Blog

Nov 03, 2023

Boosted electrochemical performance of magnetic caterpillar

Scientific Reports volume 13,

Scientific Reports volume 13, Article number: 7822 (2023) Cite this article

504 Accesses

1 Altmetric

Metrics details

Ni-incorporated MgFe2O4 (Mg0.5Ni0.5Fe2O4) porous nanofibers were synthesized using the sol–gel electrospinning method. The optical bandgap, magnetic parameters, and electrochemical capacitive behaviors of the prepared sample were compared with pristine electrospun MgFe2O4 and NiFe2O4 based on structural and morphological properties. XRD analysis affirmed the cubic spinel structure of samples and their crystallite size is evaluated to be less than 25 nm using the Williamson–Hall equation. FESEM images demonstrated interesting nanobelts, nanotubes, and caterpillar-like fibers for electrospun MgFe2O4, NiFe2O4, and Mg0.5Ni0.5Fe2O4, respectively. Diffuse reflectance spectroscopy revealed that Mg0.5Ni0.5Fe2O4 porous nanofibers possess the band gap (1.85 eV) between the calculated value for MgFe2O4 nanobelts and NiFe2O4 nanotubes due to alloying effects. The VSM analysis revealed that the saturation magnetization and coercivity of MgFe2O4 nanobelts were enhanced by Ni2+ incorporation. The electrochemical properties of samples coated on nickel foam (NF) were tested by CV, GCD, and EIS analysis in a 3 M KOH electrolyte. The Mg0.5Ni0.5Fe2O4@Ni electrode disclosed the highest specific capacitance of 647 F g−1 at 1 A g−1 owing to the synergistic effects of multiple valence states, exceptional porous morphology, and lowest charge transfer resistance. The Mg0.5Ni0.5Fe2O4 porous fibers showed superior capacitance retention of 91% after 3000 cycles at 10 A g−1 and notable Coulombic efficiency of 97%. Moreover, the Mg0.5Ni0.5Fe2O4//Activated carbon asymmetric supercapacitor divulged a good energy density of 83 W h Kg−1 at a power density of 700 W Kg−1.

The ever-increasing worldwide demand for energy is urging the development of energy storage devices and materials with impressive specific capacitance and brilliant cycle stability, such as supercapacitors1. One-dimensional (1D) nanofibers providing numerous active sites for ion absorption are potentially one of the best options as an energy storage electrode owing to their magnificent morphologies1,2. Electrospinning is an efficient, cost-effective, controllable in diameter, convenient, and rapid method to fabricate different kinds of one-dimensional nanostructures such as nanofibers, nanobelts, and nanotubes with distinguished performances like excellent cycling stability, notable capacity, and suitable ionic conductivity. Various criteria, such as solution parameters (precursors, viscosity, and solvent), flow rate, applied voltage, heating rate, and temperature, have a significant influence on the morphology of electrospun nanostructures3. Metal spinel ferrites, generally known as MFe2O4 (M: a divalent metal ion), which M and Fe ions may locate at both tetrahedral and octahedral positions in a cubic close packing of oxygen, attracted widespread attention in the past few years due to their simplicity of synthesis, high electrical conductivity, low electrical losses and inherent toxicity, physical and chemical stabilities, spontaneous magnetic and electrochemical nature resulting applications in different fields of technology4,5. Previously, the supercapacitive behavior of C/CuFe2O46, Fe2O3@SnO27, and ZnOFe2O48 nanofibers have been studied extensively.

Magnesium ferrite (MgFe2O4), possessing a band gap of 2.18 eV, is a well-known n-type semiconducting material mainly used as a microwave absorber and lithium-ion batteries due to moderate saturation magnetization and high chemical stability9,10,11. Nickel ferrite (NiFe2O4) is an n-type semiconductor, having low coercivity and high electrical resistivity12. Both MgFe2O4 and NiFe2O4 possess cubic inverse spinel structures. In inverse spinel structure, a divalent cation (Mg2+, Ni2+) occupies half of the octahedral B-sites coordination and a trivalent cation (Fe3+) locates at tetrahedral A-sites as well as half of the octahedral B-sites4,13,14,15,16,17.

