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The transition to sustainable materials and eco-efficient processes in commercial electronics is a driving force in developing green electronics. Iron-catalyzed laser-induced graphitization (IC-LIG) has been demonstrated as a promising approach for rendering biomaterials electrically conductive. To optimize the IC-LIG process and fully exploit its potential for future green electronics, it is crucial to gain deeper insights into its catalyzation mechanism and structural evolution. However, this is challenging due to the rapid nature of the laser-induced graphitization process. Therefore, multiscale preparation techniques, including ultramicrotomy of the cross-sectional transition zone from precursor to fully graphitized IC-LIG electrode, are employed to virtually freeze the IC-LIG process in time. Complementary characterization is performed to generate a 3D model that integrates nanoscale findings within a mesoscopic framework. This enabled tracing the growth and migration behavior of catalytic iron nanoparticles and their role during the catalytic laser-graphitization process. A three-layered arrangement of the IC-LIG electrode is identified including a highly graphitized top layer with an interplanar spacing of 0.343 nm. The middle layer contained γ-iron nanoparticles encapsulated in graphitic shells. A comparison with catalyst-free laser graphitization approaches highlights the unique opportunities that IC-LIG offers and discuss potential applications in energy storage devices, catalysts, sensors, and beyond., (© 2024 Wiley‐VCH GmbH.)

Wood materials incorporating new properties are of great interest, especially for advanced applications such as sustainable optics and photonics. In this work we describe a wood functionalization approach, comprising the incorporation of artificial chemiluminescent systems (phenyl oxalate ester‑hydrogen peroxide-fluorophore, and luminol-ferricyanide), resulting in light-emitting wood. By a detailed characterisation of the light emission features we point out the complex interaction between wood scaffold and chemiluminescent systems, especially the quenching effect of wood extractives (for the TCPO-H 2 O 2 -fluorophore system) and lignin (for the luminol-ferricyanide system). Moreover, we take advantage of the intrinsic anisotropic porosity and capillarity of wood tissue to study the chemiluminescent front propagation. Our results may inspire the development of novel light-emitting wood materials for a variety of applications, from fundamental studies of water uptake in wood to sensors and even design elements., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Coupling nonlinear reaction networks with soft matter building blocks holds great potential for the design of life-mimicking, time-programmable dissipative self-assembly systems. In this regard, clock reactions are especially useful triggers since they allow to autonomously generate in situ chemical stimuli such as pH changes. The methylene glycol-sulfite (MGS) is a well-known acid-to-base pH-clock reaction which is able to produce sharp and intense pH jumps (up to 5 pH units) after a reliable, yet relatively short (tens of seconds rather than minutes), induction time. Here, after an introductory discussion on the main chemical aspects of MGS and MGS-based systems, their applications for the time-programming of soft matter will be showcased - from micelles, vesicles, and droplets to supramolecular aggregates, polymers and gels. Hopefully, this will help attracting more attention and foster research on the broader field of materials programming with chemical reaction networks.

The addition of silver(i) ions to the methylene glycol-sulphite (MGS) clock reaction results in the sudden formation of metallic silver nanoparticles. Stable suspensions are obtained in the presence of poly(vinylpyrrolidone). The time delay before the appearance of the particles, as well as their size, decreases with the initial methylene glycol concentration while their monodispersity increases., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Wood is a renewable resource with excellent qualities and the potential to become a key element of a future bioeconomy. The increasing environmental awareness and drive to achieve sustainability is leading to a resurgence of research on wood materials. Nevertheless, the global climate changes and associated consequences will soon challenge the wood-value chains in several regions (e.g., central Europe). To cope with these challenges, it is necessary to rethink the current practice of wood sourcing and transformation. The goal of this review is to address the intrinsic natural diversity of wood, from its origin to its technological consequences for the present and future manufacturing of wood products. So far, industrial processes have been optimized to repress the variability of wood properties, enabling more efficient processing and production of reliable products. However, the need to preserve biodiversity and the impact of climate change on forests call for new wood processing techniques and green chemistry protocols for wood modification as enabling factors necessary for managing a more diverse wood provision in the future. This article discusses the past developments that have resulted in the current wood value chains and provides a perspective about how natural variability could be turned into an asset for making truly sustainable wood products. After briefly introducing the chemical and structural complexity of wood, the methods conventionally adopted for industrial homogenization and modification of wood are discussed in relation to their evolution toward increased sustainability. Finally, a perspective is given on technological potentials of machine learning techniques and of novel functional wood materials. Here the main message is that through a combination of sustainable forestry, adherence to green chemistry principles and adapted processes based on machine learning, the wood industry could not only overcome current challenges but also thrive in the near future despite the awaiting challenges.

