Additive-free active materials are desirable for energy storage devices as they reduce processing complexity and eliminate variability from binders or conductive additives. We report the synthesis of a highly stable, two-dimensional copper-based metal-organic framework (CuMOF) film with a tunable thickness. The exceptional adhesion of CuMOF films to electrode surfaces enables a binder-free fabrication approach, addressing a key challenge in energy storage applications, particularly in electrode design. The film exhibits a columnar morphology with well-defined grain boundaries and a high surface area, making it optimal for supercapacitor applications. Electrochemical characterization on glassy carbon electrodes yielded an areal capacitance of 2.9 mF/cm2 at a scan rate of 1 mV/s using a ∼160 nm thick CuMOF film. We investigated films as thin as 2.4 nm, where the capacitance is predominantly governed by electrical double-layer effects, highlighting the interplay between the film structure and electrochemical behavior. Thus, CuMOF films offer practical applicability, advancing efficient binder-free energy storage.

Light-emitting electrochemical cells (LECs) are gaining popularity as an easy-to-fabricate alternative to light-emitting diodes (LEDs). While Electrochemical Impedance Spectroscopy (EIS) is the standard tool for probing LEC device dynamics, it suffers from a major analytical bottleneck when two processes occur at nearly the same time constants. This problem leads to ambiguous circuit fitting. Such non-uniqueness prevents the identification of the exact underlying physical mechanism, making the interpretation difficult. We address this by implementing the Distribution of Relaxation Times (DRT) analysis. We perform EIS across a range of bias voltages on LECs using the p-type conjugated polymer MEH-PPV (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]) blended with an ionic liquid (IL). Using DRT, we successfully extract the distinct time constants of the various internal device processes. By comparing these DRT-derived time constants with traditional EIS fitting, we establish a way to get the true physical circuit.

Transition metal substitution is an effective strategy for tuning the versatile characteristics of perovskite oxides. Here, we demonstrate that transition metals like Ni, Co, and Fe doping (3%) in lanthanum manganite (LaMnO3) causes oxygen vacancies, which play a vital part in improving the material's optical, dielectric, and electrochemical performance. By causing charge imbalance and lattice distortions, dopant insertion encourages the creation of oxygen vacancies, which alter the electronic structure and carrier transport. Among the synthesized samples, Fe-doped LaMnO3 exhibited the highest dielectric constant (5823 at 100 kHz) along with reduced dielectric loss, indicating improved dielectric performance. The doped samples showed variations in magnetic susceptibility, arising from modifications in the Mn-O-Mn exchange interactions caused by dopant incorporation, while maintaining paramagnetic behavior at room temperature. With an areal capacitance of 60.36 mF cm-2 and almost 100% retention over 10,000 cycles, the Fe-doped perovskite oxide exhibits outstanding electrochemical energy-storage properties. An LCD was successfully powered by an asymmetric supercapacitor device fabricated with this electrode material, demonstrating its practical application. These results indicate that transition metal doping effectively tunes the functional properties of LaMnO3, making it a promising candidate for advanced electronics and energy storage technologies.

This study employs Distribution of Relaxation Times (DRT) analysis to elucidate the electrochemical charge dynamics within Ti3C2Tx MXene-based electrodes. Comprehensive electrochemical characterizations, including cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), were systematically conducted in various electrolytes (H2SO4, Na2SO4, and KOH) and on multiple substrates (fluorine-doped tin oxide, carbon paper, and nickel foam) to evaluate charge storage mechanisms. Through DRT analysis, distinct electron-ion transport dynamics and relaxation processes were effectively differentiated, providing deeper insight into electrolyte-substrate interactions. Results demonstrated that acidic electrolytes (H2SO4) significantly enhanced charge transfer kinetics, while highly porous substrates (nickel foam and carbon paper) improved capacitive behavior. The DRT analysis specifically identified dominant charge-transfer peaks and clarified kinetic limitations, revealing slower dynamics at higher potentials, particularly in Na2SO4. Overall, this study underscores the capability of DRT analysis to systematically unravel complex electrochemical phenomena, highlighting its importance for optimizing MXene-based energy storage systems.

