Search Results (278)

Hydrogen energy is a pivotal carrier for achieving carbon neutrality, requiring green and efficient production via water electrolysis. However, the anodic oxygen evolution reaction (OER) involves a sluggish four-electron transfer process, resulting in high overpotentials, while the prohibitive cost and complex preparation of precious metal catalysts impede large-scale commercialization. In this study, we develop a FeCo-based bimetallic deep eutectic solvent (FeCo-DES) as a multifunctional reaction medium for engineering a three-dimensional (3D) coral-like FeOOH-Co₂(OH)₃Cl/NF composite via a mild one-step impregnation approach (70 °C, ambient pressure). The FeCo-DES simultaneously serves as the solvent, metal source, and redox agent, driving the controlled in situ assembly of FeOOH-Co₂(OH)₃Cl hybrids on Ni(OH)₂/NiOOH-coated nickel foam (NF). This hierarchical architecture induces synergistic enhancement through geometric structural effects combined with multi-component electronic interactions. Consequently, the FeOOH-Co₂(OH)₃Cl/NF catalyst achieves a remarkably low overpotential of 197 mV at 100 mA cm⁻² and a Tafel slope of 65.9 mV dec⁻¹, along with 98% current retention over 24 h chronopotentiometry. This study pioneers a DES-mediated strategy for designing robust composite catalysts, establishing a scalable blueprint for high-performance and low-cost OER systems. Full article

The Mo:BiVO₄/FeOOH photoelectrode was synthesized through the deposition of FeOOH onto the surface of the Mo:BiVO₄ photoelectrode. The composite photoelectrode demonstrated a photocurrent of 1.8 mA·cm⁻², which is three times greater than that observed for pure BiVO₄. Furthermore, the glycerol conversion rate was recorded at 79 μmol·cm⁻²·h⁻¹, approximately double that of pure BiVO₄, while the selectivity for glyceraldehyde reached 49%, also about twice that of pure BiVO₄. The incorporation of Mo has been shown to enhance the stability of the BiVO₄. Additionally, Mo doping improves the efficiency of electron-hole transport and increases the carrier concentration within the BiVO₄. This enhancement leads to a greater number of holes participating in the formation of iron oxyhydroxide (FeOOH), thereby stabilizing the FeOOH co-catalyst within the glycerol conversion system. The FeOOH co-catalyst facilitates the adsorption and oxidation of the primary hydroxyl group of glycerol, resulting in the cleavage of the C−H bond to generate a carbon radical (C). The interaction between the carbon radical and the hydroxyl group produces an intermediate, which subsequently dehydrates to form glyceraldehyde (GLAD). Full article

The utilization of geothermal resources as renewable energy is a subject of interest for the regions that possess these resources. The exploitation of geothermal energy must consider local geological conditions and an integrated approach, which should include practical studies on the chemistry of geothermal waters and their effect on thermal installations. Geothermal waters from Bihor County, Romania, have a variable composition, depending on the crossed geological layers, but also on pressure and temperature. Obviously, water transport and heat transfer are involved in all applications of geothermal waters. This article aims to characterize certain geothermal waters from the point of view of composition and corrosion if used as a thermal agent. Atomic absorption spectroscopy (AAS) and UV–Vis spectroscopy were employed to analyze water specimens. Chemical composition includes calcite (CaCO₃), chalcedony (SiO₂), goethite (FeO(OH)), and magnetite (Fe₃O₄), which confirms the corrosion and scale potential of these waters. Corrosion resistance of mild carbon steel, commonly used as pipe material, was studied by the gravimetric method and through electrochemical methodologies, including chronoamperometry, electrochemical impedance spectroscopy (EIS), potentiodynamic polarization method, and open circuit potential measurement (OCP). Statistical analysis shows that the medium corrosion rate of S235 steel, expressed as penetration rate, is between 0.136 mm/year to 0.615 mm/year. The OCP, EIS, and chronoamperometry experiments explain corrosion resistance through the formation of a passive layer on the surface of the metal. This study proposes an innovative methodology and a systematic algorithm for analyzing chemical processes and corrosion phenomena in geothermal installations, emphasizing the necessity of individualized assessments for each aquifer to optimize operational parameters and ensure sustainable resource utilization. Full article