The building sector, including building operations and materials, was responsible for the emission of ∼11.9 gigatons of global energy-related CO 2 in 2020, accounting for 37% of the total CO 2 emissions, the largest share among different sectors. Lowering the carbon footprint of buildings requires the development of carbon-storage materials as well as novel designs that could enable multifunctional components to achieve widespread applications. Wood is one of the most abundant biomaterials on Earth and has been used for construction historically. Recent research breakthroughs on advanced engineered wood products epitomize this material's tremendous yet largely untapped potential for addressing global sustainability challenges. In this review, we explore recent developments in chemically modified wood that will produce a new generation of engineered wood products for building applications. Traditionally, engineered wood products have primarily had a structural purpose, but this review broadens the classification to encompass more aspects of building performance. We begin by providing multiscale design principles of wood products from a computational point of view, followed by discussion of the chemical modifications and structural engineering methods used to modify wood in terms of its mechanical, thermal, optical, and energy-related performance. Additionally, we explore life cycle assessment and techno-economic analysis tools for guiding future research toward environmentally friendly and economically feasible directions for engineered wood products. Finally, this review highlights the current challenges and perspectives on future directions in this research field. By leveraging these new wood-based technologies and analysis tools for the fabrication of carbon-storage materials, it is possible to design sustainable and carbon-negative buildings, which could have a significant impact on mitigating climate change.

Buildings are significant end-users of global energy. About 20% of the energy consumption worldwide is used for maintaining a comfortable indoor climate. Therefore, passive systems for indoor temperature and humidity regulation that can respond to environmental changes are very promising to reduce buildings' energy consumption. We developed a process to improve the responsiveness of wood to humidity changes by laser-drilling microscopic holes and incorporating a hygroscopic salt (calcium chloride). The resulting "transpiring wood" displays superior water adsorption capacity and high moisture exchange rate, allowing regulation of humidity and temperature by the exchange of moisture with the surrounding air. We proved that the hygrothermal performance of transpiring wood can be used to regulate indoor climate, with associated energy savings, for various climate types, thus favoring its application in the building sector. The reduction of temperature fluctuations, thanks to the buffering of temperature peaks, can lead to an indirect energy saving of about 10% for cooling and between 4-27% for heating depending on the climate. Furthermore, our transpiring wood meets different sustainability criteria, from raw materials to the fabrication process, resulting in a product with a low overall environmental impact and that is easy to recycle.

We demonstrate the autonomous synthesis of iron (hydr)oxide (green rust, magnetite, and lepidocrocite) nanoparticles by precipitating iron(II) ions using hydroxide ions generated in situ with the methylene glycol-sulfite (MGS) reaction, a pH-clock. We show that the nature of the products can be predetermined by tuning the initial iron(II) concentration.

Ecologically friendly wood electronics will help alleviating the shortcomings of state-of-art cellulose-based "green electronics". Here we introduce iron-catalyzed laser-induced graphitization (IC-LIG) as an innovative approach for engraving large-scale electrically conductive structures on wood with very high quality and efficiency, overcoming the limitations of conventional LIG including high ablation, thermal damages, need for multiple lasing steps, use of fire retardants and inert atmospheres. An aqueous bio-based coating, inspired by historical iron-gall ink, protects wood from laser ablation and thermal damage while promoting efficient graphitization and smoothening substrate irregularities. Large-scale (100 cm 2 ), highly conductive (≥2500 S m -1 ) and homogeneous surface areas are engraved single-step in ambient atmosphere with a conventional CO 2 laser, even on very thin (∼450 µm) wood veneers. We demonstrate the validity of our approach by turning wood into highly durable strain sensors, flexible electrodes, capacitive touch panels and an electroluminescent LIG-based device., (© 2022. The Author(s).)

Smart membranes that can open and/or close their pores in a controlled manner by external stimuli possess potential in various applications, such as water flow manipulation, indoor climate regulation, and sensing. The design of smart gating membranes with high flux, immediate response, and mechanical robustness is still an open challenge, limiting their versatility and practical applicability. Inspired by the controlled opening and closure of plant stomata, we have developed a smart gating wood membrane, taking advantage of the unique wood scaffold with its hierarchical porous structure to carry thermoresponsive hydrogel gates. Laser drilling was applied to cut channels in the wood scaffold with well-aligned pores to incorporate the smart gating membranes. In situ polymerization of poly(N-isopropylacrylamide) above its lower critical solution temperature inside the channels resulted in a hydrogel with a heterogeneous microstructure acting as a thermoresponsive gate. The wood-based smart gating membranes exhibited reversible and stable pore opening/closing under heating/cooling stimuli. The achieved rapid response and feasibility of scale-up open the venue for various practical applications. In this work, we demonstrated their potential for indoor light regulation and as a water flow manipulator., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

The development of controlled processes for continuous hydrogen generation from solid-state storage chemicals such as ammonia borane is central to integrating renewable hydrogen into a clean energy mix. However, to date, most reported platforms operate in batch mode, posing a challenge for controllable hydrogen release, catalyst reusability, and large-scale operation. To address these issues, we developed flow-through wood-based catalytic microreactors, characterized by inherent natural oriented microchannels. The prepared structured catalysts utilize silver-promoted palladium nanoparticles supported on metal-organic framework (MOF)-coated wood microreactors as the active phase. Catalytic tests demonstrate their highly controllable hydrogen production in continuous mode, and by adjusting the ammonia borane flow and wood species, we reach stable productivities of up to 10.4 cm H 2 3 min -1 cm cat -3 . The modular design of the structured catalysts proves readily scalable. Our versatile approach is applicable for other metals and MOF combinations, thus comprising a sustainable and scalable platform for catalytic dehydrogenations and applications in the energy-water nexus.

