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Optoelectronic effects differentiating absorption of right and left circularly polarized photons in thin films of chiral materials are typically prohibitively small for their direct photocurrent observation. Chiral metasurfaces increase the electronic sensitivity to circular polarization, but their out-of-plane architecture entails manufacturing and performance trade-offs. Here, we show that nanoporous thin films of chiral nanoparticles enable high sensitivity to circular polarization due to light-induced polarization-dependent ion accumulation at nanoparticle interfaces. Self-assembled multilayers of gold nanoparticles modified with l - phenylalanine generate a photocurrent under right-handed circularly polarized light as high as 2.41 times higher than under left-handed circularly polarized light. The strong plasmonic coupling between the multiple nanoparticles producing planar chiroplasmonic modes facilitates the ejection of electrons, whose entrapment at the membrane–electrolyte interface is promoted by a thick layer of enantiopure phenylalanine. Demonstrated detection of light ellipticity with equal sensitivity at all incident angles mimics phenomenological aspects of polarization vision in marine animals. The simplicity of self-assembly and sensitivity of polarization detection found in optoionic membranes opens the door to a family of miniaturized fluidic devices for chiral photonics. Chiral gold nanoparticles coated with enantiomerically pure phenylalanine were assembled into nanoporous membranes, whose ionic conductivity depends on the handedness of the incident circularly polarized light.

We demonstrate that the introduction of an elemental beam of Mn during the molecular beam epitaxial growth of Bi2Se3 results in the formation of layers of Bi2MnSe4 that intersperse between layers of pure Bi2Se3. This study revises the assumption held by many who study magnetic topological insulators (TIs) that Mn incorporates randomly at Bi-substitutional sites during epitaxial growth of Mn:Bi2Se3. Here, we report the formation of thin film magnetic TI Bi2MnSe4 with stoichiometric composition that grows in a self-assembled multilayer heterostructure with layers of Bi2Se3, where the number of Bi2Se3 layers separating the single Bi2MnSe4 layers is approximately defined by the relative arrival rate of Mn ions to Bi and Se ions during growth, and we present its compositional, structural, and electronic properties. We support a model for the epitaxial growth of Bi2MnSe4 in a near-periodic self-assembled layered heterostructure with Bi2Se3 with corresponding theoretical calculations of the energetics of this material and those of similar compositions. Computationally derived electronic structure of these heterostructures demonstrates the existence of topologically nontrivial surface states at sufficient thickness.

In this paper, a novel bimetallic Ce-Ni metal-organic frameworks (Ce-Ni-MOF) are synthesized by hydrothermal reaction, using 1,3,5-benzenetricarboxylic acid as a ligand. In particular, the bimetallic Ce-Ni-MOF with the largest specific surface area and catalytic sites was synthesized when the molar ratio of Ce3+ to Ni2+ was 3:7. Bimetallic Ce-Ni-MOF is added to the traditional conductive material of multiwall carbon nanotubes (MWCNTs) to play their synergistic effect, improve the conductivity, specific surface area, and catalytic site of the MWCNTs. A novel bisphenol A (BPA) sensor was successfully prepared by a self-assembled multilayer strategy of Ce-Ni-MOF/MWCNTs modified glassy carbon electrodes (GCE). Field emission scanning electron microscopy, powder X-ray diffraction, and transmission electron microscope were carried out to characterize the Ce-Ni-MOF/MWCNTs. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used as a sensitive analytical method for the determination of BPA, and a wider linear dynamic range of BPA determination in 0.1 μmol·L−1 to 100 μmol·L−1 with a detection limit of 7.8 nmol·L−1 (S/N = 3). The proposed method was applied to measure the content of BPA in different brands of drinking water with satisfying recovery from 97.4 to 102.4%.

