Search Results (109)

Sulfion oxidation reaction (SOR) has great potential in replacing oxygen evolution reaction (OER) and boosting highly efficient hydrogen evolution. The development of highly active and stable SOR electrocatalysts is crucial for assisting hydrogen production with low energy consumption. In this work, multiphase NiCoFe-based layered double hydroxide (namely NiCoFe-LDH) has been synthesized via a facile seed-assisted heterogeneous nucleation method. Benefiting from its unique microsized hydrangea-like structure and synergistic active phases, the catalyst delivers substantial catalytic interfaces and reactive centers for SOR. Consequently, NiCoFe-LDH electrode achieves a remarkably low potential of 0.381 V at 10 mA cm⁻² in 1 M KOH + 0.1 M Na₂S, representing a significant reduction of 0.98 V compared to conventional OER. Notably, under harsh industrial conditions (6 M KOH + 0.1 M Na₂S, 80 °C), the electrolysis system based on NiCoFe-LDH||NF pair exhibits a cell potential of only 0.71 V at 100 mA cm⁻², which shows a greater decreasing amplitude of 1.05 V compared with that of traditional OER/HER systems. Meanwhile, the NiCoFe-LDH||NF couple could maintain operational stability for 100 h without obvious potential fluctuation, as well as possessing a lower energy consumption of 1.42 kWh m⁻³ H₂. Multiphase eletrocatalysis for SOR could indeed produce hydrogen with low-energy consumption. Full article

This study investigates the influence of divalent metals—(Mg(II), Co(II), and Ni(II)) in layered double hydroxides (LDHs), with a constant trivalent Fe(III) component—on the decoloration of crystal violet and methyl blue dyes via a Fenton-type oxidation reaction. The catalysts, synthesized by co-precipitation and hydrothermal treatment, were tested in both hydroxide and oxide forms under varying agitation conditions (0 and 280 rpm). A 2² × 3 factorial design was used to analyze the effect of the divalent metal type, catalyst phase, and stirring. The Mg/Fe oxide, with the highest BET surface area (144 m²/g) and crystallite size (59.7 nm), showed superior performance—achieving up to 98% decoloration of crystal violet and 97% of methyl blue within 1 h. The kinetic analysis revealed pseudo-second-order and pseudo-first-order fits for crystal violet and methyl blue, respectively. These findings suggest that LDH-based catalysts provide a fast, low-cost, and effective option for dye removal in aqueous systems. 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

Transition metal oxides (TMOs) are considered to be highly promising materials for supercapacitor electrodes due to their low cost, multiple convertible valence states, and excellent electrochemical properties. However, inherent limitations, including restricted specific surface area and low electrical conductivity, have largely restricted their application in supercapacitors. In this paper, core–shell heterostructures of nickel–iron layered double hydroxide (NiFe-LDH) nanosheets uniformly grown on CuCo₂O₄ nanoneedles were synthesized by hydrothermal and calcination methods. It is found that the novel core–shell structure of CuCo₂O₄@NiFe-LDH improves the electrical conductivity of the electrode materials and optimizes the charge transport path. Under the synergistic effect of the two components and the core–shell heterostructure, the CuCo₂O₄@NiFe-LDH electrode achieves an ultra-high specific capacity of 323.4 mAh g⁻¹ at 1 A g⁻¹. And the capacity retention after 10,000 cycles at 10 A g⁻¹ is 90.66%. In addition, the assembled CuCo₂O₄@NiFe-LDH//RGO asymmetric supercapacitor device achieved a considerable energy density (68.7 Wh kg⁻¹ at 856.3 W kg⁻¹). It also has 89.36% capacity retention after 10,000 cycles at 10 A g⁻¹. These properties indicate the great potential application of CuCo₂O₄@NiFe-LDH in the field of high-performance supercapacitors. Full article

