Fabrication of MoS2/rGO hybrids as electrocatalyst for water splitting applications.

Environmental degradation and energy constraint are important risks to long-term sustainability in the modern world. Water splitting is a vital approach for environmentally friendly and sustainable energy storage, providing a clean way to produce hydrogen without pollutants. Preparing a catalyst that is active, bifunctional, and durable for water splitting is a difficult task. We addressed the difficulty by creating a bifunctional heterogeneous catalyst, MoS2/rGO, with an ideal weight percentage of 5 wt% by a hydrothermal process. The optimized sample showed exceptional electrocatalytic activity, requiring an overpotential of 242 mV and 120 mV to achieve a current density of 10 mA cm-2 in the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER). Furthermore, our synthesized catalyst was validated for its exceptional water-splitting capacity, with the optimized sample showing low Tafel slope values of 59 mV dec-1 for HER and 171 mV dec-1 for OER. The significant OER and HER activity seen in the 5 wt% MoS2/rGO hybrid, compared to other hybrids, is due to the many catalytic active sites that aid in charge and electron transport, as well as the synergistic interaction between MoS2 and rGO.

Efficient sorption of As(III) from water by magnetite decorated porous carbon extracted from a biowaste material.

Arsenic is a highly toxic metal that causes cancer even at a low concentration and its removal from water resources is challenging. Herein, carbon extracted from waste onion bulbs is activated to cater for porosity and functionalized with magnetite (Fe3O4) nanoparticles (named MCK6) to address the challenge of As(III) removal. Synthesized MCK6 was highly mesoporous having a surface area of 208 m2/g, where magnetite nanoparticles (≤ 10 nm) are homogeneously distributed within a porous network. The developed adsorbent inherited functional groups from the biosource and magnetic property from magnetite making it ideal for removal of As(III). Further, MCK6 showed a maximum monolayer adsorption capacity (qm) of 10.2 mg/g at 298 K and pH 7. The adsorption thermodynamics delineates a non-spontaneous and endothermic reaction, where the kinetics followed pseudo 2nd order (R2 value of 0.977), while monolayer formation is explained by the Langmuir model. Moreover, MCK6 efficiently works to remove As(III) in a competitive metal ions system including Pb+2, Cd+2, and Ca+2, making it a suitable adsorbent to tackle contaminated water.

Catalyzing Sustainable Water Splitting with Single Atom Catalysts: Recent Advances.

Electrochemical water splitting for sustainable hydrogen and oxygen production have shown enormous potentials. However, this method needs low-cost and highly active catalysts. Traditional nano catalysts, while effective, have limits since their active sites are mostly restricted to the surface and edges, leaving interior surfaces unexposed in redox reactions. Single atom catalysts (SACs), which take advantage of high atom utilization and quantum size effects, have recently become appealing electrocatalysts. Strong interaction between active sites and support in SACs have considerably improved the catalytic efficiency and long-term stability, outperforming their nano-counterparts. This review's first section examines the Hydrogen Evolution Reaction (HER) and the Oxygen Evolution Reaction (OER). In the next section, SACs are categorized as noble metal, non-noble metal, and bimetallic synergistic SACs. In addition, this review emphasizes developing methodologies for effective SAC design, such as mass loading optimization, electrical structure modulation, and the critical role of support materials. Finally, Carbon-based materials and metal oxides are being explored as possible supports for SACs. Importantly, for the first time, this review opens a discussion on waste-derived supports for single atom catalysts used in electrochemical reactions, providing a cost-effective dimension to this vibrant research field. The well-known design techniques discussed here may help in development of electrocatalysts for effective water splitting.

A zeolitic imidazolate framework (ZIF-67) and graphitic carbon nitride (g-C3N4) composite based efficient electrocatalyst for overall water-splitting reaction.

