Search Results (50)

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

To improve the low-carbon economic operation of integrated energy systems under wind power uncertainty, this paper develops an optimal scheduling model for an integrated energy system coupling oxygen-enriched combustion with hydrogen–ammonia–carbon utilization pathways. The proposed framework integrates oxygen-enriched combustion, electrolysis-based hydrogen production, methanation, hydrogen fuel cells, ammonia synthesis, urea synthesis, captured CO₂ utilization, reward–penalty ladder-type carbon trading, and IGDT-based wind power uncertainty scheduling. A deterministic scheduling model is first established to minimize the total operating cost, and Information Gap Decision Theory is then introduced to formulate risk-averse and opportunity-seeking scheduling strategies under wind power uncertainty. Simulation results show that, compared with the post-combustion carbon capture scenario and the conventional coal-fired scenario, the proposed system reduces the total operating cost by 3.37% and 8.03%, respectively, and reduces the wind curtailment cost by 40.2% and 57.0%, respectively. Compared with the post-combustion carbon capture scenario, carbon emissions are reduced by 17.7%. The hydrogen–ammonia–urea chain generates approximately 15.68 × 10⁴ CNY of urea revenue and improves carbon resource utilization. Under an IGDT deviation factor of 0.03, the risk-averse strategy increases the total operating cost by approximately 10.30 × 10⁴ CNY to enhance operational robustness, while the opportunity-seeking strategy reduces the total operating cost by approximately 10.30 × 10⁴ CNY and decreases carbon emissions by 19.6 t. These simulation results verify the effectiveness of the proposed scheduling framework under the designed case study. The proposed framework can improve the low-carbon economy, renewable energy accommodation, carbon resource utilization, and adaptability to wind power uncertainty of the studied integrated energy system. Full article

The growing demand for sustainable energy technologies has intensified interest in direct urea fuel cells as an environmentally friendly energy conversion system. In this work, a ternary NiCuZn electrocatalyst is synthesized via a single-step electrodeposition process, offering a rapid and scalable alternative to commonly used hydrothermal or multistep fabrication routes. Structural and compositional analyses (SEM, EDX) confirm the formation of coral-shaped particles of NiCuZn powders. Electrochemical evaluation in alkaline media demonstrates that powders of both tested variants exhibit clear anodic activity, with peak potentials in the range of 0.4–0.6 V_{vs Ag|AgCl (sat. KCl)}. Zinc presence was confirmed also after the process. Upon urea addition, a pronounced enhancement in anodic current density is observed. Notably, variant NiCuZn powder, which was produced using higher current density during electrodeposition, shows superior catalytic activity from approximately 0.4 V_{vs Ag|AgCl (sat. KCl)}, reaching a maximum of 10 mA/cm² near 0.75 V_{vs Ag|AgCl (sat. KCl)}, and stability, which are attributed to its highly homogeneous microstructure and dynamic surface activation mechanism uniquely by partial zinc leaching during operation. These findings demonstrate that electrodeposited NiCuZn systems can deliver competitive performance despite their structural simplicity, highlighting their potential as cost-effective and scalable anode materials for direct urea fuel cell applications. We address a critical bottleneck in fuel cell manufacturing by replacing time-intensive hydrothermal syntheses with a rapid, highly scalable electrodeposition method. Furthermore, the identification of zinc-leaching mechanisms provides crucial new insights into dynamic catalyst activation, moving beyond traditional, static anode designs. Full article

