band gap width of pure TiO 2. Interestingly, Au-N codoping may decrease the effect of photogenerated carriers, produce a new optical absorption feature in the visible region, and enhance the photocatalytic performance of TiO 2. This codoping configuration is also a promising photocatalyst for the decomposition of water using visible light without inducing unoccupied states.