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Thus, the low-cost and thermochromic superhydrophobic clay mineral/BiVO4-HP coatings presented a promising application in temperature sensors and switches with the excellent weather resistance to record and monitor the temperature changes.The magnetoelectric effect is a fundamental physical phenomenon that synergizes electric and magnetic degrees of freedom to generate distinct material responses like electrically tuned magnetism, which serves as a key foundation of the emerging field of spintronics. Here, we show by first-principles studies that ferroelectric (FE) polarization of an In2Se3 monolayer can modulate the magnetism of an adjacent transition-metal (TM)-decorated graphene layer via a ferroelectrically induced electronic transition. The TM nonbonding d-orbital shifts downward and hybridizes with carbon-p states near the Fermi level, suppressing the magnetic moment, under one FE polarization, but on reversed FE polarization this TM d-orbital moves upward, restoring the original magnetic moment. This finding of robust magnetoelectric effect in the TM-decorated graphene/In2Se3 heterostructure offers powerful insights and a promising avenue for experimental exploration of ferroelectrically controlled magnetism in two-dimensional (2D) materials.Herein, we introduce polymer nanofibers of TiO2@NiCo-LDH as interlayers into Li-S batteries. RNA Synthesis inhibitor From 0 to 60 °C, the interlayers can deliver high sulfur utilization, an outstanding rate capability, and excellent cycling life. High-temperature excitation makes it easier for the valence band electrons of TiO2 to transition to the conduction band. The electron-hole pairs formed on the surface combine with the ether group of 1,3-dioxolane in the electrolyte, which greatly reduces the decomposition and volatilization rates of the electrolyte, ensuring Li-S batteries with good cycle performance at high temperatures. The capacity can stabilize at 798.6 mAh g-1 after 100 cycles at 60 °C and 1C, and the battery can provide a capacity higher than 323.2 mAh g-1 at 0 °C. Simultaneously, the lithium metal symmetrical battery with a functional separator can be continuously cycled for 1800 and 750 h without a short circuit at the current densities of 0.65 and 1.63 mA cm-2, respectively.Numerous efforts to fabricate antimicrobial surfaces by simple yet universal protocols with high efficiency have attracted considerable interest but proved to be particularly challenging. Herein, we designed and fabricated a series of antimicrobial polymeric coatings with different functions from single to multiple mechanisms by selectively utilizing diethylene glycol diglycidyl ether (PEGDGE), polylysine, and poly[glycidylmethacrylate-co-3-(dimethyl(4-vinylbenzyl)ammonium)propyl sulfonate] (poly(GMA-co-DVBAPS)) via straightforward mussel-inspired codeposition techniques. Bactericidal polylysine endowed the modified surfaces with a high ability (∼90%) to kill attached bacteria, while PEGDGE components with unique surface hydration prevented bacterial adhesion, avoiding the initial biofilm formation. Moreover, excellent salt-responsive poly(GMA-co-DVBAPS) enabled reactant polymeric coatings to change chain conformations from shrinkable to stretchable state and subsequently release >90% attached bacteria when treated with NaCl solution, even after repeated cycles. Therefore, the obtained polymeric coatings, polydopamine/poly(GMA-co-DVBAPS) (PDA/PDV), polydopamine/polylysine/poly(GMA-co-DVBAPS) (PDA/l-PDV), and polydopamine/polylysine/poly(GMA-co-DVBAPS)/diethylene glycol diglycidyl ether (PDA/l-PDV-PEGDGE), controllably realized functions from single and dual to multiple antimicrobial mechanisms, as evidenced by long-term antifouling activity to bacteria, high bactericidal efficiency, and salt-responsive bacterial regeneration performance with several bacterial killing-release cycles. This study not only contributes to mussel-inspired chemistry for polymeric coatings with controllable functions but also provides a series of reliable and highly efficient antimicrobial surfaces for potential biomedical applications.The practical applications of Li metal batteries (LMBs) have long been limited by the obstacles of low Coulombic efficiency (CE) and formation of dendrites on Li metal electrode. Herein, we demonstrated the synthesis of a novel three-dimensional (3D) nanostructured skeleton substrate composed of nitrogen-doped hollow carbon fiber/carbon nanosheets/ZnO (NHCF/CN/ZnO) using 2-methylimidazole (2-MIZ)-coated 3D cloth as a scaffold. The mechanism of formation of this novel hierarchical structure was investigated. The multilayered hierarchical structure and abundant lithiophilic nucleation sites of the substrate provide a stable environment for the deposition and stripping of lithium metal, thus preventing the generation of lithium dendrites. Consequently, the lithium anode based on the NHCF/CN/ZnO current collector demonstrated an excellent Coulombic efficiency of 96.47% after 400 cycles at 0.5 mA cm-2. The prepared NHCF/CN/ZnO/Li electrode also showed outstanding cycling performance of over 800 h and an ultralow voltage hysteresis of less than 30 mV in a symmetric cell at 5 mA cm-2 and 5 mAh cm-2. Even at a high loading of the cathode with 10.4 mg cm-2, the full cell of NHCF/CN/ZnO/Li anode with LiFePO4 can also work very well. Our work offers a path toward the facial preparation of 3D hierarchical structure for high-performance lithium metal batteries.The physical and chemical properties of MXenes are strongly dependent on surface terminations; thus, the tailoring of surface functional groups in two-dimensional transition-metal carbides (MXenes) may extend the applicability of these compelling materials to a wider set of fields. In this work, we demonstrate the chemical modification of Ti3C2T x MXene via diazonium covalent chemistry and the subsequent effects on the electrical properties of MXene. The 4-nitrophenyl group was grafted onto the surface of MXene through a solid-liquid reaction, which was confirmed by various characterization methods, including X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, electron energy loss spectroscopy, atomic force microscopy, and transmission electron microscopy. The degree of modification of MXene is expediently tunable by adjusting the concentration of the diazonium salt solution. The work function of functionalized MXene is modifiable by regulating the quantity of grafted diazonium surface groups, with an adjustable range of around 0.
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