Direct urea–hydrogen peroxide fuel cells (DUHPFCs) are promising for sustainable power generation, but their performance is governed by highly nonlinear material and operating interactions. This study develops a machine-learning framework employing a multi-output artificial neural network (ANN) to predict cell voltage, power density (PD), and substrate-based energy efficiency (SEE) of DUHPFCs. The ANN exhibits excellent predictive accuracy, achieving coefficients of determination (R²) above 0.995 and normalized root mean square errors (NRMSE) below 1.75 × 10⁻² for all outputs. Model interpretability is enhanced by using Shapley additive explanations and partial dependence plots, which identify current density as the dominant factor affecting DUHPFC performance, followed by temperature and anolyte composition. The ANN is coupled with a multi-objective Pareto-search algorithm optimization (PAO) to resolve the trade-offs among competing performance metrics. Under different optimization objectives, a DUHPFC with an Ni_0.2Co_0.8/Ni-foam anode is predicted to achieve a maximum PD of 45.6 mW/cm² with a low SEE of 2.6% or a maximum SEE of 15.2% with a moderate PD of 40.9 mW/cm². Additionally, a balanced operating regime is identified, achieving a PD of 43.1 mW/cm² and an SEE of 13.9%. Overall, the proposed framework provides an effective decision-support tool for optimizing DUHPFC performance under competing objectives. Full article

Permeable reactive barrier (PRB) is an in situ remediation of contaminated sites mostly suitable for halogenated pollutants like halo-hydrocarbons reduced by zero-valent irons (ZVI) developed during early 1990’s. However, remediation of some nitrogen-pollutants like ammonia and urea is unsuccessful due to lack of reactants. Most recent advanced direct ammonia/urea fuel cells utilize indirect hydrogen within ammonia/urea molecules to generate electricity. Herein, a comprehensive study based on the chosen design, working principles, advantages and disadvantages of direct ammonia fuel cells for new approach of PRBs for denitrifying nitrogen-contaminant is summarized. Most surveys are carrying out in our laboratories and this work aims to review the most recent advances in ammonia fuel cells integrated with PRBs and demonstrates the proximity of this technology to future applications. Meanwhile, several challenges such as how to accumulate ammonia and urea in order to achieve satisfying energy recovery, oxidants formation, power densities and long term stability are also summarized in this review. Full article

Colistin sulfate (COL), a critical last-line antibiotic, poses a severe environmental threat due to its persistence and role in spreading mobile resistance genes. This study introduces a novel quaternary Ni-Co-Zn-Al layered double-hydroxide/activated carbon composite (Q-LDH/AC) for highly efficient COL remediation. The composite’s unique architecture, revealed through comprehensive characterization, enables an exceptional adsorption capacity of 952.52 mg·g⁻¹ under optimal conditions (pH 7, 55 °C), a value that significantly surpasses those reported for most previous adsorbents. The process was spontaneous and endothermic, with kinetics and isotherms best described by the pseudo-second-order and Langmuir–Freundlich models, respectively, indicating a complex mechanism dominated by chemisorption on both homogeneous and heterogeneous sites. A key innovative feature is the successful regeneration and reusability of the composite, which retained over 70% efficiency after five cycles, enhancing its potential for practical, cost-effective water treatment applications. The thermodynamic parameters (ΔG° = −8140.68 kJ/mol, ΔH° = +61.22 kJ/mol) indicate that the reaction is spontaneous and endothermic. The interaction mechanism of COL on Q-LDH/AC can be deduced by FT-IR including hydrogen bonding, π-π bonding, electrostatic interactions, and surface complexation. Beyond mere regeneration, this work demonstrates a pioneering circular economy strategy by repurposing the spent COL-laden adsorbent not as waste, but as a high-performance electrocatalyst. In direct urea fuel cell tests, this electrode achieved a superior and stable current density of 45.63 mA/cm² for Q-LDL/AC, substantially outperforming the pristine Q-LDH/AC/COL (206.63 mA/cm²) and highlighting how the captured pollutant enhances functionality. This dual-purpose approach successfully closes the loop, transforming the environmental liability of antibiotic-laden waste into a valuable resource for energy applications. With a production cost of 2.755 USD/g, this work presents not only a highly effective adsorbent but also a transformative, circular strategy that simultaneously addresses water pollution and energy recovery. These findings offer a promising dual-purpose solution for mitigating the environmental spread of antibiotic resistance through a sustainable cycle that enables efficient antibiotic removal from wastewater while simultaneously converting the captured pollutant into a useful energy resource. Full article

