Reticular Chemistry for Optical Sensing of Anions.

In the last few decades, reticular chemistry has grown significantly as a field of porous crystalline molecular materials. Scientists have attempted to create the ideal platform for analyzing distinct anions based on optical sensing techniques (chromogenic and fluorogenic) by assembling different metal-containing units with suitable organic linking molecules and different organic molecules to produce crystalline porous materials. This study presents novel platforms for anion recognition based on reticular chemistry with high selectivity, sensitivity, electronic tunability, structural recognition, strong emission, and thermal and chemical stability. The key materials for reticular chemistry, Metal-Organic Frameworks (MOFs), Zeolitic Imidazolate Frameworks (ZIFs), and Covalent-Organic Frameworks (COFs), and the pre- and post-synthetic modification of the linkers and the metal oxide clusters for the selective detection of the anions, have been discussed. The mechanisms involved in sensing are also discussed.

Mixed Dimensional Nanostructure (UiO-66-Decorated MWCNT) as a Nanofiller in Mixed-Matrix Membranes for Enhanced CO2 /CH4 Separation.

Mixed-matrix membranes (MMMs) with combination of two distinct dimensional nanofillers (such as 1D-3D, 2D-3D, or 3D-3D, etc.) have drawn special attention for gas separation applications due to their concerted effects on gas permeation and mechanical properties. An amine-functionalized 1D multiwalled carbon nanotube (NH2 -MWCNT) with exceptional mechanical strength and rapid gas transport was crosslinked with an amine-functionalized 3D metal-organic framework (UiO-66-NH2 ) with high CO2 affinity in a Schiff base reaction. The resultant crosslinked mixed-dimensional nanostructure was used as a nanofiller in a polysulfone (PSf) polymer matrix to explore the underlying synergy between 1D and 3D nanostructures on the gas separation performance of MMMs. Cross-sectional scanning electron microscopy and mapping revealed the homogenous dispersion of UiO-66@MWCNT in the polymer matrix. The MMM containing 5.0 wt. % UiO-66@MWCNT demonstrated a superior permeability 8.3 Barrer as compared to the 4.2 Barrer of pure PSf membrane for CO2 . Moreover, the selectivity (CO2 /CH4 ) of this MMM was enhanced to 39.5 from the 28.0 observed for pure PSf under similar conditions of pressure and temperature.

Hematite and Magnetite Nanostructures for Green and Sustainable Energy Harnessing and Environmental Pollution Control: A Review.

The optoelectrical and magnetic characteristics of naturally existing iron-based nanostructures, especially hematite and magnetite nanoparticles (H-NPs and M-NPs), gained significant research interest in various applications, recently. The main purpose of this Review is to provide an overview of the utilization of H-NPs and M-NPs in various environmental remediation. Iron-based NPs are extensively explored to generate green energy from environmental friendly processes such as water splitting and CO2 conversion to hydrogen and low molecular weight hydrocarbons, respectively. The latter part of the Review provided a critical overview to use H-NPs and M-NPs for the detection and decontamination of inorganic and organic contaminants to counter the environmental pollution and toxicity challenge, which could ensure environmental sustainability and hygiene. Some of the future perspectives are comprehensively presented in the final portion of the script, optimiztically, and it is supported by some relevant literature surveys to predict the possible routes of H-NPs and M-NPs modifications that could enable researchers to use these NPs in more advanced environmental applications. The literature collection and discussion on the critical assessment of reserving the environmental sustainability challenges provided in this Review will be useful not only for experienced researchers but also for novices in the field.

Frontiers and Challenges in Electrochemical Corrosion Monitoring; Surface and Downhole Applications.

Corrosion sensing is essential to monitor and safeguard the materials' health and control the maintenance cost of corrosion-prone materials used in various industries. The petroleum industry is a major sufferer of corrosion costs among various industries due to pipelines and downhole applications. This review article encompasses an overview of various technologies used in early detection stages for more reliable corrosion sensing and warnings. This review provides a summary of corrosion types, corrosion causing chemical species, different destructive and non-destructive technologies used in monitoring corrosion and a comprehensive overview of the state-of-the-art of various electrochemical techniques used for surface and downhole corrosion monitoring. Finally, the existing challenges for corrosion monitoring in surface and downhole conditions and prospects are discussed.

