New hierarchical bioinspired nanocomposite materials of poly­(vinyl alcohol)/poly­(acrylic acid)/carboxylate graphene oxide nanosheet@polydopamine (PVA/PAA/GO-COOH@PDA) were successfully prepared by electrospinning technique, thermal treatment, and polydopamine modification. The obtained composite membranes are composed of polymeric nanofibers with carboxylate graphene oxide nanosheets, which are anchored on the fibers by heat-induced cross-linking reaction. The preparation process demonstrate eco-friendly and controllable manner. These as-formed nanocomposites were characterized by various morphological methods and spectral techniques. Due to the unique polydopamine and graphene oxide containing structures in composites, the as-obtained composite demonstrate well efficient adsorption capacity toward dye removal, which is primarily due to the specific surface area of electrospun membranes and the active polydopamine/graphene oxide components. In addition, the composite membranes reported here are easy to regenerate. In comparison with other composite adsorbents, the preparation process of present new composite materials is highly eco-friendly and facile to operate and regulate, which demonstrates potential large-scale applications in wastewater treatment and dye removal.

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Although organic–inorganic halide perovskite solar cells (PSCs) have shown dramatically enhanced power conversion efficiencies (PCEs) in the last decade, their long-term stability is still a critical challenge for commercialization. To address this issue, tremendous research efforts have been devoted to exploring all-inorganic PSCs because of their intrinsically high structural stability. Among them, CsPbIBr2-based all-inorganic PSCs have drawn increasing attention owing to their suitable band gap and favorable stability. However, the PCEs of CsPbIBr2-based PSCs are still far from those of their organic–inorganic counterparts, thus inhibiting their practical applications. Herein, we demonstrate that by simply doping an appropriate amount of Cu2+ into a CsPbIBr2 perovskite lattice (0.5 at. % to Pb2+), the perovskite crystallinity and grain size are increased, the perovskite film morphology is improved, the energy level alignment is optimized, and the trap density and charge recombination are reduced. As a consequence, a decent PCE improvement from 7.81 to 10.4% is achieved along with an enhancement ratio of 33% with a CsPbIBr2-based PSC. Furthermore, the long-term stability of CsPbIBr2-based PSCs against moisture and heat also remarkably improved by Cu2+ doping. This work provides a facile and effective route to improve the PCE and long-term stability of CsPbIBr2-based all-inorganic PSCs.

Direct ammonia solid oxide fuel cell (DA‐SOFC) is superior to low‐temperature direct ammonia fuel cell using anion exchange membrane because of much improved anode reaction kinetics at elevated temperature. However, significant performance degradation due to severe sintering of conventional nickel cermet anode under operating conditions is a big challenge for realizing its practical use. Herein, a high‐performance anode based on La0.55Sr0.30TiO3−δ (LST) perovskite substrate with its surface decorated with in situ exsolved and strongly coupled NiCo alloy nanoparticles (NPs) is designed and fabricated for DA‐SOFCs, exhibiting superior catalytic activity for NH3 decomposition reaction due to balanced NH3 adsorption and N2 desorption processes. An electrolyte‐supported single cell with infiltrated NiCo/LST on Sm0.2Ce0.8O1.9 scaffold anode delivers a maximum power density of 361 mW cm−2 at 800 °C in NH3 fuel, superior to similar SOFCs with Ni or Co NP‐decorated LST based anodes (161 and 98 mW cm−2). Furthermore, the SOFC with this newly developed anode displays favorable operational stability without obvious performance degradation at 700 °C for a test period of ≈120 h, attributed to its high antisintering capability. This study provides some strategies to develop highly active, stable, and antisintering perovskite‐based nanocomposite for DA‐SOFCs, facilitating the practical use of this technology.

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