Search Results (493)

Sustainable water remediation requires catalytic strategies that remove contaminants efficiently while reducing chemical input, byproduct formation, and ecological disturbance. Conventional radical-dominated advanced oxidation processes can rapidly degrade pollutants, but their reliance on high oxidant dosages and freely diffusing reactive oxygen species often causes matrix quenching, non-selective oxidation, low oxidant utilization, and potential ecological risks. Mild interfacial catalysis provides a materials-chemistry strategy to regulate oxidative intensity and direct contaminant transformation under environmentally relevant conditions. In this review, mild catalysts are defined by pathway-selective, interfacially confined, and environmentally compatible oxidation rather than by low dosage alone. Representative non-radical or low-intensity pathways, including singlet oxygen generation, surface-mediated electron transfer, high-valent metal–oxo species, and direct oxidative transfer processes, are discussed in relation to active-site structure, oxidant utilization, matrix tolerance, and byproduct control. We further summarize how coordination environments, defect chemistry, heteroatom configurations, nanoconfinement, and immobilized interfaces regulate reactive-species formation and interfacial charge transfer. Key material platforms, including single-atom catalysts, heteroatom-doped carbons, defect-engineered oxides, catalytic membranes, hydrogels, and floating or immobilized composites, are evaluated from mechanistic and application-oriented perspectives. Finally, catalyst regeneration, cost, microbial community responses, algae–bacteria balance, ecotoxicity, and long-term safety are discussed to guide sustainable aquatic ecosystem restoration. Full article

Transition-metal phosphides are promising non-noble-metal electrocatalysts for alkaline hydrogen evolution, yet further improving their performance remains challenging. In this work, a Co-doped nanoporous Fe₃P self-supported electrode was fabricated by vacuum high-frequency induction and melt spinning of Fe₇₅Co₅P₂₀ precursor alloys, followed by electrochemical dealloying. Nanoporous Fe₃P prepared from Fe₈₀P₂₀ was used as the reference. Structural analyses show that dealloying selectively removes the α-Fe phase while preserving the Fe₃P framework, resulting in a three-dimensional nanoporous architecture. XPS results further confirm successful Co incorporation and reveal that Co doping modifies the local chemical environment of Fe and P. Benefiting from the combined effects of Co incorporation and the nanoporous structure, np-Co-Fe₃P exhibits significantly improved HER performance in 1.0 M KOH, requiring only 70 mV to reach 10 mA cm⁻², much lower than that of np-Fe₃P (199 mV). In addition, np-Co-Fe₃P shows a smaller Tafel slope of 94 mV dec⁻¹, lower charge-transfer resistance, and a larger double-layer capacitance of 109.4 mF cm⁻². This work demonstrates an effective strategy for enhancing the alkaline HER performance of Fe-based phosphides through the combination of Co incorporation and dealloying-derived nanoporous architecture. Full article

The development of highly efficient, stable, and cost-effective non-precious metal electrocatalysts to replace conventional platinum-based materials holds profound significance for accelerating the commercialization of advanced energy conversion devices, such as zinc–air batteries (ZABs). Herein, we propose a facile and highly efficient strategy to prepare a defect-rich, highly active nitrogen-doped porous carbon-based electrocatalyst (denoted U-Fe-N-C, urea-assisted iron–nitrogen–carbon material), via high-temperature co-pyrolysis of heme with urea. Our results demonstrate that urea not only serves as an excellent nitrogen source during pyrolysis, introducing abundant topological defects and heteroatom doping sites, but also induces the carbon substrate to form a hierarchical sponge-like porous structure with a high specific surface area. This unique microenvironment effectively prevents the agglomeration of iron species at high temperatures, achieving enhanced dispersion of iron species stabilized within the nitrogen-rich carbon matrix. Electrochemical evaluations reveal that under the optimal synthesis conditions (a precursor mass ratio of 1:3, calcination at 900 °C), U-Fe-N-C exhibits excellent oxygen reduction reaction (ORR) catalytic performance, delivering a half-wave potential of 0.731 V vs. RHE, and shows long-term operational durability that significantly surpasses that of commercial Pt/C. Furthermore, liquid rechargeable zinc–air batteries assembled with U-Fe-N-C as the air cathode deliver remarkable cycling stability, operating for up to 270 h of charge–discharge cycling without noticeable performance degradation. This study not only provides useful insights into the mechanisms of pore formation and assistance but also offers a practical perspective for the rational design and scalable synthesis of high-performance metal–nitrogen–carbon (M-N-C) electrocatalysts. Full article