Report: Antibacterial and antifungal activities of leaf extract of Achyranthes aspera (Amaranthaceae) from Pakistan.

Alcoholic extract and various fractions of Achyranthes aspera leaves, traditionally used in Pakistan for treatment of infectious diseases was screened for in vitro antibacterial and antifungal activity. The chloroform and butanol fractions were found to be the most active among the fractions, showing considerable antibacterial activity against Shigella flexneri and Escherichia coli. The highest activity was found in the ethylacetate fraction (17 mm zone of inhibition) against gram-negative (Salmonella typhi) bacteria, with MIC value as 0.29 mg/mL. In antifungal screening, moderate activity was shown by the chloroform fraction (50 % inhibition) against Microsporum canis, with MIC value as 0.25mg/mL. Considerable level of antifungal activity was depicted by crude extract, hexane and butanol fractions against Aspergillus flavus and Microsporum canis. The ability of various extracts of Achyranthes aspera to inhibit different strains of fungi and bacteria indicates its potential use for the treatment of microbial infections.

Efficient rhodamine B dye photocatalytic degradation in aqueous media using novel ZnO nanomaterials co-doped with Ce and Dy.

Water pollution caused by dyes and industrial wastewater poses a significant threat to ecosystems. The purification of such pollutants presents a major challenge. Photocatalysis based on semiconductor materials is a potential wastewater treatment process due to its safety and cost-effectiveness. In the present work, Zn1-2xCexDyxO (x = 0.01-0.05) semiconductors were prepared by the sol-gel auto-ignition method. The samples are denoted CDZO1, CDZO3, and CDZO5 for x  = 0.01-0.05, respectively. The X-ray diffraction and Raman spectroscopy results revealed the formation of ZnO hexagonal phase wurtzite structure for all synthesized compositions. Different structural properties were determined. It was found that the lattice parameters and the unit cell volume increased, while the crystallite size diminished as x varied from 0.01 to 0.05. Transmission electron microscopy observations confirmed the formation of nanoparticles with the desired chemical compositions. The specific surface area (SSA) values are found to be 39.95 m2/g, 48.62 m2/g, and 51.36 m2/g for CDZO1, CDZO5, and CDZO5 samples, respectively. The reflectance spectra were recorded to examine the optical properties of the different nanoparticles. The values of the optical band gap were 3.221, 3.225, and 3.239 eV for CDZO1, CDZO3, and CDZO5 samples, respectively. In addition, the photocatalytic performance towards RhB dye degradation for the different samples was assessed. It was established that the CDZO3 sample with a moderate SSA value exhibited the superior photocatalytic performance among the other as-prepared samples wherein the percentage of degradation efficiency, and kinetic constant rate attained their maximum values of 98.22 % and 0.0521 min-1, respectively within 75 min. As per the obtained findings, it is evident that the Zn1-2xCexDyxO photocatalyst has prominent potential for use in the degradation of dyes and offers a useful route for impeding the recombination of electron-hole pairs of zinc oxide material.

Stainless Steel Mesh in Electrochemistry: Comprehensive Applications and Future Prospects.

Stainless steel mesh (SSM) has emerged as a cornerstone in electrochemical applications owing to its exemplary versatility, electrical conductivity, mechanical robustness, and corrosion resistance. This state-of-the-art review delves into the diverse roles of SSM across a spectrum of electrochemical domains, including energy conversion and storage devices, water treatment technologies, electrochemical sensors, and catalysis. We meticulously explore its deployment in supercapacitors, batteries, and fuel cells, highlighting its utility as a current collector, electrode, and separator. The review further discusses the critical significance of SSM in water treatment processes, emphasizing its efficacy in supporting membranes and facilitating electrocoagulation, as well as its novel uses in electrochemical sensing and catalysis, which include electrosynthesis and bioelectrochemistry. Each section delineates the recent advancements, identifies the inherent challenges, and suggests future directions for leveraging SSM in electrochemical technologies. This comprehensive review showcases the current state of knowledge and articulates the novel integration of SSM with emerging materials and technologies, thereby establishing a new paradigm for sustainable and efficient electrochemical applications. Through critical analysis and insightful recommendations, this review positions itself as a seminal contribution, paving the way for researchers and practitioners to harness the full potential of SSM in advancing the electrochemistry frontiers.

Molecular interactions of 4-acetoxy-plakinamine B with peripheral anionic and other catalytic subsites of the aromatic gorge of acetylcholinesterase: computational and structural insights.

