Recovery of copper/carbon matrix nanoheteroarchitectures from recyclable electronic waste and their efficacy as antibacterial agents.

Innovative solutions are urgently needed with the growing environmental hazard of electronic waste (e-waste) and the rising global threat of bacterial infections. This study addresses both issues by using e-waste to produce copper nanoparticles within a carbon matrix (Cu/C NPs), mitigating environmental hazards while exploring their antibacterial properties. Printed circuit boards from discarded computers were collected and treated with 2 M ammonium citrate dissolved in 8% ammonia solution. The leached solution was used to synthesize copper particles using ascorbic acid. The synthesized Cu/C NPs were characterized using various techniques such as EDX, field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared (FT-IR) spectroscopy. The antibacterial activity of Cu/C NPs against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) was evaluated using colony-forming unit (CFU) reduction assay and calculating the minimum inhibitory concentrations (MICs). The Cu/C NPs were found to be effective against E. coli and S. aureus with 100% and 98% CFU reduction, respectively, with MICs ranging from 250 to 375 µg mL-1 for E. coli and 375 to 750 µg mL-1 for S. aureus, according to the bacterial load. The bactericidal kinetics showed complete bacterial elimination after 5 and 7 hours for E. coli and S. aureus, respectively. This study presents a sustainable approach for utilizing e-waste and demonstrates the potential of the recovered nanoparticles for antibacterial applications.

Electronic properties of pristine and doped graphitic germanium carbide nanomeshes.

Graphitic germanium carbide (g-GeC) is a novel material that has recently aroused much interest. Porous g-GeC can be fabricated by forming a lattice of pores in pristine g-GeC. In this work, we systematically investigate the influence of creating pores within pristine g-GeC. The pores are passivated with hydrogen, nitrogen, and oxygen, with four supercell sizes. The electronic properties are calculated using the density functional theory (DFT) formalism, which revealed that hydrogen-passivated systems have bandgaps ranging from 1.80 eV to 1.93 eV. The corresponding ranges for the nitrogen- and oxygen-passivated systems are 1.21 eV to 1.58 eV, and 1.18 eV to 1.45 eV, respectively. The bandgaps are always smaller than that of the pristine g-GeC system, and they approach the pristine value for larger supercell sizes. The studied systems have charge-trapping clusters of states located above/below the valence/conduction bands, partially localized at the pore-edge atoms. Additionally, we explore the chelation doping of the N-passivated GeC nanomesh using transition metal (Ni, Pd, Pt) three-atom clusters. Interestingly, the doped systems are dilute magnetic semiconductors. The studied systems exhibit electronic properties that may be useful for sensing and spintronics.

Designing N, P-doped graphene surface-supported Mo single-atom catalysts for efficient conversion of nitrogen into ammonia: a computational guideline.

Tuning the surroundings of single-atom catalysts (SACs) has been recognized as a successful approach to enhance their electrocatalytic efficiency. In this study, we utilized density functional theory (DFT) computations to systematically investigate how the coordination environment influences the catalytic performance of individual molybdenum atoms for the nitrogen reduction reaction (NRR) to NH3. Upon comparing an extensive array of coordination combinations, Mo-based SACs were found to feature a distinctive N, P-dual coordination. Specifically, MoN3P1G demonstrates superior performance in the conversion of nitrogen into ammonia with an exceptionally low limiting potential (-0.64 V). This MoN3P1G catalyst preferably follows the distal pathway, with the initial hydrogenation step (*N2 → *NNH) being the rate-determining step. Additionally, MoN3P1G exhibits the ability to suppress competing H2 production, showcases high thermodynamic stability, and holds significant promise for experimental preparation. These findings not only contribute to diversifying the SAC family through localized coordination control but also present cost-effective strategies for enhancing sustainable NH3 production.

A hybrid FeOx/CoOx/Pt ternary nanocatalyst for augmented catalysis of formic acid electro-oxidation.