A scalable method has been developed for synthesizing nitrogen-doped carbon-supported platinum nanoparticles. Fusarium oxysporum was utilized as reducing and stabilizing agent, and calcination was employed to produce the carbon support. The unique properties of Fusarium oxysporum facilitate the reduction of metal ions while preventing agglomeration and maintaining nanoparticle stability. An extensive investigation of the electrochemical supercapacitor and temperature-dependent dielectric properties of the nanoparticles demonstrates their suitability for supercapacitor applications. Electrochemical analysis showed N-doped C/Pt NPs with high specific capacitance, 482.77F/g at 2.0 A/g, retaining 94 % capacitance even under 20 A/g after 10,000 cycles. The symmetric supercapacitor device displayed 275F/g at 2 A/g, maintaining 61.10 Wh/kg energy density at 1000 W/kg power density, with similar to 92 % capacitance retention after 10,000 cycles. Dielectric properties of N-doped C/Pt NPs were analyzed at both ambient (300 K) and elevated (450 K) temperatures, revealing temperature-dependent characteristics and alternating current conductivity. At 0.75 MHz, the dielectric permittivity (epsilon') was measured at 31, with tangent loss at 2.01 and a.c. conductivity at 2.597 x 10(-3 O-1) m(-1). Increasing the frequency to 6.0 MHz resulted in a 2.38-fold rise in dielectric permittivity and a decrease in tangent loss to 0.77, demonstrating the temperature-sensitive nature of dielectric relaxation.

The present introduces a single step approach for enhancing supercapacitor performance by utilizing acidfunctionalized porous carbon derived from the inner skin of Arachis hypogaea as a sustainable biomass precursor. Through pyrolysis at 800 degrees C in a nitrogen atmosphere, the resulting porous carbon material demonstrates unique structural and electrochemical behavior as confirmed by FTIR, XRD, Raman spectroscopy, FE-SEM, HRTEM,EDS,BET analyses. The acid functionalized variant (FAH8) significantly outperformed the nonfunctionalized carbon (AH8), showing a fourfold increase in specific capacitance. Electrochemical evaluations revealed that FAH8 achieved a high specific capacitance of 273 Fg-1 at 0.25 Ag-1 in 3 M KOH, with an energy density of 22.5 Wh kg- 1 and a power density of 125 W kg- 1 in a three-electrode setup. The symmetrical CR2032 device of FAH8 exhibited a maximum capacitance of 98 Fg-1 and displayed excellent stability, with 98.5 % efficiency and 97.4 % capacitance retention after 7500 cycles. Notably, the device also delivered a high energy density of 23.17 Wh kg- 1 and power density of 325.0 W kg- 1. The enhanced performance attributed by the simple acid functionalization highlights the potential of this material in energy storage. Thus, the study not only emphasizes the effective use of low-cost biomass precursors but also provides a straightforward functionalization strategy to boost energy storage capabilities, paving the way for sustainable high-performance supercapacitors.

In this study, binder-free nickel cobalt oxide (NiCo2O4) nanowire arrays with a cubic spinel structure were directly grown on nickel foam (NF) via an in situ hydrothermal process. The resulting one-dimensional nanowires exhibited a uniform morphology and a favourable bandgap of approximately 1.67 eV, making them ideal candidates as electrode materials for photo-assisted supercapacitors. Electronic structure analysis revealed the coexistence of Ni2+/Ni3+ and Co2+/Co3+ redox pairs, significantly enhancing electrochemical kinetics and facilitating efficient photo-assisted charge storage. Under illumination, the NiCo2O4@NF nanowires demonstrated a remarkable 54% increase in areal capacitance, from 570 to 880 mF cm-2 at 15 mA cm-2, attributed to the efficient separation and storage of photo-generated charges driven by surface polarization effects. An asymmetric supercapacitor device was fabricated with activated carbon (AC) as the anode and NiCo2O4@NF nanowires as the photoactive cathode, maintaining 88% capacitance retention after 1000 illumination cycles. Density functional theory with the on-site Hubbard U correction (DFT + U) calculations further confirmed that nickel substitution in the Co3O4 matrix significantly reduces the bandgap and enhances the magnetic moment, supported by asymmetric spin-resolved density of states and band structure analyses. This research provides valuable insights for developing next-generation photo-assisted energy storage solutions.