We describe a preliminary investigation of the dissolution dynamics of zinc oxide nanoparticles in the presence of cyclic esters (δ-gluconolactone and propanesultone) as slow acid generators. The particles dissolution is monitored by means of turbidimetry and correlated with the evolution of pH over time. The results could be of interest for the design of chemically programmable colloidal systems.

Structural colors are produced by wavelength-dependent scattering of light from nanostructures. While living organisms often exploit phase separation to directly assemble structurally colored materials from macromolecules, synthetic structural colors are typically produced in a two-step process involving the sequential synthesis and assembly of building blocks. Phase separation is attractive for its simplicity, but applications are limited due to a lack of robust methods for its control. A central challenge is to arrest phase separation at the desired length scale. Here, we show that solid-state polymerization-induced phase separation can produce stable structures at optical length scales. In this process, a polymeric solid is swollen and softened with a second monomer. During its polymerization, the two polymers become immiscible and phase separate. As free monomer is depleted, the host matrix resolidifies and arrests coarsening. The resulting polymeric composites have a blue or white appearance. We compare these biomimetic nanostructures to those in structurally-colored feather barbs, and demonstrate the flexibility of this approach by producing structural color in filaments and large sheets.

Producing electricity from renewable sources and reducing its consumption by buildings are necessary to meet energy and climate change challenges. Wood is an excellent "green" building material and, owing to its piezoelectric behavior, could enable direct conversion of mechanical energy into electricity. Although this phenomenon has been discovered decades ago, its exploitation as an energy source has been impaired by the ultralow piezoelectric output of native wood. Here, we demonstrate that, by enhancing the elastic compressibility of balsa wood through a facile, green, and sustainable fungal decay pretreatment, the piezoelectric output is increased over 55 times. A single cube (15 mm by 15 mm by 13.2 mm) of decayed wood is able to produce a maximum voltage of 0.87 V and a current of 13.3 nA under 45-kPa stress. This study is a fundamental step to develop next-generation self-powered green building materials for future energy supply and mitigation of climate change., (Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).)

Programming supramolecular assembly in the time domain is a fundamental aspect of the design of biomimetic materials. We achieved the time-controlled sol-gel transition of a poly(vinyl alcohol)-iodine supramolecular complex by generating iodine in situ with a clock reaction. We demonstrate that both the gelation time and the mechanical properties of the resulting hydrogel can be tuned by properly selecting the clock parameters or through competitive iodine complexation.

Developing low-cost and biodegradable piezoelectric nanogenerators is of great importance for a variety of applications, from harvesting low-grade mechanical energy to wearable sensors. Many of the most widely used piezoelectric materials, including lead zirconate titanate (PZT), suffer from serious drawbacks such as complicated synthesis, poor mechanical properties (e.g., brittleness), and toxic composition, limiting their development for biomedical applications and posing environmental problems for their disposal. Here, we report a low-cost, biodegradable, biocompatible, and highly compressible piezoelectric nanogenerator based on a wood sponge obtained with a simple delignification process. Thanks to the enhanced compressibility of the wood sponge, our wood nanogenerator (15 × 15 × 14 mm 3 , longitudinal × radial × tangential) can generate an output voltage of up to 0.69 V, 85 times higher than that generated by native (untreated) wood, and it shows stable performance under repeated cyclic compression (≥600 cycles). Our approach suggests the importance of increased compressibility of bulk materials for improving their piezoelectric output. We demonstrate the versatility of our nanogenerator by showing its application both as a wearable movement monitoring system (made with a single wood sponge) and as a large-scale prototype with increased output (made with 30 wood sponges) able to power simple electronic devices (a LED light, a LCD screen). Moreover, we demonstrate the biodegradability of our wood sponge piezoelectric nanogenerator by studying its decomposition with cellulose-degrading fungi. Our results showcase the potential application of a wood sponge as a sustainable energy source, as a wearable device for monitoring human motions, and its contribution to environmental sustainability by electronic waste reduction.

Chemo-mechanical phenomena, including oscillations and peristaltic motions, are widespread in nature-just think of heartbeats-thanks to the ability of living organisms to convert directly chemical energy into mechanical work. Their imitation with artificial systems is still an open challenge. Chemical clocks and oscillators (such as the popular Belousov-Zhabotinsky (BZ) reaction) are reaction networks characterized by the emergence of peculiar spatiotemporal dynamics. Their application to polymers at interfaces (grafted chains, layer-by-layer assemblies, and polymer brushes) offers great opportunities for developing novel smart biomimetic materials. Despite the wide field of potential applications, limited research has been carried out so far. Here, we aim to showcase the state-of-the-art of this fascinating field of investigation, highlighting the potential for future developments and providing a personal outlook.