Platinum-based catalysts that have long been used as the anodes for the formic acid electro-oxidation (FAO) in the direct formic acid fuel cells (DFAFCs) were susceptible to retrogradation in performance due to CO poisoning that impaired the technology transfer in industry. This work is designed to overcome this challenge by amending the Pt surface sequentially with nanosized cobalt (nano-CoOx, fibril texture of ca. 200 nm in particle size) and iron (nano-FeOx, nanorods of particle size and length of 80 and 253 nm, respectively) oxides. This enriched the Pt surface with oxygenated groups that boosted FAO and mitigated the CO poisoning. The unfilled d-orbitals of the transition metals and their tendency to vary their oxidations states presumed their participation in a faster mechanism of FAO. Engineering the Pt surface in this FeOx/CoOx/Pt hierarchy resulted in a remarkable activity toward FAO, that exceeded four times that of the Pt catalyst with up to ca. 2.5 times improvement in the catalytic tolerance against CO poisoning. This associated a ca. - 32 mV shift in the onset potential of FAO which increased to - 40 mV with a post-activation of the same catalyst at - 0.5  in 0.2 mol L-1 NaOH, displaying the catalyst's competitiveness in reducing overpotentials in DFAFCs. It also exhibited a favorable amelioration in the catalytic durability in long-termed chronoamperometric electrolysis. The electrochemical impedance spectroscopy and the CO stripping voltammetry were employed to elucidate the origin of enhancement.

In Vitro: The Extraordinary Enhancement in Rutin Accumulation and Antioxidant Activity in Philodendron "Imperial Red" Plantlets Using Ti-Mo-Ni-O Nanotubes as a Novel Elicitor.

Rutin, a flavonoid phytochemical compound, plays a vital role in human health. It is used in treating capillary fragility and has anti-Alzheimer, anti-inflammatory, and antioxidant effects. In this study, Ti-Mo-Ni-O nanotubes (NTs) were used, for the first time, in an unprecedented plant biotechnology application, wherein in vitro Philodendron shoots (Philodendron erubescens) known as "Imperial Red" were targeted for rutin accumulation. The antioxidant responses and the accumulation of rutin were evaluated in treated Philodendron erubescens (P. erubescens) shoots using 5.0 mg/L of Ti-Mo-Ni-O NTs. The total phenolic content and total flavonoid content were estimated, and an ABTS+ assay, FRAP assay, and iron metal chelation assay were performed. The application of Ti-Mo-Ni-O NTs enhanced the rutin content considerably from 0.02 mg/g to 2.96 mg/g for dry-weight shootlet extracts. Therefore, the use of Ti-Mo-Ni-O NTs is proposed to be a superior alternative to elevate the rutin content. The aim of the current study is to target P. erubescens shoots grown in vitro for the accumulation of rutin compounds using Ti-Mo-Ni-O NT powder, to determine the quantitative and qualitative accumulation of rutin via HPLC-DAD analysis, and to estimate the antioxidant activity of P. erubescens shoot extract. This study presents a novel methodology for utilizing nano-biotechnology in the synthesis of plant secondary metabolites.

Compositionally Tunable Mn-V-Fe Phosphoselenide Nanorods with Minimal Ion-Diffusion Barrier as High Energy Density Battery Electrode Materials.