With the continuous consumption of fossil energy and the related environmental problems, clean energy, especially the hydrogen energy-derived water electrolysis, has attracted wide attention. However, as a result of the high energy consumption of water electrolysis and the limitations of single-function catalysts, there is an urgent need for cheap and simple-to-make bifunctional catalysts. In this work, based on the NiFe-LDH that is usually used for OER (Oxygen Evolution Reaction), doping of heteroatoms was carried out and a bifunctional catalyst could be then prepared using biomass as the carbon source. The preparation of catalyst precursors and in situ reduction were performed through the coupling process of hydrothermal and pyrolysis to enhance the electrolytic activity of the catalyst. Results showed that the overpotentials required to reach a current density of 10 mA·cm⁻² for the HER and OER processes were 305.2 mV and 310.4 mV, respectively, which are superior to the commercial catalysts. In the subsequent characterization, the structural characteristics of the catalyst support and their structure–activity correlation with active metals were systematically investigated by TEM, XRD, and XPS analysis, providing mechanistic insights into the catalytic behavior. The basic catalytic mechanisms of HER and OER were also obtained: the HER process was due to the formation of a Ni₃Fe alloy structure during catalyst preparation, which changed the electronic structure of the catalyst, while the OER process was induced by the formation of a NiOOH intermediate. The research results are expected to provide new ideas and data support for the preparation of bifunctional catalysts. Full article

Broad lateral size and thickness distributions impede the application of hexagonal boron nitride nanosheets (BNNSs) as friction modifiers in base oil, although they possess remarkable potential for lubrication performance promotion. In this work, a cascade centrifugation-assisted liquid-phase exfoliation approach was presented to prepare BNNSs from hexagonal boron nitride (h-BN) efficiently and scalably. Subsequently, they were ultrasonically dispersed into gas-to-liquid (GTL) base oil, and their lubrication performance promotion was evaluated by a four-ball tribotester. Tribological tests demonstrated that BNNS possesses excellent friction-reducing and anti-wear properties in GTL. Furthermore, the findings indicate that at a BNNS content of 0.8 wt.%, the system displayed the lowest COF and WSD. Particularly, with an addition of 0.8 wt.% BNNS into GTL, the AFC and WSD are reduced significantly by 40.1% and 35.4% compared to pure base oil, respectively, and the surface roughness, wear depth, and wear volume were effectively reduced by 91.0%, 68.5%, and 76.8% compared to GTL base oil, respectively. Raman, SEM-EDS, and XPS results proved that the outstanding friction-reducing and anti-wear properties of BNNS can mainly be ascribed to the presence of physical adsorption film and tribo-chemical film, which were composed of FeOOH, FeO, Fe₃O₄, and B₂O₃. Full article

In this paper, we use the facile approach for preparing novel, low-cost, efficient electrocatalysts for electrocatalytic water splitting. Interfacial engineering can significantly enhance the intrinsic performance of electrocatalysts. Herein, self-supporting FeOOH/NiFe-layered double hydroxide (LDH) nanosheet arrays were synthesized via hydrothermal and impregnation methods. The resulting FeOOH/NiFe-LDH can provide more active regions, which provide more active regions for co-reaction to proceed and accelerates electron transmit processes. Additionally, the amorphous FeOOH provides abundant active sites with low coordination, leading to excellent activity. The FeOOH/NiFe-LDH demonstrates remarkable two half-reaction electrocatalytic activity, along with excellent overpotentials of 168 mV (OER) and 155 mV (HER). This research introduces a sophisticated and scalable methodology for the creation of remarkably efficient and resilient alkaline conditions specifically designed for the HER and OER. Full article

