Room-temperature response of MOF-derived Pd@PdO core shell/γ-Fe2O3 microcubes decorated graphitic carbon based ultrasensitive and highly selective H2 gas sensor.

With the current upsurge in hydrogen economies all over the world, an increased demand for improved chemiresistive H2 sensors that are highly responsive and fast acting when exposed to gases is expected. Owing to safety concerns about explosive and highly flammable H2 gas, it is important to develop resistive sensors that can detect the leakage of H2 gas swiftly and selectively. Currently, interest in metal-organic frameworks (MOFs) for gas-sensor applications is increasing due to their open-metal sites, large surface area, and unique surface morphologies. In this research, a highly selective and sensitive H2-sensor was established based on graphitic carbon (GC) anchored spherical Pd@PdO core-shells over γ-Fe2O3 microcube (Pd@PdO/γ-Fe2O3@GC which is termed as S3) heterostructure materials. The combined solvothermal followed by controlled calcination-assisted S3 exhibited a specific morphology with the highest surface area of 79.12 m2 g-1, resulting in fast response and recovery times (21 and 29 s, respectively), and excellent sensing performance (ΔR/R0∼ 96.2 ± 1.5), outstanding long-term stability, and a 100 ppb detection limit when detecting H2-gas at room temperature (mainly in very humid surroundings). This result proves that adsorption sites provided by S3 can promote surface reactions (adsorption and desorption) for ultrasensitive and selective H2gas sensors.

Density Functional Theory Approximations and Experimental Investigations on Co1-xMoxTe2 Alloy Electrocatalysts Tuning the Overall Water Splitting Reactions.

Understanding the relationship between electronic structure, surface characteristic, and reaction process of a catalyst helps to architect proficient electrodes for sustainable energy development. The highly active and stable catalysts made of earth-abundant materials provide a great endeavor toward green hydrogen production. Herein, we assembled the Co1-xMoxTe (x = 0-1) nanoarray structures into a bifunctional electrocatalyst to achieve high-performance hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) kinetics under alkaline conditions. The designed Co0.75Mo0.25Te and Co0.50Mo0.50 electrocatalysts require minimum overpotential and Tafel slope for high-efficacy HER and OER, respectively. Furthermore, we constructed a Co0.50Mo0.50Te2∥Co0.50Mo0.50Te2 device for overall water splitting with an overpotential of 1.39 V to achieve a current density of 10 mA cm-2, which is superior to noble electrocatalyst performance, with stable reaction throughout the 50 h continuous process. Density functional theory approximations and Gibbs free energy calculations validate the enhanced water splitting reaction catalyzed by the Co0.50Mo0.50Te2 nanoarrays. The partial replacement of Co atoms with Mo atoms in the Co0.50Mo0.50Te2 structure substantially enhances the water electrolysis kinetics through the synergistic effects between the combined metal atoms and the bonded chalcogen.

Current trends and prospects in catalytic upgrading of lignocellulosic biomass feedstock into ultrapure biofuels.

Eco-friendly renewable energy sources have recommended as fossil fuel alternatives in recent years to reduce environmental pollution and meet future energy demands in various sectors. As the largest source of renewable energy in the world, lignocellulosic biomass has received considerable interest from the scientific community to advance the fabrication of biofuels and ultrafine value-added chemicals. For example, biomass obtained from agricultural wastes could catalytically convert into furan derivatives. Among furan derivatives, 5-hydroxymethylfurfural (HMF) and 2, 5-dimethylfuran (DMF) are considered the most useful molecules that can be transformed into desirable products such as fuels and fine chemicals. Because of its exceptional properties, e.g., water insolubility and high boiling point, DMF has studied as the ideal fuel in recent decades. Interestingly, HMF, a feedstock upgraded from biomass sources can easily hydrogenate to produce DMF. In the present review, the current state of the art and studies on the transformation of HMF into DMF using noble metals, non-noble metals, bimetallic catalysts, and their composites have discussed elaborately. In addition, comprehensive insights into the operating reaction conditions and the influence of employed support over the hydrogenation process have demonstrated.

Recent Advancements in Two-Dimensional Layered Molybdenum and Tungsten Carbide-Based Materials for Efficient Hydrogen Evolution Reactions.

