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Polyvinyl alcohol (PVA)/laponite (LP) nanocomposite coatings were fabricated via a facile one-step coassembly process. The formed nanocoatings contain a high concentration of LP nanosheets, which can be well aligned along the substrate surface during the coassembly process. Due to the highly orientated structure, the flexible nanocoatings exhibit ultra-high transparency and superior mechanical properties, and can also act as excellent gas barriers. Such nanocoatings can be exceptional candidates for a variety of applications, such as food packaging.

Nanosized α-zirconium phosphate (α-ZrP), unlike microcrystalline α-ZrP, takes less time to prepare and is synthesized directly in organic solvents. During the synthesis of nanosized α-ZrP, the heating step is critical because during which the particle growth/aggregation is ongoing. In order to explore more details of this step, extra water molecules were intentionally introduced to the ethanol gel of nanosized α-ZrP so that the evaporation of the solvent was slowed. To heat the gels at 65 °C for different periods (1-6 days), one could control with ease the synthesized α-ZrP in size, from 63 to 155 nm, and in morphology, from amorphous to highly crystalline. Furthermore, the heating step also affects the intercalated solvent and the dangling propionate groups on the edge of the nanosized α-ZrP, which could be deduced from the intercalation/exfoliation behavior of the nanocrystals. This modified synthesis method of nanosized α-ZrP offers an alternate means to tune the size and morphology of the nanosized α-ZrP for broad applications.

A self-assembled two-dimensional montmorillonite nanocoating enables significantly enhanced corona resistance in the Kapton film.

Surface modification is a main approach for natural polymers to gain flame retardancy. Developing a green coating system to endow natural polymers with flame retardancy and wash-durability is extremely challenging. Herein, a sandwich-like structured nanocoating system with mutual restricted network through electrostatic interaction, hydrogen bonding, and chemical bonding were designed via multi-layered coating and UV curing. The coated natural cotton fabrics demonstrated exellent flame retardancy, wash durability, and hydrophobicity. The chemicals involved include montmorillonite (MMT), ammonium polyphosphate (APP), acrylated polyurethane (PU), branched polyethylenimine (bPEI), and polydimethylsiloxane (PDMS). The concentration of bPEI governed the wash durability of the coated fabrics, and those samples with a higher concentration of bPEI possessed better wash durability. Meanwhile, bPEI served as a flammable resource to deteriorate the flame retardant performance. The systematic evaluations of the coated fabrics after washing demonstrated that this coating system can maintain balanced wash durability and flame retardancy.

A one-pot self-assembled nanocoating with a well-defined nanostructure was created consisting of polyvinyl alcohol (PVA) and montmorillonite (MMT) and applied to double-walled corrugated cardboard (CB) via spray coating. X-ray diffraction (XRD) analysis revealed the intercalation of PVA into the interstitial spaces of the MMT nanosheets and the alignment of the nanosheets. Vertical burning test, surface burning test, and horizontal burning test showed marked reductions in afterflame time, afterglow time, and flame spread, displaying quick self-extinguishing behaviors. Scanning electron microscopy (SEM) images revealed a uniform coating of the surface of CB before burning tests. After burning, the coated CB samples formed a dense char layer that protected the underlying fibers. A PVA/MMT nanocoating applied via spray coating greatly inhibited flame spread and improved flame retardancy. A one-pot coassembled nanocoating consisting of polyvinyl alcohol and montmorillonite was developed to significantly improve the flame retardancy of cardboard.

Multi-stimuli responsive (MSR) chromic materials which can exhibit a color change when exposed to external stimuli demonstrate huge potential in developing new intelligent devices. However, they commonly require complicated synthesis processes that are not suitable for mass production. To facilitate the fabrication of MSR devices, for the first time, we propose a facile 3D integration strategy to rationally assemble various commercial chromic materials, light shielding layers, and a stretchable substrate into a set of MSR devices equipped with thermo-/photo-/mechanochromic characteristics with negligible cross-interferences. Notably, the mechanochromic sensitivity can be readily adjusted to multiple levels via facile pre-stretching methods. Moreover, two types of MSR units are integrated into an interactive electronic device, which exhibits thermo-/photo-/electrochromic responses, and two levels of mechanochromic responses with color changes at 100% and 200% strain, respectively. In addition, another highly sensitive MSR unit is applied to a wearable motion/environmental monitoring chromic device, which can detect finger bending within 30% strain, and monitor environmental stimuli (UV, temperature) with thermal mapping capability. A smartphone-based colorimetric analysis app was also developed for finger bending detection. Comprehensive quantitative characterization and finite element analysis are used to elucidate the performance and intrinsic mechanisms of these MSR responses.