The commercialization of direct urea fuel cells (DUFCs) is hampered by the scarcity of low-cost, high-performance electrocatalysts for the urea oxidation reaction (UOR), while water treatment processes generate spent adsorbents as a secondary waste. This study presents a circular economy solution by transforming a waste product—spent progesterone-loaded Reishi mushroom biosorbents—into high-performance anodes for DUFCs. We demonstrate that the thermal conversion of Ganoderma lucidum into biochar (Biochar/RM), followed by its “activation” through progesterone (PG) adsorption, creates a superior electrocatalytic composite (Biochar/RM/PG). Electrochemical evaluation revealed that this spent adsorbent delivers an exceptional UOR activity, achieving a peak current density of 225.52 mA cm⁻², which is 79% higher than its pristine counterpart. This enhancement is driven by a unique synergy: the biochar provides a conductive, porous framework, while the thermally transformed PG acts as an in situ dopant, creating nitrogen-rich active sites and optimizing the surface architecture for urea electro-oxidation. The catalyst further demonstrated remarkable operational stability over 3600 s. This work establishes a pioneering “waste-to-wealth” strategy, simultaneously addressing the challenges of pharmaceutical wastewater management and the need for sustainable energy materials. Full article

Plant Microbial Fuel Cells (PMFCs) represent a promising technology that uses electroactive bacteria to convert the chemical energy in organic matter into electrical energy. The addition of carbon pellet on electrodes may increase the specific surface area for colonization via bacteria. Use of nutrients such as urea could enhance plant growth. Our study aims to address the following questions: (1) Does carbon pellet layering affect the electrical performance of PMFCs? (2) Does urea treatment of the plants used to feed the PMFCs affect the electrical performance? A new prototype of PMFC has been tested: the plant pot is on the top, drainage water percolates to the tub below, containing the Microbial Fuel Cells (MFCs). To evaluate the best layering setup, two groups of MFCs were constructed: a “Double layer” group (with carbon pellet both on the cathode and on the anode), and a “Single layer” group (with graphite only on the cathode). All MFCs were plant-fed by Spathiphyllum lanceifolium L leachate. After one year, each of the previous two sets has been divided into two subsets: one wetted with percolate from plants fertilized with urea, and the other with percolate from unfertilized plants. Open circuit voltage (mV), short circuit peak current, and short circuit current after 5 s (mA) produced values that were measured on a weekly basis. PMFCs characterized by a “Single layer” group performed better than the “Double layer” group most times, in terms of higher and steadier values for voltage and calculated power. Undesirable results regarding urea treatment suggest the use of less concentrated urea solution. The treatment may provide consistency but appears to limit voltage and peak values, particularly in the “Double layer” configuration. Full article

Extraction processes of alginates from Sargassum spp. generate a substantial number of solid residues that are commonly discarded. This study explores the sustainable transformation of these residues into nitrogen-doped biocarbon through chemical activation with KOH and nitrogen doping using urea. XRD, FTIR, SEM-EDX, Raman spectroscopy, BET surface area analysis, XPS, and CHNS elemental analysis were used to characterize the materials. The doped and activated biocarbon (BDA) demonstrated excellent physicochemical properties, including a specific surface area of 1790 m² g⁻¹ and a mesoporous structure. Electrochemical evaluation in alkaline media revealed a current density of −4.37 mA cm⁻², an onset potential of 0.922 E vs. RHE, and a half-wave potential of 0.775 E vs. RHE. Koutecky–Levich analysis indicated a two-electron reduction pathway. The superior performance was attributed to the synergistic effects of high surface area, nitrogen functionalities (pyridinic-N and pyrrolic-N), and enhanced accessibility of active sites. These results highlight the potential of waste-derived, nitrogen-doped biocarbon as a sustainable and low-cost alternative for ORR electrocatalysis in alkaline fuel cells. Full article