Designing of non-noble, cost-effective, sustainable catalysts for water splitting is essential for hydrogen production. In this research work, ZIF-67, g-C3N4, and their composite (1, 3, 5, 6, 8 wt% g-C3N4@ZIF-67) are synthesized, and various techniques, XRD, FTIR, SEM, EDX and BET are used to examine their morphological properties for electrochemical water-splitting. The linkage of ZIF-67 with g-C3N4 synergistically improves the electrochemical kinetics. An appropriate integration of g-C3N4 in ZIF-67 MOF improves the charge transfer between the electrode and electrolyte and makes it a suitable option for electrochemical applications. In alkaline media, the composite of ZIF-67 MOF with g-C3N4 over a Ni-foam exhibits a superior catalyst activity for water splitting application. Significantly, the 3 wt% g-C3N4@ZIF67 composite material reveals remarkable results with low overpotential values of -176 mV@10 mA cm-2, 152 mV@10 mA cm-2 for HER and OER. The catalyst remained stable for 24 h without distortion. The 3 wt% composite also shows a commendable performance for overall water-splitting with a voltage yield of 1.34 v@10 mA cm-2. The low contact angle (54.4°) proves the electrocatalyst's hydrophilic nature. The results of electrochemical water splitting illustrated that 3 wt% g-C3N4@ZIF-67 is an electrically conductive, stable, and hydrophilic-nature catalyst and is suggested to be a promising candidate for electrochemical water-splitting application.

Effect of Pyrolysis on iron-metal organic frameworks (MOFs) to Fe3C @ Fe5C2 for diesel production in Fischer-Tropsch Synthesis.

The Fischer-Tropsch Synthesis (FTS) is a significant catalytic chemical reaction that produces ultra-clean fuels or chemicals with added value from a syngas mixture of CO and H2 obtained from biomass, coal, or natural gas. The presence of sulfur is not considered good for producing liquid fuels for(FTS). In this study, we reveal that the presence of sulfur in ferric sulfate Fe2(SO4)3 MOF provides the high amount, 52.50% of light hydrocarbons in the carbon chain distribution. The calcined ferric nitrate Fe(NO3)3 MOF reveals the highest 93.27% diesel production. Calcination is regarded as an essential factor in enhancing liquid fuel production. Here, we probed the calcination effect of Metal Organic Framework (MOF) on downstream application syngas to liquid fuels. The XRD results of MOF. N and P. MOF.N shows the formation of the active phase of iron carbide (Fe5C2), considered the most active phase of FTS. The scanning electron microscopy (SEM) images of iron sulfate MOF catalyst (P.MOF.S) reveals that the existence of sulfur creates pores inside the particles due to the reaction of free water molecules with the sulfur derivate. The surface functional groups of prepared MOFs and tested MOFS were analyzed by Fourier transforms infrared spectroscopy (FT-IR). The thermal stability of prepared MOFS was analyzed by Thermo gravimetric analysis (TGA). The surface areas and structural properties of the catalysts were measured by N2-Physiosorption technique.

Optimization of bandgap reduction in 2-dimensional GO nanosheets and nanocomposites of GO/iron-oxide for electronic device applications.