The design and synthesis of novel heterostructured electrode materials are crucial to enable the fabrication of efficient supercapacitor devices. In this regard, transition metal phosphochalcogenides (S, Se) are promising candidates owing to their exotic electronic properties. Herein, a facile two-step hydrothermal protocol was used to synthesize binary and ternary metal phospho-selenide electrodes (Mn-Fe-P-Se, V-Fe-P-Se, Mn-V-P-Se, and Mn-Fe-V-P-Se). The chemical composition, morphology, and structure of the as-fabricated materials were fully investigated. The three-electrode electrochemical evaluation at 1.0 A g-1 demonstrated that the ternary metal electrode (MFVP-Se) exhibits a high capacity of 1968.63 C g-1. To assess the practical value of the rationally designed Mn-Fe-V-P-Se electrode material, Mn-Fe-V-P-Se was used as a positive electrode coupled with activated carbon (AC) as a negative electrode to assemble a hybrid supercapacitor device. This Mn-Fe-V-P-Se//AC device delivers a power density of 1999.96 W kg-1 with a high energy density of 149.88 Wh kg-1 coupled with no capacity loss after 5000 charging/discharging cycles. Additionally, density functional theory calculations revealed that our electrode exhibits suitable adsorption energy for OH- ions with a minimal diffusion barrier for ions.

Zeolitic imidazolate framework-8 encapsulated with Mo-based polyoxometalates as surfaces with antibacterial activity against Escherichia coli.

Bacterial infections represent a major global health concern, causing millions of deaths and a significant economic burden. The development of antibacterial nanoporous surfaces with potential mechano-bactericidal effects can revolutionize infection control practices. In this study, a hybrid material of zeolitic imidazolate framework-8 (ZIF-8) doped with phosphomolybdic acid (PMA) was synthesized and characterized by field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and N2 sorption isotherms. PMA@ZIF-8 performance as an antibacterial agent against E. coli was superior to that of its individual constituents, suggesting a synergistic effect of PMA and ZIF-8. The incorporation of PMA into ZIF-8 significantly enhanced its antibacterial efficacy, as evidenced by a twofold reduction in MIC (375 µg mL-1 vs. 750 µg mL-1) and a 4.35 times increase in the bactericidal kinetics rate constant. The time-kill curve experiment revealed that PMA@ZIF-8 achieved a 3-log reduction within 7 hours, whereas ZIF-8 required 24 hours to reach the same level of reduction. The density functional theory (DFT) calculated bandgap of PMA@ZIF-8 was significantly less than that of ZIF-8. Also, PMA@ZIF-8 has caused the elimination of 56.72% of the thiol group as detected by Ellman's assay. Accordingly, PMA@ZIF-8 can be both computationally and experimentally demonstrated as an oxidative nanozyme. PMA@ZIF-8's surface topology revealed nanorod protrusions, suggesting a potential mechano-bactericidal effect, which was confirmed by live/dead assay on PMA@ZIF-8-coated glass. This study highlights the potential of the PMA@ZIF-8 hybrid as a highly effective antibacterial agent, holding promise for creating multifunctional antibacterial surfaces.

Patterned PCL/PGS Nanofibrous Hyaluronic Acid-Coated Scaffolds Promote Cellular Response and Modulate Gene Expression Profiles.

Chronic wounds impose a significant burden on individuals and healthcare systems, necessitating the development of advanced wound management strategies. Tissue engineering, with its ability to create scaffolds that mimic native tissue structures and promote cellular responses, offers a promising approach. Electrospinning, a widely used technique, can fabricate nanofibrous scaffolds for tissue regeneration. In this study, we developed patterned nanofibrous scaffolds using a blend of poly(ε-caprolactone) (PCL) and poly(glycerol sebacate) (PGS), known for their biocompatibility and biodegradability. By employing a mesh collector, we achieved a unique fiber orientation pattern that emulated the natural tissue architecture. The average fiber diameter of PGS/PCL collected on aluminum foil and on mesh was found to be 665.2 ± 4 and 404.8 ± 16 nm, respectively. To enhance the scaffolds' bioactivity and surface properties, it was coated with hyaluronic acid (HA), a key component of the extracellular matrix known for its wound-healing properties. The HA coating improved the scaffold hydrophilicity and surface wettability, facilitating cell attachment, spreading, and migration. Furthermore, the HA-coated scaffold exhibited enhanced biocompatibility, promoting cell viability and proliferation. High-throughput RNA sequencing was performed to analyze the influence of the fabricated scaffold on the gene expression levels of endothelial cells. The top-upregulated biological processes and pathways include cell cycle regulation and cell proliferation. The results revealed significant alterations in gene expression profiles, indicating the scaffold's ability to modulate cellular functions and promote wound healing processes. The developed scaffold holds great promise for advanced wound management and tissue regeneration applications. By harnessing the advantages of aligned nanofibers, biocompatible polymers, and HA coating, this scaffold represents a potential solution for improving wound healing outcomes and improving the quality of life for individuals suffering from chronic wounds.

