Materials for Renewable and Sustainable Energy最新文献

The synthesis of δ-MnO₂, δ-MnO₂ carbon dots nanocomposite, and Fe/Cu-doped δ-MnO₂ carbon dots nanocomposite has been successfully carried out through a stirring process at room temperature and 80 °C. The synthesized powder shows a low crystallization determined through XRD and TEM analysis. Furthermore, the carbon dots are well attached to MnO₂ performing a core–shell composite material, while the doping ions Fe and Cu were incorporated into the matrix substitute Mn in the MnO₆ octahedron, although potassium ions were also detected. The manganese possess an oxidation state of + 3 and + 4, which promotes the oxygen vacancy creation ({V}_{mathrm{O}}^{cdotcdot}) denoting the conductivity decrease.

This work created, characterized, and used a magnetic biochar catalyst that is both eco-friendly and very effective. Sugarcane bagasse was selected as primary raw material for catalyst preparation, because it is renewable and ecofriendly biomass. Catalyst created by doping sugarcane bagasse biochar with magnetic material in the form of (FeSO₄·7H₂O). Thermogravimetric Analysis (TGA) and Fourier Transform Infrared spectroscopy (FTIR) were used to characterize the catalyst. In addition, physical and textural characteristics of the catalyst were identified and interpreted. The characterization outcome showed that the catalyst has good catalytic qualities. For the manufacturing of biodiesel, discarded cooking oil served as the primary feedstock. The experiment was created utilizing the Box–Behnken Design (BBD) technique. There are four variables with the following three levels each: temperature, methanol to oil ratio, catalyst concentration, and reaction time. 29 experiments in total were carried out. Using the RSM function, optimization was done. The optimal conditions for obtaining biodiesel yield—temperature, methanol to oil ratio, reaction time, and catalyst weight—were 43.597 °C, 9.975 mol/L, 49.945 min, and 1.758 wt%. A study of the produced biodiesel using a FTIR showed that the conventional biodiesel IR spectra were confirmed. All physiochemical characteristics found suggested the biodiesel complied with ASTM and EN norms. Overall, the synthesized catalyst had conducted simultaneous reactions in a single batch reactor and had demonstrated suitability for converting used cooking oil to biodiesel.

Bio-based materials represent a promising alternative in building envelope applications, with the aim of improving in-use energy efficiency. They have the advantage of being renewable, low embodied energy and CO₂ neutral or negative. In addition, they are excellent thermal regulators. This paper presents an overview of the state-of-the-art of bio-based materials used in building construction and their applications. The materials outlined include hemp, wood, date palm wood, cork, alfa and straw. Through this literature study we want to get a broad overview of the current state of theoretical and experimental studies of their hygrothermal characteristics and their thermal and energy performances. The aim is not to be exhaustive but to summarise the most important research results on these materials. This is the first part of a research work that deals with the contribution to the development of a new bio-based construction material to be used in building.

Electrochemical reduction of CO₂ is an effective method for storing intermittent renewable energy. This could result in fuel additives and chemical feedstocks such as alcohols. A challenge of electrochemical alcohol production is the transfer of electrons and protons, as well as the formation of C–C bonds. As of now, copper-based materials are the most commonly used and effective catalysts. Although CuO_x is considered a promising catalyst for electrochemical CO₂ reduction reactions (CO2RR), significant improvements in product selectivity are still needed. This paper presents some results obtained using copper oxide as a cathode, combined with 33% of ionomer, nickel iron as anode, and membrane Fumatech as electrolyte. As a result of physico-chemical experiments, morphological measurements of the cathode, electrochemical experiments carried out with a complete zero-gap cell operating under alkaline conditions, and gas-chromatographic (GC) analyses of the cathode outlet stream, we determined that methyl formate, ethanol, and propanol were mainly obtained at a rate of 116.3 μmol ({text{g}}_{text{cat}}^{-1} , {text{h}}^{-{1}}) during operation at 2.2 V.

In this work, we report that hydrogen (H₂) doped in n-type a-Si:H thin films strongly influences the electronic correlation in increasing the conversion output power of solar cells. Type n a-Si:H thin films were grown using PECVD on ITO substrates with various H2-doping, to obtain various thin films for solar-cell applications. N-type a-Si:H thin films were prepared, and then characterized using ellipsometric spectroscopy, atomic force microscopy, Fourier transform infrared spectroscopy, and transmission electron microscopy. The addition of doped-H₂ to the thin layer shows a decrease in optical conductivity, while the energy gap in the thin layer shows a significant increase in the a-Si:H-type thin layer. Our results show that H₂ doping plays a very important role in the electronic structure, which is indicated by the significant energy gap difference. On the other hand, the bond structure of each H2-doped thin film showed a change from amorphous to nanocrystalline structures which were evenly distributed in each H₂-doped bonding. Overall, we believe that the addition of doped-H₂ to our findings could help increase the power conversion output of the solar cell due to the modification of the electronic structure.