In this report we have developed different fabrication parameters to tailor the optical bandgap of graphene oxide (GO) nanosheets to make it operational candidate in electronic industry. Here we performed two ways to reduce the bandgap of GO nanosheets. First, we have optimized the oxidation level of GO by reducing amount of oxidizing agent (i.e. KMnO4) to control the sp2/sp3 hybridization ratio for a series of GO nanosheets samples. We noticed the reduction in primary band edge 3.93-3.2 eV while secondary band edge 2.98-2.2 eV of GO nanosheets as the amount of KMnO4 is decreased from 100 to 30%. Second, we have fabricated a series of 2-dimensional nanocomposites sample containing GO/Iron-oxide by using a novel synthesis process wet impregnation method. XRD analysis of synthesized nanocomposites confirmed the presence of both phases,[Formula: see text]-Fe2O3 and Fe3O4 of iron-oxide with prominent plane (001) of GO. Morphological investigation rules out all the possibilities of agglomerations of iron oxide nanoparticles and coagulation of GO nanosheets. Elemental mapping endorsed the homogeneous distribution of iron oxide nanoparticles throughout the GO nanosheets. Raman spectroscopy confirmed the fairly constant ID/IG ratio and FWHM of D and G peaks, thus proving the fact that the synthesis process of nanocomposites has no effect on the degree of oxidation of GO flakes. Red shift in G peak position of all the nanocomposites samples showed the electronic interaction among the constituents of the nanocomposite. Linear decrease in the intensity of PL (Photoluminescence) spectra with the increasing of Iron oxide nanoparticles points towards the increased interaction among the iron oxide nanoparticles and GO flakes. Optical absorption spectroscopy reveals the linear decrease in primary edge of bandgap from 2.8 to 0.99 eV while secondary edge decrease 3.93-2.2 eV as the loading of [Formula: see text]-Fe2O3 nanoparticles is increased from 0 to 5% in GO nanosheets. Among these nanocomposites samples 5%-iron-oxide/95%-GO nanosheet sample may be a good contestant for electronic devices.

A review on development of metal-organic framework-derived bifunctional electrocatalysts for oxygen electrodes in metal-air batteries.

Worldwide demand for oil, coal, and natural gas has increased recently because of odd weather patterns and economies recovering from the pandemic. By using these fuels at an astonishing rate, their reserves are running low with each passing decade. Increased reliance on these sources is contributing significantly to both global warming and power shortage problems. It is vital to highlight and focus on using renewable energy sources for power production and storage. This review aims to discuss one of the cutting-edge technologies, metal-air batteries, which are currently being researched for energy storage applications. A battery that employs an external cathode of ambient air and an anode constructed of pure metal in which an electrolyte can be aqueous or aprotic electrolyte is termed as a metal-air battery (MAB). Due to their reportedly higher energy density, MABs are frequently hailed as the electrochemical energy storage of the future for applications like grid storage or electric car energy storage. The demand of the upcoming energy storage technologies can be satisfied by these MABs. The usage of metal-organic frameworks (MOFs) in metal-air batteries as a bi-functional electrocatalyst has been widely studied in the last decade. Metal ions or arrays bound to organic ligands to create one, two, or three-dimensional structures make up the family of molecules known as MOFs. They are a subclass of coordination polymers; metal nodes and organic linkers form different classes of these porous materials. Because of their modular design, they offer excellent synthetic tunability, enabling precise chemical and structural control that is highly desirable in electrode materials of MABs.

Fabrication of cellulose paper-based counter electrodes for flexible dye-sensitized solar cells.

Here, we introduce the synthesis and deposition of organic/inorganic composite ink on cellulose paper using a rapid ultrasonic spray deposition approach that can be incorporated as a counter electrode (CE) in flexible dye-sensitized solar cells (FDSSCs). The composite ink comprised a copper indium sulfide (CuInS2) nanostructure ink and dispersion of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) in water. Fabricated counter electrodes are biodegradable, environment-friendly, flexible, and economical and meet the requirements for sustainable green energy. To evaluate the catalytic activities and power conversion efficiencies of DSSCs, the produced CuInS2/PEDOT:PSS composite ink-based CEs were compared with PEDOT:PSS counter electrodes. Cyclic voltammetry studies found that CuInS2/PEDOT:PSS had a greater cathodic charge transfer current density (Jc) (-1.23 mA cm-2). Moreover, it was found that the potential separation values are small, which indicate a stronger catalytic activity than PEDOT:PSS counter electrodes. The observed exchange current density (J0) was 3.98 mA cm-2, while the limiting current density (Jlim) increased to 45.7 mA cm-2, indicating a fast redox diffusion rate of the CuInS2/PEDOT:PSS CE. The photovoltaic performances of CuInS2/PEDOT:PSS and PEDOT: PSS-based DSSC's were measured and determined to be 5.66% and 4.41%, respectively, while the performance of CuInS2/PEDOT:PSS FDSSC composed of cellulose paper was 1.06%.