Expression of concern: Tin-zinc-oxide nanocomposites (SZO) as promising electron transport layers for efficient and stable perovskite solar cells.

Expression of concern for 'Tin-zinc-oxide nanocomposites (SZO) as promising electron transport layers for efficient and stable perovskite solar cells' by Ahmed E. Shalan et al., Nanoscale Adv., 2019, 1, 2654-2662, DOI: https://doi.org/10.1039/C9NA00182D.

Unleashing the Full Potential of Electrochromic Heterostructured Nickel-Cobalt Phosphate for Optically Active High-Performance Asymmetric Quasi-Solid-State Supercapacitor Devices.

The rational design of hybrid systems that combine capacitor and battery merits is crucial to enable the fabrication of high energy and power density devices. However, the development of such systems remains a significant barrier to overcome. Herein, we report the design of a Ni-Co phosphate (Ni3-xCox(PO4)2·8H2O) nanoplatelet-based system via a facile coprecipitation method at ambient conditions. The nanoplatelets exhibit multicomponent synergy, exceptional charge storage capabilities, rich redox active sites (ameliorating the redox reaction activity), and high ionic diffusion rate/electron transfer kinetics. The designed Ni3-xCox(PO4)2·8H2O offered a respectable gravimetric specific capacity and marvelous capability rate (966 and 595 C g-1 at 1 and 15 A g-1) over the Ni3(PO4)2·8H2O (327.3 C g-1) and Co3(PO4)2·8H2O (68 C g-1) counterparts. Additionally, the nanoplatelets showed enhanced photoactive storage performance with a 9.7% increase in the recorded photocurrent density. Upon integration of Ni3-xCox(PO4)2·8H2O as a positive pole and commercial activated carbon as a negative pole, the constructed hybrid supercapacitor device with PVA@KOH quasi-gel electrolyte exhibits great energy and power densities of 77.7 Wh kg-1 and 15998.54 W kg-1 with remarkable cycling stability of 6000 charging/discharging cycles and prominent Coulombic efficiency of 100%. Interestingly, two assembled devices are capable of glowing a red LED bulb for nearly 180 s. This research paves the way to design and fabricate electroactive species via a facile approach for boosting the design of a plethora of supercapattery devices.

A novel machine learning approach for surface roughness quantification and optimization of cast-on-strap lead-antimony alloy via two-point correlation function.

Surface roughness has a negative impact on the materials' lifetime. It accelerates pitting corrosion, increases effective heat transfer, and increases the rate of effective charge loss. However, controlled surface roughness is desirable in many applications. The automotive lead-acid battery is very sensitive to such effects. In our case study, the cast-on-strap machine has the largest effect on the surface roughness of the lead-antimony alloy. In this regard, statistical correlation functions are commonly used as statistical morphological descriptors for heterogeneous correlation functions. Two-point correlation functions are fruitful tools to quantify the microstructure of two-phase material structures. Herein, we demonstrate the use of the two-point correlation function to quantify surface roughness and optimize lead-antimony poles and straps used in the lead-acid battery as a solution to reduce their electrochemical corrosion when used in highly corrosive media. However, we infer that this method can be used in surface roughness mapping in a wide range of applications, such as pipes submerged in seawater as well as laser cutting. The possibility of using information obtained from the two-point correlation function and applying the simulated annealing procedure to optimize the surface micro-irregularities is investigated. The results showed successful surface representation and optimization that agree with the initially proposed hypothesis.

