Metal-Organic Framework-Manipulated Dielectric Genes Inside Silicon Carbonitride toward Tunable Electromagnetic Wave Absorption.

Heterointerface engineering for different identifiable length scales has emerged as a key research area for obtaining materials capable of high-performance electromagnetic wave absorption; however, achieving controllable architectural and compositional complexity in nanomaterials with environmental and thermal stabilities remains challenging. Herein, metal-containing silicon carbonitride (SiCN/M) nanocomposite ceramics with multiphase heterointerfaces were in situ synthesized via coordination crosslinking, catalytic graphitization, and phase separation processes using trace amounts of metal-organic frameworks (MOFs). The results reveal that the regulation of dielectric genes by MOFs can yield considerable lattice strain and abundant lattice defects, contributing to strong interfacial and dipole polarizations. The as-prepared SiCN/M ceramics demonstrate excellent microwave absorption performance: the minimum reflection loss (RLmin ) is -72.6 dB at a thickness of only 1.5 mm and -54.1 dB at an ultralow frequency of 3.56 GHz for the SiCN/Fe ceramics and the RLmin is -55.1 dB with a broad bandwidth of 3.4 GHz at an ultralow thickness of 1.2 mm for the SiCN/CoFe ceramic. The results are expected to provide guidance for the design of future dielectric microwave absorption materials based on heterointerface engineering while offering a paradigm for developing MOF-modified SiCN nanocomposite ceramics with desirable properties.

Freeze-Cast Ni-MOF Nanobelts/Chitosan-Derived Magnetic Carbon Aerogels for Broadband Electromagnetic Wave Absorption.

The exceptional benefits of carbon aerogels, including their low density and tunable electrical characteristics, infuse new life into the realm of creating ultralight electromagnetic wave absorbers. The clever conceptualization and straightforward production of carbon-based aerogels, which marry aligned microporous architecture with nanoscale heterointerfaces and atomic-scale defects, are vital for effective multiscale microwave response. We present an uncomplicated synthesis method for crafting aligned porous Ni@C nanobelts anchored on N, S-doped carbon aerogels (Ni@C/NSCAs), featuring multiscale structural intricacies─achieved through the pyrolysis of freeze-cast Ni-MOF nanobelts and chitosan aerogel composites. The well-ordered porous configuration, combined with multiple heterointerfaces adopting a "nanoparticles-nanobelts-nanosheets" contact schema, along with a wealth of defects, adeptly modulates conductive, polarization, and magnetic losses to realize an equilibrium in impedance matching. This magnetically doped carbon aerogel showcases an impressive effective absorption bandwidth of 8.96 GHz and a minimum reflection loss of -68.82 dB, while maintaining an exceptionally low filler content of 1.75 wt %. Additionally, the applied coating exhibits an astonishing radar cross-section reduction of 51.7 dB m2, signifying its superior radar wave scattering capabilities. These results offer key insights into the attainment of broad-spectrum microwave absorption features by enhancing the multiscale structure of current aerogels.

Thermally assisted layer-layer crosslinking towards programmable evolution of pore structures for tunable electromagnetic response capability.

The research and development of aerogel-based microwave absorbing materials with strong electromagnetic (EM) wave response is an emerging research topic in the EM wave absorption field. In order to implement light microwave absorbers with a broad bandwidth, freeze drying assisted with in situ thermally structure-directing techniques was applied to fabricate composite aerogels with orientation design. Thanks to the integration of pore structure regulation and conductive network construction, the as-prepared aerogel absorbers exhibit a tunable EM response covering a broad frequency range. In detail, the maximum reflection loss (RL) value of the CR-3 aerogel reaches -50.8 dB at 2.2 mm and its maximum effective absorption bandwidth reaches 5.4 GHz at 2.0 mm, which is in accordance with the numerical simulation results of the radar cross section (RCS), where the optimum RCS reduction of 21.4 dB m2 appears for the CR-3 aerogel when the detection theta was set as 0°. In all, this work paves the way for the exploration of high-efficiency aerogel absorbers by balancing the evolution of the pore structure and conductive connection at the same time.

Highly effective and tunable microwave absorber integrating multiscale attenuation behaviours derived from prussian blue analogue/graphene oxide aerogel.