Conversion of Plastic Waste to Carbon-Based Compounds and Application in Energy Storage Devices.

At present, plastic waste accumulation has been observed as one of the most alarming environmental challenges, affecting all forms of life, economy, and natural ecosystems, worldwide. The overproduction of plastic materials is mainly due to human population explosion as well as extraordinary proliferation in the global economy accompanied by global productivity. Under this threat, the development of benign and green alternative solutions instead of traditional disposal methods such as conversion of plastic waste materials into cherished carbonaceous nanomaterials such as carbon nanotubes (CNTs), carbon quantum dots (CQDs), graphene, activated carbon, and porous carbon is of utmost importance. This critical review thoroughly summarizes the different types of daily used plastics, their types, properties, ways of accumulation and their effect on the environment and human health, treatment of waste materials, conversion of waste materials into carbon-based compounds through different synthetic schemes, and their utilization in energy storage devices particularly in supercapacitors, as well as future perspectives. The main purpose of this review is to help the targeted audience to design their futuristic study in this desired field by providing information about the work done in the past few years.

The Development of Highly Fluorescent Hemicyanine and Dicyanoisophorone Dyes for Applications in Dye-Sensitized Solar Cells.

Ruthenium-based metal complex dyes have been employed extensively in dye-sensitized solar cells (DSSCs) as photosensitizers, but the cost and toxicity of metal complexes have promoted the development of metal-free organic dyes. The present investigation deals with the synthesis of hemicyanine and Dicyanoisophorone (DCI) based dyes adopting the D-π-A strategy, and their application on sensitization of nano-crystalline ZnO electrodes by appending the carboxyl (COOH) anchoring group as a pendant on the primary skeleton of dyes. Dyes have been characterized by UV, FTIR, and NMR spectroscopic studies. Absorption maxima (λmax) were found in the region 416-551 nm while emission wavelength (λem) was observed in the range 575-685 nm. Cyclic voltammetry and DFT calculations were used to estimate redox potential and band gap energies of dyes.

Metal-organic framework derived vanadium oxide supported nanoporous carbon structure as a bifunctional electrocatalyst for potential application in metal air batteries.

High-efficiency, sustainable, non-precious metal-based electrocatalysts with bifunctional catalytic activity for the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER) are essential for metal-air batteries. In this research, a bifunctional electrocatalyst is developed by synthesizing a novel nanoporous vanadium oxide/carbon composite (NVC-900) through pyrolysis of a highly efficient vanadium metal-organic framework, MIL-101 (V). The fabrication process was conveniently carried out by pyrolyzing the synthesized MIL-101 (V) at 900 °C, producing vanadium oxide nanoparticles embedded in the extensively distributed pores of the carbon network. The evenly distributed nanopores substantially improve the performance of the efficient electrocatalyst for both the oxygen reduction reaction and oxygen evolution reactions (ORR/OER) by increasing surface area and facilitating access to stable catalytic active sites. The unique structure was characterized by powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). For oxygen reduction reaction (ORR), the electrocatalyst established a promising limiting current density (J L) of 5.2 mA cm-2 at 1600 rpm at an onset potential of 1.18 V and a half-wave potential of 0.82 V, and for OER, a current density of 10 mA cm-2 was delivered at a potential of 1.48 V. In comparison to 10% Pt/C, the synthesized bifunctional electrocatalyst being almost equally active towards bifunctional activity, showed much better long-term cyclic stability. The one-step thermal pyrolysis strategy to synthesize the nanoporous functional material and the proposed electrocatalytic material's long-term bifunctional activity and durability make it an ideal fit for next-generation portable green metal-air batteries.

Advanced Strategies in Metal-Organic Frameworks for CO2 Capture and Separation.

