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Metal–organic frameworks (MOFs) have emerged as leading candidates for atmospheric water harvesting (AWH). Despite their high water uptake capacity, challenges persist in effective solar‐driven desorption for water collection. Addressing this, a photothermal bridge is introduced by in situ growth of Ni₃S₂ coating on a thermally conductive nickel mesh, enhancing heat transfer to the MOF and accelerating desorption kinetics. MIL‐101 (Cr) MOF in bulk form (BMOF) is bonded to the lightweight Ni─Ni3S2 mesh using adhesive, forming a dual‐layer Ni─Ni₃S₂ mesh/BMOF assembly. This hybrid retains a high water uptake of ≈0.63 g g⁻¹ at 60% relative humidity (RH) with superior sorption kinetics. Photothermally driven heat transfer from Ni─Ni₃S₂ to BMOF achieves complete water desorption within 40 min under 1 kW m−2. Compared to other configurations like foil, granules, and foam, the mesh‐based hybrid has the highest single‐cycle adsorption–desorption kinetic of 3.18 × 10⁻3 g g⁻¹ min⁻¹. Additionally, the hybrid demonstrates exceptional hydrothermal stability over 50 cycles and maintains morphological stability with airflow, ensuring consistent performance. Heat transfer simulations confirm the thermal distribution across the Ni─Ni₃S₂ mesh/BMOF, corroborating the rapid and uniform desorption. This approach paves the way for efficient AWH in high‐RH, water‐scarce regions by enhancing desorption kinetics through solar energy. [ABSTRACT FROM AUTHOR]

Li1.3Al0.3Ti1.7(PO4)3 (LATP) solid‐state electrolyte has garnered considerable interest owing to its competitive room‐temperature Li‐ion conductivity, air stability, and economic nature. Nevertheless, the successful implementation of LATP in next‐generation Li‐metal solid‐state batteries (SSBs) is impeded by its high incompatibility with Li metal. Herein, combining the Kevlar aramid nanofiber (KANF) membrane with a solidified electrolyte (SE) formed via in situ polymerization, the SE@KANF protective layer for LATP can be constructed. Such a protective layer not only effectively prevents Li metal from reducing LATP but also provides intimate interface contact and limits unnecessary electron transport. Consequently, Li symmetric battery incorporating SE@KANF layer enables an ultrahigh critical current density of 1.4 mA cm−2 and stably cycles for over 2000 h at 0.2 mA cm−2. Moreover, the full SSB coupling with LiFePO4 cathode delivers a capacity retention of 95% after 180 cycles at 0.1 C at 30 °C. The present study underscores the importance of the protective interface layer in stabilizing the LATP|Li interface. [ABSTRACT FROM AUTHOR]

The clinical use of FDA‐approved bone morphogenetic proteins (BMPs) are impeded by high costs, super‐high dosage requirement, short half‐life, and other undesirable side effects. Therefore, designing a biomaterial that can promote new bone formation without using exogenous BMPs is highly desirable in clinical applications. In the present work, a new kind of nanofibrous scaffold composed of gelatin and 45S5 bioglass (GF/45S5 BG) was prepared through thermally induced phase separation method together with the particle leach technique (TIPS&P). In addition to the significantly higher mechanical strength, the composite scaffolds (GF/45S5 BG) significantly increased osteogenic differentiation of human mesenchymal stem cells (hMSCs) in vitro compared with the neat scaffold (GF) without adding other biological agents, for example, BMPs or hormones. Most importantly, our in vivo studies also indicated that GF/45S5 BG scaffolds could directly promote ectopic bone regeneration in SD rats without exogenous BMP2. In summary, both in vitro and in vivo results indicated that the novel 45S5 bioglass functionalized GF nanofibrous scaffold is a promising alternative for bone tissue engineering. [ABSTRACT FROM AUTHOR]

Garnet‐type solid‐state lithium batteries (SSLBs) possess excellent potential owing to their safety and high energy density. However, fundamental barriers are deficient cycling stability and poor rate capability. The main concern lies in generating voids at the Li|garnet interface during Li stripping, stemming from the sluggish diffusion of Li atoms inside the bulk Li metal. Herein, a composite anode (AN@Li) containing Li–Al alloy, Li3N, and LiNO2 is designed by introducing aluminum nitrate into molten Li. The lower interfacial formation energies exhibited by Li–Al alloy, Li3N, and LiNO2 with garnet solid‐state electrolyte (SSE) enhance the wettability of AN@Li toward SSE. Meanwhile, it affords efficient conductive pathways that facilitate Li+ diffusion in the bulk anode (not just on the surface). Impressively, the resulting symmetric cell with AN@Li electrodes achieves high critical current density (1.95 mA cm−2) and long cycle life (6000 h at 0.3 mA cm−2). The SSLB coupled with LiFePO4 cathode and AN@Li anode enables stable cycling for 200 cycles at a high rate of 1 C with a retention of 96% and exhibiting outstanding rate capability (145.9 mAh g−1 at 2 C). This work provides practical insights for producing high‐performance lithium metal anode for advanced garnet‐type SSLBs. [ABSTRACT FROM AUTHOR]