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HighlightsTwo functionally different anisotropic layers are rationally assembled for highly selective and stretchable multidirectional strain sensors.Concurrently excellent selectivity, sensitivity, stretchability, and linearity up to 100% strain is demonstrated for the first time in a multidirectional strain sensor.A novel stepwise crack propagation mechanism is proposed to enable high stretchability and linearity. Flexible multidirectional strain sensors are crucial to accurately determining the complex strain states involved in emerging sensing applications. Although considerable efforts have been made to construct anisotropic structures for improved selective sensing capabilities, existing anisotropic sensors suffer from a trade-off between high sensitivity and high stretchability with acceptable linearity. Here, an ultrasensitive, highly selective multidirectional sensor is developed by rational design of functionally different anisotropic layers. The bilayer sensor consists of an aligned carbon nanotube (CNT) array assembled on top of a periodically wrinkled and cracked CNT–graphene oxide film. The transversely aligned CNT layer bridge the underlying longitudinal microcracks to effectively discourage their propagation even when highly stretched, leading to superior sensitivity with a gauge factor of 287.6 across a broad linear working range of up to 100% strain. The wrinkles generated through a pre-straining/releasing routine in the direction transverse to CNT alignment is responsible for exceptional selectivity of 6.3, to the benefit of accurate detection of loading directions by the multidirectional sensor. This work proposes a unique approach to leveraging the inherent merits of two cross-influential anisotropic structures to resolve the trade-off among sensitivity, selectivity, and stretchability, demonstrating promising applications in full-range, multi-axis human motion detection for wearable electronics and smart robotics.

Cooling in buildings is vital to human well-being but inevitability consumes significant energy, adding pressure on achieving carbon neutrality. Thermally superinsulating aerogels are promising to isolate the heat for more energy-efficient cooling. However, most aerogels tend to absorb the sunlight for unwanted solar heat gain, and it is challenging to scale up the aerogel fabrication while maintaining consistent properties. Herein, we develop a thermally insulating, solar-reflective anisotropic cooling aerogel panel containing in-plane aligned pores with engineered pore walls using boron nitride nanosheets by an additive freeze-casting technique. The additive freeze-casting offers highly controllable and cumulative freezing dynamics for fabricating decimeter-scale aerogel panels with consistent in-plane pore alignments. The unique anisotropic thermo-optical properties of the nanosheets combined with in-plane pore channels enable the anisotropic cooling aerogel to deliver an ultralow out-of-plane thermal conductivity of 16.9 mW m −1 K −1 and a high solar reflectance of 97%. The excellent dual functionalities allow the anisotropic cooling aerogel to minimize both parasitic and solar heat gains when used as cooling panels under direct sunlight, achieving an up to 7 °C lower interior temperature than commercial silica aerogels. This work offers a new paradigm for the bottom-up fabrication of scalable anisotropic aerogels towards practical energy-efficient cooling applications. Scaling up anisotropic freeze-casting processes can be challenging due to the temperature gradient farther from the cold source. Here, authors report an additive freeze-casting technique able to produce large-scale aerogel panels and demonstrate it towards practical passive cooling applications.

Flexible and easily reconfigurable supercapacitors show great promise for application in wearable electronics. In this study, multiwall C nanotubes （CNTs） decorated with hierarchical ultrathin zinc sulfide （ZnS） nanosheets （ZnS@CNT） are synthesized via a facile method. The resulting ZnS@CNT electrode, which delivers a high specific capacitance of 347.3 F·g^-1 and an excellent cycling stability, can function as a high-performance electrode for a flexible all-solid-state supercapacitor using a polymer gel electrolyte. Our device exhibits a remarkable specific capacitance of 159.6 F·g^-1, a high energy density of 22.3 W·h·kg^-1, and a power density of 5 kW·kg^-1 It also has high electrochemical performance even under bending or twisting. The all-solid-state supercapacitors can be easily integrated in series to power different commercial light-emitting diodes without an external bias voltage.