CONTEXT: A steroidal alkaloid, 4-acetoxy-plakinamine B (4APB), is a recently discovered marine natural product with inhibitory effect against acetylcholinesterase (AChE), but its mechanism of interaction with the enzyme remains to be elucidated. OBJECTIVE: The main objective was to study molecular binding mode of the compound, its interactions with catalytic subsites and molecular mechanism behind its significant inhibitory effect. MATERIALS AND METHODS: All possible interactions of ligands in the binding sites were analyzed using FRED 2.1 and the OMEGA pre-generated multi-conformer library. RESULTS: Dipole-dipole interactions were observed between the secondary amino group of 4APB and Ser200 at a distance of 3.91 Å and also with Gly117 and Gly118. A further dipole-dipole interaction was between Arg289 and the heterocyclic nitrogen. Hydrogen bonding interactions were observed between Tyr130 and secondary amino and C-4 acetyl groups as well as between heterocyclic nitrogen and Phe288 at a distance of 3.04 Å. Hydrophobic interactions were evident between rings C/D of 4APB and with Phe288, Phe330 and Phe331. The computational studies revealed 4APB's critical molecular interaction with amino acids of peripheral active (PAS) and anionic (AS) subsites. DISCUSSION: Our data provided molecular evidence for the mixed competitive inhibitory effect of 4APB. For lead optimization, structural insights revealed the N-methyl group of 4APB could be replaced by NH2 moiety to generate a more favorable hydrogen bonding with Glu199. A polar group insertion such as NH2 or OH at certain sites of the 4APB skeleton is also recommended. CONCLUSION: These computational insights explained the mixed-competitive enzyme kinetic behavior of 4APB. This study outlines a strategy for designing novel derivatives of 4APB with potentially better AChE inhibitory activities through interaction at the PAS and AS sites.

Fabrication of a Novel Co/CoO@Fe2 V4 O13 Composite Catalyst as a Photoanode for Enhanced Photoelectrochemical Water Oxidation.

Herein, the synthesis of a novel composite photocatalyst, Co/CoO@Fe2 V4 O13 , is reported by the deposition of CoO metal oxide nanoparticles on the surface of Fe2 V4 O13 bimetallic oxide. The synthesised photocatalyst exhibited a band gap of roughly 1.8 eV, rendering it responsive to the complete visible light spectrum of the sun, thereby enabling optimal absorption of solar radiation. The Co/CoO@Fe2 V4 O13 composites demonstrated an enhanced photoelectrochemical water oxidation capacity compared to pristine Fe2 V4 O13 when exposed to visible light. The enhanced performance is attributed primarily to the creation of a p-n junction at the interface of Fe2 V4 O13 and Co/CoO, as well as the Z-scheme charge transfer mechanism, which aids in the separation and transfer of photogenerated charge carriers. Light absorption by Co nanoparticles via plasmonic excitation and intra- and inter-band transitions in the composite structure is also likely, resulting in increased composite efficiency. Our findings indicate that Co/CoO@Fe2 V4 O13 composites show promising performance for solar water splitting applications and offer new perspectives for designing effective photocatalysts.

Facile deposition of FeNi/Ni hybrid nanoflower electrocatalysts for effective and sustained water oxidation.

Bimetallic iron-nickel (FeNi) compounds are widely studied materials for the oxygen evolution reaction (OER) owing to their high electrocatalytic performance and low cost. In this work, we produced thin films of the FeNi alloy on nickel foam (NF) by using an aerosol-assisted chemical deposition (AACVD) method and examined their OER catalytic activity. The hybrid FeNi/Ni catalysts obtained after 1 and 2 h of AACVD deposition show improved charge transfer and kinetics for the OER due to the strong interface between the FeNi alloy and Ni support. The FeNi/Ni-2h catalyst has higher catalytic activity than the FeNi/Ni-1h catalyst because of its nanoflower morphology that provides a large surface area and numerous active sites for the OER. Therefore, the FeNi/Ni-2h catalyst exhibits low overpotentials of 300 and 340 mV at 50 and 500 mA cm-2 respectively, and excellent stability over 100 h, and ∼0% loss after 5000 cycles in 1 M KOH electrolyte. Furthermore, this catalyst has a small Tafel slope, low charge transfer resistance and high current exchange density and thus surpasses the benchmark IrO2 catalyst. The easy, simple, and scalable AACVD method is an effective way to develop thin film electrocatalysts with high activity and stability.