NiFe2O4 and MgFe2O4 are composed of inexpensive, environmentally safe, and easily accessible materials. Studies have indicated their applicability as electrode material in supercapacitors [18,19,20, and 21]. Their electrochemical behavior is attributed to the presence of electrochemically active multivalent cations21. Despite all the interesting properties, the practical applications of these spinels for supercapacitors are still relatively restricted due to unacceptable capacitance and internal resistances. A promising way to improve the electrochemical performance of spinel ferrites is the design of novel ferrite-based nanocomposites. Hybridization by carbon nanomaterial such as graphene22 reduced graphene23,24, and carbon nanotubes25 with high conductivity can boost the specific capacitance of spinel Ferrite. Mixed ferrites are ferrite spinels that are composed of a mixture of two divalent metal ions with varying ratios. The surface properties are considerably affected by the cation distribution of mixed ferrite, making them electrochemically active26. Consequently, the ternary ferrites possess the additional composition-dependent synergistic effect of different elements. In preparation of the ternary ferrite-spinel materials, the chemical valence, structural parameters, and radius of the constituent ions should be greatly considered for minimum formation energy and composition tuning in the continuum. Interestingly, both NiFe2O4 and MgFe2O4 are isostructural and consist of isovalent Ni2+ and Mg2+, thus it is exciting to investigate the applicability of ternary Ni-Mg ferrites in the challenging field of energy storage as potential electrode materials with high electrochemical performance. Wongpratat et al. has reported the hydrothermal synthesis of Ni1-xMgxFe2O4 (x = 0, 0.25, 0.5, 0.75, and 1.00) nanoparticles using aloe vera extract solution. The results revealed that Ni0.25Mg0.75Fe2O4 electrodes show a high specific capacitance with cycling stability of 88.79% after a 1000 cycle21. Also, enhancing the surface area of the active materials by the fabrication of diverse morphology using various techniques is the most effective strategy to increase the performance of supercapacitors21. The physical properties of diverse morphology of MgFe2O4 and NiFe2O4 prepared by various methods such as hollow cubes27, core–shell28, rose-like nanoflower18, mesh-like structure19, thin film29, beehive-like nanosheets20, and nanoparticle21 have been reported earlier. One-dimensional nanomaterials, prepared via facile and low-cost electrospinning techniques, revealed superior electrochemical performance in supercapacitors owing to their unique morphology and fascinating properties, representing the great potential for boosting the performance of supercapacitors30. However, to the best of our knowledge, no reports are available focusing on the supercapacitive behavior of one-dimensional (1D) MgFe2O4 nanobelts, NiFe2O4 nanotubes, and ternary spinel Mg0.5Ni0.5Fe2O4 nanofibers. In this research, we have investigated the magnetic, optical, and electrochemical properties of these materials fabricated by the sol–gel electrospinning method. The results suggested that Mg0.5Ni0.5Fe2O4 caterpillar-like nanofibers can be used as a promising electrode for supercapacitor applications.

Magnesium nitrate (Mg(NO3)2.6H2O, > 99%, Merck), nickel nitrate (Ni(NO3)2.6H2O, > 99%, Merck), iron nitrate (Fe(NO3)3.9H2O, > 99%, Merck), N, N-Dimethylformamide (DMF), Polyvinylpyrrolidone (PVP; MW = 1,300,000, Sigma-Aldrich) and ethanol (99.8%, Merck), carbon black (Alfa Aesar), polyvinylidene difluoride (PVDF, Kynar HSV900, Arkema), N-methyl-2-pyrrolidone (NMP, > 99%, Merck), and potassium hydroxide (KOH, > 85%, chem-lab) were analytical grade and used without further purification. Deionized (DI) water (> 18.4 MΩ cm−1) from a Merck Millipore water purification system was used throughout the experiment. A flexible interconnected porous nickel foam with 1.5 mm thickness and a purity > 99% was supplied by Latech Scientific Supply Pte. Ltd. (Singapore).

MgFe2O4 (MFO), NiFe2O4 (NFO), and Mg0.5Ni0.5Fe2O4 (MNFO) nanofibers were fabricated using the sol–gel electrospinning technique. Magnesium ferrite was synthesized by adding 0.2564 g of Mg(NO3)2.6H2O and 0.4039 g Fe(NO3)3.9H2O to 10 mL ethanol/DMF (50:50 w/w) mixed solvents. After that, 1 g of PVP was added dropwise into the above solution and stirred for 12 h. The formed homogeneous sol was loaded into a syringe equipped with a 25 G blunt stainless needle and placed in a syringe pump at a distance of 12 cm from flat aluminum foil as a collector. The syringe pump and collector were connected to a high-voltage power supply, applying a voltage of 17.5 kV. The electrospinning process was done at the rate of 0.5 mL h−1 under the controlled condition at room temperature with a relative humidity of 45%. The previous method was repeated to prepare Mg0.5Ni0.5Fe2O4 ferrite, where Mg(NO3)2.6H2O (1.282 g), Ni(NO3)2.6H2O (0.1454 g), and Fe(NO3)3.9H2O (0.4039 g) were used as precursors. All of the electrospun samples were dried at 100 °C for 12 h and then calcined at 600 °C in the air for 2 h with a heating rate of 2 °C/min. The schematic representation of Mg0.5Ni0.5Fe2O4 nanofibers preparation is shown in Fig. 1.

Schematic representation of Mg0.5Ni0.5Fe2O4 nanofibers synthesized via sol–gel electrospinning method.

