Microstructural evolution of Cu–Nb oxide nanocomposite alloys during ball milling is investigated using a two-step ball-milling approach. In the first step, Cu and Nb powders are milled to create a two-phase alloy comprising a Cu-rich matrix containing a high density of 20- to 30-nm Nb precipitates. In the second step, this nanocomposite is co-milled with CuO, resulting in the reduction of CuO and the oxidation of the Nb nanoprecipitates. Transmission electron microscopy characterization shows that three distinct types of Nb oxide precipitates evolve at different levels of strain. First, nanocrystalline NbO particles (∼10 nm) are formed by dissolved Nb in Cu reacting with oxygen evolved from the CuO. Next, the Nb nanoprecipitates in Cu further reduce CuO to form Nb/Nb oxide and NbO/Nb oxide core–shell inclusions (20–30 nm). These inclusions coalesce during additional milling to form amorphous Nb oxide agglomerates (>700 nm after 50 h). The growth of Nb precipitates during step-one milling, the initial growth of NbO nanoparticles, and the formation of core–shell Nb oxide precipitates during step-two milling are attributed to the convective transport of atoms and clusters combined with shear-induced agglomeration.

SiC and Ga2O3 are promising wide band gap semiconductors for applications in power electronics because of their high breakdown electric field and normally off operation. However, lack of a suitable dielectric material that can provide high interfacial quality remains a problem. This can potentially lead to high leakage current and conducting loss. In this work, we present a novel atomic layer deposition process to grow epitaxially MgxCa1−xO dielectric layers on 4H-SiC(0001) and β-Ga2O3$\left( {\bar 201} \right)$ substrates. By tuning the composition of MgxCa1−xO toward the substrate lattice constant, better interfacial epitaxy can be achieved. The interfacial and epitaxy qualities were investigated and confirmed by cross-sectional transmission electron microscopy and X-ray diffraction studies. Mg0.72Ca0.28O film showed the highest epitaxy quality on 4H-SiC(0001) because of its closest lattice match with the substrate. Meanwhile, highly textured Mg0.25Ca0.75O films can be grown on β-Ga2O3$\left( {\bar 201} \right)$ with a preferred orientation of (111).

Nanocomposites of polyvinylidene fluoride loaded with various amounts of γ-Fe2O nanoparticles, with an average size ranging between 20 and 40 nm, have been obtained by melt mixing and investigated using various experimental techniques [Superconducting Quantum Interference Device, Mössbauer, and Thermogravimetric Analysis]. Magnetic and Mössbauer measurements confirmed the presence of maghemite and a trace of a paramagnetic iron compound. Magnetic data are consistent with a blocking temperature close to room temperature (RT), showing a decrease in the coercive field as the temperature is increased. A weak exchange bias was noticed in all nanocomposites investigated at all temperatures and tentatively ascribed to surface spin disorder. The temperature dependence of the coercive field obeys the Kneller law. The nanocomposites exhibit superparamagnetic behavior near RT. Most magnetic measurements have been performed below the blocking temperature, revealing thus a complex behavior. The dependence of the mass loss derivative versus temperature, as obtained by thermogravimetric analysis, exhibits a single peak due to the thermal degradation of the polymeric matrix. A weak increase in the thermal stability of the polymeric matrix upon loading with maghemite is reported.

This work focuses on the functionalization of agave xylan-type hemicellulose functionalized with trimethoxysilylpropylmethacrylate and crosslinked with N-vinylcaprolactam to obtain a thermoresponsive material for potential applications in drug delivery. The hydrogels showed an interconnected and porous architecture with a lower critical solution temperature (LCST) close to poly(N-vinylcaprolactam)’s (PNVCL) LCST. These materials showed a good capacity to load ciprofloxacin (in the range 9.5 × 10−3–8.4 × 10−3 mg/mL), above the minimum inhibitory concentration (MIC ≤ 0.004 × 10−3–0.5 × 10−3 mg/mL) for gram-positive and gram-negative bacteria. The hybrid hydrogel inhibited the growth of Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa.

Energy recovery from waste treatment and growing biomass is of great significance for the energy management and sustainable energy supply. It is shown that biomass and various wastes containing carbon are able to significantly contribute to the energy sector.

We describe a possible scenario for the energy development of an European country of the future. In addition to solar, wind, and hydrogen energy, priority should also be given to generating energy using small-sized gasifiers. First, it is sustainable energy since biomass and household waste are always available. Second, this approach will allow us to launch local electric power grids instead of the unified state and interstate grids, which will reduce up to three times the consumption of energy raw materials and financial resources. Third, a new design of electric motors, namely torus motors, will allow one almost halve electricity consumption and open a gateway to new technologies.

A liquid-state pyroelectric energy harvester is described and a remarkable capacity to convert a thermal gradient into electrical energy is demonstrated.

