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Converting various types of ambient mechanical energy into electricity, triboelectric nanogenerator (TENG) has attracted worldwide attention. Despite its ability to reach high open-circuit voltage up to thousands of volts, the power output of TENG is usually meager due to the high output impedance and low charge transfer. Here, leveraging the opposite-charge-enhancement effect and the transistor-like device design, we circumvent these limitations and develop a TENG that is capable of delivering instantaneous power density over 10 MW/m 2 at a low frequency of ~ 1 Hz, far beyond that of the previous reports. With such high-power output, 180 W commercial lamps can be lighted by a TENG device. A vehicle bulb containing LEDs rated 30 W is also wirelessly powered and able to illuminate objects further than 0.9 meters away. Our results not only set a record of the high-power output of TENG but also pave the avenues for using TENG to power the broad practical electrical appliances. TENG suffers from two fundamental limitations: high output impedance and low charge transfer. Herein, these limitations are circumvented by leveraging the opposite-charge-enhancement effect and transistor-like device design, thereby achieving the instantaneous power density over 10 MW/m 2 at the low frequency of ~ 1 Hz.

Two-phase (liquid, vapor) flow in confined spaces is fundamentally interesting and practically important in many practical applications such as thermal management, offering the potential to impart high thermal transport performance owing to high surface-to-volume ratio and latent heat released during liquid/vapor phase transition. However, the associated physical size effect, in coupling with the striking contrast in specific volume between liquid and vapor phases, also leads to the onset of unwanted vapor backflow and chaotic two-phase flow patterns, which seriously deteriorates the practical thermal transport performances. Here, we develop a thermal regulator consisting of classical Tesla valves and engineered capillary structures, which can switch its working states and boost its heat transfer coefficient and critical heat flux in its “switched-on” state. We demonstrate that the Tesla valves and the capillary structures serve to eliminate vapor backflow and promote liquid flow along the sidewalls of both Tesla valves and main channels, respectively, which synergistically enable the thermal regulator to self-adapt to varying working conditions by rectifying the chaotic two-phase flow into an ordered and directional flow. We envision that revisiting century-old design can promote the development of next generation cooling devices towards switchable and very high heat transfer performances for power electronic devices. Unwanted vapor backflow and chaotic two-phase flow patterns can hinder thermal transport performance in their respective systems. Here, the authors revisit the classic Tesla valve design and demonstrate a Tesla valve-based thermal regulator with capillary structures that can suppress vapor backflow and achieve directional two-phase flow.

Solar-driven evaporation offers a sustainable solution for water purification, but efficiency losses due to heat dissipation and fouling limit its scalability. Herein, we present a bilayer-structured solar evaporator ( SDWE ) with dynamic fluidic flow mechanism, designed to ensure a thin water supply and self-cleaning capability. The porous polydopamine ( PDA ) layer on a nickel skeleton provides photothermal functionality and water microchannels, while the thermo-responsive sporopollenin layer on the bottom acts as a switchable water gate. Using confocal laser microscopy and micro-CT, we demonstrate that this unique structure ensures a steady supply of thin water layers, enhancing evaporation by minimizing latent heat at high temperatures. Additionally, the system initiates a self-cleaning process through bulk water convection when temperature drops due to salt accumulation, thus maintaining increased evaporation efficiency. Therefore, the optimized p-SDWE sample achieved a high evaporation rate of 3.58 kg m −2 h −1 using 93.9% solar energy from 1 sun irradiation, and produces 18–22 liters of purified water per square meter of SDWE per day from brine water. This dynamic water transport mechanism surpasses traditional day-night cycles, offering inherent thermal adaptability for continuous, high-efficiency evaporation. Solar-driven evaporation is a sustainable water purification method, but scalability is hindered by heat loss and salt fouling. The authors introduce a bilayer-structured solar evaporator with a dynamic fluid flow mechanism, which enables self-cleaning. This approach offers continuous, high-efficiency evaporation.

Water evaporation is a natural phase change phenomenon occurring any time and everywhere. Enormous efforts have been made to harvest energy from this ubiquitous process by leveraging on the interaction between water and materials with tailored structural, chemical and thermal properties. Here, we develop a multi-layered interfacial evaporation-driven nanogenerator (IENG) that further amplifies the interaction by introducing additional bionic light-trapping structure for efficient light to heat and electric generation on the top and middle of the device. Notable, we also rationally design the bottom layer for sufficient water transport and storage. We demonstrate the IENG performs a spectacular continuous power output as high as 11.8 μW cm −2 under optimal conditions, more than 6.8 times higher than the currently reported average value. We hope this work can provide a new bionic strategy using multiple natural energy sources for effective power generation. The energy harvesting from ubiquitous natural water evaporation offers a great green energy source. Here, the authors report a bioinspired and multi-layered interfacial evaporation-driven nanogeneration strategy for efficient light-to-heat and electricity generation with continuous power output.

Developing untethered millirobots that can adapt to harsh environments with high locomotion efficiency is of interest for emerging applications in various industrial and biomedical settings. Despite recent success in exploiting soft materials to impart sophisticated functions which are not available in conventional rigid robotics, it remains challenging to achieve superior performances in both wet and dry conditions. Inspired by the flexible, soft, and elastic leg/foot structures of many living organisms, here we report an untethered soft millirobot decorated with multiple tapered soft feet architecture. Such robot design yields superior adaptivity to various harsh environments with ultrafast locomotion speed (>40 limb length/s), ultra-strong carrying capacity (>100 own weight), and excellent obstacle-crossing ability (stand up 90° and across obstacle >10 body height). Our work represents an important advance in the emerging area of bio-inspired robotics and will find a wide spectrum of applications. Despite the enormous potential of magnetically-guided soft robots for various applications, challenges related to inefficient locomotion in harsh environments hinder its development. Here, the authors demonstrate a multi-legged millirobot with excellent locomotion capability in harsh environments.