The synthesized samples as active material (80 wt.%), carbon black (10 wt.%), and PVDF (10 wt.%), were mixed and a slurry was prepared by the addition of N-methyl-2-pyrrolidone (NMP) as a solvent. Then, the prepared slurry was coated onto the nickel foam (1 × 1 cm2). Afterward, the electrodes were dried at 80 °C for 3 h. The loaded mass on Ni foam was about 1 mg.

Structural properties of prepared nanomaterials were investigated through X-ray diffraction analysis using the X'Pert Pro Philips device. The chemical bonds of nanofibers were studied by Fourier transform infrared analysis using the Alpha—Bruker device. The MIRA3TESCAN-XMU instrument was used to perform field emission scanning electron microscopy and energy dispersive spectroscopy to investigate nanofibers' morphological characteristics and elemental composition, respectively. N2 adsorption/desorption isotherms at 77 K were used to evaluate the textural properties of the samples using a BELSORP-mini II instrument. Barrett-Joyner-Halenda (BJH) and Brunauer–Emmett–Teller (BET) techniques were used to measure the pore size distribution and surface area of the samples, respectively. The optical features of samples were explored using the Scinco-S4100 device. Magnetic measurements were done using MDK (Magnetic Daghigh Kavir Co., Iran) device. A three-electrode system, consisting of a prepared electrode, Ag/AgCl, and platinum wire as working, reference, and counter electrodes in a 3 M KOH electrolyte, was used to test the electrochemical efficiency of the synthesized specimens. Using a ZAHNER-ZENNIUM device, cyclic Voltammetry, galvanostatic charge–discharge, and electrochemical impedance spectroscopy (EIS) measurements were conducted over a frequency range of 0.01–105 Hz at an AC amplitude of 10 mV. The Zview software was used to fit the EIS plot.

The X-ray diffraction patterns of synthesized MgFe2O4, NiFe2O4, and Mg0.5Ni0.5Fe2O4 nanofibers in the range of 10–80° are demonstrated in Fig. 2a–c. All diffraction peaks are well-indexed as (111), (220), (311), (400), (422), (511), (440), and (533) planes corresponding to single-phase cubic spinel structure of MgFe2O4 (JCPDS Card No. 36-0398) and NiFe2O4 (JCPDS Card No. 10-0325)22,31. No additional peaks related to any secondary phase were detected in the XRD pattern of synthesized nanofibers, indicating the high-purity phase in samples. On the XRD patterns, Rietveld fitting is conducted using MAUD software to further check the phase purity of the samples. The fitted XRD patterns are shown in Fig. 2d–f. The goodness of fit, Sig, evaluated the fitting quality of the experimental data. The Sig-goodness of those fittings was close to 1 which confirmed that the XRD patterns are compatible with a cubic spinel structure with space group symmetry Fd3m. Furthermore, the Ni2+ incorporation in magnesium ferrite not only did not disturb the spinel structure but also the sharp diffraction peaks of the Mg0.5Ni0.5Fe2O4 nanofibers suggest the enhanced crystallinity compared to MgFe2O4 and NiFe2O4 samples. The lattice constant (a) was determined from the interplanar spacing (d) for the (311) plane, using the equation for a cubic lattice structure: a = d(h2 + k2 + l2)1/2, where h, k, and l are the Miller indices. The unit cell volume of the samples is denoted in Table 1. As Ni2+ was incorporated in magnesium ferrite, the calculated lattice parameter decreased from 8.38 to 8.33 Å due to the substitution of the smaller Ni2+ ions (0.69 Å at the octahedral site and 0.55 Å at the tetrahedral site) for the larger Mg2+ ions (0.72 Å at the octahedral site and 0.57 Å at the tetrahedral site), which is in line with the results reported for Mg0.5Ni0.5Fe2O4 nanoparticles by a hydrothermal route21.

(a–c) XRD patterns of (a) MFO nanobelts, (b) NFO nanotubes, and (c) MNFO nanofibers, (d–f) Rietveld fitting of XRD patterns.

The broadening of the diffraction peak can be assigned to the small crystallite size of the sample, strain, and instrumental factors32. The average crystallite size (D) and lattice strain (ε) of prepared samples are obtained from the intercept and slope of the linear fit of the Williamson–Hall (W–H) plot (Fig. 3), which βcosθ was plotted with respect to 4sinθ according to W–H equation (Eq. 1) for preferred orientation peaks33 and the results are listed in Table 1.

where λ is the x-ray wavelength, β is the width of the peak in radians, θ is the Bragg angle, and K is a constant which is considered 0.94. The W–H plot revealed a compressive strain for the MFO sample due to lattice shrinkage.

W–H plots of (a) MFO nanobelts, (b) NFO nanotubes, and (c) MNFO nanofibers.

