A team of researchers from the North China Electric Power University and the National Institute of Metrology in China has published a perspective on a promising class of materials for extracting uranium from aqueous environments. Their work details the design and application of heterocyclic-linked covalent organic frameworks (COFs), which use light to perform this critical task. This approach holds significant potential for both cleaning up contaminated water sources and securing a sustainable supply of uranium, the primary fuel for nuclear energy, by extracting it from seawater.

The dual need for environmental remediation and resource security has spurred the development of new technologies for uranium capture. Traditional methods face challenges with selectivity and capacity. The authors explain that photocatalysis offers a distinct advantage by using light to trigger specific redox reactions, reducing soluble and mobile uranium (U(VI)) into insoluble and immobile forms (U(IV)). The success of this technique depends on creating highly efficient photocatalysts. The focus of this perspective is on COFs, which are crystalline, porous materials built from organic molecules linked by strong covalent bonds.

Implanting a device into the deep temporal cortex of a mouse without damaging the brain has long been a major challenge in neuroscience research. A team at Meijo University and Dokkyo Medical University has now overcome this barrier with a flexible sheet thinner than a human hair that slides into place without penetrating the brain.

For more than a decade, a fundamental mystery has surrounded graphene—the one-atom-thick “wonder material” known for its exceptional strength, conductivity, and transparency. Despite its seemingly simple structure, one basic question has remained unresolved: does graphene attract water, or repel it?

The answer has proven surprisingly elusive. In some experiments, water droplets bead up on graphene, suggesting a hydrophobic (water-repellent) surface. In others, water spreads out, implying hydrophilic (water-attracting) behavior. This contradiction has fueled a long-running scientific debate and created uncertainty for applications such as desalination membranes, hydrogen fuel cells, and nanoelectronic devices, where precise control of water at interfaces is essential.

With the rapid development of flexible electronics and wearable devices, there is an increasing demand for absorbing materials that exhibit high electromagnetic wave absorption efficiency and mechanical flexibility. In this work, we present a novel and effective strategy for fabricating flexible microwave absorbers via synergistically integrating a polymer framework with conductive fillers. Carbon dots (CDs) functionalized with catechol groups were first synthesized via a bottom-up approach using directed ultrasonication, employing tannic acid dispersed in acetone as the precursor. Owing to the abundant surface functional groups, the as-prepared CDs were uniformly anchored onto MXene nanosheets through chemical bonding, forming a well-dispersed MXene/CDs composite. Subsequently, this hybrid filler was incorporated into a polymer network composed of polyvinyl alcohol (PVA) and acrylamide, with water and glycerol as co-solvents, to fabricate a flexible MXene/CDs organic hydrogel. Notably, glycerol plays an important role in adjusting the polarity of the gel system, thereby effectively optimizing impedance matching. Meanwhile, the abundant heterogeneous interfaces between MXene and CDs significantly enhanced interfacial polarization, and the synergistic coupling of optimized impedance matching with strong dielectric loss endowed the MXene/CDs organic hydrogel with outstanding electromagnetic wave absorption performance. The absorber achieves a minimum reflection loss (RL_min) of − 47.9 dB at 9.46 GHz with a matching thickness of 3.1 mm, along with an effective absorption bandwidth of 3.5 GHz. Furthermore, the synergistic reinforcement of dual-crosslinked polymer chains and the MXene/CDs filler endowed the hydrogel with excellent mechanical robustness, making it suitable for flexible and wearable absorption applications.

Human cognition relies on the seamless integration of multiple senses, allowing the brain to associate, infer, and even imagine across modalities. Replicating this capability in artificial systems has long remained a challenge, particularly under strict energy constraints. This study presents a bioinspired multisensory framework that integrates vision, touch, hearing, smell, and taste within a self-powered architecture. By enabling cross-modal association and adaptive reconfiguration, the system allows one sensory input—such as touch or sound—to trigger corresponding representations in other sensory domains. Beyond conventional recognition, the framework demonstrates higher-level cognitive functions, including inference and generative pattern creation. These advances point toward a new generation of intelligent machines capable of human-like perception and cognition.

Achieving both high efficiency and high selectivity remains a central challenge in catalytic hydrogenation reactions, as rapid reactant activation often leads to overly strong binding of intermediates and unwanted over-reduction. A new photocatalytic strategy now demonstrates how this long-standing trade-off can be overcome. By harnessing nonequilibrium charge carriers generated under visible light, the system promotes efficient hydrogen dissociation while steering the reaction toward selective semihydrogenation. Active hydrogen species migrate away from their formation sites to neighboring catalytic surfaces, where product formation and desorption are energetically favored. This spatial separation of reaction steps enables near-complete conversion under ambient conditions while maintaining excellent selectivity, offering a powerful new design principle for advanced catalytic systems.

Hydrogen peroxide is a widely used chemical essential to water treatment, disinfection, and green manufacturing, yet its conventional production relies on energy-intensive and centralized processes. Recent research highlights an emerging electrochemical route that generates hydrogen peroxide directly from oxygen and water under ambient conditions. Central to this approach is the use of noble metal-free single-atom electrocatalysts, where isolated metal atoms embedded in nitrogen-doped carbon precisely steer oxygen reduction toward the desired two-electron pathway. By combining atomic-scale catalyst design with advanced reactor engineering, this strategy offers a cleaner, safer, and more flexible way to produce hydrogen peroxide on demand, opening new possibilities for decentralized and sustainable chemical manufacturing.

Breaks MOCVD’s bottleneck in high-strain quantum well epitaxy, significantly boosts 1.2 μm VECSEL performance. Atomic-scale characterization clarifies the strain compensation’s indium segregation suppression mechanism. 590 nm second harmonic output: near diffraction limit, brightness >1.65 GW·cm⁻²·sr⁻¹. Paves a new way for ultra-high-brightness yellow lasers, accelerating VECSEL’s lab-to-commercialization transition.