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Self-charging power systems (SCPSs) are envisioned as promising solutions for emerging electronics to mitigate the increasing global concern about battery waste. However, present SCPSs suffer from large form factors, unscalable fabrication, and material complexity. Herein, a type of highly stable, eco-friendly conductive inks based on poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) are developed for direct ink writing of multiple components in the SCPSs, including electrodes for miniaturized spacer-free triboelectric nanogenerators (TENGs) and microsupercapacitors (MSCs), and interconnects. The principle of “one ink, multiple functions” enables to almost fully print the entire SCPSs on the same paper substrate in a monolithic manner without post-integration. The monolithic fabrication significantly improves the upscaling capability for manufacturing and reduces the form factor of the entire SCPSs (a small footprint area of ≈2 cm × 3 cm and thickness of ≈1 mm). After pressing/releasing the TENGs for ≈79000 cycles, the 3-cell series-connected MSC array can be charged to 1.6 V while the 6-cell array to 3.0 V. On-paper SCPSs are promising to serve as lightweight, thin, sustainable, and low-cost power supplies., QC 20240514

Cellulose nanofibrils (CNF) with 2D silicate nanoplatelet reinforcement readily form multifunctional composites by vacuum-assisted self-assembly from hydrocolloidal mixtures. The final nanostructure is formed during drying. The crystalline nature of CNF and montmorillonite (MTM) made it possible to use synchrotron X-ray scattering (WAXS, SAXS) to monitor structural development during drying from water and from ethanol. Nanostructural changes in the CNF and MTM crystals were investigated. Changes in the out-of-plane orientation of CNF and MTM were determined. Residual drying strains previously predicted from theory were confirmed in both cellulose and MTM platelets due to capillary forces. The formation of tactoid platelet stacks could be followed. We propose that after filtration, the constituent nanoparticles in the swollen, solid gel already have a “fixed” location, although self-assembly and ordering processes take place during drying., QC 20231115

The nature of mass transport in plants has recently inspired the development of low-cost and sustainable wood-based electronics. Herein, we report a wood electrochemical transistor (WECT) where all three electrodes are fully made of conductive wood (CW). The CW is prepared using a two-step strategy of wood delignification followed by wood amalgamation with a mixed electron-ion conducting polymer, poly(3,4-ethylenedioxythiophene)–polystyrene sulfonate (PEDOT:PSS). The modified wood has an electrical conductivity of up to 69 Sm−1 induced by the formation of PEDOT:PSS microstructures inside the wood 3D scaffold. CW is then used to fabricate the WECT, which is capable of modulating an electrical current in a porous and thick transistor channel (1 mm) with an on/off ratio of 50. The device shows a good response to gate voltage modulation and exhibits dynamic switching properties similar to those of an organic electrochemical transistor. This wood-based device and the proposed working principle demonstrate the possibility to incorporate active electronic functionality into the wood, suggesting different types of bio-based electronic devices., QC 20230713

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., QC 20240624

Wood is a high-strength lightweight material owing to its orthotropic cellular structure and composite-like constitution. In conventional fabrication of wood-derived functional materials, the removal of the potentially beneficial components, such as lignin and hemicellulose, often leads to the disruption of the native hierarchical wood structure. Herein, we developed a facile method of in situ wood sulfonation followed by hot pressing for pine veneers to prepare high-density transparent thin films with preserved wood components and the natural fiber alignment. An optimum lignin content of the hot-pressed films was found to be 20.6% where both mechanical and optical properties were significantly enhanced with a more dense and compact structure. The hot-pressed transparent wood films also showed UV-blocking capability and could be recycled into discrete wood fibers owing to the sulfonate groups endowed by the in situ sulfonation step. The unique combination of properties achieved for thin wood films marks an important step in engineering functional wood-based materials that utilize both the structure of aligned fibers and the complex components of natural wood., QC 20230825

The high applicability of Bacterial Cellulose (BC) is often challenging due to its high production costs, which ultimately prevents its widespread use. Therefore, the present study aimed to investigate BC production using alternative feedstock to replace high-cost synthetic carbon and nitrogen sources and to evaluate the physical and structural properties of the produced BC membranes. BC was produced through a microbial consortium from kombucha, and the formulated alternative media sustained promising BC production, especially the association of apple wastes (at 10% (W/V)) with tea mixture, with a yield similar to BC produced on Hestrin–Schramm (HS) control media. Moreover, the BC samples produced in this alternative media also exhibited comparable properties to BC from HS media, with similar water-holding capacity and retention ability, thermal stability, mechanical behavior, and a crystallinity index of 87.61% and 88.08%, respectively. Thus, our findings substantiated that expensive substrates, such as glucose, peptone, and yeast extract, could be successfully replaced by apple wastes, black and green tea, for BC production while maintaining its remarkable physical and structural properties. Furthermore, besides the low-cost advantage, the bioconversion of apple waste also reduces the environmental burden caused by its disposal in landfills., QC 20230711