The continuous carbon dioxide (CO2 ) gas emissions associated with fossil fuel production, valorization, and utilization are serious challenges to the global environment. Therefore, several developments of CO2 capture, separation, transportation, storage, and valorization have been explored. Consequently, we documented a comprehensive review of the most advanced strategies adopted in metal-organic frameworks (MOFs) for CO2 capture and separation. The enhancements in CO2 capture and separation are generally achieved due to the chemistry of MOFs by controlling pore window, pore size, open-metal sites, acidity, chemical doping, post or pre-synthetic modifications. The chemistry of defects engineering, breathing in MOFs, functionalization in MOFs, hydrophobicity, and topology are the salient advanced strategies, recently reported in MOFs for CO2 capture and separation. Therefore, this review summarizes MOF materials' advancement explaining different strategies and their role in the CO2 mitigations. The study also provided useful insights into key areas for further investigations.

Electrocatalytic study of NiO-MOF with activated carbon composites for methanol oxidation reaction.

In this work, the methanol oxidation reaction is investigated on Ni based metal organic frameworks (MOF) and its composites with biomass derived activated carbon. NiO-MOF and composites with activated carbon were synthesized using hydrothermal method. SEM, EDX, and XRD, FTIR, TGA techniques were used for characterization of composites. The electrochemical activity of catalysts for oxidation of methanol was tested using cyclic voltammetry (CV) in 1 M KOH and 3 M CH3OH on glassy carbon electrode in three electrode setup. The electrochemical performance shows the effect of activated carbon concentration on methanol oxidation. The electro-oxidation catalyzed by NiO-MOF with activated carbon (40 mg) composite exhibits a peak current density of 182.72 mA/cm2 at 0.89 V potential with a scan rate of 50 mV/s making it a potential catalyst for electrocatalysis of methanol.

Electrochemical Reduction of CO2: A Review of Cobalt Based Catalysts for Carbon Dioxide Conversion to Fuels.

Electrochemical CO2 reduction reaction (CO2RR) provides a promising approach to curbing harmful emissions contributing to global warming. However, several challenges hinder the commercialization of this technology, including high overpotentials, electrode instability, and low Faradic efficiencies of desirable products. Several materials have been developed to overcome these challenges. This mini-review discusses the recent performance of various cobalt (Co) electrocatalysts, including Co-single atom, Co-multi metals, Co-complexes, Co-based metal-organic frameworks (MOFs), Co-based covalent organic frameworks (COFs), Co-nitrides, and Co-oxides. These materials are reviewed with respect to their stability of facilitating CO2 conversion to valuable products, and a summary of the current literature is highlighted, along with future perspectives for the development of efficient CO2RR.

Designing and theoretical study of fluorinated small molecule donor materials for organic solar cells.

A recently synthesized photoactive donor named fluorinated thienyl-substituted benzodithiophene (DRTB-FT), modified with four novel end capped acceptor molecules, has been investigated through different electrical, quantum, and spectrochemical techniques for its enhanced electro-optical and photovoltaic properties. DRTB-FT was connected to 2-methylenemalononitrile (D-1), 2-methylene-3-oxobutanenitrile (D-2), 2-(2-methylene-3-oxo-2,3-dihydro-1H-inden-1-ylidene) malononitrile (D-3), and 3-methyl-5methylene-2-thioxothiazolidin-4-one (D-4) as terminal acceptor moieties. The architectural D-1 and D-3 molecules owe reduced optical band gap of 2.45 and 2.28 eV benefited from A-D-A configuration and have broaden maximum absorption band (λmax) at 617 and 602 nm in polar organic solvent (chloroform). Reduced optical band gap sets the ease for enhanced absorption. Reorganization energy of electron (λe) of D-3 molecule (0.00397 eV) was smaller among all which disclosed its greater mobility of conducting electrons (ICT). Larger values of dipole moment (µ) of D-1 (5.939 Debye) and D-3 (3.661 Debye) molecules in comparison to R indicated greater solubilities of the targeted molecules. Among the tailored molecules, D-3 showed the lowest binding energy of 0.25 eV in solvent phase and 0.08 eV in gaseous phase. The voltaic strength of the designed molecules was examined with respect to fullerene derivative (PC61BM) which exposed that D-1 is the best choice for achieving higher PCE. TDM (transition density matrix), DOS (density of states) analysis, and binding energies all were estimated at MPW1PW91/6-31G (d, p) level of DFT (density functional theory). All the architecture molecules show reduced band gap and high electron transfer rate due to the lowest reorganization energy (RE) of electron. The results show that there is greater contribution of acceptor and conjugated donor core towards the total absorption into the visible region of the spectrum. When tailored molecules D-1, D-2, D-3, and D-4 were blended with fullerene derivative polymer (PC61BM), they give high values of voltage at zero current level (Voc) compared to R.