The development of bifunctional air electrodes with high activity and durability is essential for advancing flexible zinc–air batteries. Herein, a hierarchical electrode structure is designed by growing N-doped carbon nanotubes (CNTs) on copper foam, where CNTs serve as highly active oxygen reduction reaction (ORR) sites. The controlled deposition of NiFeCo-layered double hydroxide (LDH) nanosheets, optimized to maintain ORR activity while enhancing oxygen evolution reaction (OER) performance, enables a finely tuned bifunctional catalyst. This architecture achieves outstanding electrochemical properties, requiring only 0.897 V vs. RHE and 1.446 V vs. RHE to reach 10 mA cm⁻² in 1 M KOH, thereby minimizing overpotentials. When implemented as an air electrode in a quasi-solid-state zinc–air battery, the system demonstrates remarkable cycling stability, sustaining performance for over 300 h. Furthermore, a 16 cm² pouch-type zinc–air battery delivers a high discharge capacity of 0.62 Ah, highlighting the scalability of this design. This work presents a robust and scalable strategy for developing high-performance bifunctional air electrodes, offering a promising route for next-generation flexible energy storage systems. Full article

The construction of high-performance catalysts for overall water splitting (OWS) is crucial. Nickel–iron-layered double hydroxide (NiFe LDH) is a promising catalyst for OWS. However, the slow kinetics of the HER under alkaline conditions seriously hinder the application of NiFe LDH in OWS. This work presents a strategy to optimize OWS performance by adjusting the entropy of multi-metallic LDH. Quaternary NiFeCrCo LDH was constructed, which exhibited remarkable OWS activity. The OER and HER of NiFeCrCo LDH were stable for 100 h and 80 h, respectively. The OWS activity of NiFeCrCo LDH//NiFeCrCo LDH only required 1.42 V to reach 10 mA cm⁻², and 100 mA cm⁻² required 1.54 V. Under simulated seawater conditions, NiFeCrCo LDH//NiFeCrCo LDH required 1.57 V to reach 10 mA cm⁻² and 1.71 V to reach 100 mA cm⁻². The introduction of Co into the structure induced Cr to provide more electrons to Fe, which regulated the electronic state of NiFeCrCo LDH. The appropriate electronic state of the structure is essential for the remarkable performance of OWS. This work proposes a new strategy to achieve excellent OWS performance through entropy-increase engineering. Full article

A supercapacitor’s energy storage capability is greatly dependent on electrode materials. Layered double hydroxides (LDHs) were extensively studied as battery-type electrodes because of their 2D structure and quick intercalation/deintercalation of electrolyte ions. However, the energy storage capability for pristine LDHs is limited by their large aggregation tendency and poor electrical conductivity. Herein, a novel NiCoMn-LDH/SWCNTs (single-walled carbon nanotubes) composite electrode material, with ultrathin NiCoMn-LDH nanosheets dispersedly grown among the highly conductive networks of SWCNTs, was prepared via a facile zeolitic imidazolate framework-67 (ZIF-67)-derived in situ etching and deposition procedure. The NiCoMn-LDH/SWCNTs electrode demonstrates a specific capacitance as large as 1704.3 F g⁻¹ at 1 A g⁻¹, which is ascribed to its exposure of more active sites than NiCoMn-LDH. Moreover, the assembled NiCoMn-LDH/SWCNTs//BGA (boron-doped graphene aerogel) hybrid supercapacitor exhibits a superior capacitance of 167.9 F g⁻¹ at 1.0 A g⁻¹, an excellent energy density of 45.7 Wh kg⁻¹ with a power density of 700 W kg⁻¹, and an outstanding cyclic stability with 82.3% incipient capacitance maintained when subjected to 5000 charge and discharge cycles at the current density of 10 A g⁻¹, suggesting the significant potential of NiCoMn-LDH/SWCNTs as the electrode material applicable in supercapacitors. Full article