Nature has evolved elegant ways to alter the wood cell wall structure through carbohydrate-active enzymes, offering environmentally friendly solutions to tailor the microstructure of wood for high-performance materials. In this work, the cell wall structure of delignified wood is modified under mild reaction conditions using an oxidative enzyme, lytic polysaccharide monooxygenase (LPMO). LPMO oxidation results in nanofibrillation of cellulose microfibril bundles inside the wood cell wall, allowing densification of delignified wood under ambient conditions and low pressure into transparent anisotropic films. The enzymatic nanofibrillation facilitates microfibril fusion and enhances the adhesion between the adjacent wood fiber cells during densification process, thereby significantly improving the mechanical performance of the films in both longitudinal and transverse directions. These results improve the understanding of LPMO-induced microstructural changes in wood and offer an environmentally friendly alternative for harsh chemical treatments and energy-intensive densification processes thus representing a significant advance in sustainable production of high-performance wood-derived materials., QC 20230627

The drawbacks of amorphous hard carbon are its low conductivity and structural instability, due to its large volume change and the occurrence of side reactions with the electrolyte during cycling. Here, we propose a simple and rapid method to address these disadvantages; we used an emulsion solvent-evaporation method to create hierarchically structured microparticles of hard carbon nanoparticles, derived from soot, and multi-walled-carbon-nanotubes at a very low threshold of 2.8 wt%. These shrub-ball like microparticles have well-defined void spaces between different nanostructures of carbon, leading to an increased surface area, lower charge-resistance and side reactions, and higher electronic conductivity for Na+ insertion and de-insertion. They can be slurry cast to assemble Na+ anodes, exhibiting an initial discharge capacity of 713.3 mA h g(-1) and showing long-term stability with 120.8 mA h g(-1) at 500 mA g(-1) after 500 cycles, thus outperforming neat hard carbon nanoparticles by an order of magnitude. Our work shows that hierarchical self-assembly is attractive for increasing the performance of microparticles used for battery production., QC 20220502

Wood pulp fibres are promising reinforcements for biocomposites due to their renewable resource origin and mechanical properties. An oriented and dense fibre reinforcement structure is beneficial for biocomposite properties. We present a method of modifying fibres (e.g. to increase strain to failure) in pre-formed oriented high-density paper structures intended for biocomposites or as hot-pressed fibre materials. Mildly delignified, well-preserved holocellulose fibres from softwood are used. Cold alkali treatment (hemicellulose removal) and mercerisation (conversion to cellulose II) were carried out successfully on oriented fibre sheets. Controlled anisotropy and sheet density are achieved from untreated and straight fibres in the sheet formation step. High mechanical properties and increased ductility of mercerised sheets were observed, which may be valuable for hot-pressed fibre materials (E ≈ 7.1 GPa, strength of 108 MPa and strain to failure of 5.3%) and biocomposites. In contrast, modified wood pulp fibres were difficult to orient, resulting in higher sheet porosity and weak interfibre bonding., QC 20230524

2,2,6,6-Tetramethylpiperidin-1-yl oxyl (TEMPO)-oxidized beta-chitin nanofibrils (T-ChNF) are novel nanofibrils of high strength and stiffness and can also enhance the adsorption of chitosan in materials for biomedical applications. This study presents the preparation, structure, and properties of T-ChNF based on squid pens. Our nanofibrils have a zeta potential of -25.3 mV at neutral pH and a carboxylic content of 0.17 mmol/g, making hydrocolloid suspension stable at alkaline and neutral pH. It was demonstrated that positively charged chitosan could be adsorbed on the negatively charged surface of T-ChNF, leading to charge neutralization. The key to strong squid pen T-ChNF is the initial raw squid chitin properties and the high degree of acetylation (DA = 99.9%). The T-ChNF diameter is similar to 4.4 nm, and the length is in the micrometer range. The length and diameter are similar to those of squid pen beta-chitin fibrils prepared under mild conditions. These qualities of fibrils resulted in high-strength (176 MPa) chitin films prepared using the rapid vacuum filtration and drying technique. T-ChNF-based films are ductile, flexible, and transparent., QC 20210601

Inspired by a wood-like multicomponent structure, an interface-reinforced method was developed to fabricate high-performance cellulose nanofibril (CNF)/carbon nanotube (CNT) nanocomposites. Holocellulose nanofibrils (HCNFs) with core-shell structure were first obtained from bagasse via mild delignification and mechanical defibration process. The well-preserved native hemicellulose as the amphiphilic shell of HCNFs could act as a binding agent, sizing agent, and even dispersing agent between HCNFs and CNTs. Remarkably, both the tensile strength at high relative humidity (83% RH) and electrical conductivity of the HCNF/CNT nanocomposites were significantly improved up to 121 MPa and 321 S/m, respectively, demonstrating great superiority compared to normal CNF/CNT composite films. Furthermore, these HCNF/CNT composites with outstanding integrated performances exhibited great potential in the field of flexible liquid sensing., QC 20210111