Metal Organic Frameworks Derived Sustainable Polyvinyl Alcohol/Starch Nanocomposite Films as Robust Materials for Packaging Applications.

Bio-nanocomposites-based packaging materials have gained significance due to their prospective application in rising areas of packaged food. This research aims to fabricate biodegradable packaging films based upon polyvinyl alcohol (PVA) and starch integrated with metal-organic frameworks (MOFs) or organic additives. MOFs offer unique features in terms of surface area, mechanical strength, and chemical stability, which make them favourable for supporting materials used in fabricating polymer-based packaging materials. zeolitic imidazolate frameworks (ZIFs) are one of the potential candidates for this application due to their highly conductive network with a large surface area and high porosity. Present research illustrates a model system based on ZIF-67 (C8H10N4Co) bearing 2-10 wt.% loading in a matrix of PVA/starch blend with or without pyrolysis to probe the function of intermolecular interaction in molecular packing, tensile properties, and glass transition process. ZIF-67 nanoparticles were doped in a PVA/starch mixture, and films were fabricated using the solution casting method. It was discovered through scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and Fourier transform infrared spectroscopy (FTIR) that addition of ZIF-67 and pyrolyzed ZIF-67 changed and enhanced the thermal stability of the membrane. Moreover, 2-10 wt.% loading of ZIF-67 effected the thermal stability, owing to an interlayer aggregation of ZIF-67. The membranes containing pyrolyzed ZIF-67 showed mechanical strength in the order of 25 MPa in a moderate loading of pyrolyzed ZIF-67 (i.e., at 4 wt.%). The crystallinity enhanced by an increment in ZIF-67 loading. On the other hand, pyrolyzed ZIF-67 carbon became amorphous because of the inert environment and elevated temperature. The surface area also increased after the pyrolysis, which helped to increase the strength of the composite films.

Electrocatalytic performance of NiNH2BDC MOF based composites with rGO for methanol oxidation reaction.

Present work comprehensively investigated the electrochemical response of Nickel-2 Aminoterephthalic acid Metal-Organic Framework (NiNH2BDC) and its reduced graphitic carbon (rGO) based hybrids for methanol (CH3OH) oxidation reaction (MOR) in an alkaline environment. In a thorough analysis of a solvothermally synthesized Metal-Organic Frameworks (MOFs) and its reduced graphitic carbon-based hybrids, functional groups detection was performed by FTIR, the morphological study by SEM, crystal structure analysis via XRD, and elemental analysis through XPS while electrochemical testing was accomplished by Chronoamperometry (CA), Cyclic Voltametric method (CV), Electrochemically Active Surface Area (EASA), Tafel slope (b), Electron Impedance Spectroscopy (EIS), Mass Activity, and roughness factor. Among all the fabricated composites, NiNH2BDC MOF/5 wt% rGO hybrid by possessing an auspicious current density (j) of 267.7 mA/cm2 at 0.699 V (vs Hg/HgO), a Tafel slope value of 60.8 mV dec-1, EASA value of 15.7 cm2, and by exhibiting resistance of 13.26 Ω in a 3 M CH3OH/1 M NaOH solution displays grander electrocatalytic activity as compared to state-of-the-art platinum-based electrocatalysts.

A comprehensive and critical review of the recent progress in electrocatalysts for the ethanol oxidation reaction.