Increasing the sustainability of energy generation can be pursued by harvesting extremely low enthalpy sources: low temperature differences between cold and hot reservoirs are easily achieved in every industrial process, both at large and small scales, in plants as well as in small appliances, vehicles, natural environments, and human bodies. This paper presents the assessment and efficiency estimate of a liquid-state pyroelectric energy harvester, based on a colloid containing barium titanate nanoparticles and ferrofluid as a stabilizer. The liquid is set in motion by an external pump to control velocity, in a range similar to the one achieved by Rayleigh–Bénard convection, and the colloid reservoir is heated. The colloid is injected into a Fluorinated Ethylene Propylene pipe where titanium electrodes are placed to collect electrical charges generated by pyroelectricity on the surface of the nanoparticles, reaching 22.4% of the ideal Carnot efficiency of a thermal machine working on the same temperature drop. The maximum extracted electrical power per unit of volume is above 7 mW/m3 with a ΔT between electrodes of 3.9 K.

Hydrogen is a versatile energy storage medium with significant potential for integration into the modernized grid.

Advanced materials for hydrogen energy storage technologies including adsorbents, metal hydrides, and chemical carriers play a key role in bringing hydrogen to its full potential.

The U.S. Department of Energy Hydrogen and Fuel Cell Technologies Office leads a portfolio of hydrogen and fuel cell research, development, and demonstration activities, including hydrogen energy storage to enable resiliency and optimal use of diverse domestic energy resources.

Today, the technology around generating and storing efficient and sustainable energy is rapidly evolving and hydrogen technologies offer versatile options. This perspective provides an overview of the U.S. Department of Energy's (DOE) Hydrogen and Fuel Cell Technologies Office's R&D activities in hydrogen storage technologies within the Office of Energy Efficiency and Renewable Energy, with a focus on their relevance and adaptation to the evolving energy storage needs of a modernized grid, as well as discussion of identified R&D needs and challenges. The role of advanced materials research programs focused on addressing energy storage challenges is framed in the context of DOE's H2@Scale initiative, which will enable innovations to generate cost-competitive hydrogen as an energy carrier, coupling renewables, as well as nuclear, fossil fuels, and the grid, to enhance the economics of both baseload power plants and intermittent solar and wind, to enhance resiliency and avoid curtailment. Continued growth and engagement of domestic and international policy stakeholders, industry partnerships, and economic coalitions supports a positive future outlook for hydrogen in the global energy system.

Nanostructures of plasmonic metals naturally combine strong light–matter interactions with catalytic activity, enabling new opportunities for light harvesting, catalytic chemistry, and artificial photosynthesis. Numerous studies have demonstrated that the optical excitation of localized surface plasmons generates hot electrons that can activate adsorbates triggering or facilitating chemical reactions on the surface of the nanoparticle. Going beyond such hot-electron-activated chemistry, a body of studies has shown that electron and hole carriers can be harvested from a plasmonically excited nanoparticle and utilized as redox equivalents for driving chemical reactions involving charge transfer. This article reviews such photoredox chemistry driven by plasmonic excitation of metal nanoparticles. Under certain conditions, a plasmonically excited nanoparticle can catalyze multielectron, multiproton transformations such as the photosynthesis of CO2 to hydrocarbons. We describe how the free energy of plasmonically generated charge carriers can be harvested and utilized for thermodynamically uphill reactions involving the formation of energy-rich chemical bonds or the development of molecular complexity. We end with a discussion of future opportunities in plasmon-excitation-driven photoredox chemistry.

Detailed report on MOFs for CO2 adsorption on the basis of ligands employed, OMSs, and structures. Systematic report on the high- and low-pressure CO2 capture. Report on the mechanism of CO2 capture.

A review on the promising field of MOF-based carbon capture and storage is presented. We discuss here the main features of MOFs applicable for CO2 capture and separation, the linker functionalization role, and the most important CO2-binding sites as also the most efficient and significant technologies, and a systematic report on the high- and low-pressure CO2 capture.

A comparison between electrochemical carbon dioxide conversion and reforestation is presented. By comparing thermodynamic and forestry data, recommendations for technology development can be made.

With the global average temperature steadily increasing due to anthropogenic emission of greenhouse gases into the atmosphere, there has been increasing interest worldwide in new technologies for carbon capture, utilization, and storage (CCUS). This coincides with the decrease in cost of deployment of intermittent renewable electricity sources, specifically solar energy, necessitating development of new methods for energy storage. Carbon dioxide conversion technologies driven by photovoltaics aim to address both these needs. To adequately contribute to greenhouse gas reduction, the carbon dioxide conversion technology deployed should have a substantially higher rate of carbon dioxide removal than planting an equivalent-sized forest. Using consistent methodologies, we analyze the effectiveness of model photovoltaic-driven carbon dioxide conversion technologies that produce liquid alcohols as compared to planting an equivalent forest. This analysis serves to establish an energy use boundary for carbon dioxide conversion technology, in order to be a viable alternative as a net carbon negative technology.