Green and renewable energy is the key to overcoming energy-related challenges such as fossil-fuel depletion and the worsening of environmental habituation. Among the different clean energy sources, hydrogen is considered the most impactful energy carrier and is touted as an alternate fuel for clean energy needs. Even though noble metal catalysts such as Pt, Pd, and Au exhibit excellent hydrogen evolution reaction (HER) activity in acid media, their earth abundance and capital costs are highly debatable. Hence, developing cost-effective, earth-abundant, and conductive electrocatalysts is crucial. In particular, various two-dimensional (2D) transition metal carbides and their compounds are gradually emerging as potential alternatives to noble metal-based catalysts. Owing to their improved hydrophilicity, good conductivity, and large surface areas, these 2D materials show superior stability and excellent catalytic performances during the HER process. This review article is a compilation of the different synthetic protocols, their impact, effects of doping on molybdenum and tungsten carbides and their derivatives, and their application in the HER process. The paper is more focused on the detailed strategies for improving the HER activity, highlights the limits of molybdenum and tungsten carbide-based electrocatalysts in electro-catalytic process, and elaborates on the future advancements expected in this field.

Metal Organic Framework-Derived ZnO@GC Nanoarchitecture as an Effective Hydrogen Gas Sensor with Improved Selectivity and Gas Response.

Although they are not as favorable as other influential gas sensors, metal-oxide semiconductor-based chemiresistors ensure minimal surface reactivity, restricting their gas selectivity, gas response, and reaction kinetics, particularly when functioning at room temperature (RT). A hybrid design, which includes metal-oxide/carbon nanostructures and passivation with specific gas filtration layers, can address the concerns of surface reactivity. We present a novel hierarchical nanostructured zinc oxide (ZnO), decorated with graphitic carbon (GC) and synthesized via a wet-chemical strategy, which is then followed by the self-assembly of a zeolitic imidazolate framework (ZIF-8). Because of its large surface area, high porosity, and efficient inspection of other analyte (interfering) gases, the ZnO@GC can provide intensified surface reactivity at RT. In the present study, such a hybrid sensor confirmed extraordinary gas sensing properties, which was characterized by excellent H2 selectivity, fast response, rapid recovery kinetics, and high gas response (ΔR/R0 ∼ 124.6%@10 ppm), particularly in extremely humid environments. The results reveal that adsorption sites provided by the ZIF-8 template-based ZnO@GC frameworks facilitate the adsorption and desorption of H2.

Fundamentals and comprehensive insights on pulsed laser synthesis of advanced materials for diverse photo- and electrocatalytic applications.

The global energy crisis is increasing the demand for innovative materials with high purity and functionality for the development of clean energy production and storage. The development of novel photo- and electrocatalysts significantly depends on synthetic techniques that facilitate the production of tailored advanced nanomaterials. The emerging use of pulsed laser in liquid synthesis has attracted immense interest as an effective synthetic technology with several advantages over conventional chemical and physical synthetic routes, including the fine-tuning of size, composition, surface, and crystalline structures, and defect densities and is associated with the catalytic, electronic, thermal, optical, and mechanical properties of the produced nanomaterials. Herein, we present an overview of the fundamental understanding and importance of the pulsed laser process, namely various roles and mechanisms involved in the production of various types of nanomaterials, such as metal nanoparticles, oxides, non-oxides, and carbon-based materials. We mainly cover the advancement of photo- and electrocatalytic nanomaterials via pulsed laser-assisted technologies with detailed mechanistic insights and structural optimization along with effective catalytic performances in various energy and environmental remediation processes. Finally, the future directions and challenges of pulsed laser techniques are briefly underlined. This review can exert practical guidance for the future design and fabrication of innovative pulsed laser-induced nanomaterials with fascinating properties for advanced catalysis applications.

Impact of Molybdenum Dichalcogenides on the Active and Hole-Transport Layers for Perovskite Solar Cells, X-Ray Detectors, and Photodetectors.

