The main prerequisite of an active visible-light-driven photocatalyst is to effectively utilize the visible light to induce electron-hole (e-/h+) pairs of expanded lifetime. To this end, for the first time, the ternary heterojunctions of CeO2/Fe3O4 /Graphene oxide and Ce3+/ Fe3O4 /Graphene oxide (CeO2/Fe3O4/GO and Fe2.8Ce0.2O4/GO) were prepared via facile ultrasonic-assisted procedures and employed for destruction of oxytetracycline (OTC) under visible light irradiation. The changes in the relative crystal structure, morphology, atomic and surface functional group composition, magnetic, and optic properties of magnetite were uncovered by various techniques. The substantial degradation and mineralization of OTC via visible light/Fe2.8Ce0.2O4/GO system were thoroughly discussed in terms of narrowed band gap energy, the principal function of Ce3+/Ce4+ and Fe2+/Fe3+ redox pairs and GO platelets, enhanced charge separation and transfer, and enlarged active surface area. Furthermore, the performance of visible light/Fe2.8Ce0.2O4/GO system was evaluated for treating real wastewater and its efficiency was investigated using a number of enhancers and scavengers. Finally, the generated byproducts in the course of photodegradation were determined and the oxidation pathway, photocatalytic kinetics, and plausible mechanism were proposed. The results confirmed that the introduced Ce ions and graphene oxide sheets boost the photo-catalytic efficiency of magnetite for photodegradation of OTC.
Herein, it is aimed to develop a high-performance monolithic adsorbent to be utilized in methyl orange (MO) adsorption. Therefore, amino-functionalized three-dimensional graphene networks (3D-GNf) fulfilling the requirements of reusability and high capacity have been fabricated via hydrothermal self-assembly approach followed by a double-crosslinking strategy. The potential utilization of 3D-GNf as an adsorbent for removal MO has been assessed using both batch-adsorption studies and an artificial neural network (ANN) approach. Graphene oxide sheets have been amino-functionalized and cross-linked, by ethylenediamine (EDA) during hydrothermal treatment, following the glutaraldehyde has used as a double-crosslinking agent to facilitate the crosslinking of architecture. The successful fabrication of 3D-GNf has been confirmed by field-emission scanning electron microscopy (FESEM), Fourier transform infrared (FT-IR), Raman and X-ray photoelectron spectroscopy (XPS). Moreover, N2 adsorption/desorption isotherms have revealed the high specific surface area (1015 m2 g-1) with high pore volume (1.054 cm3 g-1) and hierarchical porous structure of 3D-GNf. The effect of initial concentration, contact time, and temperature on adsorption capacity have been thoroughly studied, and the kinetics, isotherms, and thermodynamics of MO adsorption have been modelled. The MO adsorption has been well defined by the pseudo-second-order kinetic model and Langmuir isotherm model with a monolayer adsorption capacity of 270.27 mg g-1 at 25 °C. The thermodynamic findings have revealed MO adsorption has occurred spontaneously with an endothermic process. The Levenberg-Marquardt backpropagation algorithm has been implemented to train the ANN model, which has used the activation functions of tansig and purelin functions at the hidden and output layers, respectively. An optimum ANN model with high-performance metrics (coefficient of determination, R2 = 0.9995; mean squared error, MSE = 0.0008) composed of three hidden layers with 5 neurons in each layer was constructed to forecast MO adsorption. The findings have shown that experimental results are consistent with ANN-based data, implying that the suggested ANN model may be used to forecast cationic dye adsorption.
Heavy metal pollution remains a global environmental challenge that poses a significant threat to human life. Various methods have been explored to eliminate heavy metal pollutants from the environment. However, most methods are constrained by high expenses, processing duration, geological problems, and political issues. The immobilization of metals, phytoextraction, and biological methods have proven practical in treating metal contaminants from the soil. This review focuses on the general status of heavy metal contamination of soils, including the excessive heavy metal concentrations in crops. The assessment of the recent advanced technologies and future challenges were reviewed. Molecular and genetic mechanisms that allow microbes and plants to collect and tolerate heavy metals were elaborated. Tremendous efforts to remediate contaminated soils have generated several challenges, including the need for remediation methodologies, degrees of soil contamination, site conditions, widespread adoptions and various possibilities occurring at different stages of remediation are discussed in detail.