Effect of Synthetic Methodology on the Physicochemical Attributes and Electrocatalytic Activity of NiAl-LDHs for the Oxygen Evolution Reaction.

Layered double hydroxides (LDHs) are promising materials for oxygen evolution reactions (OERs), a key component of water splitting to produce hydrogen and oxygen via water electrolysis. However, the performance of LDHs can be limited by their low surface area and poor accessibility of active sites. In this work, we synthesized highly exfoliated 2D NiAl-LDHs by aqueous miscible solvent treatment method (AMOST) and compared its electrocatalytic efficiency with its analogue synthesised via slow urea hydrolysis. We demonstrate that the exfoliated 2D LDHs prepared by AMOST method have a higher surface area and more active sites than the crystalline LDHs obtained through urea hydrolysis, resulting in a superior OER activity and efficiency. The exfoliated 2D LDHs required a lower overpotential of 280 mV to reach a current density of 50 mA cm-2 and it also outperformed IrO2 , a benchmark OER catalyst, in terms of overpotential and stability. We demonstrate that the physicochemical properties of nanosheets derived from NIAl-LDH-based materials are strongly influenced by the synthetic methodology, which affects the exfoliation degree, surface area and active site density. These factors are crucial for improving the OER catalytic performance of these materials, as shown by our results.

CO2 Adsorption on Biomass-Derived Carbons from Albizia procera Leaves: Effects of Synthesis Strategies.

CO2 capture is a useful strategy for controlling the risks associated with global warming. The design of an adsorbent is essential for clean and potentially energy-efficient adsorption-based carbon capture processes. This study reports a facile and moderately temperature single-stage combined pyrolysis and activation strategy for the synthesis of nitrogen-doped carbons for high-performance CO2 capture. Using nitrogen-rich Albizia procera leaves as the precursor and carrying out single-stage pyrolysis and activation at temperatures of 500, 600, and 700 °C in the presence NaHCO3 as an activating agent, carbons with different surface characteristics and ultrahigh weight percentage (22-25%) of nitrogen were obtained. The subtle differences in surface characteristics and nitrogen content had a bearing on the CO2 adsorption performance of the resultant adsorbents. Outstanding results were achieved, with a CO2 adsorption capacity of up to 2.5 mmol/g and a CO2 over N2 selectivities reaching 54. The isotherm results were utilized to determine the performance indicators for a practical vacuum swing adsorption process. This study provides a practical strategy for the efficient synthesis of nitrogen-doped carbons for various adsorption applications.

Sn-doped BiOCl for photoelectrochemical activities and photocatalytic dye degradation under visible light.

In this work, bismuth oxychloride (BiOCl) and Sn-doped BiOCl (SBCl) with improved visible light photocatalytic activity were synthesized via the co-precipitation method. The XRD analysis determined the tetragonal phase of BiOCl, 1 %, 5 %, and 10 % SBCl. The crystallite sizes were in the range of 20-34 nm. These results confirmed that the Sn ion was successfully incorporated into the BiOCl lattice. This was further confirmed by FT-IR and Raman analysis. The optical properties, such as the band gap energy, were studied using UV-vis DRS. It was found that doping BiOCl with Sn has a minor effect on the band gap tuning. BET shows that the SBCl samples have acquired a larger specific surface area (14.66-42.20 m2/g) than BiOCl (13.49 m2/g). The photocatalytic performance showed that SBCl samples have higher photocatalytic activity than BiOCl in degrading Rhodamine B (RhB) dye under visible light irradiation. Among the SBCl samples, 5 % SBCl exhibited the highest photocatalytic efficiency which degraded 91.2 % of the RhB dye in 60 min. Moreover, the photoelectrochemical activities of the as-synthesized BiOCl and SBCl were investigated using linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) in the dark and under visible light irradiation. Both studies showed that SBCl exhibits enhanced photoelectrochemical activities than BiOCl. Hence, it can be suggested that SBCl possesses visible light active properties and can be potentially used as a photocatalyst and photoelectrode material.

CO2 Adsorption on Pore-Engineered Carbons Derived from Jute Sticks.

