Search Results (3,239)

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

CO₂ methanation with renewable hydrogen is a promising strategy for carbon valorization and synthetic natural gas (SNG) production. However, the molecular mechanisms behind catalyst-dependent adsorption and mass transport in zeolite-confined spaces are still not fully elucidated. Herein, we performed comparative molecular simulations on HZSM-5, Ni/ZSM-5 and Ru/ZSM-5 by combining density functional theory (DFT), grand canonical Monte Carlo (GCMC) and molecular dynamics (MD) methods, aiming to clarify the thermodynamic and mass transport mechanisms of reactant enrichment and product desorption in CO₂ methanation. The electronic structures of the three systems were systematically evaluated via Mulliken charge analysis, differential charge density mapping, and frontier molecular orbital calculations. We further quantified the adsorption thermodynamics and diffusion kinetics of reactants and products, focusing specifically on the effects of temperature and framework Si/Al ratio for Ni/ZSM-5. The results show that Ni doping greatly modulates the local electronic environment of the ZSM-5 framework, enhancing the adsorption of CO₂ (−121.9 kJ·mol⁻¹) and H₂ (−81.6 kJ·mol⁻¹) and weakening the adsorption of CH₄ and H₂O. A higher Si/Al ratio reduces CO₂ adsorption capacity, while elevated temperatures inhibit reactant adsorption and lower the diffusion selectivity of CH₄. This demonstrates that moderately low temperatures and moderate Si/Al ratios can optimize the adsorption and diffusion behaviors of reactants and products. This work provides molecular-level insights into the adsorption and diffusion behaviors of Ni/ZSM-5 and offers theoretical references for the rational development of high-performance CO₂ methanation catalysts. Full article

Nanostructured catalysts have become a core component of energy conversion in electrocatalysis and photocatalysis; however, successfully translating their performance from laboratory scale to industrial applications remains a long-standing challenge. This paper provides a critical assessment of the field, systematically tracing the entire development trajectory from catalyst design to practical application. We focus on five major classes of catalysts—monometallic catalysts, bimetallic/multimetallic alloy catalysts, metal compound catalysts, carbon-based composite catalysts, and single-atom catalysts—and explore synthetic strategies for achieving precise structural control, including hydrothermal/solvothermal methods, electrodeposition, template-assisted and MOF-derived syntheses, high-temperature pyrolysis, and post-treatment defect engineering. This paper delves into the mechanisms and performance descriptors governing the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), oxygen reduction reaction (ORR), urea oxidation, photocatalytic water splitting, and CO₂ reduction. Based on the above analysis, this paper lays the mechanistic foundation for five core strategies to improve catalyst performance: morphology control, elemental doping, heterostructure and interface engineering, defect and vacancy engineering, and support modification. Furthermore, this paper provides an in-depth evaluation of the applications of these catalysts in water splitting, CO₂ valorization, fuel cells, metal–air batteries, and energy-saving electrolysis, with a particular focus on earth-abundant alternatives to precious metals. We argue that in many well-studied reactions, intrinsic activity may no longer be the primary bottleneck restricting their development; instead, the core challenge now lies in maintaining excellent catalytic performance under harsh and industrially relevant conditions, especially under high-current densities, impurity-containing feed systems, and long-term operating conditions. In response to this shift in research focus, this paper clearly identifies the key obstacles hindering the industrial application of catalysts and proposes practical directions for future research. Full article

Developing cost-effective alternatives to platinum-based catalysts remains paramount for commercializing anion exchange membrane fuel cells (AEMFCs). We report a metal-free nitrogen-doped carbon catalyst derived from a rationally designed polyurea–polyimine copolymer that outperforms commercial 20 wt% Pt/C in superior relative durability and methanol tolerance. Strategic integration of polyurea’s pore-forming capability with polyimine’s thermal stability enabled the synthesis of a catalyst (NC-1000N) featuring ultrahigh surface area (1276.5 m² g⁻¹), optimal nitrogen speciation (20.5% pyridinic-N, 45.3% graphitic-N), and enhanced graphitization, which improves the electrical conductivity of catalysts. NC-1000N exhibited exceptional oxygen reduction performance with an onset potential of 0.96 V, almost four-electron selectivity (n = 3.87), a medium Tafel slope (105 mV dec⁻¹), and minimal charge transfer resistance (46.74 Ω). When evaluated in single-cell AEMFCs, NC-1000N delivered a peak power density of 372.1 mW cm⁻², which is 26% higher than Pt/C at equivalent loading, while demonstrating superior stability (94.8% retention after 7 h) and complete methanol tolerance. Systematic pyrolysis temperature optimization (800–1000 °C) revealed critical structure–property relationships governing catalyst evolution from disordered precursor to highly graphitic, nitrogen-enriched carbon with precisely engineered active sites. This work establishes polymer-derived carbons and provides design principles for scalable synthesis of high-performance metal-free electrocatalysts for sustainable energy conversion technologies. Full article