Use of MXenes (Ti3 C2 Tx ), which belongs to the family of two-dimensional transition metal nitrides and carbides by encompassing unique combination of metallic conductivity and hydrophilicity, is receiving tremendous attention, since its discovery as energy material in 2011. Owing to its precursor selective chemical etching, and unique intrinsic characteristics, the MXene surface properties are further classified into highly chemically active compound, which further produced different surface functional groups i. e., oxygen, fluorine or hydroxyl groups. However, the role of surface functional groups doesn't not only have a significant impact onto its electrochemical and hydrophilic characteristics (i. e., ion adsorption/diffusion), but also imparting a noteworthy effect onto its conductivity, work function, electronic structure and properties. Henceforth, such kind of inherent chemical nature, robust electrochemistry and high hydrophilicity ultimately increasing the MXene application as a most propitious material for overall environment-remediation, electrocatalytic sensors, energy conversion and storage application. Moreover, it is well documented that the role of MXenes in all kinds of research fields is still on a progress stage for their further improvement, which is not sufficiently summarized in literature till now. The present review article is intended to critically discuss the different chemical aptitudes and the diversity of MXenes and its derivates (i. e., hybrid composites) in all aforesaid application with special emphasis onto the improvement of its surface characteristics for the multidimensional application. However, this review article is anticipated to endorse MXenes and its derivates hybrid configuration, which is discussed in detail for emerging environmental decontamination, electrochemical use, and pollutant detection via electrocatalytic sensors, photocatalysis, along with membrane distillation and the adsorption application. Finally, it is expected, that this review article will open up new window for the effective use of MXene in a broad range of environmental remediation, energy conversion and storage application as a novel, robust, multidimensional and more proficient materials.
Recently, the growing demand for a renewable and sustainable fuel alternative is contingent on fuel cell technologies. Even though it is regarded as an environmentally sustainable method of generating fuel for immediate concerns, it must be enhanced to make it extraordinarily affordable, and environmentally sustainable. Hydrogen (H2 ) synthesis by electrochemical water splitting (ECWS) is considered one of the foremost potential prospective methods for renewable energy output and H2 society implementation. Existing massive H2 output is mostly reliant on the steaming reformation of carbon fuels that yield CO2 together with H2 and is a finite resource. ECWS is a viable, efficient, and contamination-free method for H2 evolution. Consequently, developing reliable and cost-effective technology for ECWS was a top priority for scientists around the globe. Utilizing renewable technologies to decrease total fuel utilization is crucial for H2 evolution. Capturing and transforming the fuel from the ambient through various renewable solutions for water splitting (WS) could effectively reduce the need for additional electricity. ECWS is among the foremost potential prospective methods for renewable energy output and the achievement of a H2 -based economy. For the overall water splitting (OWS), several transition-metal-based polyfunctional metal catalysts for both cathode and anode have been synthesized. Furthermore, the essential to the widespread adoption of such technology is the development of reduced-price, super functional electrocatalysts to substitute those, depending on metals. Many metal-premised electrocatalysts for both the anode and cathode have been designed for the WS process. The attributes of H2 and oxygen (O2 ) dynamics interactions on the electrodes of water electrolysis cells and the fundamental techniques for evaluating the achievement of electrocatalysts are outlined in this paper. Special emphasis is paid to their fabrication, electrocatalytic performance, durability, and measures for enhancing their efficiency. In addition, prospective ideas on metal-based WS electrocatalysts based on existing problems are presented. It is anticipated that this review will offer a straight direction toward the engineering and construction of novel polyfunctional electrocatalysts encompassing superior efficiency in a suitable WS technique.
The increasing demand for searching highly efficient and robust technologies in the context of sustainable energy production totally rely onto the cost-effective energy efficient production technologies. Solar power technology in this regard will perceived to be extensively employed in a variety of ways in the future ahead, in terms of the combustion of petroleum-based pollutants, CO2 reduction, heterogeneous photocatalysis, as well as the formation of unlimited and sustainable hydrogen gas production. Semiconductor-based photocatalysis is regarded as potentially sustainable solution in this context. g-C3 N4 is classified as non-metallic semiconductor to overcome this energy demand and enviromental challenges, because of its superior electronic configuration, which has a median band energy of around 2.7 eV, strong photocatalytic stability, and higher light performance. The photocatalytic performance of g-C3 N4 is perceived to be inadequate, owing to its small surface area along with high rate of charge recombination. However, various synthetic strategies were applied in order to incorporate g-C3 N4 with different guest materials to increase photocatalytic performance. After these fabrication approaches, the photocatalytic activity was enhanced owing to generation of photoinduced electrons and holes, by improving light absorption ability, and boosting surface area, which provides more space for photocatalytic reaction. In this review, various metals, non-metals, metals oxide, sulfides, and ferrites have been integrated with g-C3 N4 to form mono, bimetallic, heterojunction, Z-scheme, and S-scheme-based materials for boosting performance. Also, different varieties of g-C3 N4 were utilized for different aspects of photocatalytic application i. e., water reduction, water oxidation, CO2 reduction, and photodegradation of dye pollutants, etc. As a consequence, we have assembled a summary of the latest g-C3 N4 based materials, their uses in solar energy adaption, and proper management of the environment. This research will further well explain the detail of the mechanism of all these photocatalytic processes for the next steps, as well as the age number of new insights in order to overcome the current challenges.