CO2 capture is a practical approach to mitigating the impacts of global warming. Adsorption-based carbon capture is a clean and potentially energy-efficient method whose performance greatly depends on adsorbent design. In this study, we explored the use of jute-derived carbon as a high-performance adsorbent for CO2 capture. The carbons were produced by pyrolyzing powdered jute sticks with NaHCO3 as an activating agent at 500-700 °C. Impressive adsorption capacities of up to 2.5 mmol ⋅ g-1 and CO2 /N2 selectivities of up to 54 were achieved by adjusting the pore size distribution and surface functionalization. Based on the isotherm results, the working capacities, regenerabilities, and potentials for CO2 separation were determined for a practical vacuum swing adsorption process. The adsorbent materials were characterized by XRD, FTIR, Raman, FESEM and N2 sorption at 77 K. This study provides a general approach for designing adsorbents for various gas-separation applications.

Photoassisted degradation of a herbicide derivative, dinoseb, in aqueous suspension of titania.

The titanium dioxide (TiO(2)) photoassisted degradation of herbicide dinoseb has been examined in aqueous suspensions under UV light irradiation. The degradation kinetics were studied under various conditions such as substrate concentration, type of catalyst, catalyst dosage, pH, and light intensity as well as in presence of electron acceptors such as hydrogen peroxide, potassium bromate, and potassium persulphate under continuous air purging, and the degradation rates were found to be strongly influenced by these parameters. The Degussa P25 was found to be more efficient photocatalyst as compared to other photocatalysts tested. Dinoseb was found to degrade efficiently in acidic pH and all the electron acceptors studied enhanced the degradation rate. The results manifested that the photocatalysis of dinoseb followed pseudo-first-order kinetics. A qualitative study of the degradation products generated during the process was performed by GC-MS, and a degradation mechanism was proposed.

ZSM-5 Catalysts for MTO: Effect and Optimization of the Tetrapropylammonium Hydroxide Concentration on Synthesis and Performance.

Light olefin production from methanol using various zeolite catalysts has industrial and economic importance considering the growth of the petrochemical market. Zeolites are generally synthesized using various organic templates as structure-directing agents (SDAs). In this study, synthesis of a series of ZSM-5 zeolites was performed systematically using the microwave-assisted crystallization method, and these samples were analyzed in detail to understand the effect of the SDA concentration. Powder diffraction, N2 adsorption, scanning electron microscopy, ammonia adsorption desorption, and 27Al and 29Si NMR spectroscopies were used for the characterization. The organic SDA tetrapropyl ammonium hydroxide (TPAOH/SiO2 mole ratio = 0.0500) is found to have an optimum concentration against the silica precursor for achieving the highest crystallinity, suitable morphology, ideal pore size, effective pore volume, and tuned microporous/mesoporous area. For samples with a template concentration ratio of 0.050 or higher, 29Si and 27Al NMR data revealed the presence of an intact ZSM-5 structure. Using a fixed bed reactor at 500 °C and atmospheric pressure, the catalytic performance of the selected catalysts from the series is investigated for the methanol-to-olefin conversion reaction. The sample with the highest crystallinity showed the best conversion, selectivity toward light olefins, and time on stream stability. It is also worth noting that the highest crystallinity, micropore area, and micropore volume are reached for the optimum value rather than the highest template concentration. This allows for a reduction in the template concentration and a move closer to a synthesis pathway benign to environment and economics.

Zr, La-dual doped silver niobate for photocatalytic degradation of dyes under visible light irradiation.

Sol-gel-assisted synthesis of silver niobate, 1%, 5%, and 10% Zr, La-dual doped silver niobates were carried out. Analysis done using XRD showed that increasing Zr and La dual doping caused the synthesized materials to adopt an AgNbO3-like structure. This is also supported by FT-IR results. FESEM revealed that the silver niobate has a prism-like morphology while Zr, La-dual doped samples are irregular in shape. EDX mapping of the 10% Zr, La dual silver niobate confirmed the presence of Nb, Ag, Zr, and La metals. When compared with the silver niobate, the band gap energy of Zr, La-dual doped silver niobates are narrower, as shown by UV-Vis DRS measurements. It was revealed that dual doping of silver niobates with Zr and La has significantly improved the photocatalytic degradation of methylene blue (MB) and Rhodamine B (RhB) dyes. The 1% Zr, La-dual doped silver niobate showed the best photocatalytic results in terms of degrading MB while 10% Zr, La-dual doped silver niobate achieved the best performance when degrading RhB.