Non-noble metal electrocatalysts for the hydrogen oxidation reaction (HOR) that are both highly active and low-cost are essential for the widespread use of fuel cells. Herein, a simple two-step method for creating an in-plane heterostructure of Ni₃N/MoSe₂ loaded on N-doped reduced graphene oxide (Ni₃N/MoSe₂@N-rGO) as an effective electrocatalyst for the HOR is described. The process involves hydrothermal treatment of the Ni and Mo precursors with N-doped reduced graphene oxide, followed by the annealing with urea. The Ni₃N/MoSe₂@N-rGO catalyst exhibits high activities for the HOR, with current densities of 2.15 and 3.06 mA cm⁻² at 0.5 V vs. the reversible hydrogen electrode (RHE) in H₂-saturated 0.1 M KOH and 0.1 M HClO₄ electrolytes, respectively, which is comparable to a commercial 20% Pt/C catalyst under similar experimental conditions. Furthermore, the catalyst demonstrates excellent durability, maintaining its performance during accelerated degradation tests for 5000 cycles. This work offers a practical framework for the designing and preparing of non-precious metal electrocatalysts for the HOR in fuel cells. Full article

The climate crisis has become the most serious concern of human beings and environments worldwide in the 21st century. Global concerns about cancer epidemiology mainly originate from anthropogenic activities, particularly fossil-based operations. A key solution to this problem is the use of fuel cells—devices—capable of the direct conversion of fuel chemical energies like urea into electricity. To make their commercialization reasonable, one of the problems that needs to be solved is the development of anodic materials. The majority of investigations on urea oxidation are based on nickel, but its inadequate activity limits the efficiency of these devices. In this work, we propose and synthesize a Ni-Cu-Fe ternary electrocatalyst for urea oxidation through a fast and facile electrodeposition method. The properties of the synthesized material are examined by Scanning Electron Microscopy (SEM) conjugated with Energy Dispersive X-ray Spectroscopy (EDS), Transmission Electron Microscopy (TEM), and X-ray Diffraction (XRD). Its electrochemical properties were also examined in a 1 M KOH solution with and without 0.15 M urea. We found that the prepared powder is active in the electro-oxidation of urea, with 1.65 V_{vs RHE} required for a current density of 10 mA cm⁻² and a stable potential of 2.38 V_{vs RHE} required for 3 h of polarization at 10 mA cm⁻². Full article

Cobalt-based catalysts are recognized as promising electrocatalysts for oxygen reduction reactions (ORRs) in fuel cells that operate within acidic electrolytes. A synthesis process involving a cobalt complex, nanocellulose, and dopamine, followed by pyrolysis at 500 °C under a nitrogen atmosphere, was used to create a cobalt and nitrogen-doped carbonaceous material. Additionally, urea was incorporated to enhance nitrogen doping in the carbonaceous material. The morphology and structure of the material were examined using Scanning Electron Microscopy (SEM) and X-ray Diffraction (XRD), where SEM unveiled dispersed metal oxides within the carbonaceous framework. Energy Dispersive X-ray Spectroscopy (EDS) analysis showed an even distribution of elements across the cobalt-doped carbonaceous material. X-ray Photoelectron Spectroscopy (XPS) analysis further highlighted significant alterations in the elemental composition due to pyrolysis. The electrochemical behavior of the cobalt-doped carbonaceous material, with respect to the oxygen reduction reaction (ORR) in an acidic medium, was investigated via cyclic voltammetry (CV), revealing an ORR peak at 0.30 V against a reversible hydrogen reference electrode, accompanied by a notably high current density. The catalyst’s performance was evaluated across different pH levels and with various layers deposited, showing enhanced effectiveness in acidic conditions and a more pronounced reduction peak with uniformly applied electrode layers. Rotating disk electrode (RDE) studies corroborated the mechanism of a four-electron reduction of oxygen to water, emphasizing the catalyst’s efficiency. Full article