Biochar is a solid product generated through the pyrolysis of biomass materials under anaerobic or hypoxic conditions, and it is characterized by its strong adsorption capacity. To investigate the phosphorus adsorption performance of biochar derived from wheat straw, bamboo, and water hyacinth in wastewater, iron modification treatments were applied to these biochars, and the most effective modified biochar was identified. The physicochemical properties of the modified biochars were characterized using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), and scanning electron microscopy (SEM). The results showed that optimal modification was achieved with an iron–carbon mass ratio of 0.70 for wheat straw biochar (Fe-WBC) and 0.45 for both bamboo biochar (Fe-BBC) and water hyacinth biochar (Fe-HBC). The maximum phosphorus adsorption capacities of the three modified biochars were as follows: 31.76 mg g⁻¹ (Fe-WBC) > 27.14 mg g⁻¹ (Fe-HBC) > 25.31 mg g⁻¹ (Fe-BBC). It was demonstrated that the adsorption behavior of Fe-BBC was predominantly multi-molecular layer adsorption, whereas the adsorption behavior of Fe-WBC and Fe-HBC was primarily monolayer adsorption. All three types of modified biochars reached adsorption equilibrium within 30 min, with Fe-WBC exhibiting the best adsorption performance. Analysis revealed that the modified biochars contained a large number of unsaturated C bonds and aromatic rings, indicating relatively stable structures. The surfaces of the modified biochars were rich in hydroxyl and carbonyl groups, which contributed to their strong adsorption properties. Post-modification analysis indicated that iron in the biochars predominantly existed in forms such as goethite (FeOOH) and hematite (Fe₂O₃). The iron content in each type of modified biochar constituted approximately 3.08% for Fe-WBC, 5.94% for Fe-BBC, and 5.68% for Fe-HBC relative to their total elemental composition. Overall, the iron-modified biochars employed in this study significantly enhanced the adsorption capacity and efficiency for phosphorus removal in wastewater. Full article

The oxygen evolution reaction (OER) is pivotal in hydrogen production via water electrolysis, yet its sluggish kinetics, stemming from the four-electron transfer process, remain a major obstacle, with overpotential reduction being critical for enhancing efficiency. This work addresses this challenge by developing a novel approach to stabilize and activate non-precious metal catalysts for OER. Specifically, we synthesized a three-dimensional flake NiFe-LDH/ZIF-L composite catalyst on a flexible nickel foam (NF) substrate through a room temperature soaking and hydrothermal method, leveraging the mesoporous structure of ZIF-L to increase the specific surface area and optimizing electron transfer pathways via interfacial regulation. Continuous linear sweep voltammetry (LSV) scanning induced structural self-reconstruction, forming highly active NiOOH species enriched with oxygen vacancies, which significantly boosted catalytic performance. Experimental results demonstrate an overpotential of only 221 mV at 10 mA cm⁻² and a Tafel slope of 56.3 mV dec⁻¹, alongside remarkable stability, attributed to the catalyst’s hierarchical nanostructure that accelerates mass diffusion and charge transfer. The innovation lies in the synergistic effect of the mesoporous ZIF-L structure and interfacial regulation, which collectively enhance the catalyst’s activity and durability, offering a promising strategy for advancing large-scale water electrolysis hydrogen production technology. Full article

Hydrogen energy holds great promise for alleviating energy and environmental issues, with alkaline electrochemical water splitting being a key approach for hydrogen production. However, the high cost and limited availability of noble-metal catalysts hinder its widespread application. This study presents a novel method to fabricate a NiFeP-CoP/CF electrode. By growing CoOOH nanosheets on Co foam at low temperatures and filling the gaps between nanosheets with Ni and Fe phosphides, the prepared electrode exhibits outstanding electrocatalytic performance. For the oxygen evolution reaction (OER) in alkaline media, it requires overpotentials of only 235 mV and 290 mV to reach current densities of 10 mA cm⁻² and 100 mA cm⁻², respectively. In the case of the hydrogen evolution reaction (HER), overpotentials of 89 mV and 172 mV are needed to achieve current densities of −10 mA cm⁻² and −100 mA cm⁻². The NiFeP-CoP/CF-based electrolytic cell requires a cell voltage of only 1.70 V to achieve a current density of 100 mA cm⁻² for overall water splitting. Moreover, during long-term continuous operation at 100 mA cm⁻², the overpotential for OER remains constant while that for HER decreases. The low-temperature growth of CoOOH nanosheets on Co foam provides a new strategy for large-scale electrode production applicable in electrochemical processes and pollutant degradation. Significantly, filling the nanosheet gaps with phosphides effectively enhances the electrocatalytic performance of the system. This work offers a facile and cost-effective technique for the large-scale production of metallic (oxyhydr)hydroxides for electrocatalytic water splitting, showing great potential for industrial applications. Full article