Figure 4 represents the Fourier transform infrared spectra of prepared nanofibers, revealing valuable information about the different functional groups. In general, the spinel ferrite structure consists of two sub-lattices in which divalent ions (Ni2+ and Mg2+) occupy octahedral B-sites and trivalent ions (Fe3+) are equally distributed among tetrahedral A-sites and octahedral B-sites34. The bands at 438 and 465 cm−1 correspond to the intrinsic stretching vibration of the octahedral sites of Mg-O and Ni–O (νo); also the band at 580 cm−1 represents the intrinsic stretching vibration of the tetrahedral site of Fe–O (νt), respectively, confirming the formation of the spinel structure of MgFe2O4 and NiFe2O422,35. In the MNFO sample, the metal–oxygen absorption bands slightly shifted with the Ni2+ incorporation. This may be due to Mg, Ni, and Fe cations redistribution on both sites. The broad band around 3419 and the less intense band around 1637 cm−1 indicated the characteristic vibrational modes of O–H groups and vibrations of the absorbed water molecules, respectively36. The bands observed at 2859 and 2937 cm−1 disclosed the asymmetric and symmetric stretching vibrations of methylene (–CH2) groups, respectively12. The band at 1380 cm−1 was ascribed to the carboxylate group37. The bands in the range of 1000 to 1250 cm−1 correspond to nitrate ion traces as well as C–O bonding22,38. After calcination, they become weaker. Another band located around 2359 cm−1 was reasonably attributed to the anti-symmetrical vibration of carbon dioxide absorbed from the environment, observed only in the as-spun MgFe2O4 sample39.

FTIR spectra of (a) as-spun MFO, (b) MFO nanobelts, (c) NFO nanotubes, and (d) MNFO nanofibers.

FESEM images of the prepared MgFe2O4, NiFe2O4, and Mg0.5Ni0.5Fe2O4 samples calcined at 600 °C are represented at three different magnifications in Fig. 5. It can be found that all of the samples possess one-dimensional arrays. The MgFe2O4 sample demonstrates long and continuous solid inner belt-like morphology with rectangular cross-sections that possess an average diameter of 65 nm (Fig. 5a–c). In other terms, the collapse of the as-spun polymeric precursor fibers during the calcination led to nanobelts morphology40. The NiFe2O4 depicts short and broken hollow-interior uniform nanotubes (Fig. 5d–f). It has been reported that fast solvent evaporation rate and phase separation during electrospinning tend to the production of hollow nanofibers after calcination41. As clearly observed in Fig. 5g–i, the Ni incorporation in MgFe2O4 causes the formation of roughly porous caterpillar-like nanofibers with numerous grain boundaries. The formation of the rough surface is attributed to the properties of precursor solution, which will be valuable for electrochemical applications where the surface area has a huge impact on determining their performance41,42.

FESEM images of (a–c) MFO nanobelts, (d–f) NFO nanotubes, (g–i), and MNFO nanofibers in low, moderate, and high-magnification.

Figure 6 showed the EDS spectra of prepared samples, which revealed the presence of desired elements such as magnesium (Mg), nickel (Ni), iron (Fe), and oxygen (O) and confirmed the chemical purity of samples43. Au peak was normally detected at ~ 2 keV due to the coating of Au thin layer over prepared samples to reduce charging influence44.

EDS spectra of (a) MFO nanobelts, (b) NFO nanotubes, and (c) MNFO nanofibers.

The nitrogen adsorption–desorption isotherms of samples are shown in Fig. 7. The isotherm exhibited a typical type-IV behavior with an H3-type hysteresis loop, indicating the presence of mesoporous structure45. The formation of mesoporous structure is due to the removal of PVP polymeric matrix after calcination at temperature of 600 °C. The BET specific surface area and average pore diameter of the samples are listed in Table 1. The BET surface area value is calculated as 17.8, 25.0, and 40.2 m2 g−1 for MFO, NFO, and MNFO samples, respectively. Insets of Fig. 7a–c demonstrates the pore size distribution based on the BJH procedure. The average pore diameter of MNFO fibers was around 7.3 nm. The high surface area of MNFO will be useful for the diffusion of electrolytes, which is vital for the enhancement of electrochemical properties46.

N2 adsorption–desorption isotherms of (a) MFO, (b) NFO and (c) MNFO samples (the insets show the corresponding pore size distribution).

In order to investigate the optical properties of prepared nanofibers, the UV–vis-DRS spectra were recorded in the region of 300–900 nm (Fig. 8a). Kubelka–Munk function (\(\mathrm{F}\left(\mathrm{R}\right)=\frac{{(1-R)}^{2}}{2R}\)) of each sample was utilized to calculate the optical band gap using Tauc equation (Eq. 2)47

where α, h, \(\nu\), and A represent the material's absorption coefficient proportional to F(R), Planck's constant, the light frequency, and the constant parameters-containing characteristics of the bands, respectively. Also, n = 1/2 is considered to determine the direct optical band gap (Eg) of MgFe2O4 and NiFe2O4, and the plot of (αhν)2 versus hν is shown in Fig. 8b. It is known that the structural parameters, crystallite size, and impurities are potential factors that affect the band gap value44. The band gap of MFO nanobelts, NFO nanotubes, and MNFO caterpillar-like nanofibers was found to be 1.90, 1.80, and 1.85 eV, respectively. It is seen that the band gap of MNFO nanofibers is narrower than the MFO nanobelts sample because adding nickel in the MNFO preparation process induces inner states in the band gap, providing additional levels between the conduction and the valence bands17,44. The calculated band gap value of MNFO nanocomposite lies between the values obtained for the band gap of magnesium ferrite and nickel ferrite due to alloying effect and indicated suitable substitution of Ni ions on Mg sites in MgFe2O4. The band gap narrowing of magnesium ferrite nanoparticles by Ni substitution was reported by other researchers11,48.