HighlightsHighly porous aerogel with longitudinally aligned channels and whisker-like ligaments is constructed by solvent-assisted unidirectional freezing.The thermal insulation and solar reflection capabilities of the composite aerogel reach a state-of-the-art level.The composite aerogel capable of infrared stealth and temperature preservation presents great potential for application in energy-saving buildings.With the mandate of worldwide carbon neutralization, pursuing comfortable living environment while consuming less energy is an enticing and unavoidable choice. Novel composite aerogels with super thermal insulation and high sunlight reflection are developed for energy-efficient buildings. A solvent-assisted freeze-casting strategy is used to produce boron nitride nanosheet/polyvinyl alcohol (BNNS/PVA) composite aerogels with a tailored alignment channel structure. The effects of acetone and BNNS fillers on microstructures and multifunctional properties of aerogels are investigated. The acetone in the PVA suspension enlarges the cell walls to suppress the shrinkage, giving rise to a lower density and a higher porosity, accompanied with much diminished heat conduction throughout the whole product. The addition of BNNS fillers creates whiskers in place of disconnected transverse ligaments between adjacent cell walls, further ameliorating the thermal insulation transverse to the cell wall direction. The resultant BNNS/PVA aerogel delivers an ultralow thermal conductivity of 23.5 mW m−1 K−1 in the transverse direction. The superinsulating aerogel presents both an infrared stealthy capability and a high solar reflectance of 93.8% over the whole sunlight wavelength, far outperforming commercial expanded polystyrene foams with reflective coatings. The anisotropic BNNS/PVA composite aerogel presents great potential for application in energy-saving buildings.

The effects of carbon nanotubes (CNTs) on the mechanical and fracture properties of ramie fiber-reinforced epoxy composites were investigated. Three-point bending, short beam shear, single-edge-notch bending, and Charpy impact tests were employed to evaluate the properties of ramie fiber-reinforced composites without and with CNTs modification. The fracture mechanisms were revealed with the aid of the dynamic mechanical analysis, Fourier transform infrared, and X-ray photoelectron spectroscopy. It was found that the mechanical and fracture properties of ramie fiber-reinforced composites were enhanced by incorporating multiwalled carbon nanotubes, except the impact fracture toughness. The unique chemical compositions and the multiscaled nanosized microstructures of natural fibers brought into focus new mechanisms for the improvement of the mechanical properties of natural fiber-reinforced composites.

Electrically conductive porous structures are ideal candidates for lightweight and absorption-dominant electromagnetic interference (EMI) shielding. In this review, we summarize the recent progress in developing porous composites and structures from emerging two-dimensional (2D) graphene and MXene nanosheets for EMI shielding applications. Important properties contributing to various energy loss mechanisms are probed with a critical discussion on their correlations with EMI shielding performance. Technological approaches to constructing bulk porous structures, such as 2D porous films, three-dimensional (3D) aerogels and foams, and hydrogels, are compared to highlight important material and processing parameters required to achieve optimal microstructures. A comprehensive comparison of EMI shielding performance is also carried out to elucidate the effects of different assembly techniques and microstructures. Distinctive multifunctional applications in adaptive EMI shielding, mechanical force attenuation, thermal management, and wearable devices are introduced, underlining the importance of unique compositions and microstructures of porous composites. The process-structure-property relationships established in this review would offer valuable guidance and insights into the design of lightweight EMI shielding materials.

Smart windows, capable of tailoring light transmission, can significantly reduce energy consumption in building services. While mechano-responsive windows activated by strains are promising candidates, they face long-lasting challenges in which the space for the light scatterer’s operation has to be enlarged along with the window size, undermining the practicality. Recent attempts to tackle this challenge inevitably generate side effects with compromised performance in light modulation. Here, we introduce a cuttlefish-inspired design to enable the closing and opening of pores within the 3D porous structure by through-thickness compression, offering opacity and transparency upon release and compression. By changing the activation mode from the conventional in-plane to through-thickness direction, the space requirement is intrinsically decoupled from the lateral size of the scatterer. Central to our design is the asymmetry of pore orientation in the 3D porous structure. These inclined pores against the normal direction increase the opaqueness upon release and improve light modulation sensitivity to compression, enabling transmittance regulation upon compression by an infinitesimal displacement of 50 μ m. This work establishes a milestone for smart window technologies and will drive advancements in the development of opto-electric devices. Strain-responsive smart windows represent a green technology for transparency control but demand large space to activate. Here, a new material structure activated by compression is proposed, yielding strong optical regulation with minute deformation