Advanced oxidation processes (AOPs) based on activated persulfate (PS) are gradually being employed in the treatment of novel pollutants. In this study, an efficient and reliable CoNiFe-layered double hydroxide (LDH) was prepared by a hydrothermal method, which could effectively activate peroxomonosulfate (PMS) and cause free sulfate radical (SO₄^•−) oxidation to decompose atrazine (ATZ). The degradation rate of ATZ was greater than 99% within 60 min at pH 7 when the initial concentration of ATZ was 10 mg·L⁻¹, and the dosages of PMS and activator were 0.6 mM and 80 mg·L⁻¹. The analysis of ATZ degradation confirmed the reusability of the activator and its strong structural stability. The generation of four free radicals was analyzed and confirmed, and the influence on the degradation reaction was SO₄^•− > O₂^•− > ¹O₂ > •OH. The analytical results showed that the metal ions reacted with HSO₅⁻ in PMS to cause an oxidation–reduction cycle change in the valence state of the metal ions and generated the primary factor affecting the degradation reaction—SO₄^•−. Nine degradation intermediates with reduced toxicity were detected and possible ATZ degradation pathways were deduced, thus confirming the activation mechanism of CoNiFe-LDH. Full article

Hydrogen plays a vital role in the global shift toward cleaner energy solutions, with water electrolysis standing out as one of the most promising techniques for generating hydrogen. Despite its potential, the oxygen evolution reaction (OER) involved in this process faces significant challenges, including high overpotentials and slow reaction rates, which underscore the need for advanced electrocatalytic materials to enhance efficiency. Noble metal catalysts are effective but expensive, so transition-metal-based electrocatalysts like nickel–cobalt layered double hydroxides (NiCo LDHs) have become promising alternatives. In this research, a series of NiCo LDH catalysts doped with Fe, Mn, Cu, and Zn were effectively produced using a one-step hydrothermal technique. Among the catalysts, the Fe-doped NiCo LDH exhibited OER activity, achieving a lower overpotential (289 mV) at a current density of 50 mA/cm², which was far better than the 450 mV of the undoped NiCo LDH. The Mn-, Cu-, and Zn-NiCo LDHs also exhibited lower overpotentials of 414 mV, 403 mV, and 357 mV, respectively, at this current density. The Fe-doped NiCo LDH had a 3D layered nanoflower structure, increasing the surface area for reactant adsorption. The electrochemically active surface area (ECSA), as indicated by the double-layer capacitance (C_dl), was larger in the doped samples. The C_dl value of the Fe-doped NiCo LDH was 3.72 mF/cm², significantly surpassing the 0.82 mF/cm² of the undoped NiCo LDH. These changes improved charge transfer and optimized reaction kinetics, enhancing the overall OER performance. This study offers significant contributions to the development of efficient electrocatalysts for the OER, advancing the understanding of key design principles for enhanced catalytic performance. Full article

Heavy metal cations such as Ag⁺, Pb²⁺, and Hg²⁺ can accumulate in living organisms, posing severe risks to biological systems, including humans. Therefore, removing heavy metal cations from wastewater is crucial before discharging them to the environment. However, trace levels and high-capacity removal of the heavy metals remain a critical challenge. This work demonstrates the synthesis and characterization of [Mo₂S₁₂]²⁻ intercalated cobalt aluminum-layered double hydroxide, CoAl―Mo₂S₁₂―LDH (CoAl―Mo₂S₁₂), and its remarkable sorption properties for heavy metals. This material shows high efficiency for removing over 99.9% of Ag⁺, Cu²⁺, Hg²⁺, and Pb²⁺ from 10 ppm aqueous solutions with a distribution constant, K_d, as high as 10⁷ mL/g. The selectivity order for removing these ions, determined from the mixed ion state experiment, was Pb²⁺ < Cu²⁺ ≪ Hg²⁺ < Ag⁺. This study also suggests that CoAl―Mo₂S₁₂ is not selective for Ni²⁺, Cd²⁺, and Zn²⁺ cations. CoAl―Mo₂S₁₂ is an efficient sorbent for Ag⁺, Cu²⁺, Hg²⁺, and Pb²⁺ ions at pH~12, with the removal performance of both Ag⁺ and Hg²⁺ cations retaining > 99.7% across the pH range of ~2 to 12. Our study also shows that the CoAl―Mo₂S₁₂ is a highly competent silver cation adsorbent exhibiting removal capacity (q_m) as high as ~918 mg/g compared with the reported data. A detailed mechanistic analysis of the post-treated solid samples with Ag⁺, Hg²⁺, and Pb²⁺ reveals the formation of Ag₂S, HgS, and PbMoO₄, respectively, suggesting the precipitation reaction mechanism. Full article