(a) DRS spectra, and (b) Tauc plots of prepared samples.

Optimization of the magnetic properties of ferrites has played a decisive role in the application of the magnetic materials group. The vibrating sample magnetometer (VSM) was utilized to measure the magnetization (M) of prepared nanomaterials as a function of the applied magnetic field (H). The hysteresis loops of prepared samples measured at room temperature are demonstrated in Fig. 9. The magnetization was enhanced with an increasing applied magnetic field and saturated at an extremely small value of the applied magnetic field. Also, the small coercivity observed in all hysteresis loops confirms the soft ferromagnetic nature of the synthesized nanofibers13. From these hysteresis curves, the value of saturation magnetization (Ms), remnant magnetization (Mr), coercivity (Hc), and the magnetic moment (\({\mu }_{B}\)) are tabulated in Table 2. The obtained data indicated that the substitution of Mg2+ by Ni2+ ions in the host MgFe2O4 lattice had enhanced the value of saturation magnetization from 16.4 to 22.0 emu/g, whereas this value for NiFe2O4 nanotubes is found to be 23.6 emu/g. The obtained saturation magnetization values of MgFe2O4 nanobelts and NiFe2O4 nanotubes are smaller than bulk values of 27 and 47 emu/g, but comparable to the reported values for nanoparticles49,50. The reduction of Ms relatively to bulk can be attributed to the decreased particle size (enhanced surface/volume ratio) and spin canting at the surface of nanoparticles49,50. It is known that the crystallinity, surface imperfection, chemical composition, and cation distribution variation on octahedral and tetrahedral sites have a huge impact on the saturation magnetization of spinel ferrite nanostructures9,13. The increase in the Ms value of the MFO by Ni incorporation can be attributed to the larger magnetic moments of Ni2+ (2.83 \({\mu }_{B}\)) as compared to the Mg2+ (0 \({\mu }_{B}\)) at the octahedral site51. The magnetic moment (\({\mu }_{B}\)) is calculated using the \({\mu }_{B}=\frac{M \times {M}_{s}}{5585}\) equation, where Ms and M represent the saturation magnetization and the molecular weight of the sample52 (See Table 2). Moreover, the coercive field, Hc, was increased from 0.40 for the MgFe2O4 nanotubes to 3.26 Oe for the MNFO sample. The increase of the surface anisotropy of small crystallites contributed to the enhancement of coercivity51,53. This sort of increase in saturation magnetization for nickel-substituted magnesium ferrite has also been reported earlier54,55.

Room temperature VSM plot of MFO nanobelts, NFO nanotubes, and MNFO nanofibers. The inset shows magnified view of M–H curves.

The electrochemical performance of MgFe2O4, NiFe2O4, and Mg0.5Ni0.5Fe2O4 electrodes was tested using a three-electrode system in 3 M KOH. The Cyclic Voltammetry (CV) of prepared samples at various scan rates of 10, 30, 50, and 80 mV s−1 with a potential window of 0–0.5 V is shown in Fig. 10a–c. The CV profiles with distinct anodic and cathodic redox peaks demonstrate the supercapacitive nature of prepared nanomaterials. As it is known, the enhancement of ion-electrode interaction (diffusion–reaction at the electrolyte and electrode interface) leads to excellent capacitive behavior 56. The energy storage mechanism of prepared samples is suggested by the following reactions57,58:

CV plots of (a) MFO nanobelts, (b) NFO nanotubes, and (c) MNFO nanofibers. (d) The specific capacitance of samples at scan rates of 10, 30, 50, and 80 mV s−1.

The shape of the cyclic voltammogram of samples remains unchanged as the sweep rate increases from 10 to 80 mV s−1, revealing excellent electrochemical reversibility and prominent high-rate performance. However, the shifts of redox peaks towards lower/higher potentials may be attributed to the polarization effect. The specific capacitance from the CV profile was calculated according to the following equation:

where Csp, \(\smallint IdV\), m, \(\nu\), and ∆V denote the specific capacitance (F g−1), the integrated area under the CV plot, the mass of active material (g), the scan rate (V s−1), and the potential window (V), respectively59. The specific capacitance values of MgFe2O4, NiFe2O4, and Mg0.5Ni0.5Fe2O4 at the scan rate of 10 mV s−1 were 98, 385, and 965 F g−1, respectively, as shown in Fig. 10d. The specific capacitance is significantly influenced by the scan rate enhancement. The calculated data of Csp exhibited a higher specific capacitance at lower scan rates. This implies that the electrolyte ions had sufficient time to penetrate and access all the inner microstructures of the electrode material for charge storage60.