Tunable and efficient absorption of graphene-based microwave absorbers are essential on the realms of electromagnetic compatibility and protection in various application scenarios. However, challenges arise owing to their limited microwave attenuation behaviors. Herein, CoNiFe Prussian blue analogue (PBA)-derived magnetic alloy@carbon nanocubes anchored on N-doped reduced graphene oxide (rGO) aerogels were achieved via CoNiFe-PBA nanocubes assisting assembly of GO and subsequent thermal annealing approach. Such three-dimensional (3D) graphene-based macroscopic architecture integrates multiple attenuation behaviours occurred across multiple length scales. Attributed to the synergy of multiple scattering, conduction loss, multiple heterogeneous interface and dipolar polarizations, and magnetic loss, the optimized CoNiFe-PBA/GO aerogel derivative simultaneously exhibits strong reflection loss and wide effective bandwidth with an ultralow filling content (1.1 wt%) at both X band (-66.01 dB and 5.2 GHz at 3.2 mm) and Ku band (-66.23 dB and 6.6 GHz at 2.6 mm). Multiscale assembly strategy of graphene-based electromagnetic functional materials from molecular level to macroscale proposed and demonstrated by this work shows promise for exploring tunable and efficient microwave absorbers.

Nanolayered Ceramic-Confined Graphene Aerogel with Conformal Heterointerfaces for Low-Frequency Microwave Absorption.

Graphene-based aerogels have garnered considerable attention for their lightweight and efficient microwave absorption (MA) properties; however, optimizing the relationship between impedance matching and attenuation capability at low frequencies remains a challenge. In this study, a three-dimensional (3D) silicon carbonitride (SiCN) nanoceramic-coated graphene aerogel with conformal heterogeneous interfaces is constructed by precursor infiltration and pyrolysis to optimize MA performance at low frequencies. Thanks to the enhanced impedance matching and significant interfacial polarization of the two-dimensional sandwiched SiCN/graphene/SiCN cell walls and multiple scattering occurring within the 3D porous skeleton, the aerogel achieves a minimum reflection loss of -57.9 dB at an ultralow frequency of 4.92 GHz (C-band) and a broad bandwidth of 5.0 GHz at an ultralow thickness of 1.7 mm. The strategy developed here provides a method for enhancing dielectric polarization loss in graphene aerogels by the joint optimization of interfacial polarization and impedance matching, inspiring the design of high-performance graphene-based materials for low-frequency MA.

Harnessing Pseudo-Jahn-Teller Disordering of Monoclinic Birnessite for Excited Interfacial Polarization and Local Magnetic Domains.

The symmetry in a polymorph is one of the most important elements for determining the inherent lattice nature. The MnO2 host tends to high-symmetry MnO6 octahedra as a result of the electronic structure t2g 3 eg 0 of Mn4+ ions, displaying an ordered structure accompanying with poor polarization loss and limiting its application toward high-performance microwave absorbers. Here, a pseudo-Jahn-Teller (PJT) distortion and PJT disordering design with abundant self-forming interfaces and local magnetic domains in the monoclinic birnessite-MnO2 host is first reported. The PJT distortion can give rise to asymmetric MnO6 octahedra, inducing the formation of interfaces and increased electron spin magnetic moment in the lattice. The resultant birnessite with PJT distortions and PJT disordering delivers an outstanding reflection loss value of -42.5 dB at an ultralow thickness of 1.7 mm, mainly derived from the excited interfacial polarization and magnetic loss. This work demonstrates an effective approach in regulating the lattice structure of birnessite for boosting microwave absorption performance.

Ultralight Magnetic and Dielectric Aerogels Achieved by Metal-Organic Framework Initiated Gelation of Graphene Oxide for Enhanced Microwave Absorption.