The human craving for energy is continually mounting and becoming progressively difficult to gratify. At present, the world's massive energy demands are chiefly encountered by nonrenewable and benign fossil fuels. However, the development of dynamic energy cradles for a gradually thriving world to lessen fossil fuel reserve depletion and environmental concerns is currently a persistent issue for society. The discovery of copious nonconventional resources to fill the gap between energy requirements and supply is the extreme obligation of the modern era. A new emergent, clean, and robust alternative to fossil fuels is the fuel cell. Among the different types of fuel cells, the direct ethanol fuel cell (DEFCs) is an outstanding option for light-duty vehicles and portable devices. A critical tactic for obtaining sustainable energy sources is the production of highly proficient, economical and green catalysts for energy storage and conversion devices. To date, a broad range of research is available for using Pt and modified Pt-based electrocatalysts to augment the C2H5OH oxidation process. Pt-based nanocubes, nanorods, nanoflowers, and the hybrids of Pt with metal oxides such as Fe2O3, TiO2, SnO2, MnO, Cu2O, and ZnO, and with conducting polymers are extensively utilized in both acidic and basic media. Moreover, Pd-based materials, transition metal-based materials, as well as transition metal-based materials are also points of interest for researchers nowadays. This review article delivers a broad vision of the current progress of the EOR process concerning noble metals and transition metals-based materials.

Metal-organic framework based electrode materials for lithium-ion batteries: a review.

Metal-organic frameworks (MOFs) with efficient surface and structural properties have risen as a distinctive class of porous materials through the last few decades, which has enabled MOFs to gain attention in a wide range of applications like drug delivery, gas separation and storage, catalysis and sensors. Likewise, they have also emerged as efficient active materials in energy storage devices owing to their remarkable conducting properties. Metal-organic frameworks (MOFs) have garnered great interest in high-energy-density rechargeable batteries and super-capacitors. Herein the study presents their expanding diversity, structures and chemical compositions which can be tuned at the molecular level. It also aims to evaluate their inherently porous framework and how it facilitates electronic and ionic transportation through the charging and discharging cycles of lithium-ion batteries. In this review we have summarized the various synthesis paths to achieve a particular metal-organic framework. This study focuses mainly on the implementation of metal-organic frameworks as efficient anode and cathode materials for lithium-ion batteries (LIBs) with an evaluation of their influence on cyclic stability and discharge capacity. For this purpose, a brief assessment is made of recent developments in metal-organic frameworks as anode or cathode materials for lithium-ion batteries which would provide enlightenment in optimizing the reaction conditions for designing a MOF structure for the battery community and electrochemical energy storage applications.

A TiO2 composite with graphitic carbon nitride as a photocatalyst for biodiesel production from waste cooking oil.

Semiconductor-based photocatalysts have attracted a lot of interest due to their environmental friendliness and high stability. Waste cooking oil can be converted to biodiesel by the process of transesterification. A TiO2/g-C3N4 combination was prepared by using a wet impregnation process. The photocatalyst was analyzed by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray spectroscopy (EDX), Thermogravimetric analysis (TGA), and Ultraviolet-visible spectroscopy (UV-vis). For effective transesterification, WCO was collected and acid-esterified to reduce the FFA concentration (below 3%). For the transesterification reaction, esterified WCO was used and the reactions were carried out under solar irradiation at 60 °C with an oil to methanol ratio of 1 : 9 and stirred for 1 hour, using different TiO2/g-C3N4 catalysts (10, 20 & 30%) with different catalyst concentrations of 1%, 2% and 3%. The results showed that TiO2/20% g-C3N4 with 2% catalyst concentration gives the highest yield of biodiesel production (89.5%) as compared to other catalyst concentrations used. In addition to (FTIR), additional fuel characteristics such as density, viscosity, flashpoint, acid value, and pH were tested to determine the quality of the generated biodiesel and were found to comply with fuel standards. With high stability and good catalytic activity, the synthesized composite TiO2/g-C3N4 is a viable option for producing biodiesel from WCO.