The galvanostatic charge–discharge (GCD) profiles of prepared nanomaterials were recorded at a current density of 1, 3, 5, 7, and 10 A g−1 demonstrated in Fig. 11a–c. To prevent an oxygen evolution reaction (OER) at a higher potential during the charging process in an aqueous electrolyte, the GCD test voltage was set in the range of 0–0.4 V. The specific capacitance was calculated from the GCD profile using the following equation:

where Csp, I, ∆t, m, and ∆V denote the current (A), the time of a full discharge (s), the mass of the active material (g), and the potential window (V)59. The specific capacitance of prepared samples at various current densities of 1, 3, 5, 7, and 10 A g−1 is exhibited in Fig. 11d. The specific capacitance values of MgFe2O4, NiFe2O4, and Mg0.5Ni0.5Fe2O4 at the current density of 1 A g−1 were obtained 97, 240, and 647 F g−1, respectively, which declined to 75, 150, and 325 F g−1 at the current density of 10 A g−1 due to reduced accessibility of active sites in high diffusion rate.

GCD plots of (a) MFO nanobelts, (b) NFO nanotubes, and (c) MNFO nanofibers. (d) The specific capacitance at the current density of 1, 3, 5, 7, 10 A g−1.

In both CV and GCD tests, the significantly high specific capacitance value of the MNFO samples is attributed to two main convincing reasons: (i) By adding nickel into the magnesium ferrite, the Ni2+ ions enhanced the electrochemical activities by enriching the redox states, and the whole process prominently improved the electrochemical chemical performance of the material61,62,63. (ii) The unique morphology of porous nanofibers, including high surface area and grain boundaries, played a major role in the electrochemical activities and capacitive energy storage of prepared materials64,65. The electrochemical behavior of nickel or magnesium-based ferrite has also been reported in the literature and some of them are listed in Table 3, indicating that obtained specific capacitance values are higher than those reported earlier by some authors.

Long-term cycling stability as a criterion is also studied (see Fig. 12a). The prepared electrodes of MFO, NFO, and MNFO samples exhibited capacitance retention of about 81, 87, and 91% after 3000 cycles at 10 A g−1, respectively. The Coulombic efficiency is also estimated according to the below equation:

where η, \({t}_{D}\), and \({t}_{C}\) represent the Coulombic efficiency, charge time (s), and discharge time (s), respectively73. The Coulombic efficiency of prepared samples at various current densities of 1, 3, 5, 7, and 10 A g−1 is exhibited in Fig. 12b. The MgFe2O4 nanobelts, NiFe2O4 nanotubes, and Mg0.5Ni0.5Fe2O4 nanofibers demonstrated high Coulombic efficiency of 92, 95, and 97%, respectively, at the current density of 10 A g−1. Herein, the superior Coulombic efficiency of MNFO may be attributed to the appropriate formation of 1D surface area and designed architecture with high surface area, which cause the unique reversibility of the charge–discharge process of the prepared sample46,74.

(a) Cycling stability of samples at the current density of 10 A g−1 after 3000 cycles. (b) Coulombic efficiency at the current densities of 1, 3, 5, 7, and 10 A g−1. (c) EIS plots MFO nanobelts, NFO nanotubes, and MNFO nanofibers, insets show the curves in the high-frequency range and the equivalent circuit.

The electrochemical impedance spectroscopy (EIS) measurements of prepared nanomaterials were carried out in the frequency range of 0.01 Hz to 100 kHz.

The Nyquist plot and the equivalent circuit diagram consist of charge transfer resistance (Rct), solution resistance (sum of electrolyte ionic resistance, electrode-to-current collector contact resistance, and electrode material intrinsic resistance; Rs), Warburg resistance (Zw), and the constant phase element (CPE) are displayed in Fig. 12c. The intercept and semicircle diameter on the real axis in the Nyquist plot denotes the solution resistance and the Faradaic charge transfer resistance, respectively46,61. The RS value of electrodes is very low, allowing the electrolyte to access the electrodes surface efficiently75. The Rct of MFO, NFO, and MNFO was calculated to be 6.64, 4.79, and 3.16 Ω, respectively. The lowest Rct value of nickel-substituted magnesium ferrite revealed that Ni incorporation in magnesium ferrite structure facilitates the charge transfer efficiency at the interface of electrode and electrolyte, affirming the higher specific capacitance of this electrode46,75. Also, steeper slopes of the plot in the low-frequency regions imply that the Mg0.5Ni0.5Fe2O4 sample has lower Warburg resistance (greater ionic conductivity) than other samples. Therefore, nickel incorporation in MgFe2O4 provided better ionic and electronic conductivity in the Mg0.5Ni0.5Fe2O4 sample.