The emergence and the growing influence of contaminants in wastewater has driven the development of advanced and efficient treatment technologies. Catalysts based on biochar have become a promising material because of their cheapness, adjustable physicochemical characteristics, and environmental compatibility. This study comprehensively reviews recent developments in biochar-based catalytic processes to treat wastewater with an emphasis on AOPs and photocatalysis. The main categories of catalysts including metal-loaded biochar, heteroatom-doped biochar, biochar-supported semiconductor composites, and magnetic biochar are extensively discussed with regard to their synthesis, structure, and performance in the elimination of organic, emerging, and heavy metal contaminants. Emphasis is placed on catalytic reactions, radical (•OH, SO₄•⁻) and non-radical (singlet oxygen and electron transfer) reactions, as well as the effect of functional groups on the surface, defects, and electronic features in the control of activity. Engineered biochar has a better performance in charge separation, reactive species generation, and synergistic interactions between adsorption and degradation. Nevertheless, there are issues such as heterogeneity in biochar properties, insufficient understanding of structure–activity interactions, catalyst stability, and the absence of studies of biochar under real wastewater conditions. The future perspectives focus on rational catalyst design, integration of processes, and scaling up to practical applications. Overall, biochar-based catalysts have emerged as a sustainable platform for advanced wastewater treatment, but additional studies are needed to enable their large-scale use. Full article

Direct emission of low-concentration methane not only aggravates global warming but also causes serious energy waste. Catalytic combustion is considered an effective strategy for methane abatement because it enables methane oxidation at relatively low temperatures. In this work, a series of Mn–Ce–Cu/γ-Al₂O₃ catalysts with different nominal Mn/Ce ratios were prepared by the incipient wetness impregnation method and applied to low-concentration methane catalytic combustion. The results showed that Mn–Ce co-modification significantly improved the activity of Cu/γ-Al₂O₃ catalysts, and the catalytic performance strongly depended on the Mn/Ce ratio. Among all samples, 7Mn-3Ce-10Cu exhibited the best activity, with the temperatures required for 10%, 50% and 90% methane conversion (T₁₀, T₅₀ and T₉₀) of 380.8, 427.3 and 478.7 °C, respectively. Apparent activation energy (E_a) analysis further showed that 7Mn-3Ce-10Cu possessed the lowest E_a value of 83.81 kJ mol⁻¹, indicating that the optimized Mn/Ce ratio effectively lowered the apparent kinetic barrier for methane oxidation. X-ray diffraction (XRD), transmission electron microscopy (TEM) and nitrogen (N₂) adsorption–desorption results suggested that Mn–Ce co-modification changed the phase composition, improved the dispersion state of active oxide species and generated a more favorable pore structure for reactant diffusion. Oxygen temperature-programmed desorption (O₂-TPD) and X-ray photoelectron spectroscopy (XPS) results further indicated that the enhanced activity of 7Mn-3Ce-10Cu was closely associated with improved oxygen desorption behavior, a higher proportion of surface oxygen species and favorable surface redox characteristics of Cu, Mn and Ce species. Moreover, 7Mn-3Ce-10Cu maintained methane conversion above 90% during a 50 h stability test at 500 °C, and the inhibition caused by 5% H₂O was partially reversible. These results demonstrate that Mn–Ce co-modification is an effective strategy for improving low-cost Cu-based catalysts for low-concentration methane combustion. Full article

The oxygen reduction reaction (ORR) is a key process in electrochemical energy conversion technologies such as fuel cells and metal–air batteries; however, its sluggish kinetics and reliance on precious metal catalysts limit large-scale application. This review provides a comprehensive overview of recent advances in non-precious nanoscale electrocatalysts for ORR in alkaline media. Particular emphasis is placed on reaction mechanisms, including dominant pathways, kinetics, and key intermediates, as well as the advantages of alkaline electrolytes over acidic systems. The performance of various catalyst classes is systematically discussed, including transition metal-based materials (Fe, Co, Zn, Cu, and bimetallic systems) and metal-free carbon-based electrocatalysts. Special attention is given to heteroatom-doped carbon materials, carbon nanostructures, and emerging hybrid systems such as MXene-based composites. Comparative analysis highlights the relationship between catalyst composition, structure, and electrochemical performance metrics, including half-wave potential, onset potential, Tafel slope, number of electron transfer, and operational stability. Overall, non-precious catalysts demonstrate promising activity and durability, approaching that of noble metals under alkaline conditions. The insights summarized in this review guide the rational design of efficient, cost-effective ORR electrocatalysts and support the development of sustainable energy technologies. Full article

