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With the rapid development of soft electronics, flexible and stretchable strain sensors are highly desirable. However, coupling of high sensitivity and stretchability in a single strain sensor remains a challenge. Herein, a kind of conductive elastomer is constructed with poly(dimethylsiloxane) (PDMS) and silylated cellulose nanocrystal (SCNC)/carbon nanotube (CNT) nanohybrids through a facile one-pot solution-casting method. The hydrophobic SCNCs can effectively facilitate the dispersion of CNTs in PDMS and synergistically improve the interfacial compatibility between CNTs and the PDMS matrix, resulting in favorable stress and electron transfer in the polymer network. Due to the outstanding electrical conductivity of CNTs and the excellent dispersity and high mechanical performance of SCNCs, combined with the good compatibility between SCNC-mediated carbon nanotubes (SCNC-CNTs) and PDMS, the resulting composite elastomer (SCNC-CNT/PDMS) shows high electrical conductivity (∼2.77 S m–1), tensile strength (∼5.72 MPa), and fatigue resistance properties. The strain sensor assembled by SCNC-CNT/PDMS demonstrates a high strain range above 100%, appealing strain sensitivity with a gauge factor of 37.11 at 50–100% strain, and long-term stability and durability, which is capable of monitoring both real-time human motions and acoustic vibrations. This work paves a new way for the design and controllable preparation of flexible and stretchable conductive elastomers, demonstrating promising applications in wearable devices and intelligent electronics.

Most materials used for optical lighting applications need to produce a uniform illumination and require high mechanical and hydrophobic properties. However, they are rarely eco-friendly. Herein, a bio-based, polymer matrix-free, luminescent, and hydrophobic film with excellent mechanical properties for optical lighting purposes is demonstrated. A template is prepared by turning a wood veneer into porous scaffold from which most of the lignin and half of the hemicelluloses are removed. The infiltration of quantum dots (CdSe/ZnS) into the porous template prior to densification resulted in almost uniform luminescence (isotropic light scattering) and could be extended to various quantum dot particles, generating different light colors. In a subsequent step, the luminescent wood film is coated with hexadecyltrimethoxysilane (HDTMS) viachemical vapor deposition. The presence of the quantum dots coupled with the HDTMS coating renders the film hydrophobic (water contact angle ≈ 140°). This top-down process strongly eliminates lumen cavities and preserves the orientation of the original cellulose fibrils to create luminescent and polymer matrix-free films with high modulus and strength in the direction of fibers. The proposed optical lighting material could be attractive for interior designs (e.g., lamps and laminated cover panels), photonics, and laser devices.

Next-generation electronics (e.g., substrate and conductor) need to be high performance, multifunctional, and environmentally friendly. Here, we report the creation of a fully wood-based flexible electronics circuit meeting these requirements, where the substrate, a strong, flexible and transparent wood film, is printed with a lignin-derived carbon nanofibers conductive ink. The wood film fabrication involves extensive removal of lignin and hemicellulose to tailor the nanostructure of the material followed by collapsing of the cell walls. This process preserves the original alignment of the cellulose nanofibers and promotes their binding. The film is flexible, yet strong in fiber direction with a Young’s modulus and a tensile strength of 49.9 GPa and 469.9 MPa, respectively. Furthermore, a sustainable and bio-based conductive ink is formulated with lignin-derived carbon nanofibers. The bio-based ink is printed on transparent wood film, and a strain sensor application of the printed circuit is demonstrated. Combining the transparent wood film with the conductive ink produces environmental friendly and sustainable wood-based electronics for potential applications such as flexible circuits and sensors. Moreover, we envision the potential for a scalable and continuous fabrication process as well as end-of-life recyclability.

Pure organic ultralong room temperature phosphorescent (URTP) materials have garnered significant attention for applications in luminescent materials, biosensing, and information encryption. These materials offer advantages over heavy metal phosphorescent materials, such as lower cost, reduced biological toxicity, and minimal environmental impact. Herein, for the first time, we demonstrate a series of organic RTP materials based on spiro[fluorene-9,9′-xanthene] (SFX) hole-transporting molecules, specifically X59and X55. Our research presents that incorporating more rigid SFX units significantly extends RTP lifetime and enhances photoluminescence quantum yield (PLQY). The large steric hindrance of the rigid SFX structures suppresses nonradiative molecular motions, thereby prolonging phosphorescence emission. Compared to the baseline molecule X1, experimental results show that molecule X59extends the phosphorescence lifetime by 230 ms, while X55achieves an extension of 260 ms. Furthermore, we highlight the potential of this series of RTP molecules for use in transparent, programmable luminescent tags. Our work not only expands the molecular types of organic RTP materials but also provides innovative strategies for designing long-lived, high-quantum-yield RTP molecules. We envision that this will advance the smart device field of organic phosphorescent materials and their practical applications, such as intelligent labels, tags, and optical sensors.

Tremendous efforts have been dedicated to developing effective and eco-friendly approaches for separation of oil–water mixtures. Challenges remain in terms of complex processing, high material cost, low efficiency, and scale-up problems. Inspired by the tubular porosity and hierarchical organization of wood, a strong, mesoporous, and hydrophobic three-dimensional wood structure is created for selective oil/water separation. A delignified wood template with hydrophilic characteristics is obtained by removal of lignin. The delignified wood template is further functionalized by a reactive epoxy–amine system. This wood/epoxy biocomposite reveals hydrophobic/oleophilic functionality and shows oil absorption as high as 15 g/g. The wood/epoxy biocomposite has a compression yield strength and modulus up to 18 and 263 MPa, respectively, at a solid volume fraction of only 12%. This is more than 20 times that of cellulose-based foams/aerogels reconstructed from cellulose nanofibrils. The favorable performance is ascribed to the natural hierarchical honeycomb structure of wood. Oil can be selectively absorbed not only from below but also from above the water surface. High oil/water absorption capacity of both types of wood structures (delignified template and polymer-modified biocomposite) allows for applications in oil/water separation.

Eco-friendly materials need “green” fire-retardancy treatments, which offer opportunity for new wood nanotechnologies. Balsa wood (Ochroma pyramidale) was delignified to form a hierarchically structured and nanoporous scaffold mainly composed of cellulose nanofibrils. This nanocellulosic wood scaffold was impregnated with colloidal montmorillonite clay to form a nanostructured wood hybrid with high flame-retardancy. The nanoporous scaffold was characterized by scanning electron microscopy and gas adsorption. Flame-retardancy was evaluated by cone calorimetry, whereas thermal and thermo-oxidative stabilities were assessed by thermogravimetry. The location of well-distributed clay nanoplatelets inside the cell walls was confirmed by energy-dispersive X-ray analysis. This unique nanostructure dramatically increased the thermal stability because of thermal insulation, oxygen depletion, and catalytic charring effects. A coherent organic/inorganic charred residue was formed during combustion, leading to a strongly reduced heat release rate peak and reduced smoke generation.

•Emerging technologies for the development of wood products toward extended carbon storage and capture are overviewed.•The developing technologies of engineered wood products are summarized with the objective of extending wood carbon storage.•Wood nanotechnologies are highlighted for manufacturing high-performance products as potential alternatives of fossil-based plastics.