The interface architectures of inorganic-organic halide perovskite-based devices play key roles in achieving high performances with these devices. Indeed, the perovskite layer is essential for synergistic interactions with the other practical modules of these devices, such as the hole-/electron-transfer layers. In this work, a heterostructure geometry comprising transition-metal dichalcogenides (TMDs) of molybdenum dichalcogenides (MoX2  = MoS2 , MoSe2 , and MoTe2 ) and perovskite- or hole-transfer layers is prepared to achieve improved device characteristics of perovskite solar cells (PSCs), X-ray detectors, and photodetectors. A superior efficiency of 11.36% is realized for the active layer with MoTe2 in the PSC device. Moreover, X-ray detectors using modulated MoTe2 nanostructures in the active layers achieve 296 nA cm-2 , 3.12 mA (Gy cm2 )-1 and 3.32 × 10-4 cm2 V-1 s-1 of collected current density, sensitivity, and mobility, respectively. The fabricated photodetector produces a high photoresponsivity of 956 mA W-1 for a visible light source, with an excellent external quantum efficiency of 160% for the perovskite layer containing MoSe2 nanostructures. Density functional theory calculations are made for pure and MoX2 doped perovskites' geometrical, density of states and optical properties variations evidently. Thus, the present study paves the way for using perovskite-based devices modified by TMDs to develop highly efficient semiconductor devices.

Unveiling the Redox Electrochemistry of MOF-Derived fcc-NiCo@GC Polyhedron as an Advanced Electrode Material for Boosting Specific Energy of the Supercapattery.

Metal organic frameworks (MOFs), which constitute a new class of porous organic-inorganic hybrid materials, have gained considerable attention in the fields of electrochemical energy storage and conversion devices owing to their open topological structures, large surface areas, tunable morphologies, and extreme redox activity. A synthesis protocol that comprises coprecipitation followed by controlled calcination processes to design a battery-type electrode is used. This electrode consists of three-dimensional (3D), ant cave-like polyhedrons of nickel-cobalt alloy on graphitic carbon (GC; NiCo@GC) nanostructures; trimesic acid is used as a potential MOF-linker. The developed NiCo@GC sample exhibits mesoporous characteristics with the maximum surface area of 94.08 m2 g-1 at 77 K. In addition, the redox activity at different sweep rates reveals the battery-type charge storage behavior of the NiCo@GC electrode; its three-electrode assembly provides 444 C g-1 specific capacity at 2 A g-1 with long-term capacity retention. The constructed supercapattery (SC) devices (i.e., AC//NiCo@GC) achieved capacity, specific energy, and specific power are 74.3 mAh g-1 , 39.5 Wh kg-1 , and 665 W kg-1 , respectively. Owing to its reasonable electrochemical characteristics, the prepared NiCo@GC material is a promising candidate for supercapattery electrodes for portable electronic devices.

Bifunctional iron molybdate as highly effective heterogeneous electro-Fenton catalyst and Li-ion battery anode.

Three-dimensional materials have attracted considerable interest in energy and environmental remediation fields. Iron molybdate (FMO) materials have prepared via a facile hydrothermal technique with glycerol assistance, and their structural and chemical composition confirmed using various physico-chemical techniques. The prepared bi-functional material is a strong candidate for energy storage and electrocatalytic degradation of Methylene blue and Congo red. Experimental results confirmed the synthesized FMO-10 catalyst was extremely efficient for methylene blue and Congo red breakdown, achieving 91 % and 96 % degradation in 36 h, respectively. This high catalytic activity was attributed to FMO significant visible light absorption, and reactive OH formation from H2O2 synergistically triggered by both Fe3+ and MoO42-. Prepared FMO samples demonstrated excellent potential as negative electrode material for lithium ion batteries. Electrode specific capacity initially dropped then rebounded to 1265 mAh g-1 after 100 cycles at 100 mA g-1 change rate between 0.01 and 3.0 V.

Fabrication strategies and surface tuning of hierarchical gold nanostructures for electrochemical detection and removal of toxic pollutants.

The intensive research on the synthesis and characterization of gold (Au) nanostructures has been extensively documented over the last decades. These investigations allow the researchers to understand the relationships between the intrinsic properties of Au nanostructures such as particle size, shape, morphology, and composition to synthesize the Au nano/hybrid nanostructures with novel physicochemical properties. By tuning the properties above, these nanostructures are extensively employed to detect and remove trace amounts of toxic pollutants from the environment. This review attempts to document the achievements and current progress in Au-based nanostructures, general synthetic and fabrication strategies and their utilization in electrochemical sensing and environmental remediation applications. Additionally, the applications of Au nanostructures (e.g., as adsorbents, sensing platforms, catalysts, and electrodes) and advancements in the field of electrochemical sensing of different target analytes (e.g., proteins, nucleic acids, heavy metals, small molecules, and antigens) are summarized. The literature survey concludes the existing methods for the detection of toxic contaminants at various concentration levels. Finally, the existing challenges and future research directions on electrochemical sensing and degradation of toxic contaminants using Au nanostructures are defined.