The composition of the surface, optical response, and size of the carbon dots synthesized from Valencia orange peels (Citrus sinensis L. Osbeck) were studied. The peels used in the hydrothermal synthesis were at three ripeness stages, and the synthesis was carried out at 220 °C and 3 MPa. Infrared spectroscopy results showed that carbon dots synthesized from the peels of unripe oranges are functionalized with oxygenated groups, and the carbonization process was effective. Instead, carbon dots obtained from peels of ripe oranges exhibit a nitrogen-functionalized surface. These results were confirmed by the bond-breakdown analysis in photoelectron spectroscopy. Additionally, the self-doped surface modified the optical response of the carbon dots, exhibiting an enhancement of the absorption band located at 283 nm corresponding to the contribution from n-π* transitions in nitrogen. Also, the excitation and emission wavelengths present a red shift for the ripe peels. Based on the above and the transmission electron microscopy results, it is concluded that the emission mechanism is associated with surface states and not particle size. Statistical analysis yielded an average size of less than 10 nm, regardless of the orange peels’ ripeness stage. It was observed that the CDs-N3 sample has more crystalline nuclei, which is justified because ripe peels follow a shorter carbonization pathway. Full article

High-entropy alloy (HEA) coatings exhibit enhanced chemical stability when doped with carbon, primarily due to the strong bonding between carbon and transition metals. Typical transition metals used in these coatings include Cr, Fe, Co, Ni, Cu, Ti, V, W, Nb, Ta, and Zr. Owing to their excellent chemical stability, HEA coatings are widely employed to protect component surfaces operating in highly corrosive environments. Against this backdrop, the present study investigates the effect of carbon doping introduced via methane gas flow during the physical vapor deposition of TiAlTaZrNb HEA coatings on corrosion resistance. The morphology and structure of the coatings were analyzed by field emission scanning electron microscopy, X-ray diffraction, and Raman spectroscopy. Corrosion protection and coating resistance were assessed through potentiodynamic polarization and electrochemical impedance spectroscopy. While increasing the methane flow resulted in an approximately 34% reduction in coating thickness, the overall coating resistance increased by one order of magnitude, reaching a maximum at a methane flow rate of 9 sccm, corresponding to the carbon solubility limit. This improvement was evidenced by a decrease in the corrosion rate from 8.02 × 10⁻² mm y⁻¹ for the uncoated H13 steel to 8.00 × 10⁻⁴ mm y⁻¹ for the HEA-coated samples. However, at higher methane flow rates, carbon precipitation and the formation of parallel microcracks contributed to an increase in corrosion rate. Full article

Transition-metal sulfides are promising electrode materials for high-performance supercapacitors but are often limited by poor conductivity, particle agglomeration, and insufficient active sites. Herein, Co-doped NiS₂ with tunable sulfur vacancies was directly grown on flexible carbon cloth via a facile one-step solvothermal method by systematically controlling sulfur source ratio, Ni:Co ratio, temperature, and reaction time. Structural analyses reveal that the optimized conditions of S:(Ni + Co) = 3:1, Ni:Co = 2:1, 160 °C, and 15 h promote the formation of phase-pure Co-doped NiS₂ hierarchical microspheres with enhanced crystallinity and abundant active sites from the synergistic interaction between Ni and Co. Consequently, the optimized electrode delivers an impressive capacitance of 1296 F g⁻¹ at a current density of 1 A g⁻¹, along with excellent rate performance, retaining more than 88% of its capacitance after 1500 charge/discharge cycles at current densities ranging from 2 to 20 A g⁻¹. This work highlights the critical role of synthesis parameter engineering in regulating defect chemistry, structure, and electrochemical performance in advanced energy storage applications. Full article

Carbon aerogels possess continuous three-dimensional conductive networks, hierarchical pore architectures, and tunable surface chemistry. These structural characteristics make them suitable electrode materials for alkali-metal-ion batteries. This review examines the controlled synthesis and heteroatom doping of carbon aerogels. The discussion links framework construction, electronic-structure modulation, and storage mechanism matching with their electrochemical behavior. The rational design of carbon aerogels should move beyond the simple pursuit of high specific surface area or high dopant content. Effective electrodes require the coordinated regulation of pore architecture, conductive continuity, heteroatom-doped sites, and ion-storage pathways. The current application status of carbon aerogels in alkali-metal-ion batteries is also analyzed from an industrial perspective. A mechanism-oriented and application-oriented framework is therefore required to translate carbon aerogel-based electrodes from structural optimization to a practical battery. Full article

