Air-permeable, antibacterial, fireproof, electromagnetic shielding polymeric textile-based wearable heaters with exceptional electrothermal and photothermal conversion performance were developed for future health management and protection.
Thermal camouflage has attracted increasing attention owing to the rapid development of infrared (IR) surveillance technologies. Various materials and systems have been developed to date, but the realization of high-temperature thermal camouflage using ultrathin film/coating remains a great challenge; this is of great significance, especially for IR stealth in military equipment. This work demonstrates a series of ultrathin Ti 3 C 2 T x MXene films (as low as 1 µm) with superior high-temperature indoor/outdoor thermal camouflage performance: wide camouflage temperature range (from below −10 °C to over 500 °C), large reduction in radiation temperature (exceeding 300 °C for objects with temperatures over 500 °C), long-term high-temperature or fire stability, multifunctionality including disguised Joule heating capability, and high electromagnetic interference shielding efficiency. The superior high-temperature thermal camouflage performance of the ultrathin MXene film is attributed to its low mid-IR emissivity (0.19), which is comparable to that of stainless steel but far below that of other 2D nanomaterials, such as graphene. The multifunctional ultrathin MXene films prepared through simple vacuum-assisted filtration provide a feasible method for efficient high-temperature thermal camouflage using ultrathin films, demonstrating the great promise of MXene materials for thermal camouflage, IR stealth, counter-surveillance, and security protection.
Three ZnAl2O4 samples were prepared via a modified polyacrylamide gel method using a citric acid solution with different aluminum salt starting materials, including AlCl3∙6H2O, Al2(SO4)3∙18H2O, and Al(NO3)3∙9H2O under identical conditions. The influence of different aluminum salts on the morphologies, phase purity, and optical and fluorescence properties of the as-prepared ZnAl2O4 nanoparticles were studied. The experimental results demonstrate that the phase purity, particle size, morphology, and optical and fluorescence properties of ZnAl2O4 nanoparticles can be manipulated by the use of different aluminum salts as starting materials. The energy bandgap (Eg) values of ZnAl2O4 nanoparticles increase with a decrease in particle size. The fluorescence spectra show that a major blue emission band around 400 nm and two weaker side bands located at 410 and 445 nm are observed when the excitation wavelength is 325 nm. The ZnAl2O4 nanoparticles prepared from Al(NO3)3∙9H2O exhibit the largest emission intensity among the three ZnAl2O4 samples, followed in turn by the ZnAl2O4 nanoparticles prepared from Al2(SO4)3∙18H2O and AlCl3∙6H2O. These differences are attributed to combinational changes in Eg and the defect types of the ZnAl2O4 nanoparticles.
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