Owing to its 100% theoretical salt rejection capability, membrane distillation (MD) has emerged as a promising seawater desalination approach to address freshwater scarcity. Ideal MD requires high vapor permeate flux established by cross-membrane temperature gradient (∆T) and excellent membrane durability. However, it’s difficult to maintain constant ∆T owing to inherent heat loss at feedwater side resulting from continuous water-to-vapor transition and prevent wetting transition-induced membrane fouling and scaling. Here, we develop a Ti 3 C 2 T x MXene-engineered membrane that imparts efficient localized photothermal effect and strong water-repellency, achieving significant boost in freshwater production rate and stability. In addition to photothermal effect that circumvents heat loss, high electrically conductive Ti 3 C 2 T x MXene also allows for self-assembly of uniform hierarchical polymeric nanospheres on its surface via electrostatic spraying, transforming intrinsic hydrophilicity into superhydrophobicity. This interfacial engineering renders energy-efficient and hypersaline-stable photothermal membrane distillation with a high water production rate under one sun irradiation. Membrane distillation is susceptible to thermal inefficiency and membrane wetting issues during seawater desalination. Here, authors design a MXene-engineered membrane that imparts efficient localized photothermal effect and strong water repellency, achieving sustainable freshwater production.

The Leidenfrost effect, namely the levitation of drops on hot solids 1 , is known to deteriorate heat transfer at high temperature 2 . The Leidenfrost point can be elevated by texturing materials to favour the solid–liquid contact 2 – 10 and by arranging channels at the surface to decouple the wetting phenomena from the vapour dynamics 3 . However, maximizing both the Leidenfrost point and thermal cooling across a wide range of temperatures can be mutually exclusive 3 , 7 , 8 . Here we report a rational design of structured thermal armours that inhibit the Leidenfrost effect up to 1,150 °C, that is, 600 °C more than previously attained, yet preserving heat transfer. Our design consists of steel pillars serving as thermal bridges, an embedded insulating membrane that wicks and spreads the liquid and U-shaped channels for vapour evacuation. The coexistence of materials with contrasting thermal and geometrical properties cooperatively transforms normally uniform temperatures into non-uniform ones, generates lateral wicking at all temperatures and enhances thermal cooling. Structured thermal armours are limited only by their melting point, rather than by a failure in the design. The material can be made flexible, and thus attached to substrates otherwise challenging to structure. Our strategy holds the potential to enable the implementation of efficient water cooling at ultra-high solid temperatures, which is, to date, an uncharted property. Structured thermal armours on the surface of a solid inhibit the Leidenfrost effect, even when heated to temperatures in excess of 1,000 °C, pointing the way towards new cooling strategies for high-temperature solids.

The design of smart surfaces with switchable adhesive properties in a wet environment has remained a challenge in adhesion science and materials engineering. Despite intense demands in various industrial applications and exciting progress in mimicking the remarkable wet adhesion through the delicate control of catechol chemistry, polyelectrolyte complex, and supramolecular architectures, the full recapitulation of nature’s dynamic function is limited. Here, we show a facile approach to synthesize bioinspired adhesive, which entails the reversible, tunable, and fast regulation of the wet adhesion on diverse surfaces. The smart wet adhesive takes advantage of the host–guest molecular interaction and the adhesive nature of catechol chemistry, as well as the responsive polymer, allowing for screening and activation of the interfacial interaction simply by a local temperature trigger in an on-demand manner. Our work opens up an avenue for the rational design of bioinspired adhesives with performances even beyond nature. Many industrial applications require switchable adhesive properties in wet conditions, but this still remains challenging to achieve. Here the authors synthesize an adhesive based on host-guest interactions that exhibits reversible, tunable and fast regulation of the wet adhesion on diverse surfaces.

The directed, long-range and self-propelled transport of droplets on solid surfaces is crucial for many applications from water harvesting to bio-analysis1–9. Typically, preferential transport is achieved by topographic or chemical modulation of surface wetting gradients that break the asymmetric contact line and overcome the resistance force to move droplets along a particular direction10–16. Nonetheless, despite extensive progress, directional droplet transport is limited to low transport velocity or short transport distance. Here we report the high-velocity and ultralong transport of droplets elicited by surface charge density gradients printed on diverse substrates. We leverage the facile water droplet printing on superamphiphobic surfaces to create rewritable surface charge density gradients that stimulate droplet propulsion under ambient conditions17 and without the need for additional energy input. Our strategy provides a platform for programming the transport of droplets on flat, flexible and vertical surfaces that may be valuable for applications requiring a controlled movement of droplets17–19.

Developing versatile, scalable, and durable coatings that resist the accretion of matters (liquid, vapor, and solid phases) in various operating environments is important to industrial applications, yet has proven challenging. Here, we report a cellular coating that imparts liquid-repellence, vapor-imperviousness, and solid-shedding capabilities without the need for complicated structures and fabrication processes. The key lies in designing basic cells consisting of rigid microshells and releasable nanoseeds, which together serve as a rigid shield and a bridge that chemically bonds with matrix and substrate. The durability and strong resistance to accretion of different matters of our cellular coating are evidenced by strong anti-abrasion, enhanced anti-corrosion against saltwater over 1000 h, and maintaining dry in complicated phase change conditions. The cells can be impregnated into diverse matrixes for facile mass production through scalable spraying. Our strategy provides a generic design blueprint for engineering ultra-durable coatings for a wide range of applications. The design and scalable fabrication of durable superhydrophobic coatings that prevent accretion of matter is challenging. Here the authors developed a generic cellular design for ultra-durable coatings that provides liquid-repellence, vapor imperviousness, and solid-shedding capabilities.