This study provides a rigorous analysis of the phase stability, mechanical behavior, and surface integrity of a non-equiatomic (FeCoNiCr)₈₅Ga₁₅ high-entropy alloy (HEA). By transitioning from the conventional equiatomic design to a gallium-doped 3d-transition metal matrix, we explore the interplay between lattice distortion and phase separation. Synthesized via vacuum arc melting, the as-cast alloy exhibits a non-homogeneous dendritic morphology consisting of a Cr-Fe-Co rich face-centered cubic (FCC) matrix and Ni-Ga rich body-centered cubic (BCC) interdendritic regions. While global thermodynamic criteria (δ = 3.65, ΔH_mix = −9.28 kJ/mol, and Ω = 2.23) favor single-phase solid solution stability, the Valence Electron Concentration (VEC = 7.46) precisely forecasts this dual-phase structure. Following low-temperature annealing at 250 °C for 24 h, high lattice strain energy drives a significant morphological transformation where the continuous interdendritic network resolves into discrete, phase-separated B2/BCC “islands”. Mechanical and tribological characterizations reveal that this low-temperature thermal activation triggers precipitate hardening; the macro-hardness increases from 146 ± 11 HB to 153 ± 7.5 HB and the micro-hardness rises from 186 ± 4 HV_0.5 to 206 ± 17.5 HV_0.5, yielding enhanced resistance to oxidation-delamination wear. However, electrochemical evaluation in a 3.5 wt.% NaCl solution highlights a fundamental trade-off: the formation of localized galvanic micro-cells between the phase-separated islands and the matrix causes the corrosion current density (i_corr) to increase from ≈10⁻⁹ A/cm² in the as-cast state to ≈10⁻⁶ A/cm² post-heat treatment, accompanied by a heightened susceptibility to localized pitting. These findings elucidate the primary role of electronic structure and minor p-block additions in regulating the lifecycle performance of transition metal HEAs under extreme conditions. Full article

Understanding lithium distribution and transport within Li-ion battery components is critical in improving battery longevity, safety and performance. This study investigates lithium concentration profiles across the interface of an aluminum-doped Li₇La₃Zr₂O₁₂ (Al-LLZO) solid electrolyte and a lithium metal anode using Nuclear Reaction Analysis (NRA), a non-destructive depth-profiling technique. The Al-LLZO electrolyte was synthesized via electrospinning, producing nanofibers, which were subsequently sintered into pellets of average thickness 380 µm. These pellets were integrated into a Li|Al-LLZO|NMC-111 half-cell and cycled at 0.1 C for 1, 3, and 10 cycles, indicating pronounced lithium accumulation at the electrolyte–anode interface. Using NRA, this study provided a clear pathway for better understanding lithium transport and interfacial behavior, by quantitatively measuring the lithium distribution at the Al-LLZO electrolyte–electrode interface, and to look at the changes at this interface over the battery cycles. Full article

The search for efficient photocatalysts for sustainable hydrogen production has driven growing interest in barium titanate (BaTiO₃)-based materials, particularly through polymorph control, surface engineering, and nonmetal and transition-metal doping. In this work, we provide an atomic-scale understanding of structural modifications in nitrogen-, fluorine-, and rhodium-doped BaTiO₃ using Density Functional Theory (DFT), as well as pristine and fluorine-substituted BaTiO₃ using reactive force-field molecular dynamics (ReaxFF-MD) simulations. DFT results for pristine and doped tetragonal BaTiO₃, as well as pristine hexagonal BaTiO₃, reveal that nitrogen and rhodium substitutions enhance the covalent character of Ti-N and Rh-O bonds and promote the redistribution of electron density, as evidenced by noncovalent interaction (NCI) and critical point (QTAIM) analyses, whereas fluorine substitution leads to more ionic Ti-F bonding. ReaxFF-MD simulations of pristine and fluorine-substituted BaTiO₃ in contact with water molecules demonstrate that fluorine substitution suppresses interfacial O-H bond formation and promotes ordered molecular hydration layers near titanium sites, as reflected in bond statistics and radial distribution functions. This study provides molecular insights into the role of N, F, and Rh doping in BaTiO₃ using DFT, and the role of fluorine doping in BaTiO₃ at the water–solid interface using ReaxFF-MD simulations, demonstrating that this integrated computational approach provides a solid basis for the rational design of next-generation materials for energy-related applications. Direct calculations of photocatalytic activity, charge transfer rates, and ferroelectric polarization effects were not performed in this work and remain important directions for future study. Full article