Further exploration is done to study the accurate potential of MNFO sample in real applications, assembling two-electrode cell utilizing MNFO and Active Carbon (AC) as positive and negative electrodes, respectively, in a 3 M KOH electrolyte. At first, the electrochemical properties of AC electrode were investigated by the standard three-electrode system. Figure 13a demonstrates the CV curves of individual AC and MNFO electrodes at a scan rate of 30 mV s−1 and complementary potentials within − 1 to 0 V and 0–0.5 V, respectively. As shown in Fig. 13b, the stable potential windows of MNFO//AC asymmetric supercapacitor (ASC) are capable of being extended to 1.5 V, displaying cyclic voltammograms along with weak redox peaks with no polarization. As the scanning rate increases, the enlargement of the CV curves occurs, manifesting the suitable rate performance of the cell. The specific capacitance of MNFO//AC is 306, 206, 150, 126, 100, and 86 F g−1 at 1, 2, 3, 4, 5, and 7 A g−1 obtained from GCD results (Fig. 13c). The energy density (E) and power density (P) of MNFO//AC were calculated using Eqs. (9) and (10)17, as the Ragone plot is demonstrated in Fig. 13d.

(a) CV curves of AC and MNFO//AC at the scan rate of 30 mV s−1, (b) CV curves of the MNFO//AC cell at various scan rates, (c) GCD curves of the MNFO //AC cell at different current densities, and (d) Ragone plot of the MNFO//AC cell.

Where, Csp (F g−1) is the specific capacitance, ∆V (V) is the working voltage window, and ∆t (s) is the discharge time of the MNFO//AC cell. The results revealed a high energy density of 83 W h Kg−1 and a power density of 700 W Kg−1 at a current density of 1 A g−1.

In this work, an attempt has been made to achieve the superior electrocapacitive performance from the novel and well-designed ternary Mg0.5Ni0.5Fe2O4 spinel ferrite nanofibers compared to pure MgFe2O4 nanobelts and NiFe2O4 nanotubes prepared by electrospinning technique. The XRD, FTIR, FESEM, EDS, DRS, and VSM studies are also done to show the maximum functionality of samples. XRD and FTIR results showed the well-crystallized cubic spinel phase and metal–oxygen bonds of the samples on the octahedral and tetrahedral sites, respectively. The optical band gap of Mg0.5Ni0.5Fe2O4 was narrower than MgFe2O4 nanobelts. The enhancement of saturation magnetization and coercivity of MgFe2O4 nanobelts via Ni2+ ions substation was confirmed using the VSM test. The electrochemical study revealed that although the specific capacitance obtained for the pristine magnesium ferrite nanobelts was small, the incorporation of nickel into its structure caused the formation of a novel ternary ferrite with a significant capacitance. The highest specific capacitance of 647 F g−1 for Mg0.5Ni0.5Fe2O4 with outstanding cycling stability of 91% after 3000 cycles at 10 A g−1 was achieved which is far greater than pristine MgFe2O4 and NiFe2O4. Furthermore, the Mg0.5Ni0.5Fe2O4//Activated carbon asymmetric supercapacitor cell could be cycled reversibly in the high-voltage range of 0 to 1.5 V and divulged intriguing performances with an energy density of 83 W h Kg−1 at a power density of 700 W Kg−1. Mg0.5Ni0.5Fe2O4 electrode with safe and suitable electrochemical performance is promising for practical application in energy storage devices and might play an important role in renewable energy, potentially reducing pollution and decreasing the consumption of hydrocarbon fuels. We hope that this work can open up new possibilities for exploring novel ternary ferrite spinels as electrode materials for application in the energy storage field.

All data generated or analyzed during this study are included in this published article, and the datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.

Malaie, K. & Ganjali, M. R. Spinel nano-ferrites for aqueous supercapacitors; Linking abundant resources and low-cost processes for sustainable energy storage. J. Energy Storage 33, 102097. https://doi.org/10.1016/J.EST.2020.102097 (2021).

Article Google Scholar

Wei, Q. et al. Porous one-dimensional nanomaterials: design, Fabrication and applications in electrochemical energy storage. Adv. Mater. 29, 1602300. https://doi.org/10.1002/adma.201602300 (2017).

Article CAS Google Scholar

Huang, Z. M., Zhang, Y. Z., Kotaki, M. & Ramakrishna, S. A review on polymer nanofibers by electrospinning and their applications in nanocomposites. Compos. Sci. Technol. 63, 2223–2253. https://doi.org/10.1016/S0266-3538(03)00178-7 (2003).

Article CAS Google Scholar

Agú, U. A. et al. Synthesis and characterization of a mixture of CoFe2O4 and MgFe2O4 from layered double hydroxides: Band gap energy and magnetic responses. J. Magn. Magn. Mater. 369, 249–259. https://doi.org/10.1016/j.jmmm.2014.06.046 (2014).