Bioenergy is one of several renewable energy options derived from biomass that can help satisfy our energy needs.  Anaerobic digestion is a viable method for producing bioenergy in the form of biogas from biomass. The anaerobic digestion process is challenged with low biogas recovery, and low-quality effluent or CO₂ emission, which contribute to environmental pollution and the carbon footprint in the atmosphere. Computational process modelling and simulation can provide realistic information for dealing with the technological challenges involved with anaerobic digestion. In this study, modeling and simulation of the simplified anaerobic digestion process were done using SuperPro Designer software fed with biomass feedstock containing carbohydrates, proteins, and fats, as well as yeast, at 37 °C mesophilic temperature. The anaerobic digestion process yielded 89.655% of CH₄ and 10.345% of CO₂ and confirmed that the carbohydrate feedstock produces more CH₄ composition in the biogas. Mineralization of CO₂ using MgO yielded 0.23% MgCO₃, consuming > 99% of the CO₂ produced during the anaerobic digestion process. Environmental impact assessment of the effluent discharge yielded 0.142 kg Slds/L volatile solid with 6.01% COD reduction per batch of the anaerobic digestion process in an anaerobic digester with 90% (1.925 kg/batch) feedstock dosage. The data indicate that single-batch effluent cannot be discharged into the environment, hence indicating the possible recycling for multiple anaerobic digestion processing. The results are a significant guide for the realistic scalable production of high-quality biogas for bioenergy application, CO₂ mineralization, and environmental remediation.

Nowadays, addressing the drawbacks of liquid electrolyte-based batteries is a hot and challenging issue, which is supposed to be fulfilled through solid electrolyte systems such as polymer electrolytes. Polymer blend electrolytes (PBEs) are widely investigated as viable options to solve the undesired characteristics of their liquid counterparts and also the poor ionic conductivity of homopolymer-based electrolytes. Even though PBEs outperform homopolymer-based electrolytes in terms of performance, the conductivity of pristine PBEs is quite low for practical applications (i.e. below 10^–3 S/cm at room temperature). A very promising approach to solve this limitation is to incorporate additives into the electrolyte systems, to select suitable polymeric materials and to employ the desired synthesizing techniques as the performance of PBEs is strongly dependent on the selection of polymeric materials (i.e. on the inherent properties of polymers), the nature and amount of salts and other additives, and also the techniques employed to synthesize the polymer blend hosts and/or polymer blend electrolytes, determining the functionality, amorphousness, dielectric constant, dimensional stability, and, ultimately, the electrochemical performances of the system. This paper reviews the different factors affecting the miscibility of polymer blends, PBEs synthesizing techniques, the thermal, chemical, mechanical and electrochemical characteristics of PBEs, and also the challenges and opportunities of PBEs. Moreover, the paper presents the current progress of polymer blend electrolytes as well as future prospects for advancing polymer blend electrolytes in the energy storage sectors.

In this study, new polypyrrole films (ppy) were synthesized using a physical plasma deposition (PAPVD) system; where the equipment design and methodology for plasma-assisted pyrrole polymerization were improvement. The morphology, functional groups, and thermal stability of the polymer network films were characterized by X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC) techniques, respectively. The electrochemical properties of the films as capacitor were evaluated by cyclic voltammetry and electrochemical impedance spectroscopy. The results observed by SEM showed that the ppy 100W-1 and ppy 100W-2 films present uniformity in their structure. The analyses of TGA and DSC confirmed the improvement in stability; meanwhile for 100W-1 film, the presence of ppy bonds was corroborated by XPS. Plasma-activated ppy 100W-1 film exhibited higher capacitance and minor Rct resistance than that obtained for ppy 100W-2 film. The specific capacitances values of ppy 100W-1 and ppy 100w-2 films are 196 and 150 F/g in 1 M KCl. After charging and discharging tests of 1000 cycles at 5 mA cm⁻² current density of ppy 100W-1 film retains 89% of its initial capacitance. Therefore, ppy 100W-1 film showed to be a promising material for use as an electrochemical capacitor.

Doping TiO₂ with noble metals, transition metals, cations, anions have yielded very promising results in enhancing photocatalytic activity of TiO₂ in the visible region and its role in generating alternate forms of energy. Noble metals in general can effectively slow down carrier recombination. However, the study of Pd and Ni as dopant can lead to a reliable and versatile TiO₂-modified photocatalyst. In this paper, we explore the optical properties of Pd- and Ni-doped TiO₂ by doping with 4.17% Ni and Pd dopant concentrations. The optical properties prove that Ni-doped TiO₂ can absorb well in the visible region with an absorption coefficient of 1 × 10⁵ cm⁻¹. Hence, Ni-doped TiO₂ can successfully alter the electronic and optical properties of TiO₂ for favorable future applications. In the visible region, absorption coefficient of Pd-doped TiO₂ supercell is around 1.2 × 10⁵ cm⁻¹ which is comparatively greater than that of pure TiO₂ confirming its utility as a versatile and viable visible light photocatalyst. The other optical properties like reflectivity, refractivity, extinction coefficient and electron energy loss spectrum have also been studied.

In this study, different Cobalt–Copper mixed oxides compositions for supercapacitor electrodes have been prepared, by means of electrodeposition and thermal annealing. The chemical–physical and electrochemical characterization of electrodes, as well as the effect of different Co/Cu in the ratios on the crystal lattice, electrode morphologies, and electrochemical performance of the electrodes, were investigated using X-ray diffraction (XRD), scanning electron microscopic (SEM) and cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge (GCD) tests. The results indicated that the electrode prepared from 0.06 M CoSO₄·7H₂O + 0.04 M CuSO₄·5H₂O solution (CC4) had a better electrochemical performance. The initial capacity of the CC4 electrode was 28.3 mAh/g at a scan rate of 5 mV/s with a coulombic efficiency of 94%. CC4 electrode featured capacity retention of 79.2% at a constant current density of 1 A/g after 5000 cycles.