Ternary Zn1-xNixSe nanostructures as efficient photocatalysts for detoxification of hazardous Congo red, methyl orange, and chrome yellow dyes in wastewater sources.

Water contamination by hazardous organic pollutants poses an extreme threat to the environment and globally endangers aquatic life and human health. Hence, the removal of toxic organic effluents from water sources is necessary to ensure a healthy green environment. To this end, a new class of emerging, visible-light-driven Zn- and Ni-based ternary metal-selenide (Zn1-xNixSe) nanophotocatalysts, with tunable nanostructures via regulation of the stoichiometric ratios of Zn and Ni, were synthesized for efficient water purification by a facile one-pot hydrothermal process. These catalysts exhibit outstanding porous properties, with large surface areas and average particle sizes of around 80 ± 10 nm. The as-prepared ternary Zn1-xNixSe catalysts enable improved optical properties, intrinsic conductivity, bandgap reductions, and large numbers of active sites compared with pristine materials, thereby exhibiting outstanding degradation properties against various dye molecules, including Congo red, methyl orange, and chrome-IV upon visible light irradiation. The improved photodegradation capabilities of the Zn1-xNixSe catalysts may be attributed to the synergistic combinations of Zn and Ni selenides, which in turn minimize the recombination rates of the photogenerated carriers compared to their individual constituents. These findings clearly demonstrate that the proposed ternary Zn1-xNixSe catalysts could be potentially used to remove toxic organic contaminants from industrial wastewater.

Hexagonal nanostructured cobalt oxide @ nitrogen doped multiwalled carbon nanotubes/polypyyrole composite for supercapacitor and electrochemical glucose sensor.

Hexagonal nanostructured cobalt oxide @ N-doped MWCNT /polypyyrole (Co3O4/PPy@N-MWCNT) composite was produced by an ultrasonication-mediated solvothermal method for electrochemical supercapacitor and glucose sensor applications. The structural and electrochemical properties of the Co3O4/PPy@N-MWCNT were confirmed by various spectroscopic and microscopic techniques. The as-prepared electrode showed an excellent capacitance of ∼872 F/g at 0.5 A/g with a capacitance retention of 96.8 %, even after 10,000 cycles. In addition, analysis of the sensing activity of the composite materials towards the glucose detection showed excellent electrochemical sensing performance that includes the glucose linear limit of (10 to 0.15) µm, detection sensitivity of 195.72 µA/cm2/mM, and lower detection value of S = 0.07327 µA/cm2 @ R2 = 0.99. The as-prepared composite material can be a promising candidate for the electrochemical supercapacitor and the efficient sensing of glucose.

Application of advanced materials in sonophotocatalytic processes for the remediation of environmental pollutants.

Significant advances in various industrial processes have resulted in the discharge of toxic pollutants into the environment. Consequently, it is essential to develop efficient wastewater treatment processes to reduce water contamination and increase recycling/reuse. Photocatalytic degradation is considered as an efficient method for the degradation of toxic pollutants in industrial wastewater. However, the use of photocatalytic approaches is associated with numerous limitations, such as lengthy procedures and the necessity for large amounts of catalysts. Hence, it has been proposed that photocatalysis could be combined with other techniques, including sonolysis, electrochemical, photothermal, microwave, ultrafiltration, and biological reactor. The integration of photocatalysis with sonolysis could be remarkably beneficial for environmental remediation. The combination of these processes has the advantages of using uniformly dispersed catalysts, regeneration of the catalyst surface, improved mass transfer, enhanced surface area due to smaller catalyst particles, and production of more active radicals for the degradation of organic pollutants. In this review, an overview on employing sonophotocatalysis for the removal of toxic organic contaminants from aqueous environments is provided. Additionally, the limitations of photocatalysis alone and the fundamental sonophotocatalytic mechanistic pathways are discussed. The importance of utilizing advanced two-dimensional (2D) semiconductor materials in sonophotocatalysis and the common synthetic approaches for the preparation of 2D materials are also highlighted. Lastly, the review provides comprehensive insights into different materials based on metal oxides, chalcogenides, graphene, and metal organic frameworks (MOFs), which are involved in sonophotocatalytic processes employed for the remediation of environmental pollutants.

Influence of selenium precursors on the formation of iron selenide nanostructures (FeSe2): Efficient Electro-Fenton catalysts for detoxification of harmful organic dyestuffs.