HIGHLIGHTS: Metal-organic frameworks (MOFs) are used to directly initiate the gelation of graphene oxide (GO), producing MOF/rGO aerogels. The ultralight magnetic and dielectric aerogels show remarkable microwave absorption performance with ultralow filling contents. The development of a convenient methodology for synthesizing the hierarchically porous aerogels comprising metal-organic frameworks (MOFs) and graphene oxide (GO) building blocks that exhibit an ultralow density and uniformly distributed MOFs on GO sheets is important for various applications. Herein, we report a facile route for synthesizing MOF/reduced GO (rGO) aerogels based on the gelation of GO, which is directly initiated using MOF crystals. Free metal ions exposed on the surface of MIL-88A nanorods act as linkers that bind GO nanosheets to a three-dimensional porous network via metal-oxygen covalent or electrostatic interactions. The MOF/rGO-derived magnetic and dielectric aerogels Fe3O4@C/rGO and Ni-doped Fe3O4@C/rGO show notable microwave absorption (MA) performance, simultaneously achieving strong absorption and broad bandwidth at low thickness of 2.5 (- 58.1 dB and 6.48 GHz) and 2.8 mm (- 46.2 dB and 7.92 GHz) with ultralow filling contents of 0.7 and 0.6 wt%, respectively. The microwave attenuation ability of the prepared aerogels is further confirmed via a radar cross-sectional simulation, which is attributed to the synergistic effects of their hierarchically porous structures and heterointerface engineering. This work provides an effective pathway for fabricating hierarchically porous MOF/rGO hybrid aerogels and offers magnetic and dielectric aerogels for ultralight MA.

Conductive substrates-based component tailoring via thermal conversion of metal organic framework for enhanced microwave absorption performances.

Component tailoring, especially for the conductive substrates-based composites, acts as a significant role in optimizing the electromagnetic (EM) parameters and improving the EM response capability. Here, Fe-based metal oxides modified rGO microwave absorbers with component evolution were fabricated through hydrothermal treatment and subsequent pyrolysis process. The synergistic effects of the dielectric loss (multi-relaxations) and the magnetic loss (resonance and eddy current) are found to be effective in promoting the microwave absorption property of Fex-1Ox/C/rGO absorbers. As the thermal treatment temperature reaches 500 °C, the as-prepared composite sample shows ideal microwave absorption performance, where the reflection loss value is -25.94 dB, and the effective bandwidth reaches 5.84 GHz at 1.9 mm. In addition, CST simulation was employed to analyze the microwave absorption capability in the actual far field. When the scattering angle is 0° and 20°, the radar cross section (RCS) reduction of S-500/PEC layers is 8.11 dB m2 and 8.80 dB m2, respectively. This study exhibits the importance of component tailoring in enhancing the performances of substrates-based microwave absorption materials.

[Up-conversion luminescent materials of Y2O3: RE(RE=Er or Er/Yb) prepared by sol-gel combustion synthesis].

Y2O3 powders doped with rare-earth ions were synthesized by sol-gel combustion synthesis. Effects of different calcinating temperatures, Er+ doping concentration and Yb3+ doping concentration were investigated. It was shown that the single well crystallized Y2O3 powders could be obtained at 800 degrees C; as the calcinating temperature increased, the crystallinity and upconversion luminescence intensity were higher; the particle size was uniform around 1 microm at 900 degrees C; when Er3+ doping concentration was 1 mol%, the green upconversion luminescence intensity reached the maximum, but for red upconversion luminescence, when Er3+ doping concentration was 4 mol%, its luminescence intensity reached the maximum; as the ratio of Yb3+ to Er3+ was 4:1, the green emission intensity reached the maximum, while the red emission intensity was always increasing as Yb3+ doping concentration increased.

Mobilization and distribution of lead originating from roof dust and wet deposition in a roof runoff system.

In this research, the mobilization and distribution of lead originating in roof dust and wet deposition were investigated within a roof dust-rooftop-runoff system. The results indicated that lead from roof dust and wet deposition showed different transport dynamics in runoff system and that this process was significantly influenced by the rainfall intensity. Lead present in the roof dust could be easily washed off into the runoff, and nearly 60 % of the total lead content was present in particulate form. Most of the lead from the roof dust was transported during the late period of rainfall; however, the lead concentration was higher for several minutes at the rainfall beginning. Even though some of the lead from wet deposition, simulated with a standard isotope substance, was adsorbed onto adhered roof dust and/or retained on rooftop in runoff system, most of it (50-82 %) remained as dissolved lead in the runoff for rainfall events of varying intensity. Regarding the distribution of lead in the runoff system, the results indicated that it could be carried in the runoff in dissolved and particulate form, be adsorbed to adhered roof dust, or remain on the rooftop because of adsorption to the roof material. Lead from the different sources showed different distribution patterns that were also related to the rainfall intensity. Higher rainfall intensity resulted in a higher proportion of lead in the runoff and a lower proportion of lead remaining on the rooftop.