A facile, highly efficient approach to obtain molybdenum trioxide (MoO 3 )-doped tungsten trioxide (WO 3 ) is reported. An annealing process was used to transform ammonium tetrathiotungstate [(NH 4 ) 2 WS 4 ] to WO 3 in the presence of oxygen. Ammonium tetrathiomolybdate [(NH 4 ) 2 MoS 4 ] was used as a dopant to improve the film for use in an electrochromic (EC) cell. (NH 4 ) 2 MoS 4 at different concentrations (10, 20, 30, and 40 mM) was added to the (NH 4 ) 2 WS 4 precursor by sonication and the samples were annealed at 500 °C in air. Raman, X-ray diffraction, and X-ray photoelectron spectroscopy measurements confirmed that the (NH 4 ) 2 WS 4 precursor decomposed to WO 3 and the (NH 4 ) 2 MoS 4 –(NH 4 ) 2 WS 4 precursor was transformed to MoO 3 -doped WO 3 after annealing at 500 °C. It is shown that the MoO 3 -doped WO 3 film is more uniform and porous than pure WO 3 , confirming the doping quality and the privileges of the proposed method. The optimal MoO 3 -doped WO 3 used as an EC layer exhibited a high coloration efficiency of 128.1 cm 2 /C, which is larger than that of pure WO 3 (74.5 cm 2 /C). Therefore, MoO 3 -doped WO 3 synthesized by the reported method is a promising candidate for high-efficiency and low-cost smart windows.

Structure pulverization and poor electrical conductivity of metal dichalcogenides result in serious capacity decay both in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). To resolve the above problems, a combination of metal dichalcogenides with conductive scaffolds as high-performance electrode materials has aroused tremendous interest recently. Herein, we synthesize a 3D honeycomb-like rGO anchored with SnS 2 quantum dots (3D SnS 2 QDs/rGO) composite via spray-drying and sulfidation. The unique 3D-ordered honeycomb-like structure can confine the volume change of SnS 2 QDs in the lithiation/delithiation and sodiation/desodiation processes, provide enough space for electrolyte reservoirs, promote the conductivity of the SnS 2 QDs, and improve the electron transfer. As a result, the 3D SnS 2 QDs/rGO composite electrode delivers a high capacity and long cycling stability (862 mAh/g for LIB at 0.1 A/g after 200 cycles, 233 mAh/g for SIB at 0.5 A/g after 200 cycles). This study provides a feasible synthesis route for preparing 3D-ordered porous networks in varied materials for the development of high-performance LIBs and SIBs in future.

Infrared (IR) light photodetection based on two dimensional (2D) materials of proper bandgap has attracted increasing attention. However, the weak IR absorption in 2D materials, due to their ultrathin attribute and indirect bandgap in multilayer structures, degrades their performance when used as IR photodetectors. In this work, we utilize the fact that few-layer MoTe 2 flake has a near-IR (NIR) bandgap and demonstrate a ~ 60-fold enhancement of NIR response by introducing a gold hollow nanorods on the surface. Such gold hollow nanorods have distinct absorption peak located also at the NIR regime, therefore induces strong resonance, benefitting NIR absorption in MoTe 2 , resulting in strong near-field enhancement. With the evidence from steady and transient state optical spectra, we confirm that the enhancement of NIR response originates only photon absorption, rather than electron transport at interfaces as observed in other heterostructures, therefore, precluding the requirement of high-quality interfaces for commercial applications.