Achieving efficient overall water splitting with non-precious metal catalysts remains a significant challenge due to the sluggish kinetics of both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). Herein, we report a nickel–iron bimetallic doped geopolymer electrocatalyst (Ni_0.9Fe_0.1-GP) fabricated via a one-step alkali activation method on 316L stainless steel. Structural characterizations reveal that Fe³⁺ incorporation alters the distribution of Na⁺ and Ni²⁺ within the geopolymer network and modulates the Ni electronic structure. Electrochemical measurements show that Ni_0.9Fe_0.1-GP delivers an HER overpotential of 332.42 mV and an OER overpotential of 227.31 mV at 10 mA cm⁻², outperforming Ni-GP and bare 316L SS. The practical operating voltage of Ni_0.9Fe_0.1-GP is 1.81 V, while the two-electrode electrolyzer delivers a comparable current density at 1.90 V (after accounting for uncompensated system resistances). Long-term stability tests demonstrate the superior durability of Ni_0.9Fe_0.1-GP during HER, OER, and overall water splitting. Mechanistic studies reveal the dual role of Fe³⁺: substantially increasing the electrochemical active surface area (ECSA) while modulating the Ni electronic structure, and improving structural stability through strong chemical anchoring within the geopolymer network. This work provides new insights into cost-effective bifunctional electrocatalysts and expands the application of geopolymers as functional catalytic supports for water splitting. Full article

Faced with a global energy crisis and ecological degradation, overall water splitting (OWS) is a pivotal approach for renewable energy conversion and storage. However, its industrial application is hindered by the high energy barriers/sluggish kinetics of the anodic oxygen evolution reaction (OER), as well as the scarcity of precious metal catalysts limiting large-scale deployment. Herein, a cobalt-based layered double hydroxide (Co-LDH) was used as the precursor, and a multi-strategy synergistic modification (hydrothermal synthesis, Fe doping, sulfurization, and external magnetic field magnetization) was applied to fabricate the Fe-Co₃S₄-MS-20 min electrocatalyst. This strategy establishes Fe-Co bimetallic synergistic active centers, and magnetic treatment modulates the electron configuration of Fe 3d orbitals without changing the material’s lattice spacing or morphology. Structural characterizations and electrochemical measurements were used to investigate the effects of combined modifications on the catalyst’s phase structure, morphology, electronic structure, and trifunctional catalytic performance toward the hydrogen evolution reaction (HER), OER, and urea oxidation reaction (UOR). The Fe-Co₃S₄-MS-20 min catalyst exhibits a larger electrochemical active surface area, lower charge transfer resistance, and smaller Tafel slope in 1 M KOH, it achieves overpotentials of 165 mV for HER (10 mA·cm⁻²) and 310 mV for OER (100 mA·cm⁻²), along with superior UOR performance and long-term stability. In situ impedance and Raman spectroscopy confirm that magnetization accelerates charge transfer and promotes in situ reconstruction. Synergistic multi-strategy regulation optimizes the electronic structure of active centers, reducing electrocatalytic energy barriers. This work provides new insights into designing high-performance non-precious metal electrocatalysts and offers experimental support for external magnetic field regulation in electrocatalyst modification. Full article

Carbon quantum dots (CQDs) exhibit multiple antibacterial mechanisms, making them more effective than conventional antibiotics, which typically act through a single mode of action. These mechanisms include membrane disruption, biofilm inhibition, reactive oxygen species (ROS) generation, and photodynamic (PDT) or photothermal (PTT) effects under light irradiation. Extensive research has been conducted to reinforce these mechanisms and improve the antibacterial performance of CQDs, aiming to reduce required CQD dosages and combat bacterial resistance. This review systematically summarizes structural and functional design strategies reported since 2020. We categorized these strategies into selecting antibacterial molecules as precursors, controlling particle size, surface modification, doping with non-metal and metal elements, and forming functional composites to enable light activation, synergetic effects, and multifunctionality. For each category, we provide representative CQD examples, in terms of their preparation, physicochemical properties contributing to antibacterial performance, and possible structure–activity relationships. Finally, the review highlights limitations and proposes future research directions for developing antibacterial CQDs for clinical translation. Full article