Environmental pollution due to the excessive consumption of fossil fuels for energy production is a critical global issue. Fuel cells convert chemical energy directly into electricity in a clean and silent electrochemical process, but face challenges related to hydrogen storage, handling, and transportation. The direct borohydride fuel cell (DBFC), utilizing sodium borohydride as a liquid fuel, is a promising alternative to overcome such issues but requires the design of cost-effective nanostructured electrocatalysts. In this study, we synthesized nitrogen-doped graphene anchoring Ni nanoparticles (Ni@NG) by thermal degradation of polyethylene terephthalate bottle waste with urea and metallic Ni, and evaluated it as a sustainable carbon support. Electrocatalysts were prepared by incorporating ultralow amounts (0.09 to 0.27 wt.%) of Pd into the Ni@NG support. The resulting PdNi@NG electrocatalysts were characterized using ICP-OES, XPS, TEM, N₂-sorption analysis, XRD, and Raman and FTIR spectroscopy. Voltammetry assessed the materials’ electrocatalytic activity for oxygen reduction and borohydride oxidation reactions in alkaline media, corresponding to the anodic and cathodic reactions in DBFCs. The electrocatalyst with 0.27 wt.% Pd loading (PdNi_15@NG) exhibited the best performance for both reactions. Consequently, it was employed as an anodic and cathodic material in a lab-scale DBFC, achieving a specific power of 3.46 kW g_Pd⁻¹. Full article

Nickel-based catalysts have been widely recognized as highly promising electrocatalysts for oxidation. Herein, we designed a catalyst surface based on iron oxide electrodeposited on NiCo₂O₄ spinel oxide. Nickel foam was used as a support for the prepared catalysts. The modified surface was characterized by different techniques like electron microscopy and X-ray photon spectroscopy. The activity of the modified surface was investigated through the electrochemical oxidation of different organic molecules such as urea, ethanol, and ethylene glycol. Therefore, the modified Fe@ NiCo₂O₄/NF current in 1.0 M NaOH and 1.0 M fuel concentrations reached 31.4, 27.1, and 17.8 mA cm⁻² for urea, ethanol, and ethylene glycol, respectively. Moreover, a range of kinetic characteristics parameters were computed, such as the diffusion coefficient, Tafel slope, and transfer coefficient. Chronoamperometry was employed to assess the electrode’s resistance to long-term oxidation. Consequently, the electrode’s activity exhibited a reduction ranging from 17% to 30% over a continuous oxidation period of 300 min. Full article

The production of green hydrogen using water electrolysis is widely regarded as one of the most promising technologies. On the other hand, the oxygen evolution reaction (OER) is thermodynamically unfavorable and needs significant overpotential to proceed at a sufficient rate. Here, we outline important structural and chemical factors that affect how well a representative nickel ferrite-modified graphene oxide electrocatalyst performs in efficient water splitting applications. The activities of the modified pristine and graphene oxide-supported nickel ferrite were thoroughly characterized in terms of their structural, morphological, and electrochemical properties. This research shows that the NiFe₂O₄@GO electrode has an impact on both the urea oxidation reaction (UOR) and water splitting applications. NiFe₂O₄@GO was observed to have a current density of 26.6 mA cm⁻² in 1.0 M urea and 1.0 M KOH at a scan rate of 20 mV s⁻¹. The Tafel slope provided for UOR was 39 mV dec⁻¹, whereas the GC/NiFe₂O₄@GO electrode reached a current of 10 mA cm⁻² at potentials of +1.5 and −0.21 V (vs. RHE) for the OER and hydrogen evolution reaction (HER), respectively. Furthermore, charge transfer resistances were estimated for OER and HER as 133 and 347 Ω cm², respectively. Full article