Significance Smart devices characterized by micro-/nanotopographies, such as cracks, wrinkles, folds, etc., have been fabricated for widespread application. Here, with the combination of multiscale hierarchical architecture, ultrathin metal nanocoatings with high optical/photothermal tunability and morphological versatility, and surface/interface engineering, a set of multifunctional devices with multistimuli responsiveness was fabricated. These devices can adapt to external stimuli with reversible and instantaneous responses in optical signals, which include strain-regulated light-scattering properties, photothermal-responsive wrinkled surface coupled with moisture-responsive structural color, and mechanically controllable light-shielding properties. The structural designs that rationally overlay micro-/nanostructured ultrathin nanocoatings with other elements are the key to realize this advanced system, which provides avenues for designing versatile, tunable, and adaptable multifunctional devices., Inspired by the intriguing adaptivity of natural life, such as squids and flowers, we propose a series of dynamic and responsive multifunctional devices based on multiscale structural design, which contain metal nanocoating layers overlaid with other micro-/nanoscale soft or rigid layers. Since the optical/photothermal properties of a metal nanocoating are thickness dependent, metal nanocoatings with different thicknesses were chosen to integrate with other structural design elements to achieve dynamic multistimuli responses. The resultant devices demonstrate 1) strain-regulated cracked and/or wrinkled topography with tunable light-scattering properties, 2) moisture/photothermal-responsive structural color coupled with wrinkled surface, and 3) mechanically controllable light-shielding properties attributed to the strain-dependent crack width of the nanocoating. These devices can adapt external stimuli, such as mechanical strain, moisture, light, and/or heat, into corresponding changes of optical signals, such as transparency, reflectance, and/or coloration. Therefore, these devices can be applied as multistimuli-responsive encryption devices, smart windows, moisture/photothermal-responsive dynamic optics, and smartphone app–assisted pressure-mapping sensors. All the devices exhibit high reversibility and rapid responsiveness. Thus, this hybrid system containing ultrathin metal nanocoatings holds a unique design flexibility and adaptivity and is promising for developing next-generation multifunctional devices with widespread application.

Energy collection and molecular separation are two emerging applications based on membrane technologies. It remains a challenge to improve the separation performance of molecular channels. Meanwhile, the application of membranes is typically impeded by their poor stability under practical hydrous conditions. Herein, we present the fabrication of a uniformly lamellar membrane using montmorillonite nanosheets as building blocks. We managed to achieve nanofluidic ion transport and molecular separation simultaneously. The membrane nanochannels possess nanofluidic ion transport properties with an output power density of up to 0.18 W m−1 at a membrane thickness of 11.2 μm under a 1000-fold transmembrane concentration difference. The membrane also shows a water permeance of 429 L m−2 h−1 atm−1 at a thickness of 2.5 μm and high separation efficiency for both cationic and anionic dyes. Moreover, the montmorillonite-based membranes can maintain high stability under aqueous conditions with soaking, shaking, and even ultrasonication.

CsxWO3 nanorods can be used to sensitize the single layer g-C3N4, where full spectrum light harvesting excited electrons to drive the photocatalytic reduction of N2 into NH3. Under UV light, both water splitting and solar ammonia synthesis reaction exhibit high activity. However, selectivity towards ammonia over hydrogen is realized under NIR irradiation. With the control of methanol, O2 can directly decide the NH3 or H2 evolution on photocatalyst. The origin is the strong capture of O2 with the electrons from the photocatalyst under light irradiation to yield the oxygen active species, which transfer electrons subsequently with help of methanol to generate NH3. However, H2 production will be suppressed by O2. And with its sacrifice, methanol preserves the produced NH3 from oxidation. The O2-sacrificial agent mediated NH3 evolution reaction found here provides insights in the promotion role of them in other catalysis.

The electrostatic combination of anionic block copolymers with cationic gold(i) complexes leads to the formation of spherical micelles, where gold(i)-containing ionic cores were formed with anionic blocks and further stabilized by neutral blocks of polystyrene or poly(ethylene oxide). This self-assembled strategy induces remarkable phosphorescence enhancement of the gold(i) complexes in solution. The emissive intensity increases unexpectedly with increasing molecular weight of the anionic block that is not coordinated onto the gold(i) complexes. The intensely phosphorescent micelles formed in water can be utilized as a luminescence bioimaging probe in living cells.

The organic insulator-metal interface is the most important junction in flexible electronics. The strong band offset of organic insulators over the Fermi level of electrodes should theoretically impart a sufficient impediment for charge injection known as the Schottky barrier. However, defect formation through Anderson localization due to topological disorder in polymers leads to reduced barriers and hence cumbersome devices. A facile nanocoating comprising hundreds of highly oriented organic/inorganic alternating nanolayers is self-coassembled on the surface of polymer films to revive the Schottky barrier. Carrier injection over the enhanced barrier is further shunted by anisotropic 2D conduction. This new interface engineering strategy allows a significant elevation of the operating field for organic insulators by 45% and a 7× improvement in discharge efficiency for Kapton at 150 °C. This superior 2D nanocoating thus provides a defect-tolerant approach for effective reviving of the Schottky barrier, one century after its discovery, broadly applicable for flexible electronics.