electricity on a large scale with ultralow greenhouse gases emission. [2] Uranium is the most critical ingredient for the production of nuclear power. In order for nuclear power to be a sustainable energy generation in the future, economically viable sources of uranium beyond terrestrial ores must be developed. [3] The oceans hold ≈4.5 billion tons of uranium, [4] making them a potential huge resource to support nuclear power production for hundreds of years. [5] All that is required is the ability to capture this element from seawater in cost-and energy-efficient ways. In the last decades, researchers worldwide have tried various methods to recover uranium from seawater and aqueous solution, such as coprecipitation, [6] ion-exchange, [7] adsorption via porous organic polymers, [8,9] and organic-inorganic hybrid adsorbents. [10][11][12][13][14][15][16] Among these technologies, the adsorption approach, particularly by using fiber-based adsorbents, is recognized as the most feasible process in terms of practicality, processability, cost, and environmental concerns. [3,17] In the 1990s, Japan Atomic Energy Agency (JAEA) research teams had successfully captured over 1083 g of uranium directly from ocean by using nonwoven fabric adsorbent, firmly establishing the practicality of uranium recovery from the oceans in appreciable quantities. [3,18] Uranium extraction from seawater via fiber adsorption has recentlyThe oceans contain hundreds of times more uranium than terrestrial ores. Fiber-based adsorption is considered to be the most promising method to realize the industrialization of uranium extraction from seawater. In this work, a pre-amidoximation with a blow spinning strategy is developed for mass production of poly(imide dioxime) nanofiber (PIDO NF) adsorbents with many chelating sites, excellent hydrophilicity, 3D porous architecture, and good mechanical properties. The structural evidences from 13 C NMR spectra confirm that the main functional group responsible for the uranyl binding is not "amidoxime" but cyclic "imidedioxime." The uranium adsorption capacity of the PIDO NF adsorbent reaches 951 mg-U per g-Ads in uranium (8 ppm) spiked natural seawater. An average adsorption capacity of 8.7 mg-U per g-Ads is obtained after 56 d of exposure in natural seawater via a flowthrough column system. Moreover, up to 98.5% of the adsorbed uranium can be rapidly eluted out and the adsorbent can be regenerated and reused for over eight cycles of adsorption-desorption. This new blow spun PIDO nanofabric shows great potential as a new generation adsorbent for uranium extraction from seawater.

Solar‐driven conversion of CO2 into high value‐added fuels is expected to be an environmental‐friendly and sustainable approach for relieving the greenhouse gas effect and countering energy crisis. Metal sulfide semiconductors with wide photoresponsive range and favorable band structures are suitable photocatalysts for CO2 photoreduction. This review summarizes the recent progress on metal sulfide semiconductors for photocatalytic CO2 reduction. First, the fundamentals, mechanisms and some principles, like product selectivity, of photocatalytic CO2 reduction are introduced. Then, according to the elemental composition, the metal sulfide photocatalysts applied for CO2 reduction are classified into binary (CdS, ZnS, MoS2, SnS2, Bi2S3, In2S3,Cu2S, NiS/NiS2, and CoS2), ternary (ZnIn2S4, CdIn2S4, CuInS2, Cu3SnS4, and CuGaS2), and quaternary (Cu2ZnSnS4) systems, in which their crystal structures, photochemical characteristics, and photocatalytic CO2 reduction applications are systematically demonstrated. Especially, the diverse modification strategies for improving the activity and product selectivity of photocatalytic CO2 reduction on these metal sulfides are summarized. Finally, the current challenges and future directions for the development of metal sulfide photocatalysts for CO2 reduction are proposed. This review is expected to serve as a powerful reference for exploiting high‐efficiency metal sulfide photocatalysts for CO2 conversion and furthering related mechanism understanding.

Advanced ceramic sponge materials with temperature-invariant high compressibility are urgently needed as thermal insulators, energy absorbers, catalyst carriers, and high temperature air filters. However, the application of ceramic sponge materials is severely limited due to their complex preparation process. Here, we present a facile method for large-scale fabrication of highly compressible, temperature resistant SiO 2-Al 2 O 3 composite ceramic sponges by blow spinning and subsequent calcination. We successfully produce anisotropic lamellar ceramic sponges with numerous stacked microfiber layers and density as low as 10 mg cm −3. The anisotropic lamellar ceramic sponges exhibit high compression fatigue resistance, strain-independent zero Poisson's ratio, robust fire resistance, temperatureinvariant compression resilience from −196 to 1000°C, and excellent thermal insulation with a thermal conductivity as low as 0.034 W m −1 K −1. In addition, the lamellar structure also endows the ceramic sponges with excellent sound absorption properties, representing a promising alternative to existing thermal insulation and acoustic absorption materials.

Electrochromic smart windows (ECSWs) are considered as the most promising alternative to traditional dimming devices. However, the electrode technology in ECSWs remains stagnant, wherein inflexible indium tin oxide and fluorine-doped tin oxide are the main materials being used. Although various complicated production methods, such as high-temperature calcination and sputtering, have been reported, the mass production of flexible and transparent electrodes remains challenging. Here, a nonheated roll-to-roll process is developed for the continuous production of flexible, extralarge, and transparent silver nanofiber (AgNF) network electrodes. The optical and mechanical properties, as well as the electrical conductivity of these products (i.e., 12 Ω sq at 95% transmittance) are comparable with those AgNF networks produced via high-temperature sintering. Moreover, the as-prepared AgNF network is successfully assembled into an A4-sized ECSW with short switching time, good coloration efficiency, and flexibility.