Herein, based on the principle of biomineralization and a layer-by-layer self-assembly (LBL) method combined with a sol-gel method, a chitosan–SiO 2 film was formed on the wood surface. Polycationic chitosan was used as a mineralization inducer and self-assembled multilayer polyelectrolyte on the substrate surfaces. This inducer accelerated the deposition of silicon dioxide (SiO 2 ) in the cell wall and intercellular space of the wood and a chitosan–SiO 2 film was formed, which was confirmed by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The appearance of Si–O–Si and Si–O–C peaks in the Fourier transform infrared (FTIR) spectra, which were confirmed by X-ray photoelectron spectroscopy (XPS), indicated the formation of an organic–inorganic structure on the mineralized wood. Thermogravimetric analysis showed that the carbon residue ratio of the control wood was 10%. In contrast, with an increase in the number of self-assembled layers, the carbon residue ratio of the mineralized wood increased, reaching a maximum of 58%. The highest peak in cone calorimetry (CONE) indicated that heat release rate of the mineralized wood was significantly reduced after mineralization, with microcalorimetry experiments demonstrating a similar outcome. Moreover, the moisture absorption and physical and mechanical strength of the mineralized wood were reduced and increased, respectively. Based on the principle of biomineralization, combining LBL with sol-gel method provides a new idea for the preparation of wood-inorganic composites and the preparation process is non-toxic, non-hazardous, green. Highlights In this study, based on the principle of biomineralization, the layer self-assembly method was combined with the sol–gel method. The rapid deposition of silica on the cell wall of wood induced by chitosan to form a chitosan-SiO 2 film layer improved the flame retardant properties and physical-mechanical properties of wood. It provides an idea and a way to prepare wood–inorganic composites.

Transfusion medicine is a field that has developed in the second half of the last century. Very rapidly, however, it became clear that this approach also carried its problems, such as the incompatibility of red blood cells and plasma between donors and recipients, and the possibility of transmitting viral and bacterial infections. An immunomagnetic biosensor for the label-free detection of a bacterial model, Escherichia coli , is described and compared to a self assembled multilayer system reported previously. The paramagnetic nanoparticles layer attracted to, and formed on, the gold electrode surface via a magnetic field up to 300 mT is not totally blocking for the redox probe comparing to the thiol self assembled monolayer (a biotin thiol and a spacer thioalcohol). Moreover, the modeling of the Nyquist spectra obtained by electrochemical impedance spectroscopy for increasing concentrations of E. coli shows for both system a sigmoid variation of the polarization resistance with increasing logarithmic concentration of bacteria. A sensitivity slope of 10.675 was obtained for the immunomagnetic sensor compared to 6.832 for the self assembled multilayer process, this indicating the higher sensitivity of the paramagnetic nanoparticles biosensor.

Rescuing the compromised function of periodontal ligament stem cells (PDLSCs) due to hyperglycemia-induced oxidative stress and reducing the risk of postoperative infection around the interface of scaffold materials are of prime importance for periodontal regeneration in diabetes mellitus. To this end, a facile and green approach for the establishment of surfaces with antioxidative and antibacterial properties was developed in this work. Briefly, the surfaces of polystyrene (PS) plate were pre-modified with polydopamine and then coated with a genipin crosslinked layer-by-layer (LbL) assembly, which was established by using the antibacterial polyelectrolytes carboxymethyl chitosan (CMC) and polylysine (PLL) as building block. Metformin as an antioxidative agent was incorporated into the discrete nanolayers to achieve sustainable release. Our research showed that metformin-loaded LbL assembly presented favorable cytocompatibility. The released metformin could partially rescue the impaired osteogenic function of human PDLSCs induced by high glucose in vitro. Meanwhile, owing to the antibacterial activity of CMC and PLL, the colonization of common pathogenic bacteria related to periodontal disease could be disturbed on the surface of developed coatings. Accordingly, the presented strategy for surface functionalization of materials in our study holds a promising potential for periodontal regeneration application in diabetic patients. Graphical abstract

The reactivities of various fatty monoacids and diacids on copper metal-containing surfaces were investigated through reflection–absorption infrared spectroscopy. The formation of copper carboxylates is detected on pure copper surfaces, while copper and zinc carboxylates are simultaneously formed on brass surfaces. Following the decrease of acid carbonyl and the formation of carboxylate infrared bands, it is shown that fatty monoacids C8 and C10 react with clean/polished copper and its zinc alloy within 2–4 h, while those with chains > C12 react within days. At the end of the processes, only the corresponding metal carboxylates are detected in all cases. An explanation for the above is offered on a molecular mobility and acidity basis, where the lower monoacids (liquids in room temperature), also having lower pKa values, favor higher reaction rates. Furthermore, it is argued that longer-chain fatty monoacids, when deposited from their solutions, allow for favorable orientation resulting in self-assembled monolayer-type molecular packing on the copper surface, which may additionally rationalize the slower reaction. Interestingly, fatty diacids do not form any carboxylate products under the same conditions, as it is argued that their molecules may efficiently pack as self-assembled multilayers on copper and ultimately protect it. The possible implications of the fatty monoacid and diacid behavior on the archaeological organic residues level and regarding the stability of copper alloys are discussed.