In this investigation, a sequences of iron diselenide (FeSe2) nanomaterials as the competent and highly stable catalysts for the detoxification of aqueous organic dye pollutants such as Congo red (CR) and methylene blue (MB) through Electro-Fenton (EF) process using hydrogen peroxide as an initiator have been studied. The utilized selenium precursors include selenium metal, selenious acid (H2SeO3) and selenium dioxide (SeO2) which were employed for the synthesis of FeSe2 catalysts through a wet chemical strategy. It has been observed that based on the employed precursors, different morphologies ranges of the FeSe2 catalysts were obtained: microgranualr particles to nano-stick to nanoflakes. The crystalline nature and phase purity of the obtained FeSe2 catalysts were determined through XRD, Raman and HR-TEM analyses which confirmed their orthorhombic ferroselite structure. Among the prepared FeSe2 catalysts, FS-2 (using H2SeO3) displayed better porous properties as compared to other catalysts and achieved the highest surface area of 74.68 m2g-1. The narrow bandgap (0.88 eV) and fast conversion of Fe2+/Fe3+ cycle of FeSe2 led CR and MB degradation of 93.3% and 90.4%, respectively. The outcome of this study demonstrates improved catalytic properties of FeSe2 nanostructures for the efficient detoxification of hazardous and toxic effluents.

ZIF-8 templated assembly of La3+-anchored ZnO distorted nano-hexagons as an efficient active photocatalyst for the detoxification of rhodamine B in water.

The use of lanthanum-anchored zinc oxide distorted hexagon (La@ZnO DH) nanoclusters as an active material for the photodegradation of rhodamine B (Rh-B) dye via hydrogen bonding, electrostatic, and π-π interactions is examined herein. The active photocatalyst is derived from porous zeolite imidazole frameworks (ZIF-8) via a combined ultrasonication and calcination process. The distorted hexagon nanocluster morphology with controlled surface area is shown to provide excellent catalytic activity, chemical stability and demarcated pore volume. In addition, the low bandgap (3.57 eV) of La@ZnO DH is shown to expand the degradation of Rh-B under irradiation of UV light as compared to the pristine ZIF-8-derived ZnO photocatalyst due to inhibited recombination of electrons and holes. The outstanding physicochemical stability and enhanced performance of La@ZnO DH could be ascribed to the synergistic interaction among La3+ particles and the ZnO nanoclusters and provide a route for their utilization as a promising catalyst for the detoxification of Rh-B.

Highly dispersive Co3O4 nanoparticles incorporated into a cellulose nanofiber for a high-performance flexible supercapacitor.

Transition metal oxides used as electrode materials for flexible supercapacitors have attracted huge attention due to their high specific capacitance and surface-to-volume ratio, specifically for cobalt oxide (Co3O4) nanoparticles. However, the low intrinsic electronic conductivity and aggregation of Co3O4 nanoparticles restrict their electrochemical performance and prevent these electrode materials from being commercialized. Herein, a facile, advantageous, and cost effective sol-gel synthetic route for growing Co3O4 nanoparticles uniformly over a low cost and eco-friendly one-dimensional (1D) hydrophilic cellulose nanofiber (CNF) surface has been reported. This exhibits high conductivity, which enables the symmetric electrode to deliver a high specific capacitance of ∼214 F g-1 at 1 A g-1 with remarkable cycling behavior (∼94% even after 5000 cycles) compared to that of pristine CNF and Co3O4 electrodes in an aqueous electrolyte. Furthermore, the binder-free nature of 1D Co3O4@CNF (which was carbonized at 200 °C for about 20 min under a H2/Ar atmosphere) shows great potential as a hybrid flexible paper-like electrode and provides a high specific capacitance of 80 F g-1 at 1 A g-1 with a superior energy density of 10 W h kg-1 in the gel electrolyte. This study provides a novel pathway, using a hydrophilic 1D CNF, for realizing the full potential of Co3O4 nanoparticles as advanced electrode materials for next generation flexible electronic devices.

Recent Advances in Nanostructured Transition Metal Carbide- and Nitride-Based Cathode Electrocatalysts for Li-O2 Batteries (LOBs): A Brief Review.