This study reports the preparation of a nanocomposite using a black cumin surface as a carbon framework on which zinc oxide-doped manganese ferrite nanoparticles were deposited and grown. A simple precipitation method was used to prepare the nanocomposite. The resulting composite was characterized using various characterization analyses such as FTIR, XRD, EDX, SEM, TEM, and TGA. The composite surface was highly conformed with functional groups, and the nanocomposite was formed due to electrostatic and non-electrostatic interactions between the carbon framework and the nanoparticles. X-ray analysis revealed a crystalline structure with crystal sizes up to 45 nm. Microscopic images revealed the surface morphology, confirming the irregular distribution of particles within the composite. The resulting composite material was used for adsorption application. The composite material was tested for the removal of Congo red dye from water. It was found that under optimal conditions, a dose of 2 g per liter of absorbent removed nearly 100% of dye from a 10 mL volume of 10 mg per liter Congo red solution within 90 min and 7 pH. A monolayer adsorption was confirmed by the isotherm analysis. The monolayer adsorption capacity for the present study was ~13.0 mg per gram. The adsorption kinetics suggested the fitting of pseudo-second order. Based on the findings, it was concluded that the chemical mechanism was responsible for the present adsorption process. The regeneration study demonstrates the stability of current adsorbent up to two cycles only. This nanocomposite is the first of its kind which promotes the creation of nanocomposites in the future by using natural materials and reduces the dependency on activated carbon. Full article

Titanium-doped diamond-like carbon (DLC:Ti) films were deposited by magnetron sputtering. The effects of Ti concentration on the microstructure, phase composition and piezoresistive properties of the films were systematically investigated. The surface morphology, crystal structure and chemical bonding states of the samples were characterized using SEM, XRD and XPS. The piezoresistive properties were then assessed by monitoring the resistance change in the thin films using a precision resistance meter under controlled external stimulation. The results demonstrate that the sp²/sp³ ratio of the DLC:Ti films increases with rising Ti concentration, and both Ti–C and Ti–Ti chemical bonds are formed within the films. An excessive β-Ti phase forms when the Ti concentration exceeds 39.7 at.%. The electrical resistance of DLC:Ti films decreases linearly as the applied normal stress increases from 0 to 35 MPa, with a maximum piezoresistive coefficient of −9.0 × 10⁻² GPa⁻¹ achieved for the film with a Ti doping concentration of 12.9 at.%. One hundred cyclic loading–unloading tests induce the structural transition from sp³ to sp², resulting in the graphitization of DLC:Ti films. In addition, external stress facilitates the fracture of Ti–C bonds and the relaxation of residual stress in the DLC:Ti films; the β- to α-Ti phase transformation induced by external loading is also observed in the films. Cyclic piezoresistive tests reveal that the piezoresistive stability of the DLC:Ti films is enhanced with increasing Ti concentration, which is attributed to the increased formation of Ti–C bonds in the films. Full article

The development of sustainable electrocatalysts for clean energy by modifying biomass-derived activated carbon with nitrogen and transition metals is presented. Activated carbon (AWC) material was obtained using alder wood char as a precursor, while nitrogen and cobalt or copper nanoparticles were incorporated with the aim of creating efficient materials for hydrazine oxidation (HzOR) and direct hydrazine–hydrogen peroxide fuel cells (DHHPFC, N₂H₄–H₂O₂). The composition, structure, and surface morphology of the created materials were examined using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The activity of the AWC, AWC–Co–N, and AWC–Cu–N catalysts for HzOR was investigated using cyclic voltammetry (CV) and linear sweep voltammetry (LSV). N₂H₄–H₂O₂ fuel-cell tests were performed by applying the catalysts as both the anode and cathode. It was found that all materials retained a hierarchical porous carbon framework, while metal incorporation altered surface compactness. Cobalt doping produced well-dispersed Co nanoparticles and abundant Co–N–C coordination sites, whereas Cu introduction resulted in moderately compact structures with uniformly distributed Cu-based nanoparticles. Electrochemical measurements demonstrated that both metal dopants enhanced HzOR activity, with the catalytic performance following the order of AWC–Co–N > AWC–Cu–N > AWC. Fuel-cell testing further confirmed this trend: AWC–Co–N achieved the highest maximum power density (30.4 mW cm⁻²), outperforming AWC–Cu–N (17.7 mW cm⁻²). These results identify AWC–Co–N as a highly effective bifunctional electrocatalyst for DHHPFCs. Full article

