Passive radiative cooling is emerging as a sustainable strategy to reduce energy consumption by emitting heat directly through Earth’s atmospheric transparency window. Here, we demonstrate transparent wood-based biocomposite coatings as an eco-friendly solution for passive radiative cooling under direct sunlight. We fabricated freestanding, micron-thick coatings using wood scaffolds functionalized with ZnO nanoparticles, followed by thiol–ene in situ polymerization to improve transparency and mechanical resilience. These coatings exhibit high visible transparency combined with exceptionally strong mid-infrared emissivity (∼0.95). When applied onto silicon substrates exposed to direct sunlight, ZnO-functionalized coatings effectively lowered the substrate temperature by ∼6–7 °C. This was primarily attributed to enhanced thermal radiation, highlighting their potential for mitigating overheating in solar cells and other sunlight-exposed structures. Additionally, the enhanced mechanical properties of these biocomposites provide versatility for structural and optical applications, positioning them as a cost-effective, bio-based alternative to traditional cooling technologies.

Metallic wood combines the unique structural benefits of wood and the properties of metals and is thus promising for applications ranging from heat transfer to electromagnetic shielding to energy conversion. However, achieving metallic wood with full use of wood structural benefits such as anisotropy and multiscale porosity is challenging. A key reason is the limited mass transfer in bulk wood where fibers have closed ends. In this work, programmed removal of cell-wall components (delignification and hemicellulose extraction) was introduced to improve the accessibility of cell walls and mass diffusion in wood. Subsequent low-temperature electroless Cu plating resulted in a uniform continuous Cu coating on the cell wall, and, furthermore, Cu nanoparticles (NPs) insertion into the wood cell wall. A novel Cu NPs-embedded multilayered cell-wall structure was created. The unique structure benefits compressible metal-composite foam, appealing for stress sensors, where the multilayered cell wall contributes to the compressibility and stability. The technology developed for wood metallization here could be transferred to other functionalizations aimed at reaching fine structure in bulk wood.

Converting omnipresent environmental energy through the assistance of spontaneous water evaporation is an emerging technology for sustainable energy systems. Developing bio-based hydrovoltaic materials further pushes the sustainability, where wood is a prospect due to its native hydrophilic and anisotropic structure. However, current wood-based water evaporation-assisted power generators are facing the challenge of low power density. Here, an efficient hydrovoltaic wood power generator is reported based on wood cell wall nanoengineering. A highly porous wood with cellulosic network filling the lumen is fabricated through a green, one-step treatment using sodium hydroxide to maximize the wood surface area, introduce chemical functionality, and enhance the cell wall permeability of water. An open-circuit potential of ≈140 mV in deionized water is realized, over ten times higher than native wood. Further tuning the pH difference between wood and water, due to an ion concentration gradient, a potential up to 1 V and a remarkable power output of 1.35 µW cm−2 is achieved. The findings in this study provide a new strategy for efficient wood power generators.

Hydrovoltaic energy harvesting offers the potential to utilize enormous water energy for sustainable energy systems. Here, we report the utilization and tailoring of an intrinsic anisotropic 3D continuous microchannel structure from native wood for efficient hydrovoltaic energy harvesting by Fe3O4 nanoparticle insertion. Acetone-assisted precursor infiltration ensures the homogenous distribution of Fe ions for gradience-free Fe3O4 nanoparticle formation in wood. The Fe3O4/wood nanocomposites result in an open-circuit voltage of 63 mV and a power density of ∼52 μW/m2 (∼165 times higher than the original wood) under ambient conditions. The output voltage and power density are further increased to 1 V and ∼743 μW/m2 under 3 suns solar irradiation. The enhancement could be attributed to the increase of surface charge, nanoporosity, and photothermal effect from Fe3O4. The device exhibits a stable voltage of ∼1 V for 30 h (3 cycles of 10 h) showing good long-term stability. The methodology offers the potential for hierarchical organic-inorganic nanocomposite design for scalable and efficient ambient energy harvesting.

Owing to the hierarchical structure, easy multi-functionalization and favorable mechanical properties, wood could harvest electricity from mechanical energy through piezoelectric behavior. In this work, a scalable method to synthesize wood/ZnO composite with multilayered ZnO morphologies is reported for efficient mechanical energy conversion. The synthesis includes charged wood template fabrication, precursor infiltration, and ZnO hydrothermal growth, resulting in controlled ZnO morphologies and distributions while maintaining the hierarchical structure of the wood. Stereo-digital image correlation (stereo-DIC) investigated the relationship between deformation and piezoelectric performance, which revealed the homogeneous distribution of multilayered ZnO enhance piezoelectric performance. The output voltage of wood/ZnO was 1.5 V under periodic mechanical compression (8–10 N) for 300 cycles, while the output current was 2.91 nA. The scalable synthesis strategy and piezoelectric performance are significant for the design of advanced wood nanocomposites for sustainable and efficient energy conversion systems.