When coating different dielectrics on polymer surfaces, the surface morphology could be changed to wrinkles or cracks. The wrinkles or cracks are self-formed during the process of heating and cooling. The presented experimental results show that the wrinkles can be self-aligned between two nearest patterns. The direction of aligned wrinkles can be tuned to parallel, perpendicular and required degrees according to the different array-based patterns. The number of wrinkles can also be controlled by changing the size of the patterns. In a limited range, a larger size pit has more wrinkles.

Dopamine (DA) is an important neurotransmitter which indicates the risk of several neurological diseases. The selective determination with low detection limit is necessary for early diagnosis and prevention of neurological diseases associated with abnormal concentration of DA. The purpose of this study is to fabricate a poly(3-aminobenzylamine)/poly(sodium 4-styrenesulfonate) (PABA/PSS) multilayer thin film for use as an electrochemical DA biosensor. The PABA was firstly synthesized using a chemical oxidation method of 3-aminobenzylamine (ABA) monomer with ammonium persulfate (APS) as an oxidant. For electrochemical biosensor, the PABA/PSS thin film was fabricated on fluorine doped tin oxide (FTO)-coated glass substrate using the layer-by-layer (LBL) self-assembly method. The optimized number of bilayers was achieved using SEM and cyclic voltammetry (CV) results. The electroactivity of the optimized LBL thin film toward detection of DA in neutral solution was studied by CV and amperometry. The PABA/PSS thin film showed good sensitivity for DA sensing with sensitivity of 6.922 nA·cm−2·µM−1 and linear range of 0.1–1.0 µM (R2 = 0.9934), with low detection limit of 0.0628 µM, long-term stability and good reproducibility. In addition, the selectivity of the PABA/PSS thin film for detection of DA under the common interferences (i.e., ascorbic acid, uric acid and glucose) was also presented. The prepared PABA/PSS thin film showed the powerful efficiency for future use as DA biosensor in real sample analysis.

Silk-based medical products have a long history of use as a material for surgical sutures because of their desirable mechanical properties. However, silk fibroin fabric has been reported to be haemolytic when in direct contact with blood. The layer-by-layer self-assembly technique provides a method for surface modification to improve the biocompatibility of silk fibroin fabrics. Regenerated silk fibroin and alginate, which have excellent biocompatibility and low immunogenicity, are outstanding candidates for polyelectrolyte deposition. In this study, silk fabric was degummed and positively charged to create a silk fibroin fabric that could undergo self-assembly. The multilayer self-assembly of the silk fibroin fabric was achieved by alternating the polyelectrolyte deposition of a negatively charged alginate solution (pH = 8) and a positively charged regenerated silk fibroin solution (pH = 2). Finally, the negatively charged regenerated silk fibroin solution (pH = 8) was used to assemble the outermost layer of the fabric so that the surface would be negatively charged. A stable structural transition was induced using 75% ethanol. The thickness and morphology were characterised using atomic force microscopy. The properties of the self-assembled silk fibroin fabric, such as the bursting strength, thermal stability and flushing stability, indicated that the fabric was stable. In addition, the cytocompatibility and haemocompatibility of the self-assembled silk fibroin fabrics were evaluated. The results indicated that the biocompatibility of the self-assembled multilayers was acceptable and that it improved markedly. In particular, after the self-assembly, the fabric was able to prevent platelet adhesion. Furthermore, other non-haemolytic biomaterials can be created through self-assembly of more than 1.5 bilayers, and we propose that self-assembled silk fibroin fabric may be an attractive candidate for anticoagulation applications and for promoting endothelial cell adhesion for vascular prostheses.