Catalytic Cracking of n-Dodecane to Chemicals: Effect of Variable-Morphological ZSM-5 Zeolites Synthesized Using Various Silica Sources.

This study emphasizes tuning the synthesis conditions of MFI zeolites to achieve better catalytic properties by optimizing the mesoporosity, the balance between Brønsted and Lewis sites, and the zeolite particle sizes. The MFI zeolites were hydrothermally synthesized at various temperatures employing different silica sources. The synthesis temperature was varied between 110 to 180 °C at constant synthesis time (15 h). Different silicon sources led to variations in structure, morphology, and size of the MFI zeolite along with tuned Lewis and Brønsted acid sites in parallel correlation with shape selectivity of the reaction. The catalytic activities of synthesized zeolites were investigated in the catalytic cracking of n-dodecane to produce value-added chemicals. The zeolite synthesized at 180 °C using fumed silica presented the highest catalytic conversion (96.6%), while maximum light olefin gaseous products (73.1%) were obtained for the sample synthesized at 140 °C using tetraethyl orthosilicate as the silica source. The MFI zeolite synthesized at 180 °C employing tetraethyl orthosilicate as a silica source facilitated the formation of both naphthenes and aromatics (71.3%) as major liquid products.

Prognostic significance of serum bilirubin in stroke.

BACKGROUND: Oxidative injury is an important cause of the neurologic lesion in stroke. Serum bilirubin is considered a natural antioxidant that may affect the prognosis of stroke. The purpose of this study was to evaluate the prognostic significance of bilirubin in stroke patients. METHODS: A prospective cross-sectional study was conducted in Medical Units of Khyber Teaching Hospital, Peshawar. Inpatients admitted with acute attack of stroke were included in this study. Data regarding serum bilirubin and concurrent cerebrovascular risk factors were collected. National Institutes of Health Stroke Scale (NIHSS) and modified Rankin Scale (mRS) were used to analyse stroke's severity and functional outcomes, respectively. RESULTS: Hypertension, diabetes mellitus and heart diseases were the most common risk factors. Patients were divided into 3 groups on the basis of serum bilirubin, i.e., < or = 0.6 mg/dl (Group-1), 0.7-0.9 mg/dl (Group-2), and > or = 1.0 mg/dl (Group-3). The mean pre-hospitalisation NIHSS score for Groups 1, 2 and 3 was 5.62, 11.66 and 25.33, respectively; and post-hospitalisation score was 0.875, 3.76 and 16.26, respectively. The pre-hospitalisation mRS score was 4 for Group-1, 4.52 for Group-2 and 4.93 for Group-3; while post-hospitalisation Mrs Score was 1.50, 2.38 and 4.26, respectively. Average serum bilirubin level was significantly higher in patients with poor outcomes as compared with good outcomes (p < 0.01). CONCLUSIONS: This study suggests that higher serum bilirubin levels were associated with increased stroke severity, longer hospitalisation and poor prognosis.

Aerosol-Assisted Chemical Vapor Deposition Growth of NiMoO4 Nanoflowers on Nickel Foam as Effective Electrocatalysts toward Water Oxidation.

The fabrication of active and durable catalysts derived from transition metals is highly desired for the realization of efficient water oxidation reactions. This is particularly important to address the slow oxygen evolution reaction (OER) kinetics and hence can contribute to the conversion and storage of sustainable energy. In this study, the deposition of crystalline flowerlike 2D nanosheets of nickel molybdate (NiMoO4) directly on nickel foam (NF) through an aerosol-assisted chemical vapor deposition process is reported. The NiMoO4 nanosheets were developed on NF by altering the deposition time for 60 and 120 min at a fixed temperature of 480 °C. The structural determination by XRD and XPS analyses revealed a highly crystalline single phase NiMoO4. The micrographs of NiMoO4 show that the surface consisted of vertically aligned 2D nanosheets assembled into flowerlike structures. The nanosheets produced after 60 min deposition time on a network of NF is found to perform better for OER as compared to the one developed for 120 min. A reference current density of 10 mA cm-2 was achieved at an overpotential (η) of 320 mV, which was better as compared to that reported for the benchmark OER catalyst in 1.0 M KOH. Moreover, a small Tafel value (75 mV dec-1) and good OER stability for >15 h were also observed.