Converting CO₂ and green hydrogen into products such as methane and methanol not only has a negative carbon effect, but also stores renewable energy into energy chemicals. This represents a promising route for hydrogen energy storage technologies. The hydrogenation of CO₂ to methane and methanol, which represent strongly exothermic reactions, are thermodynamically favored at low temperatures. However, the inherent inertness of CO₂ makes it difficult to activate CO₂ at low temperatures. Both reactions face the challenge of activating CO₂ at low temperature, so catalysts exhibiting high activity under such conditions are a critical need. Layered double hydroxides (LDHs) have attracted considerable interest owing to their regular layered structure and uniform dispersion of multiple metallic components. However, there are few studies on the same effects of promoters over LDHs-derived catalysts. Here, we investigated the same effects of promoters on two LDHs-derived catalysts in different CO₂ hydrogenation reactions to illustrate the effects of promoters on facilitating low-temperature CO₂ activation in LDHs-derived catalysts. By adding promoters Fe and Mn to the catalysts NiAl-Fe and CuZnAl-Mn, the crystal lattices were expanded, surface areas were increased 38% and 25%, and the reduction temperatures were decreased to 97 °C and 10 °C, respectively. These promoters significantly enhanced the CO₂ adsorption and activation of the catalysts NiAl-Fe and CuZnAl-Mn. The methanation catalyst NiAl-Fe achieved a CO₂ conversion of 80.8% at 200 °C and 2 MPa, while the methanol synthesis catalyst CuZnAl-Mn exhibited a CO₂ conversion of 21.3% and a methanol selectivity of 61.8% under the conditions of 250 °C and 3 MPa. The influence of the LDHs precursors’ structure and the addition of promoters Fe and Mn on the catalytic performance were studied by XRD, N₂ adsorption–desorption, H₂-TPR, H₂-TPD, and CO₂-TPD. Full article

NiFe-layered double hydroxide (NiFe-LDH) and La-, Mo- or W-doped NiFe-LDH microparticles (NiFeX-LDH, X = La, Mo, W) were synthesized via the co-precipitation method. Their adsorption characteristics were evaluated by the removal of methyl orange (MO) and hexavalent chromium (Cr⁶⁺). The effects of the metal ion doping type, doping concentration (0–3at%), pH and temperature on the MO adsorption properties were systematically studied. The results show that W-doped NiFe-LDH exhibits superior MO removal capacity compared to undoped or La- or Mo-doped NiFe-LDH at the same 1at% doping level, which is attributed to the increased layer charge density and strong affinity for the π-electron systems of MO molecules. The NiFeW-LDH-1at% sample demonstrated the best MO adsorption performance within the W-doping range of 0–3at%, achieving a superior adsorption capability of 666.67 mg/g with a significantly shorter equilibrium time (10–120 min) compared to the similar LDH. NiFeW-LDH-1at% showed promising reusability, with its adsorption efficiency remaining 78.3% of its initial level after five adsorption–desorption cycles. The MO uptake onto NiFeX-LDH was attributed to the combined effect of anion exchange and the attraction of layer charge. In addition, the adsorption of NiFeW-LDH-1at% matched well with the Langmuir isotherm model and pseudo-second-order kinetic model, indicating a monolayer and chemical adsorption. Furthermore, NiFeW-LDH-1at% effectively adsorbed of Cr₂O₇²⁻ in the aqueous solution, revealing that W doping significantly enhances Cr(VI) removal performance. The maximum theoretical adsorption capacity onto NiFeW-LDH-1at% reached 63.25 mg/g, which was notably higher than that of the pristine NiFe-LDH adsorbent (53.56 mg/g). Overall, the W-doped NiFe-LDH material, as a low-cost and highly efficient adsorbent, shows great potential for wastewater treatment application. Full article