Hematite (Fe₂O₃) has been accepted as a promising and potential photo(electro)catalyst. However, its poor carrier separation and transfer efficiency has limited its application for photoelectrocatalytic (PEC) water oxidation. Herein, a S-doped FeOOH (S:FeOOH) layer was rationally designed and grown on Fe₂O₃ to construct a S:FeOOH/Fe₂O₃ composite photoanode. The obtained S:FeOOH/Fe₂O₃ photoanodes were fully characterized. The surface injection efficiency for Fe₂O₃ was then significantly increased with a high η_surface value of 92.8%, which increases to 2.98 times for Fe₂O₃ and 2.16 times for FeOOH/Fe₂O₃, respectively. With 2.43 mA cm^‒2 at 1.23 V, the optimized S:FeOOH/Fe₂O₃ photoanode was entrusted with a higher photocurrent density. The onset potential for S:FeOOH/Fe₂O₃ cathodically shifts 70 mV over Fe₂O₃. The improved PEC performance suggests that the S:FeOOH layer acts as ultrafast transport channels for holes at the photoanode/electrolyte interface, suppressing surface charge recombination. A Z-scheme band alignment between Fe₂O₃ and S:FeOOH was deduced from the UV–Vis and UPS spectra to promote charge transfer. This method provides an alternative for the construction of photoanodes with enhanced PEC water splitting performance. Full article

This study focuses on the nameplate of Vila D. Bosco, a modern building in Macau from the time of Portuguese rule, and looks at the types of metal materials and surface coatings used, as well as how they corrode due to the tropical marine climate affecting the building’s metal parts. The study uses different techniques, such as X-ray fluorescence spectroscopy (XRF), scanning electron microscopy/energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), attenuated total internal reflectance Fourier transform infrared spectroscopy (ATR-FTIR), and cross-sectional microscopic analysis, to carefully look at the metal, corrosion products, and coating of the nameplate. The results show that (1) the nameplate matrix is a resulfurized steel with a high sulfur content (Fe up to 97.3% and S up to 1.98%), and the sulfur element is evenly distributed inside, which is one of the internal factors that induce corrosion. (2) Rust is composed of polycrystalline iron oxides such as goethite (α-FeOOH), hematite (α-Fe₂O₃), and magnetite (Fe₃O₄) and has typical characteristics of atmospheric oxidation. (3) The white and yellow-green coatings on the nameplate are oil-modified alkyd resin paints, and the color pigments are TiO₂, PbCrO₄, etc. The surface layer of the letters is protected by a polyvinyl alcohol layer. The paint application process leads to differences in the thickness of the paint in different regions, which directly affects the anti-rust performance. The study reveals the deterioration mechanism of resulfurized steel components in a subtropical polluted environment and puts forward repair suggestions that consider both material compatibility and reversibility, providing a reference for the protection practice of modern and contemporary architectural metal heritage in Macau and even in similar geographical environments. Full article