Boosted formic acid electro-oxidation on platinum nanoparticles and "mixed-valence" iron and nickel oxides.

The modification of Pt nanoparticles (nano-Pt, assembled electrochemically onto a glassy carbon (GC) substrate) with hybrid multivalent nickel (nano-NiOx) and iron (nano-FeOx) oxide nanostructures was intended to steer the mechanism of the formic acid electro-oxidation (FAO) in the desirable dehydrogenation pathway. This binary modification with inexpensive oxides succeeded in mediating the reaction mechanism of FAO by boosting reaction kinetics "electron transfer" and amending the surface geometry of the catalyst against poisoning. The sequence of deposition was optimized where the a-FeOx/NiOx/Pt/GC catalyst (where "a" denotes a post-activation step for the catalyst at -0.5 V in 0.5 mol L-1 NaOH) reserved the best hierarchy. Morphologically, while nano-Pt appeared to be spherical (ca. 100 nm in average diameter), nano-NiOx appeared as flowered nanoaggregates (ca. 56 nm in average diameter) and nano-FeOx (after activation) retained a plate-like nanostructure (ca. 38 nm in average diameter and 167 nm in average length). This a-FeOx/NiOx/Pt/GC catalyst demonstrated a remarkable catalytic efficiency (125 mA mgPt-1) for FAO that was ca. 12.5 times that of the pristine Pt/GC catalyst with up to five times improvement in the catalytic tolerance against poisoning and up to -214 mV shift in the FAO's onset potential. Evidences for equipping the a-FeOx/NiOx/Pt/GC catalyst with the least charge transfer resistance and the highest stability among the whole investigated catalysts are provided and discussed.

Boosting selectivity towards formate production using CuAl alloy nanowires by altering the CO2 reduction reaction pathway.

Understanding the fundamentals behind an electrocatalyst's selectivity enables the ability to steer product formation. Herein, we study Cu nanowires doped with a small amount of Al (12%) for CO2R, which enhances formate production by 16.9% over pure Cu nanowires. Density functional theory calculations and COR were employed to posit the preference of the formate formation pathway as a result of the Al doping.

Optimized Fabrication of Bimetallic ZnCo Metal-Organic Framework at NiCo-Layered Double Hydroxides for Multiple Storage and Capability Synergy All-Solid-State Supercapacitors.

Rational design and structural regulation of hybrid nanomaterials with superior electrochemical performance are crucial for developing sustainable energy storage platforms. Among these materials, NiCo-layered double hydroxides (NiCo-LDHs) demonstrate an exceptional charge storage capabilities owing to their tunable 2D lamellar structure, large interlayer spacing, and rich redox electrochemically active sites. However, NiCo-LDHs still suffer from sever agglomeration of their particles with limited charge transfer rates, resulting in an inadequate rate capability. In this study, bimetallic ZnCo-metal organic framework (MOF) tripods were grown on the surface of NiCo-LDH nanowires, which significantly reduced the self-agglomeration and stacking of the NiCo-LDH nanowire arrays, offering more accessible active sites for charge transfer and shortening the path for ion diffusion. The fabricated hybrid ZnCo-MOF@NiCo-LDH and its individual counterparts were tested as supercapacitor electrodes. The ZnCo-MOF@NiCo-LDH electrode demonstrated a remarkable specific capacitance of 1611 F g-1 at 2 A g-1 with an enhanced rate capability of 66% from 2 to 20 A g-1. Moreover, an asymmetric all solid-state supercapacitor device was constructed using ZnCo-MOF@NiCo-LDH and palm tree-derived activated carbon (P-AC) as positive and negative poles, respectively. The constructed device can store a high specific energy of 44.5 Wh Kg-1 and deliver a specific power of 876.7 W Kg-1 with outstanding Columbic efficiency over 10,000 charging/discharging cycles at 15 A g-1.