To overcome the disadvantage of difficult recovery of powder catalysts and improve catalyst utilization, the selection of foam metal substrates as supports can reduce the difficulty of material recovery and effectively inhibit the leaching of metal ions. Herein, CoMnNi-layered double hydroxide (LDH) derived from Co-Mn ZIF was immobilized onto nickel foam (NF) through in situ synthesis. The results of XRD and SEM analyses of the samples indicated that the LDH was successfully grown on the nickel foam matrix, and the material could maintain its original morphology to the maximum extent after loading. By comparing the XPS of the material before and after the reaction, it was confirmed that the surface hydroxyl group and C=O of the material were involved in the activation of peroxymonosulfate (PMS). The results of the quenching reaction showed that SO₄^•− and ¹O₂ are the main active substances in the oxidation of enrofloxacin (ENR). When the dosage of NF@CoMnNi-LDH was 0.4 g/L, the pH of the solution was 6.82, and when the dosage of PMS was 2.0 mM, the degradation rate of ENR reached 82.6% within 30 min. This research offers novel insights into the degradation of antibiotics from water using a monolithic catalyst supported by metal foam. Full article

Heavy metals enter river basins through industrial effluents, agricultural wastes, surface run-offs, and other human activities, negatively impacting aquatic and terrestrial life by bioaccumulating in the food chain. This problem is on a continuous rise in under-developed and developing countries, such as in Pakistan. Therefore, the current study was aimed to determine concentrations of heavy metals, essential trace elements, and macrominerals (Zn, Pb, Ni, Mn, Mg, Fe, Cu, Cr, Co, Cd, Ca, and As) in the water, sediments, and tissues (gills, liver, and muscles) of Bagarius bagarius and Bagre marinus in the Jhelum River, Pakistan. The hematological and biochemical profiles of these fish across two sampling sites (Jhelum Bridge Khushab, upstream, and Langarwala Pull—downstream) were also evaluated. Results showed greater bioaccumulation of heavy metals in fish downstream, correlating with higher concentrations of these metals in water and sediments downstream. In the case of B. marinus, the highest concentration observed was 16.59 mg/g (Ca), and the lowest concentration was 9.51 mg/g (Fe). In the case of B. bagarius, the highest concentration observed was 17.47 mg/g (Ca), and the lowest concentration was 7.95 mg/g (Mg). Increased activities of alkaline phosphatase (ALP), alanine aminotransferase (ALT), aspartate aminotransferase (AST), and lactate dehydrogenase (LDH) were observed downstream. Hematological changes included increased white blood cells (WBCs) and decreased red blood cells (RBCs), lymphocytes, hemoglobin (Hb), platelets (Plt), and hematocrit (Hct). A significant correlation was observed among heavy metals across the water, sediment, and different tissues of B. marinus and B. bagarius. Moreover, principal component analysis (PCA) for both species along both sampling sites illustrated the relationship between fish tissues and metals. The current study concluded that the fish accumulated a significantly higher concentration of heavy metals downstream, which might be linked with dumping of the domestic wastes and industrial and agricultural runoff, adversely affecting both fish and human health. Full article

In this study, a three-dimensional (3D) interconnected porous Ni/SiC skeleton (3D Ni/SiC) was synthesized by binder-free hydrogen bubble template-assisted electrodeposition in an electrolyte containing Ni²⁺ ions and SiC nanopowders. This 3D Ni/SiC skeleton served as a substrate for directly synthesizing nickel–cobalt layered double hydroxide (LDH) nanosheets via electrodeposition, allowing the formation of a nickel–cobalt LDH nanosheet-decorated 3D Ni/SiC skeleton (NiCo@3D Ni/SiC). The multiscale hierarchical structure of NiCo@3D Ni/SiC was attributed to the synergistic interaction between the pseudocapacitor (3D Ni skeleton and Ni–Co LDH) and electrochemical double-layer capacitor (SiC nanopowders). It provided a large specific surface area to expose numerous active Ni and Co sites for Faradaic redox reactions, resulting in an enhanced pseudocapacitance. The as-fabricated NiCo@3D Ni/SiC structure demonstrated excellent rate capability with a high areal capacitance of 1565 mF cm⁻² at a current density of 1 mA cm⁻². Additionally, symmetrical supercapacitor devices based on this structure successfully powered commercial light-emitting diodes, indicating the potential of as-fabricated NiCo@3D Ni/SiC in practical energy storage applications. Full article