A large volume of research on lithium-oxygen (Li-O2) batteries (LOBs) has been conducted in the recent decades, inspired by their high energy density and power density. However, these future generation energy-storage devices are still subject to technical limitations, including a squat round-trip efficiency and a deprived rate-capability, due to the slow-moving electrochemical kinetics of both the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) over the surface of the cathode catalyst. Because the electrochemistry of LOBs is rather complex, only a limited range of cathode catalysts has been employed in the past. To understand the catalytic mechanisms involved and improve overall cell performance, the development of new cathode electrocatalysts with enhanced round-trip efficiency is extremely important. In this context, transition metal carbides and nitrides (TMCs and TMNs, respectively) have been explored as potential catalysts to overcome the slow kinetics of electrochemical reactions. To provide an accessible and up-to-date summary for the research community, the present paper reviews the recent advancements of TMCs and TMNs and its applications as active electrocatalysts for LOBs. In particular, significant studies on the rational design of catalysts and the properties of TMC/TMN in LOBs are discussed, and the prospects and challenges facing the continued development of TMC/TMN electrocatalysts and strategies for attaining higher OER/ORR activity in LOBs are presented.

Ionic Liquid-Based Electrolytes for Energy Storage Devices: A Brief Review on Their Limits and Applications.

Since the ability of ionic liquid (IL) was demonstrated to act as a solvent or an electrolyte, IL-based electrolytes have been widely used as a potential candidate for renewable energy storage devices, like lithium ion batteries (LIBs) and supercapacitors (SCs). In this review, we aimed to present the state-of-the-art of IL-based electrolytes electrochemical, cycling, and physicochemical properties, which are crucial for LIBs and SCs. ILs can also be regarded as designer solvents to replace the more flammable organic carbonates and improve the green credentials and performance of energy storage devices, especially LIBs and SCs. This review affords an outline of the progress of ILs in energy-related applications and provides essential ideas on the emerging challenges and openings that may motivate the scientific communities to move towards IL-based energy devices. Finally, the challenges in design of the new type of ILs structures for energy and environmental applications are also highlighted.

Synthesis and Antibacterial Properties of Novel ZnMn2O4-Chitosan Nanocomposites.

The development of productive antibacterial agents from nontoxic materials via a simple methodology has been an immense research contribution in the medicinal chemistry field. Herein, a sol-gel one-pot reaction was used to synthesize hybrid composites of hausmannite-chitosan (Mn3O4-CS) and its innovative derivative zinc manganese oxide-chitosan (ZnMn2O4-CS). Fixed amounts of CS with different metal matrix w/v ratios of 0.5%, 1.0%, 1.5%, and 2.0% for Mn and Zn precursors were used to synthesize ZnMn2O4-CS hybrid composites. X-ray diffraction analysis indicated the formation of polycrystalline tetragonal-structured ZnMn2O4 with a CS matrix in the hybrids. Fourier-transform infrared spectroscopic analysis confirmed the formation of ZnMn2O4-CS hybrids. Detailed investigations of the surface modifications were conducted using scanning electron microscopy; micrographs at different magnifications revealed that the composites' surface changed depending on the ratio of the source materials used to synthesize the ZnMn2O4-CS hybrids. The antibacterial activity of the Mn3O4-CS and ZnMn2O4-CS composites was tested against various bacterial species, including Bacillus subtilis, Escherichia coli, Salmonella typhi, and Pseudomonas aeruginosa. The zone of inhibition and minimum inhibitory concentration values were deduced to demonstrate the efficacy of the ZnMn2O4-CS nanocomposites as antibacterial agents.

Ni(OH)2-decorated nitrogen doped MWCNT nanosheets as an efficient electrode for high performance supercapacitors.

In this study, nickel hydroxide nanoparticles (NPs) decorated with nitrogen doped multiwalled carbon nanotubes (N-MWCNT) hybrid composite was synthesized by thermal reduction process in the presence of cetyl ammonium bromide (CTAB) and urea. The as-synthesized Ni(OH)2@N-MWCNT hybrid composite was characterized by FTIR, Raman, XRD, BET, BJH and FE-TEM analyses. These prepared porous carbon hybrid composite materials possessed high specific surface area and sheet like morphology useful for active electrode materials. The maximum specific capacitance of Ni(OH)2@N-MWCNT hybrid nanocomposite in the two electrode system showed 350 Fg-1 at 0.5 A/g,energy density ~43.75 Wkg-1 and corresponds to power density 1500 W kg-1 with excellent capacity retention after 5000 cycles. The results suggest that the prepared two-dimensional hybrid composite is a promising electrode material for electrochemical energy storage applications.