Structural Design for EMI Shielding: From Underlying Mechanisms to Common Pitfalls.

Modern human civilization deeply relies on the rapid advancement of cutting-edge electronic systems that have revolutionized communication, education, aviation, and entertainment. However, the electromagnetic interference (EMI) generated by digital systems poses a significant threat to the society, potentially leading to a future crisis. While numerous efforts are made to develop nanotechnological shielding systems to mitigate the detrimental effects of EMI, there is limited focus on creating absorption-dominant shielding solutions. Achieving absorption-dominant EMI shields requires careful structural design engineering, starting from the smallest components and considering the most effective electromagnetic wave attenuating factors. This review offers a comprehensive overview of shielding structures, emphasizing the critical elements of absorption-dominant shielding design, shielding mechanisms, limitations of both traditional and nanotechnological EMI shields, and common misconceptions about the foundational principles of EMI shielding science. This systematic review serves as a scientific guide for designing shielding structures that prioritize absorption, highlighting an often-overlooked aspect of shielding science.

Peroxymonosulfate assisted pesticide breakdown: Unveiling the potential of a novel S-scheme ZnO@CoFe2O4 photo-catalyst, anchored on activated carbon.

A ternary hetero-junction was prepared by anchoring ZnO@CoFe2O4 (ZCF) on activated carbon (AC) and employed as a UV-assisted peroxymonosulfate (PMS) activator to boost the degradation of diazinon (DZN) pesticide. The structure, morphology, and optical properties of the ZCFAC hetero-junction were characterized through a series of techniques. The highest degradation efficiency of DZN (100% in 90 min) was achieved by the PMS-mediated ZCFAC/UV system, superior to other single or binary catalytic systems due to the strong synergistic effect between ZCFAC, PMS, and UV. The operating reaction conditions, synergistic effects, and the possible pathways of DZN degradation were investigated and discussed. Optical analysis showed that the band-gap energy of the ZCFAC hetero-junction not only enhanced the absorption of UV light but also reduced the recombination of photo-induced electron/hole pairs. Both radical and non-radical species (HO•, SO4•-, O2•-, 1O2, and h+) took part in the photo-degradation of DZN, assessed by scavenging tests. It was found that AC as a carrier not only improved the catalytic activity of CF and ZnO nanoparticles and conferred high stability for the catalyst but also played a crucial role in accelerating the catalytic PMS activation mechanism. Moreover, the PMS-mediated ZCFAC/UV system showed good reusability, universality, and practical applicability potential. Overall, this work explored an efficient strategy for the best use of hetero-structure photo-catalysts towards PMS activation to achieve high performance in decontaminating organic compounds.

A novel, Z-scheme ZnO@AC@FeO photocatalyst, suitable for the intensification of photo-mediated peroxymonosulfate activation: Performance, reactivity and bisphenol A degradation pathways.

In this study, the intensification of a UVC-based PMS activation treatment is performed by a novel photocatalyst. Using ZnO nanoparticles coupled with activated carbon (AC), impregnated by ferroferric oxides (FO, magnetite), as an effective Z-scheme photocatalyst (ZACFO), the effective Bisphenol A (BP-A) removal was attained. Several techniques were applied for the characterization of the as-prepared catalyst and proved the successful preparation of ZACFO. The photocatalytic activity of pristine ZnO was significantly improved after its combination with ACFO. It was found that the fabrication of ZACFO heterostructures could inhibit the charge carriers recombination and also accelerate the charge separation of photo-induced e-/h+ pairs. Under this UVC-based photocatalysis-mediated PMS activation system, ZACFO showed an excellent potential as compared to the single constituent catalysts. The complete degradation of 20 mg/L concentration of BP-A was attained in just 20 min with excellent reaction rate constant of 27.3 × 10-2 min-1. Besides, over 60% of TOC was eliminated by the integrated ZACFO/PMS/UV system within 60 min of reaction. The minor inhibition by most matrix components, the high recycling capability with minor metals' leaching and the effectiveness in complex matrices, constitute this composite method an efficient and promising process for treating real wastewater samples. Finally, based on the photo-produced reactive intermediates and by-products identified, the Z-scheme photocatalytic mechanism and the plausible pathway of BP-A degradation were proposed comprehensively. The presence and role of radical and non-radical pathways in the decontamination process of BP-A over ZACFO/PMS/UV system was confirmed.

Exploring the visible light-assisted conversion of CO2 into methane and methanol, using direct Z-scheme TiO2@g-C3N4 nanosheets: synthesis and photocatalytic performance.