The performance of energy storage devices is largely determined by the properties of their electrode materials, making it essential to develop well-designed materials capable of delivering high efficiency across various applications. In this study, monoclinic-phase Bismuth Vanadate (Bi4V2O11) nanostructures were synthesized via a facile hydrothermal method and doped with varying weight percentages of Thulium (Tm). The structural and morphological characteristics of Tm-doped Bi4V2O11 were analyzed using XRD, Raman spectroscopy, XPS, HRTEM, FESEM, and subsequently evaluated as electrode materials for electrochemical energy storage. Tm doping induces structural distortions and oxygen vacancies, leading to improved crystallinity, enhanced ionic conductivity, and superior electrochemical stability. Among the synthesized materials, 6 % Tm/Bi4V2O11 demonstrated exceptional electrochemical performance, achieving a high areal capacitance of 112.7 mF/cm2 at a scan rate of 10 mV/s-significantly surpassing pristine Bi4V2O11 (4.6 mF/cm2). Additionally, it exhibited an impressive energy density of 9.4 mWh/cm2 at a power density of 2500 mW/cm2. Furthermore, the material demonstrated remarkable cycling stability, retaining 110 % of its initial capacitance after 10,000 cycles at 25 mA/cm2. Electrochemical analysis revealed a decrease in diffusion-controlled capacitance with increasing scan rate, highlighting the diffusion-processed charge storage mechanism governed by the materials. To evaluate practical applicability, an asymmetric supercapacitor (ASC) was fabricated using 6 % Tm/Bi4V2O11 as the cathode and activated carbon (AC) as the anode. The assembled device demonstrated robust cyclic stability, retaining 85 % capacitance and 100 % coulombic efficiency after 10,000 cycles. These results establish 6 % Tm/ Bi4V2O11 as a promising nanostructured electrode material with superior electrochemical characteristics, making it a promising electrode for next-generation energy storage applications.

Flexible, high-performance supercapacitors are critical for the future generation of portable and wearable electronics. In this research, we present, for the first time, the synthesis and design of a flexible supercapacitor device using ZnO hexagonal prism-decorated MXene synthesized via a hydrothermal method, serving as a highly efficient electrode material. Pristine MXene suffers from restacking, limiting its electrochemical performance; however, decorating it with ZnO hexagonal prism mitigates this issue by enhancing interlayer spacing and improving ion transport. The unique hexagonal prism morphology of ZnO, combined with the layered MXene structure, significantly enhances electrical conductivity while preventing restacking. The resulting material achieved an impressive specific capacitance of 140 F g-1 at 0.5 A g-1, greatly surpassing pristine MXene (73 F g-1). Furthermore, it exhibited outstanding cycling stability, with 97.2 % capacitance retention after 12,000 cycles at 3 A g-1. A flexible symmetric supercapacitor fabricated using this material demonstrated excellent mechanical flexibility, maintaining reliable electrochemical performance under bending angles of 0 degrees, 60 degrees, 90 degrees, and 180 degrees. The device also delivered a high energy density of 6.33 Wh kg-1 and a power density of 600 W kg-1, showcasing the potential of ZnO hexagonal prism decorated MXene as a promising material for advanced energy storage applications.

This study investigates the potential of perovskite oxides for supercapacitor applications, focusing on AgNbO3 synthesized via the solid-state route and doped with Lanthanum (La) at concentrations of 0 %, 5 %, and 9 %. The doped nanomaterials were characterized using XRD, FESEM, HRTEM, XPS, FTIR, Raman, and UV-Vis spectroscopy to confirm the crystal structure, morphology and the optical properties of the synthesized materials. Electrochemical analysis demonstrated that La doping significantly enhances the capacitance of the perovskite material, with the areal capacitance increasing from 4.8 mF/cm2 at 0 % La to 22.5 mF/cm2 at 9 % La at a scan rate of 5 mV/s. Moreover, an asymmetric supercapacitor device was fabricated using the activated carbon (AC) as the anode and La-doped AgNbO3 as the cathode. This device demonstrated remarkable electrochemical performance, maintaining robust cyclic stability over an extensive 4000 charge-discharge cycles at 5 mA/cm2. This study underscores the viability of La doping is a feasible approach for optimizing the energy storage properties of AgNbO3 and also paves the way for further investigation and improvement of perovskite-based materials in high-performance energy systems.