A multifunctional soft material with high ionic and electrical conductivity, combined with high mechanical properties and the ability to change shape can enable bioinspired responsive devices and systems. The incorporation of all these characteristics in a single material is very challenging, as the improvement of one property tends to reduce other properties. Here, a nanocomposite film based on charged, high-aspect-ratio 1D flexible nanocellulose fibrils, and 2D Ti3C2Tx MXene is presented. The self-assembly process results in a stratified structure with the nanoparticles aligned in-plane, providing high ionotronic conductivity and mechanical strength, as well as large water uptake. In hydrogel form with 20 wt% liquid, the electrical conductivity is over 200 S cm−1 and the in-plane tensile strength is close to 100 MPa. This multifunctional performance results from the uniquely layered composite structure at nano- and mesoscales. A new type of electrical soft actuator is assembled where voltage as low as ±1 V resulted in osmotic effects and giant reversible out-of-plane swelling, reaching 85% strain.

Functional metal oxide particles are often added to the polymers to prepare flexible functional polymer com-posites with adequate mechanical properties. ZnO and cellulose nanofibrils (CNF) outstand among these metal oxides and the polymer matrices respectively due to their various advantages. Herein, we in situ prepare ZnO microrods in the presence of CNF, which resultes in a layered composite structure. The ZnO microrods are sandwiched between the CNF layers and strongly bind to highly charged CNF, which provides a better stress transfer during mechanical activity. Digital image correction (DIC) and finite element analysis-based computa-tional homogenization methods are used to investigate the relationship between mechanical properties and composite structure, and the stress transfer to the ZnO microrods. Full-field strain measurements in DIC reveal that the in situ ZnO microrods preparation leads to their homogenous distribution in the CNF matrix unlike other methods, which require external means such as ultrasonication. The computational homogenization technique provides a fairly good insight into the stress transfer between constituents in microstructure as well as a good prediction of macroscopic mechanical properties, which otherwise, would be challenging to be assessed by any ordinary mechanical testing in the layered composites. Finally, we also demonstrate that these composites could be used as physiological motion sensors for human health monitoring.

Cellulose nanofibril (CNF) materials are candidates for the sustainable development of high mechanical performance nanomaterials. Due to inherent hydrophilicity and limited functionality range, most applications require chemical modification of CNF. However, targeted transformations directly on CNF are cumbersome due to the propensity of CNF to aggregate in non-aqueous solvents at high concentrations, complicating the choice of suitable reagents and requiring tedious separations of the final product. This work addresses this challenge by developing a general, entirely water-based, and experimentally simple methodology for functionalizing CNF, providing aliphatic, allylic, propargylic, azobenzylic, and substituted benzylic functional groups. The first step is NaIO4 oxidation to dialdehyde-CNF in the wet cake state, followed by oxime ligation with O-substituted hydroxylamines. The increased hydrolytic stability of oximes removes the need for reductive stabilization as often required for the analogous imines where aldehyde groups react with amines in water. Overall, the process provides a tailored degree of nanofibril functionalization (2-4.5 mmol/g) with the possible reversible detachment of the functionality under mildly acidic conditions, resulting in the reformation of dialdehyde CNF. The modified CNF materials were assessed for potential applications in green electronics and triboelectric nanogenerators. Water is a standing challenge in the chemical modification of cellulose nanofibrils. Here, authors employ oxime-ligation to solve this by direct covalent chemistry on dialdehyde-CNF in water and assess the material for potential applications in green electronics and triboelectric nanogenerators.

Sustainable energy technologies require the development of sustainable composites using novel methods and materials with a minimal environmental impact. Piezoelectric effect-based mechanical energy harvesting (MEH) and sensing offer great potential as a sustainable technology for low-grade mechanical energy harvesters and self-powered sensors. Herein, we utilize ZnO to functionalize the delignified wood surface for MEH and vibration sensing applications, where wood act as robust support to well adhered piezoelectric ZnO nanoparticles. This surface functionalization strategy is a reasonable substitute for the bulk ZnO films, which offer optimal utilization of active material at relatively low content. The wood/ZnO composite device is utilized for vibration sensing and MEH. The device (25 cm2) resulted in a peak to peak output voltage of ~15 mV and a peak to peak current of ~2.2 nA under the influence of mechanical vibrations from the periodic motion of a linear motor operating at the acceleration of 50 ms-2. The scalable fabrication approach signifies the practical use of wood-based composites for piezoelectric mechanical energy harvesting.

Functional wood materials often rely on active additives due to the weak piezoelectric response of wood itself. Here, we chemically modify wood to form functionalized, eco-friendly wood veneer for self-powered vibration sensors. Only the piezoelectricity of the cellulose microfibrils is used, where the drastic improvement comes only from molecular and nanoscale wood structure tuning. Sequential wood modifications (delignification, oxidation, and model fluorination) are performed, and effects on vibration sensing abilities are investigated. Wood veneer piezoelectricity is characterized by the piezoresponse force microscopy mode in atomic force microscopy. Delignification, oxidation, and model fluorination of wood-based sensors provide output voltages of 11.4, 23.2, and 60 mV by facilitating cellulose microfibril deformation. The vibration sensing ability correlates with improved piezoelectricity and increased cellulose deformation, most likely by large, local cell wall bending. This shows that nanostructural wood materials design can tailor the functional properties of wood devices with potential in sustainable nanotechnology.