Rising global demand for safe, high-quality foods has accelerated the development of rapid, sensitive, and cost-effective analytical technologies for detecting harmful substances and quality markers. Electrochemical sensors have emerged as promising tools for food safety monitoring due to their high sensitivity, fast response, portability, and affordability compared with conventional laboratory methods. This review highlights recent advances in nanostructured electrochemical sensors for detecting key food analytes, including antioxidants, mycotoxins, allergens, and flavor compounds in diverse food matrices. It examines advanced nanomaterials such as metal oxides, MXenes, doped carbon nitrides, and noble metal-decorated graphene, which enhance sensor performance through improved surface area, conductivity, and electrocatalytic activity. Integrated with screen-printed or glassy carbon electrodes, these materials achieve ultra-low detection limits, wide linear ranges, and strong selectivity in complex food systems. The review also explores next-generation applications such as NFC-enabled smart packaging for continuous, non-invasive monitoring across the supply chain. Emerging trends in miniaturization, multiplex sensing, and artificial intelligence are discussed, along with key challenges in translating laboratory innovations into practical commercial solutions for global food safety. Full article

Cobalt oxide (Co₃O₄), a transition metal oxide with a cubic spinel structure, shows high potential in peroxymonosulfate (PMS) activation, while its catalytic efficiency is often limited by sluggish interfacial charge transfer. In this study, a chlorine-doped Co₃O₄ (Cl-Co₃O₄) was synthesized via a hydrothermal method for the degradation of bisphenol A (BPA) through PMS activation. Systematic characterizations and electrochemical tests demonstrated that chlorine doping could effectively modulate the surface electronic structure of the catalyst, significantly reducing the interfacial charge transfer resistance. Degradation performance evaluations revealed that, compared to pristine Co₃O₄, Cl-Co₃O₄ exhibited a significantly enhanced BPA degradation, achieving near-complete removal of BPA within 15 min under neutral to weakly alkaline conditions. The optimal operational parameters were determined as catalyst dosage of 0.20 g/L, PMS concentration of 0.10 mM and initial pH of 7.0–9.0, with the pseudo-first-order rate constant reaching 0.37 min⁻¹. High-concentration NO₃⁻ showed weak inhibition, while Cl⁻ showed moderate inhibition; 50 mM HCO₃⁻ drastically reduced the rate constant to 0.05 min⁻¹ and almost completely suppressed the reaction. Sulfate (SO₄•⁻) and superoxide (O₂•⁻) radicals were the primary reactive species in this system, explicitly excluding the role of the non-radical electron transfer pathway. Furthermore, three plausible BPA degradation pathways involving C-C bond cleavage, hydroxylation and C-O bond breakage were proposed with 19 intermediates identified. Ecotoxicological assessments based on ECOSAR verified that both acute and chronic toxicity of the intermediates to fish, daphnid and green algae decreased gradually, and the final small-molecule products exhibited significantly lower toxicity than the parent BPA. This study provides a novel strategy for enhancing the PMS activation performance of cobalt-based catalysts by modulating their electronic structures via halogen doping. Full article

The lithium battery recycling industry is developing rapidly, and the rapid oxidation and degradation of dimethyl carbonate (DMC) in the wastewater generated by this industry is of crucial importance. In this study, Fe and Cu dopants were controlled and the C-SiO₂ framework with porous structures was constructed to synthesize FeCuC-SiO₂ and C-SiO₂ catalysts. The former could achieve 91.65% of DMC degradation within 60 min through peroxymonosulfate (PMS) activation, and the degradation rate was increased to 4.44 times compared to C-SiO₂ without Fe and Cu doping. And under optimized conditions, a DMC degradation rate of 90.57% can be achieved within 10 min by FeCuC-SiO₂. The catalyst has good stability and the catalytic activity can be maintained during reuse process for five times with over 70% of DMC degradation rate, 58.9% of mineralization rate, and a relatively low amount of metal leaching. Moreover, the degradation rate can still remain above 70% with the existence of impurity anions, demonstrating a strong salt resistance. Hydroxyl radicals (OH^•), sulfate radicals (SO₄^•−), and ¹O₂ were found to dominant the reaction in the FeCuC-SiO₂-PMS system, which were involved in both free radical and non-free radical pathways and led to excellent catalytic oxidation performance and environmental adaptability. In general, a novel design for a Fenton-like catalyst was presented, providing a theoretical basis for the improvement of oxidation efficiency and the regulation of reaction pathways in Fenton-like reactions. Full article