The development of multifunctional nanomaterials with both superior dielectric and electrochemical properties is crucial for advancing modern electronic and energy storage technologies. In this study, hexanediamine-functionalized zinc oxide nanoparticles (ZnO NPs) were synthesized and systematically investigated. ZnO nanoparticles were successfully functionalized with 1,6-hexanediamine, and comprehensive analysis confirmed modifications in structural, optical, chemical, and morphological properties, validating the effectiveness of the functionalization process. PXRD confirmed enhanced crystallinity and increased crystallite size upon capping, while FTIR verified successful amine functionalization through characteristic NH and CH2 vibrations. Optical studies revealed a blue shift in absorption and reduced trap emissions in capped ZnO NPs due to quantum confinement, with band gaps of 3.02 eV (pure) and 2.87 eV (capped). TEM analysis confirmed improved morphology and dispersion in capped ZnO NPs with hexagonal shape and reduced agglomeration. The dielectric behavior of the functionalized ZnO NPs showed real and imaginary dielectric permittivity of 115 and 99 at 1 MHz, respectively. Additionally, the material exhibited an AC conductivity of 0.0056 Ω-1 mm-1, highlighting its potential for advanced electronic application. Furthermore, an asymmetric device was fabricated to investigate the electrochemical properties, which displayed cyclic stability. After 15,000 cycles at a current density of 15 mA cm-2, the device retained 81

High-performance sodium-ion batteries (NIBs) are an essential alternative for sustainable energy storage amid growing concerns about limited lithium resources. Two-dimensional transition metal oxides (TMOs) particularly vanadium pentoxide (V2O5)-show great promise as electrode materials for NIBs. In this work, we report the firstever sol-gel-assisted green synthesis of V2O5 using Trachyspermum ammi (L.) leaf extract, offering an eco-friendly route free from hazardous chemicals. The green-synthesized V2O5 (GS-V2O5) and its composite with single-walled carbon nanotubes (SWCNT) (GS-V2O5/SWCNT) exhibited reduced crystallite size and lower agglomeration compared to chemically synthesized V2O5 (CS-V2O5), demonstrating superior structural properties. The GS-V2O5/ SWCNT composite exhibits a remarkable specific capacity of 527 mAh g(-1) at a current density of 50 mA g(-1), significantly outperforming pristine GS-V2O5 (193 mAh g(-1)). It also achieves a 60.46 % initial coulombic efficiency (ICE), significantly higher than the 6.14 % for GS-V2O5 alone. Electrochemical impedance spectroscopy (EIS) reveals a sharp reduction in charge transfer resistance (Rct) from 1822 Omega to 31 Omega upon SWCNT addition, and GITT analysis confirms a Na-ion diffusion coefficient of 1.53 x 10(-1)0 cm(2) s(-1). Postmortem studies indicate that SWCNT incorporation preserves electrode integrity, enhances electrical percolation, and maintains stability during cycling. Collectively, these findings highlight the strong potential of bio-synthesized nanocomposites for safer, long-lasting, and higher-performance energy storage applications.

This study provides a comprehensive analysis of a biofabricated nanomaterial derived from Sansevieria trifasciata root extract, evaluating its structural, morphological, and optical properties for use in asymmetric supercapacitors. The nanomaterial comprises pristine ZnO nanoparticles (ZnO NPs) and a 1% Ag-doped ZnO nanocomposite (Ag@ZnO NC), synthesized through a green-assisted sol-gel autocombustion method. Employing techniques such as X-ray diffraction, ultraviolet-visible near-infrared, scanning electron microscopy-energy-dispersive X-rayspectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, and transmission electron microscopy, the study confirms a hexagonal wurtzite structure and nanocrystallites with spherical and hexagonal shapes (30 nm). Optical analysis reveals a red shift in the band gap with Ag doping, indicating improved conductivity. The material shows potential applications in solar cells, optoelectronics, spintronics, wastewater treatment, and high-performance asymmetric supercapacitors. Raman spectra validate the wurtzite phase and identify intrinsic defects. Electrochemical tests demonstrate remarkable supercapacitive behavior with a 94% capacitance retention after 10,000 cycles, highlighting its promise as advanced asymmetric supercapacitors.