Steel fiber-reinforced concrete structures designed for marine environments can become compromised by the ingress of water and ions. Water and ion transport through the pores between steel fibers and concrete gels significantly affects the durability of such structures, but the mechanisms of this transport are not sufficiently understood. Reported here is a molecular dynamics-based investigation of the transport of water, NaCl, Na₂SO₄, and mixed solutions of NaCl and Na₂SO₄ through γ–FeOOH/CSH pores. The effect of pore width on the capillary transport of NaCl + Na₂SO₄ solutions was also investigated and reported. It is shown that the depth of water penetration in NaCl solution increases parabolically with time. It is further shown that the CSH surface forms bonds with different ions to form Na–O_CSH, Cl–Ca_CSH, and S–Ca_CSH compounds, which results in reduced rates of solution transport. The mixed NaCl + Na₂SO₄ solution was found to have the lowest transport rate. A reduction in pore width was found to reduce the transport rate of water molecules and diminish the transport of ions. In pores smaller than 2.5 nm in width, the immobilized ions aggregate into clusters, occupying pore inlets and blocking more ions from entering the channels. Compared with the matrix on both sides, solutions are transported significantly faster along the CSH side than along the γ–FeOOH side, indicating that the addition of steel fibers can effectively slow down the transport of water molecules and ions in concrete. These data on the difference in the transport of solutions along the two sides of the matrix may provide molecular-level insights to support studies on the durability of concrete materials. Full article

Developing high-performance oxygen evolution reaction (OER) electrocatalysts remains a critical challenge for sustainable hydrogen production via water electrolysis. Herein, we present a self-supported atomic iridium-decorated FeOOH nanostructure on iron foam (Ir-FeOOH/IF) by a facile impregnation reduction method. The self-supported Ir-FeOOH/IF electrode integrates the high electrical conductivity and outstanding mass transfer performance of IF. The FeOOH features abundant active sites, while the Ir modification regulated the electronic structure of FeOOH. As a result, the as-prepared Ir-FeOOH/IF catalyst (with the optimized synthesis time) achieves a low overpotential of 145 and 284 mV at current densities of 0.1 and 1 A cm⁻², respectively, and exhibits excellent long-term catalytic stability for 135 h at 0.1 A cm⁻² in a 1 M KOH solution. This work provides a new strategy for the design of low-cost and highly stable OER electrocatalysts. Full article

Passive films that form on Alloy 600 and Alloy 690 during four hours in simulated Primary Water (PW) of Pressurized Water Nuclear Reactors (PWRs) at 320 °C were investigated by in situ surface-enhanced Raman spectroscopy (SERS). Similar tests conducted on unalloyed nickel, unalloyed chromium, and laboratory alloys of Ni-10Cr, Ni-20Cr, Ni-5Cr-8Fe, and Ni-10Cr-8Fe aided in assigning the peaks in the surface-enhanced Raman (SER) spectra of the passive films of Alloy 600 and Alloy 690. SERS indicates an inner layer (IL) of Cr₂O₃/CrOOH forms on both Alloy 600 and Alloy 690 and that Alloy 690’s IL was more protective against corrosion due to its greater resistance to ion transport. The outer layer (OL) of Alloy 600 consists of NiO and spinels, FeCr₂O₄—M(Cr,Fe)₂O₄. The OL of Alloy 690 contains no spinel. A comparison of SER spectra in 320 °C PWR PW to the spectra following cooling down to room temperature and after exposure to air indicates some differences between in situ films and ex situ films. Full article

A facile low temperature hydrothermal-calcination approach was developed for the fabrication of β-FeOOH nanorods (NRs) and hollow-structure α-Fe₂O₃ magnetic nanorods (MNRs), and the products were characterized using SEM, TEM, XRD and VSM techniques. To achieve smaller-sized β-FeOOH NRs, the effects of Fe³⁺ concentration, the volume ratio of ethanol to water in solution, hydrothermal temperature, and hydrothermal time on the structure of the precursors were systematically investigated, and the nanorods with an average length 104 nm and diameter 36 nm were fabricated at hydrothermal temperature of 100 °C for 2 h using 0.15 M ferric chloride hexahydrate in 50% ethanol solution. Subsequently, the hollow-structure α-Fe₂O₃ MNRs with an average length of 67 nm, diameter of 20 nm, and thickness of 5 nm were successfully obtained via the calcination process at 400 °C for 2.5 h for versatile applications. Full article