Synthetic structural materials with exceptional mechanical performance suffer from either large weight and adverse environmental impact (for example, steels and alloys) or complex manufacturing processes and thus high cost (for example, polymer-based and biomimetic composites). Natural wood is a low-cost and abundant material and has been used for millennia as a structural material for building and furniture construction. However, the mechanical performance of natural wood (its strength and toughness) is unsatisfactory for many advanced engineering structures and applications. Pre-treatment with steam, heat, ammonia or cold rolling followed by densification has led to the enhanced mechanical performance of natural wood. However, the existing methods result in incomplete densification and lack dimensional stability, particularly in response to humid environments, and wood treated in these ways can expand and weaken. Here we report a simple and effective strategy to transform bulk natural wood directly into a high-performance structural material with a more than tenfold increase in strength, toughness and ballistic resistance and with greater dimensional stability. Our two-step process involves the partial removal of lignin and hemicellulose from the natural wood via a boiling process in an aqueous mixture of NaOH and NaSO followed by hot-pressing, leading to the total collapse of cell walls and the complete densification of the natural wood with highly aligned cellulose nanofibres. This strategy is shown to be universally effective for various species of wood. Our processed wood has a specific strength higher than that of most structural metals and alloys, making it a low-cost, high-performance, lightweight alternative.

Sodium-ion batteries are emerging as a highly promising technology for large-scale energy storage applications. However, it remains a significant challenge to develop an anode with superior long-term cycling stability and high-rate capability. Here we demonstrate that the Na þ intercalation pseudocapacitance in TiO 2 /graphene nanocomposites enables high-rate capability and long cycle life in a sodium-ion battery. This hybrid electrode exhibits a specific capacity of above 90 mA h g -1 at 12,000 mA g -1 (B36 C). The capacity is highly reversible for more than 4,000 cycles, the longest demonstrated cyclability to date. First-principle calculations demonstrate that the intimate integration of graphene with TiO 2 reduces the diffusion energy barrier, thus enhancing the Na þ intercalation pseudocapacitive process. The Na-ion intercalation pseudocapacitance enabled by tailor-deigned nanostructures represents a promising strategy for developing electrode materials with high power density and long cycle life.

Reducing human reliance on energy-inefficient cooling methods such as air conditioning would have a large impact on the global energy landscape. By a process of complete delignification and densification of wood, we developed a structural material with a mechanical strength of 404.3 megapascals, more than eight times that of natural wood. The cellulose nanofibers in our engineered material backscatter solar radiation and emit strongly in mid-infrared wavelengths, resulting in continuous subambient cooling during both day and night. We model the potential impact of our cooling wood and find energy savings between 20 and 60%, which is most pronounced in hot and dry climates.

Solar evaporation is an ancient technology that has regained tremendous attention because of the abundance of solar energy, widely available water sources, and facile facilities in combination with substantial improvements of conversion efficiency enabled by improved photothermal materials, thermal management, and interfacial heating system designs in recent years. In this review, we discuss recent developments in photothermal materials, with a focus on their photothermal conversion mechanisms as light absorbers. We also explore the diverse structural design and engineering strategies that are being used to improve evaporation performance, including the design principles for high-efficiency light-to-heat conversion, optimization of thermal management, water transport, interface wettability, and anti-saltblocking structures. We describe the potential applications of this attractive technology in a variety of energy and environmental fields. The current challenges and future research opportunities are also discussed, providing a roadmap for the future development of solar evaporation technology.

Emerging solar desalination by interfacial evaporation shows great potential in response to global water scarcity because of its high solar‐to‐vapor efficiency, low environmental impact, and off‐grid capability. However, solute accumulation at the heating interface has severely impacted the performance and long‐term stability of current solar evaporation systems. Here, a self‐regenerating solar evaporator featuring excellent antifouling properties using a rationally designed artificial channel‐array in a natural wood substrate is reported. Upon solar evaporation, salt concentration gradients are formed between the millimeter‐sized drilled channels (with a low salt concentration) and the microsized natural wood channels (with a high salt concentration) due to their different hydraulic conductivities. The concentration gradients allow spontaneous interchannel salt exchange through the 1–2 µm pits, leading to the dilution of salt in the microsized wood channels. The drilled channels with high hydraulic conductivities thus function as salt‐rejection pathways, which can rapidly exchange the salt with the bulk solution, enabling the real‐time self‐regeneration of the evaporator. Compared to other salt‐rejection designs, the solar evaporator exhibits the highest efficiency (≈75%) in a highly concentrated salt solution (20 wt% NaCl) under 1 sun irradiation, as well as long‐term stability (over 100 h of continuous operation).