E-waste recycled materials as efficient catalysts for renewable energy technologies and better environmental sustainability.

Waste from electrical and electronic equipment exponentially increased due to the innovation and the ever-increasing demand for electronic products in our life. The quantities of electronic waste (e-waste) produced are expected to reach 44.4 million metric tons over the next five years. Consequently, the global market for electronics recycling is expected to reach $65.8 billion by 2026. However, electronic waste management in developing countries is not appropriately handled, as only 17.4% has been collected and recycled. The inadequate electronic waste treatment causes significant environmental and health issues and a systematic depletion of natural resources in secondary material recycling and extracting valuable materials. Electronic waste contains numerous valuable materials that can be recovered and reused to create renewable energy technologies to overcome the shortage of raw materials and the adverse effects of using non-renewable energy resources. Several approaches were devoted to mitigate the impact of climate change. The cooperate social responsibilities supported integrating informal collection and recycling agencies into a well-structured management program. Moreover, the emission reductions resulting from recycling and proper management systems significantly impact climate change solutions. This emission reduction will create a channel in carbon market mechanisms by trading the CO2 emission reductions. This review provides an up-to-date overview and discussion of the different categories of electronic waste, the recycling methods, and the use of high recycled value-added (HAV) materials from various e-waste components in green renewable energy technologies.

Impact of innovative nanoadditives on biodigesters microbiome.

Nanoparticles (NPs) supplementation to biodigesters improves the digestibility of biowaste and the generation of biogas. This study investigates the impact of innovative nanoadditives on the microbiome of biodigesters. Fresh cow manure was anaerobically incubated in a water bath under mesophilic conditions for 30 days. Three different NPs (zinc ferrite, zinc ferrite with 10% carbon nanotubes and zinc ferrite with 10% C76 fullerene) were separately supplemented to the biodigesters at the beginning of the incubation period. Methane and hydrogen production were monitored daily. Manure samples were collected from the digesters at different time points and the microbial communities inside the biodigesters were investigated via real-time PCR and 16 S rRNA gene amplicon-sequencing. The results indicate that zinc ferrite NPs enhanced biogas production the most. The microbial community was significantly affected by NPs addition in terms of archaeal and bacterial 16 S rRNAgene copy numbers. The three ZF formulations NPs augmented the abundance of members within the hydrogenotrophic methanogenic phyla Methanobacteriaceae. While Methanomassiliicoccacaea were enriched in ZF/C76 supplemented biodigester due to a significant increase in hydrogen partial pressure, probably caused by the enrichment of Spirochaetaceae (genus Treponema). Overall, NPs supplementation significantly enriched acetate-producing members within Hungateiclostridiaceae in ZF/CNTs, Dysgonomonadaceae in ZF and Spirochaetaceae ZF/C76 biodigesters.

Antiviral Electrospun Polyamide Three-Layered Mask Filter Containing Metal Oxide Nanoparticles and Black Seed Oil.

Upon the tremendous spread of coronavirus, there is a need to develop biodegradable, multifunctional, antiviral masks that can be safely used without polluting the environment as conventional surgical masks do. In this study, a three-layered mask filter is designed and fabricated. The first two layers contain electrospun polyamide with dispersed nanoparticles (NPs) of TiO2 and ZnO prepared via breakdown anodization. The third layer is composed of Nigella sativa oil (black seed oil) electrospun with polyamide and blended with chitosan to form an effective antiviral three-layered mask filter. The morphological characterization revealed the nanoscale features of the fabricated nanofibers with the ZnO and TiO2 NPs being embedded in the polymeric matrix. The specimens showed good wettability, which is necessary for virus attachment and its subsequent decay. The assembled mask has shown very good mechanical properties. The cytotoxicity results revealed that the proposed mask filter has less cytotoxic effect on the A549 cell line than the commercial KN95 mask filter with maintaining a cell viability of 65.3%. The antiviral activity test showed a variable virucidal effect against human adenovirus on A549 cells. The proposed mask showed the highest effect on the virus followed by PA-ZnO and PA-TiO2 films, which supports the assumption that the used NPs may have broad and promising effects on viruses when combined with the electrospun films.

