Although various bio inspired materials with outstanding mechanical, acoustic and optic properties have been developed, bio inspired microwave absorbing materials are rarely reported. Herein, under the inspiration of the opal, for the first time a kind of Co@Co3O4/nitrogen-doped (N-doped) mesoporous carbon spheres (Co@Co3O4/NMCS) with periodic three-dimensional (3D) structure toward microwave absorption of Co@Co3O4/NMCS was designed and synthesized. The microwave absorption performance was optimized with respect to the contents of Co@Co3O4 nanoparticles. Co@Co3O4/NMCS with ~20wt% Co@Co3O4 content achieves the -53.8 dB at 5.7 GHz with a thickness of 3.5 mm. The simulated radar cross section result demonstrated the Co@Co3O4/NMCS can efficiently suppress the strong electromagnetic scattering from metal groove structure. This periodic porous structures of nitrogen-doped mesoporous carbon spheres combined with the magnetic Co@Co3O4 nanoparticles contribute to the excellent absorbing performance.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.Whereas small siRNA nanocarriers with a size of 10-20 nm exert high tissue-permeability, they encounter the challenge of inefficient adsorption on the cell surface, resulting in poor cellular uptake of siRNA. To solve this dilemma, this study aims to control the hydrophobicity of a small siRNA nanocarrier, unimer polyion complex (uPIC), with a size of ∼10 nm. The uPICs are fabricated to consist of a single pair between siRNA and a smart triblock copolymer comprising hydrophilic poly(2-ethyl-2-oxazoline) (PEtOx), thermoswitchable poly(2-n-propyl-2-oxazoline) (PnPrOx), and cationic poly(l-lysine) (PLL). The PnPrOx segment is dehydrated at 37 °C (>lower critical solution temperature) to enhance the hydrophobicity of uPICs. The uPICs with a hydrophobic domain facilitates cellular uptake of the siRNA payload through stronger binding to the cell surface, compared with control uPICs without a PnPrOx segment, leading to a significantly enhanced gene silencing effect in cultured cancer cells.We employed first-principles calculations to investigate the effect of structural disorders on the Li storage capacity of graphene nanomaterials. Our calculations first revealed that the Li storage capacity of a graphene monolayer does not necessarily increase with the size of a C vacancy created but is largely determined by the local geometry of the defect sites. Our electronic structure analysis further revealed that the enhanced Li storage capacity by the C vacancy defect is mainly attributed to the increased number of the unoccupied electronic density of states lying near the Fermi level, which can be substantially increased by raising the number of bond rotations within the vacancy sites. Furthermore, it was also found that the Li storage capacity of graphene can be effectively enhanced by increasing the degree of local ring disorders without the presence of any vacancy defect. The amorphous graphene structure was shown to possess a relatively higher Li storage capacity compared to pristine graphene, primarily owing to the presence of many nonhexagonal rings randomly distributed in the graphene lattice. These nonhexagonal rings can create many electron-deficient regions on the graphene surface to effectively accommodate more electrons from Li, thereby substantially enhancing the Li storage capacity of graphene nanomaterials.Mixed oxygen ionic and electronic conduction is a vital function for cathode materials of solid oxide fuel cells (SOFCs), ensuring high efficiency and low-temperature operation. However, Fe-based layered double perovskites, as a classical family of mixed oxygen ionic and electronic conducting (MIEC) oxides, are generally inactive toward the oxygen reduction reaction due to their intrinsic low electronic and oxygen-ion conductivity. Herein, Zn doping is presented as a novel pathway to improve the electrochemical performance of Fe-based layered double perovskite oxides in SOFC applications. The results demonstrate that the incorporation of Zn ions at Fe sites of the PrBaFe2O5+δ (PBF) lattice simultaneously regulates the concentration of holes and oxygen vacancies. Consequently, the oxygen surface exchange coefficient and oxygen-ion bulk diffusion coefficient of Zn-doped PBF are significantly tuned. The enhanced mixed oxygen ionic and electronic conduction is further confirmed by a lower polarization resistance of 0.0615 and 0.231 Ω·cm2 for PrBaFe1.9Zn0.1O5+δ (PBFZ0.1) and PBF, respectively, which is measured using symmetric cells at 750 °C. Moreover, the PBFZ0.1-based single cell demonstrates the highest output performance among the reported Fe-based layered double perovskite cathodes, rendering a peak power density of 1.06 W·cm-2 at 750 °C and outstanding stability over 240 h at 700 °C. https://www.selleckchem.com/products/Ilginatinib-hydrochloride.html The current work provides a highly effective strategy for designing cathode materials for next-generation SOFCs.