The present work summarizes the fabrication of an amine-functionalized cadmium-based metal-organic framework (MOF), {[Cd(AT)(BP)]·4DMF}n or Cd_AT-BP, by adopting a simple solvothermal approach using 2-aminoterephthalic acid (AT) as the main linker, while 4,4'-bipyridyl (BP) as an auxiliary linker. The structure of Cd_AT-BP was validated by the single-crystal X-ray diffraction technique that revealed the formation of an overall three-dimensional network with BP acting as a bridge between the 2D sheets of the MOF. The robust framework of Cd_AT-BP decorated with a free amine functional group was utilized for energy storage application. The electrochemical measurements of Cd_AT-BP revealed a maximum areal capacitance of 9.8 mF/cm2 at a scan rate of 5 mV/s. Further, to enhance the practical utility of Cd_AT-BP in energy storage devices, two composites of Cd_AT-BP with reduced graphene oxide (rGO) and multiwalled carbon nanotubes (CNTs), viz., Cd_AT-BP/rGO and Cd_AT-BP/CNT, were prepared by adopting a facile ultrasonication approach. The synthesized Cd_AT-BP/rGO and Cd_AT-BP/CNT composites displayed an impressive areal capacitance of 117 and 37 mF/cm2 (58.5 and 17.5 F/g) at a scan rate of 5 mV/s, respectively, and a capacitance retention of up to 118 and 100% after 5000 cycles at a constant current density of 5 mA/cm2. The highest energy density of about 4.23 mW h/cm2 (2.12 W h/kg) at a current density of 1 mA/cm2 was shown by Cd_AT-BP/rGO among all the three materials attributable to the layered structure of rGO, providing a larger surface area accessible for ion adsorption. Enticed by the remarkable outcomes exhibited by Cd_AT-BP/rGO, we fabricated a two-electrode asymmetric supercapacitor (ASC) device. The developed ASC device revealed energy and power densities of 26.7 mW h/cm2 (13.4 W h/kg) and 3760 mW/cm2 (1880 W/kg), respectively, with a galvanostatic charge-discharge stability of up to 10,000 cycles. The findings identify Cd_AT-BP/rGO as a potential contender for future-generation supercapacitors.

This work presents an innovative and environmentally friendly biological synthesis approach for producing alpha-Fe2O3 nanoparticles (NPs) and the successful synthesis of alpha-Fe2O3/reduced graphene oxide (rGO) nanocomposites (NCs). This novel synthesis route utilizes freshly extracted albumin, serving as both a reducing agent and a stabilizing agent, rendering it eco-friendly, cost-effective, and sustainable. A combination of characterization techniques including X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, and field emission scanning electron microscopy (FE-SEM) was employed to predict and confirm the formation of the as-synthesized alpha-Fe2O3 NPs and alpha-Fe2O3/rGO NCs. Transmission electron microscopy (TEM) verified the anisotropic nature of the synthesized nanoparticles. To gain insight into the enhanced capacitance of the alpha-Fe2O3/rGO NCs, a series of electrochemical tests, namely cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), electrochemical impedance spectroscopy (EIS), and stability assessments, were conducted in a conventional three-electrode configuration. Furthermore, a two-electrode asymmetric supercapacitor (ASC) device was fabricated to assess the practical viability of this material. The alpha-Fe2O3/rGO NCs exhibited a remarkable potential window of 2 V in an aqueous electrolyte, coupled with exceptional cycling stability. Even after undergoing 10 000 cycles, the capacitive retention exceeded 100%, underlining the promising potential of this material for advanced energy storage applications.

The growing need for cleaner air is gaining a lot of attention, and therefore, the removal of organosulfur compounds from fuel with a concentration less than 15 ppm is becoming the need of the hour. To fulfill this expectation, we have synthesized an emergent class of magnetic hybrid nanomaterials (Fe3O4/rGO and Ni/Fe3O4/rGO) through a sol-gel-assisted green synthetic technique that shows remarkable adsorptive desulfurization of dibenzothiophene (DBT). The structural feature of the magnetic nanomaterial was identified through various characterization techniques like PXRD, FTIR, Raman, XPS, TGA, BET, SEM, and TEM. The magnetization of Ni/Fe3O4/rGO confirmed that the adsorbents performed well in magnetic separation. Further, doping with various concentrations of Ni enhances its magnetization, thereby making the recovery of nanocomposites easy, eco-friendly, and inexpensive with the help of an external magnet. In contrast to an undoped nanocomposite, Ni-doped Fe3O4/rGO exhibits superior properties. Also, Ni-doped Fe3O4/rGO shows enhanced desulfurization with an effective removal efficiency of 73% as compared with a pristine nanocomposite (45%). This is because as the doping concentration of Ni metal was increased, active Lewis acid sites were remarkably increased which were favorably available for the transfer of lone pair electrons on S atoms or pi-electrons in the aromatic ring of thiophene to form strong S-Ni bonding or pi-complexation. With regard to academic, industrial, and environmental considerations, Ni/Fe3O4/rGO is found to be a promising adsorbent and can be the best replacement for adsorptive desulfurization due to its relatively high adsorption capacity, improved magnetization, and simple magnetic separation efficiency.