To integrate high chromaticity with visible-light-driven antibacterial functionality in yellow inorganic pigments, carbon-doped BiVO₄ (C-BiVO₄) pigments were synthesized via a one-step self-propagating combustion synthesis (SCS) using citric acid as a fuel and carbon source. The effects of citric acid dosage on phase composition, morphology, chromatic performance, and antibacterial activity were systematically investigated. The results indicate that carbon doping induces lattice expansion and oxygen vacancy formation, modulates the electronic band structure, and significantly suppresses photogenerated electron-hole recombination. At an optimal citric acid to BiVO₄ molar ratio of 1.2, the pigment exhibits excellent yellow chromaticity (b* = 79.71). Under visible-light irradiation, C-BiVO₄ achieves a methylene blue photodegradation rate of 96.63% and an E. coli inactivation efficiency of 99.99%, substantially outperforming undoped BiVO₄. Moreover, the C-BiVO₄ yellow pigment shows good dispersibility and thermal stability in PMMA and glass matrices and passes acute skin irritation and dermal toxicity tests, confirming its low toxicity and non-irritating nature. This work provides a new strategy for developing environmentally friendly inorganic pigments that combine high chromaticity with photocatalytic antibacterial functionality. Full article

A nitrogen/sulfur co-doped reduced graphene oxide (N,S-RGO) material was rationally prepared via a modified Hummers method followed by microwave-assisted reduction. The resulting material was uniformly deposited onto a glassy carbon electrode (GCE) to fabricate an electrochemical sensor for nitrobenzene (NB) detection. The prepared N,S-RGO material was characterized in detail using Fourier-transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy, confirming the successful incorporation of heteroatoms. Furthermore, electrochemical studies, including cyclic voltammetry (CV) and linear sweep voltammetry (LSV), revealed the enhanced electrical conductivity of the material. The fabricated N,S-RGO/GCE sensor exhibited remarkable electroanalytical performance, achieving a low detection limit (LOD) of 7 nM within a linear concentration range of 0.05 to 147 µM. The enhanced sensing performance is attributed to the synergistic effect of nitrogen and sulfur doping, which improves electron transfer kinetics and abundant active sites for NB reduction. Furthermore, the sensor demonstrated outstanding selectivity toward NB in the presence of common interfering substances. Its practical applicability was confirmed through the successful detection of NB in environmental water samples, yielding convincing recovery rates. These results highlight the potential of the N,S-RGO/GCE platform as an efficient and reliable electrochemical sensor for environmental monitoring of NB contamination. Full article

Biomass-derived carbons are promising sustainable anode materials for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) because biomass is renewable, abundant, low-cost, and naturally diverse in composition and morphology. Lignocellulosic frameworks, intrinsic heteroatoms, and biomass-derived inorganic species can be converted through carbonization, activation, graphitization, and doping into carbon architectures with tunable porosity, carbon ordering, and surface chemistry. This review first summarizes the compositional and structural features of biomass precursors and explains how processing conditions convert them into carbon frameworks. Recent advances in biomass-derived carbon anodes are then discussed by comparing the distinct design requirements for LIBs and SIBs. For LIBs, accessible surface area, hierarchical porosity, heteroatom-derived active sites, and improved electronic conductivity are generally beneficial for enhancing Li⁺ storage and rate capability. In contrast, SIB hard carbons require controlled surface exposure, expanded turbostratic spacing, and closed or latent pores to improve Na⁺ storage reversibility and initial Coulombic efficiency. These comparisons emphasize that biomass-derived carbon anodes should be designed according to system-specific storage mechanisms rather than a universal carbon design strategy. Full article

Dry reforming of methane (DRM) is an attractive route for H₂ production and simultaneous CO₂ utilization, but its practical implementation is limited by catalyst deactivation. This study experimentally investigates the catalytic performance of Ni/Al₂O₃ and Gd-doped ceria-promoted Ni/GDC–Al₂O₃ catalysts for DRM in a fixed-bed quartz reactor over 400–800 °C at gas residence times of 0.1 s and 0.4 s. Increasing temperature and residence time enhanced CH₄ and CO₂ conversion as well as H₂ and CO yields for both catalysts. The GDC-promoted catalyst exhibited markedly improved activity, achieving conversions and product yields at 0.1 s comparable to those of Ni/Al₂O₃ at 0.4 s and reaching complete CH₄ conversion at about 650 °C, approximately 100 °C lower than the Ni/Al₂O₃ catalyst. Long-term testing at 650 °C showed stable catalytic behavior of the Ni/GDC–Al₂O₃ catalyst, while operational observations qualitatively suggested the absence of significant carbon deposition, consistent with equilibrium calculations. Full article