Radiative cooling is a passive thermal management strategy that leverages the natural ability of materials to dissipate heat through infrared radiation. It has significant implications for energy efficiency, climate adaptation, and sustainable technology development, with applications in personal thermal management, building temperature regulation, and aerospace engineering. However, radiative cooling performance is susceptible to environmental aging and special environmental conditions, limiting its applicability in extreme environments. Herein, a critical review of extreme environmental radiative cooling is presented, focusing on enhancing environmental durability and cooling efficiency. This review first introduces the design principles of heat exchange channels, which are tailored based on the thermal flow equilibrium to optimize radiative cooling capacity in various extreme environments. Subsequently, recent advancements in radiative cooling materials and micro-nano structures that align with these principles are systematically discussed, with a focus on their implementation in terrestrial dwelling environments, terrestrial extreme environments, aeronautical environments, and space environments. Moreover, this review evaluates the cooling effects and anti-environmental abilities of extreme radiative cooling devices. Lastly, key challenges hindering the development of radiative cooling devices for extreme environmental applications are outlined, and potential strategies to overcome these limitations are proposed, aiming to prompt their future commercialization.

Rechargeable aqueous metal-ion batteries are promising alternative energy storage devices in the post-lithium-ion era due to their inherent safety and environmental compatibility. Among them, aqueous zinc ion batteries (AZIBs) stand out as next-generation energy storage systems, offering low cost, high safety, and eco-friendliness. Nevertheless, the instability of Zn metal anodes, manifested as Zn dendrite growth, interfacial side reactions, and hydrogen (H₂) evolution, remains a major obstacle to commercialization. To address these challenges, extensive research has been conducted to understand and mitigate these issues. This review comprehensively summarizes recent advances in Zn anode stabilization strategies, including artificial solid electrolyte interphase (SEI) layers, structural optimization, electrolyte modification, and bioinspired designs. These approaches collectively aim to achieve uniform Zn deposition, suppress parasitic reactions, and enhance cycling stability. Furthermore, it critically evaluates the advantages and feasibility of different strategies, discuss potential synergistic effects of multi-strategy integration, and provide perspectives for future research directions.

Symmetric solid oxide fuel cells (SSOFCs) have emerged as promising energy conversion devices due to their low fabrication cost and outstanding durability. Ammonia (NH₃), a carbon‑free hydrogen carrier with high energy density and ease of storage, serves as an ideal fuel for such systems. In this study, a bifunctional electrode material, Pr_0.32Sr_0.48Fe_0.75Ni_0.2Ru_0.05O_3-δ (PSFNRu), is synthesized by doping 5 mol% Ru into the parent perovskite Pr_0.32Sr_0.48Fe_0.8Ni_0.2O_3-δ (PSFN). The resulting PSFNRu exhibits abundant oxygen vacancies and enables the in‑situ exsolution of alloy nanoparticles (ANPs) under reducing conditions, which act as additional active sites to enhance electrochemical performance. The PSFNRu‑based SSOFC delivers peak power densities of 736 mW cm^-2 with H₂ and 547 mW cm^-2 with NH₃ at 800 °C, significantly outperforming its undoped counterpart. Furthermore, the cell maintains stable performance for over 172 h at 700 °C under NH₃ fuel, confirming excellent operational durability. These findings underscore the potential of PSFNRu as a high‑performance symmetric electrode for direct ammonia SSOFCs (DA‑SSOFCs).

The overall energy efficiency is critical for commercializing promising electrochemical technologies such as the CO₂ reduction reaction (CO₂RR). Despite the rapid development of advanced catalysts and reactors for CO₂RR, its commercial potential is still hindered by the sluggish oxygen evolution reaction (OER), which causes high cell voltages and low energy efficiencies. Herein, we have developed a NiOOH@Ni₃S₂ catalyst on the surface of nickel foam (NF) via an electrochemical surface reconstruction strategy. We observe that the oxidation of glycerol to formate is more thermodynamically favorable than the OER on the developed NiOOH@Ni₃S₂/NF catalysts. The Ni²⁺/Ni³⁺ redox couples within the NiOOH@Ni₃S₂ heterojunction enhance the charge transfer kinetics between the active sites and adsorbed reaction intermediates, facilitating the highly selective and active generation of formate from glycerol oxidation reaction (GOR), with a remarkable Faradaic efficiency (FE) of 94% achieved at 100 mA cm^-2. Comprehensive mechanistic studies identified that the reaction pathway towards formate generation starts from glyceraldehyde intermediates and the glycolate was considered as the key species. Moreover, benefited from the efficient conversion of CO₂ to formate on bismuth nanosheets, the GOR//CO₂RR paired electrolysis system realizes a remarkable overall FE of ca. 190% for formate co-production at 160 mA cm^-2 (cathodic FE: 91.25%; anodic FE: 98.70%). This proceeds at a cell voltage of ca. 2.32 V, which is ca. 0.85 V lower than that of OER-assisted CO₂RR system at the same current density. This work provides new insights for co-upgrading CO₂ and biomass to value-added chemicals.

This review examines inflammation as a physiological defense mechanism against infectious agents, physical trauma, reactive oxygen species (ROS), and metabolic stress, which, under dysregulated conditions, may progress into chronic diseases. Nanomedicine, which integrates nanotechnology with medicine, suppresses inflammatory signaling pathways and overexpressed pro-inflammatory cytokines, such as ROS, to address inflammation-related pathologies. Current advances in nanomaterial design and synthesis strategies are systematically analyzed, with parallel discussions on toxicity mechanisms, influencing factors, and evaluation methods that are critical for clinical translation. Applications of functional nanomaterials are highlighted in the context of refractory inflammatory conditions, including wound healing, gastrointestinal disorders, and immune, neurological, or circulatory diseases, along with targeted delivery strategies. Persistent challenges in nanomedicine development, such as biocompatibility optimization, precise biodistribution control, and standardized toxicity assessment, are critically assessed. By bridging material innovation with therapeutic efficacy, this review establishes a framework for advancing nanomedicine to improve treatment outcomes while addressing translational barriers.

Since the Corona era, people's interest in health management has increased significantly compared to before. In addition, the emergence of multidrug-resistant bacteria through antibiotics has begun to have a great impact on human health. Therefore, the research team would like to report the synergy effect of antibacterial activity using wearable organic light-emitting diodes and natural antibacterial substances against staphylococcus aureus. This is research on a platform that is more convenient than past treatment methods and can suppress the development of multidrug-resistant staphylococcus aureus.

Silicon (Si) is a promising anode material for rechargeable batteries due to its high theoretical capacity and abundance, but its practical application is hindered by the continuous growth of porous solid-electrolyte interphase (SEI), leading to capacity fade. Herein, a LiF-Pie structured SEI is proposed, with LiF nanodomains encapsulated in the inner layer of the organic cross-linking silane matrix. A series of advanced techniques such as cryogenic electron microscopy, time-of-flight secondary ion mass spectrometry, and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry have provided detailed insights into the formation mechanism, nanostructure, and chemical composition of the interface. With such SEI, the capacity retention of LiCoO₂||Si is significantly improved from 49.6% to 88.9% after 300 cycles at 100 mA g⁻¹. These findings provide a desirable interfacial design principle with enhanced (electro) chemical and mechanical stability, which are crucial for sustaining Si anode functionality, thereby significantly advancing the reliability and practical application of Si-based anodes.