Herein we report on the excellent, supercapacitor performance and flexible device application of a robust, new polymeric metal-ligand complex, which is readily synthesized at room temperature via a straightforward, one-step protocol using the N4 donor, namely 3,3 '-diaminobenzidine (DAB) and gadolinium(III) nitrate. Thus, the coordination polymer (Gd-DAB) complex synthesized in a facile and economically feasible synthesis route paves the way for realizing a new class of affordable, durable energy devices for storage applications. The results of complementary characterization techniques not only corroborated the proposed structure but also revealed a potential two-dimensional (2D)/sheet-like organization similar to the coordination polymer (COP). The elec-trochemical tests performed on the as-prepared sample, in the form of an electrode active component, showed brilliant supercapacitive characteristics with the capacitive retention exceeding over 100% even after 5000 cycles. The complex has been used as an active media for the fabrication of an interdigitated flexible and symmetric supercapacitor. The electrochemical storage device evaluation, under different bending angles (up to 180o) and twisting conditions at the current density of 10 mu A/cm2 for 5000 cycles, revealed the capacitive retention of-50% after 5000 cycles.

The present investigation is aimed to develop hybrid nanocomposites of polyetherimide (PEI)/silicone rubber (85:15 wt:wt) incorporated with fixed loading (3 wt%) of halloysite nanotubes (HNTs) and 0.0, 0.1, 0.3, and 0.5 wt% loadings of reduced graphene oxide (RGO) by melt mixing process using a twin-screw extruder. In comparison with RGO, it is observed that the HNTs disperse sparingly in PEI/silicone rubber mixtures in spite of having similar Physico-chemical structures. SEM studies reveal that the addition of RGO increases the dispersion of HNTs in PEI/silicone rubber to a greater extent, which results in an improvement in tensile strength from 41 to 59 MPa and tensile modulus from 658 to 715 MPa on the addition of 0.3 wt% of graphene. This synergistic effect of both the nanofillers is also reflected by significant improvements in flexural modulus (from 3217 to 4156 MPa), impact strength (56 to 78 J/m), Rockwell hardness (89 to 104), and thermal properties of nanocomposite; the highest storage modulus (7290 MPa) was observed for 0.3 wt% and lowest (5390 MPa) for 0.0 wt% loading of graphene at 50 °C temperature. It is due to the rigidity in polymer chains movement because of dispersion of RGO that improves the interfacial interaction, as well as thermal vibrations of the C–C bond, which are restricted of the polymer matrix.

Indian Mutual Fund Industry (IMFI) is growing day-by-day since its evolution in 1963 and ready to cross total assets value from ₹35trillion very soon. In present study, the gross resource mobilized (GRM) by private, public and UTI schemes has been studied from FY2009-2010 to FY2018-2019. The Regression analysis has been performed using various models on the basis of selected independent variables. Subsequently, the optimum models have been suggested to predict the value of GRM by private, public and UTI schemes. The paper enhances the understanding of IMFI and GRM relations with various predictors.

The present investigation is targeted to prepare nanocomposites based on binary blends of polyetherimide (PEI)-silicone rubber incorporated with varied loadings of nanotitanium dioxide particles. Nanocomposites have been prepared by melt blending process using twin screw extruder. Thermal properties of the developed nanocomposites have been investigated with the help of thermogravimetric analyzer (TGA) and dynamic mechanical analyzer (DMA). Scanning electron microscopy (SEM) is used to analyze the morphological properties of the impact strength) of the nanocomposites have been evaluated by universal testing machine (UTM). Mechanical testing results reveal that there is 35% increase in tensile strength, 3% increase in tensile modulus and 41% increase in impact strength at 1 phr loading of nanotitanium into blend polymer matrix. The nanocomposite having 1 phr nano-titanium has got the highest thermal stability than the others. DMA results indicate that at 50 degrees C nanocomposites having 1 phr nano-titanium reveals 69% increase in storage modulus as compared to pure blend system. SEM micrographs clearly indicate that the nanocomposite with 1 phr loading of nano titanium has the smallest domain size as compared to other nanocomposites .This may be due to uniform and homogeneous dispersion of 1 phr nanotitanium in polymer matrix followed by fairly good polymer filler interaction.