The rapid growth of carbon dioxide (CO2) emissions raises concern about the possible consequences of atmospheric CO2 increase, such as global warming and greenhouse effect. Photocatalytic CO2 conversion has attracted researchers' interests to find a sustainable route for its elimination. In the present study, a direct Z-scheme TiO2/g-C3N4 composite (T-GCN) was fabricated via a facile hydrothermal route for the photocatalytic reduction of CO2 into methane (CH4) and methanol (CH3OH), under visible light irradiation without an electron mediator. The microstructure of the as-obtained TiO2/g-C3N4 nanocomposites was fully characterized for its physicochemical, structural, charge separation, electronic, and photo-excited carrier separation properties. The effect of CO2 and H2O partial pressure was studied to find the best operational conditions for obtaining maximum photocatalytic efficiency; the PCO2 and PH2O were 75.8 and 15.5 kPa, respectively, whereas, by increasing the light intensity from 20 to 80 mW/cm2, a remarkable improvement in the reduction rate takes place (from 11.04 to 32.49 µmol.gcat-1.h-1 methane production, respectively). Finally, under the most favorable light, PCO2 and PH2O conditions, high methanol and methane rates were obtained from the CO2 photocatalytic reduction through T-GCN (1.44 µmol.gcat.-1.h-1 and 32.49 µmol.gcat.-1.h-1, respectively) and an integrated proposition for the Z-scheme mechanism of photocatalytic reduction was proposed. This study offers a promising strategy to synthesize a Z-scheme T-GCN heterojunction with high photocatalytic performance for effective CO2 conversion.

Sono-photocatalytic degradation of tetracycline and pharmaceutical wastewater using WO3/CNT heterojunction nanocomposite under US and visible light irradiations: A novel hybrid system.

In this paper, in-situ fabrication of tungsten oxide (WO3) on carbon nano-tube (CNT) was performed via sol-gel/hydrothermal method to prepare WO3/CNT nanocomposites and then coupled with visible light and ultrasound (US) irradiations for sono-photocatalytic removal of tetracycline (TTC) and pharmaceutical wastewater treatment. The as-prepared catalysts were characterized by FT-IR, XRD, TEM, UV-VIS DRS, FESEM, EDS, TGA, BET, BJH, EIS, and EDX techniques. The characterization tests, indicated successful incorporation of CTNs into the WO3 framework and efficient reduction of charge carries recombination rate after modifying with CNT. The investigation of experimental parameters verified that 60 mg/L TTC could be perfectly degraded at optimum operational parameters (WO3/CNT: 0.7 g/L, pH: 9.0, US power: 250 W/m2, and light intensity: 120 W/m2 over 60 min treatment. Trapping experiments results verified that HO radicals and h+ were the main oxidative species in degradation of TTC. The as-prepared photocatalysts could be reused after six successive cycles with an approximately 8.8 % reduction in removal efficiency. Investigation of the effect of real pharmaceutical wastewater revealed that this system is able to eliminate 83.7 and 90.6 % of TOC and COD, respectively after 220 min of reaction time. Some compounds with lower toxic impact and molecular weight, compared to raw pharmaceutical wastewater, were detected after treatment by sono-photocatalysis process. The biodegradability of real pharmaceutical wastewater was improved significantly after treatment by WO3/CNT sono-photocatalysis.

Photocatalytic decontamination of phenol and petrochemical wastewater through ZnO/TiO2 decorated on reduced graphene oxide nanocomposite: influential operating factors, mechanism, and electrical energy consumption.

ZnO/TiO2 anchored on a reduced graphene oxide (rGO) ternary nanocomposite heterojunction was synthesized via the multi-step method including hydrothermal, solvothermal and sol-gel methods. XRD, Raman, FESEM, EDX, Dot Mapping EDS, BET, FTIR, UV-VIS, TGA, and EIS techniques were utilized for characterizing as-synthesized catalysts. The XRD and Raman data proved the formation of anatase phase TiO2 and wurtzite phase ZnO in the prepared samples. Further, the UV-Vis spectrum confirmed that the band gap value of ZnO/TiO2 diminished on introduction of graphene oxide. Photocatalytic performance of the fabricated catalysts was investigated by decontamination of phenol in aqueous solutions. The effect of different operational factors such as pH, catalyst dosage, phenol concentration, and light illumination was investigated to find the optimum decontamination conditions. According to the results, complete degradation of phenol was achieved at pH = 4, catalyst dosage of 0.6 g L-1, light intensity of 150 W, and phenol initial concentration of 60 ppm at 160 min under visible light illumination. With the addition of graphene oxide to the composite, a significant increase was detected in the photocatalytic performance due to the higher available surface area and lower electron/hole recombination rate. In addition, the scavenging experiments revealed that the ·OH is responsible for the degradation of phenol during the reaction. The degradation mechanism, economic performance, mineralization, and recyclability were also investigated. Kinetic studies confirmed that photocatalytic degradation process followed the pseudo-first-order kinetic model. A case of real wastewater treatment was used to examine the performance of the catalyst for real case studies.