Fabrication of polyhedral Cu-Zn oxide nanoparticles by dealloying and anodic oxidation of German silver alloy for photoelectrochemical water splitting.

A significant effort has been dedicated to the synthesis of Cu-Zn oxide nanoparticles as a robust photocathode material for photoelectrochemical water splitting. Cu-Zn oxide nanoparticles were formed by controlled anodization of German silver (Cu-Zn-Ni) alloy in an aqueous electrolyte. Scanning electron microscopy (SEM) demonstrates the dependence of the obtained nanostructures on the anodization time. The X-ray diffraction (XRD) patterns showed the formation of copper oxide (CuO) and zinc oxide (ZnO) nanoparticles with good stability. This was also confirmed by the compositional X-ray photoelectron spectroscopy (XPS) analysis. The obtained polyhedral nanoparticles showed high optical activity with adequate bandgap energy. These optimized nanoparticles achieved boosted photocurrent of - 0.55 mA/cm2 at - 0.6 V vs. SCE under AM 1.5 illumination, confirming the role of the optimized dealloying and thermal treatment in tuning the photoelectrochemical performance of the material.

A mesoporous ternary transition metal oxide nanoparticle composite for high-performance asymmetric supercapacitor devices with high specific energy.

We report on the optimized fabrication and electrochemical properties of ternary metal oxide (Ti-Mo-Ni-O) nanoparticles as electrochemical supercapacitor electrode materials. The structural, morphological, and elemental composition of the fabricated Ti-Mo-Ni-O via rapid breakdown anodization are elucidated by field emission scanning electron microscopy, Raman, and photoelectron spectroscopy analyses. The Ti-Mo-Ni-O nanoparticles reveal pseudocapacitive behavior with a specific capacitance of 255.4 F g-1. Moreover, the supercapacitor device Ti-Mo-Ni-O NPs//mesoporous doped-carbon (TMN NPs//MPDC) device exhibited a superior specific energy of 68.47 W h kg-1 with a corresponding power density of 2058 W kg-1. The supercapacitor device shows 100% coulombic efficiency with 96.8% capacitance retention over 11 000 prolonged charge/discharge cycles at 10 A g-1.

Computational and experimental elucidation of the boosted stability and antibacterial activity of ZIF-67 upon optimized encapsulation with polyoxometalates.

Water microbial purification is one of the hottest topics that threats human morbidity and mortality. It is indispensable to purify water using antimicrobial agents combined with several technologies and systems. Herein, we introduce a class of nanosized metal organic framework; Zeolitic imidazolate framework (ZIF-67) cages encapsulated with polyoxometalates synthesized via facile one-step co-precipitation method. We employed two types of polyoxometalates bioactive agents; phosphotungstic acid (PTA) and phosphomolybdic acid (PMA) that act as novel antibacterial purification agents. Several characterization techniques were utilized to investigate the morphological, structural, chemical, and physical properties such as FESEM, EDS, FTIR, XRD, and N2 adsorption/desorption isotherms techniques. The antibacterial assessment was evaluated using colony forming unit (CFU) against both Escherichia coli and Staphylococcus aureus as models of Gram-negative and Gram-positive bacteria, respectively. The PTA@ZIF-67 showed higher microbial inhibition against both Gram-positive and Gram-negative bacteria by 98.8% and 84.6%, respectively. Furthermore, computational modeling using density functional theory was conducted to evaluate the antibacterial efficacy of PTA when compared to PMA. The computational and experimental findings demonstrate that the fabricated POM@ZIF-67 materials exhibited outstanding bactericidal effect against both Gram-negative and Gram-positive bacteria and effectively purify contaminated water.