Article ADS CAS Google Scholar

Kumar, A. M., Ragavendran, V., Mayandi, J., Ramachandran, K. & Jayakumar, K. Phase dependent electrochemical characteristics of bismuth ferrite: A bifunctional electrocatalyst for supercapacitors and dye-sensitized solar cells. Coll. Surf. A Physicochem. Eng. Asp. 656, 130529. https://doi.org/10.1016/J.COLSURFA.2022.130529 (2023).

Article CAS Google Scholar

Nilmoung, S. et al. Electrospun carbon/CuFe2O4 composite nanofibers with improved electrochemical energy storage performance. J. Alloys Compd. 688, 1131–1140. https://doi.org/10.1016/j.jallcom.2016.06.251 (2016).

Article CAS Google Scholar

Safari, M., Mazloom, J. & Boustani, K. Hierarchical Fe2O3 hexagonal nanoplatelets anchored on SnO2 nanofibers for high-performance asymmetric supercapacitor device. Sci. Rep. 12, 14919. https://doi.org/10.1038/s41598-022-18840-2 (2022).

Article ADS CAS PubMed PubMed Central Google Scholar

Agyemang, F. O. & Kim, H. Electrospun ZnFe2O4-based nanofiber composites with enhanced supercapacitive properties. Mater. Sci. Eng. B Solid-State Mater. Adv. Technol. 211, 141–148. https://doi.org/10.1016/j.mseb.2016.06.011 (2016).

Article CAS Google Scholar

Gaba, S., Kumar, A. & Rana, P. S. Influence of Ce3+ ion doping on structural and magnetic properties of magnesium nanoferrite. J. Supercond. Nov. Magn. 32, 1465–1474. https://doi.org/10.1007/s10948-018-4846-x (2019).

Article CAS Google Scholar

Satapathy, S. et al. MgFe2O4/(Ba0·85Ca0.15) (Zr0·1Ti0.9)O3 lead free ceramic composite: A study on multiferroic and magnetoelectric coupling properties at room temperature. J. Alloys Compd. 853, 156960. https://doi.org/10.1016/j.jallcom.2020.156960 (2021).

Article CAS Google Scholar

Shobana, M. K., Kim, K. & Kim, J. H. Impact of magnesium substitution in nickel ferrite: Optical and electrochemical studies. Phys. E Low-Dimens. Syst. Nanostruct. 108, 100–104. https://doi.org/10.1016/j.physe.2018.12.013 (2019).

Article ADS CAS Google Scholar

Menelaou, M., Georgoula, K., Simeonidis, K. & Dendrinou-Samara, C. Evaluation of nickel ferrite nanoparticles coated with oleylamine by NMR relaxation measurements and magnetic hyperthermia. Dalt. Trans. 43, 3626–3636. https://doi.org/10.1039/c3dt52860j (2014).

Article CAS Google Scholar

Feng, Y. et al. Preparation and characterization of MgFe2O4 nanocrystallites via PVA sol-gel route. J. Alloys Compd. 699, 521–525. https://doi.org/10.1016/j.jallcom.2016.12.432 (2017).

Article CAS Google Scholar

Naik, M. Z. & Salker, A. V. Tailoring the super-paramagnetic nature of MgFe2O4 nanoparticles by In3+ incorporation, Mater. Sci. Eng. B Solid-State Mater. Adv. Technol. 211, 37–44. https://doi.org/10.1016/j.mseb.2016.05.019 (2016).

Article CAS Google Scholar

Zhou, D. et al. Investigation of electronic and local structural changes during lithium uptake and release of nano-crystalline NiFe2O4 by X-ray absorption spectroscopy. J. Power Sour. 342, 56–63. https://doi.org/10.1016/j.jpowsour.2016.12.038 (2017).

Article ADS CAS Google Scholar

Zhang, X. et al. Binder-free NiFe2O4/C nanofibers as air cathodes for Li-O2 batteries. J. Power Sour. 377, 136–141. https://doi.org/10.1016/j.jpowsour.2017.12.002 (2018).

Article ADS CAS Google Scholar

Sharifi, S., Yazdani, A. & Rahimi, K. Incremental substitution of Ni with Mn in NiFe2O4 to largely enhance its supercapacitance properties. Sci. Rep. 10, 1–15. https://doi.org/10.1038/s41598-020-67802-z (2020).

Article CAS Google Scholar

Ganjali, K. M. M. R. & Norouzi, T. A. P. Hydrothermal growth of magnesium ferrite rose nanoflowers on Nickel foam; application in high-performance asymmetric supercapacitors. J. Mater. Sci. Mater. Electron. 29, 650–657. https://doi.org/10.1007/s10854-017-7958-3 (2017).

Article CAS Google Scholar

Patil, P. D. et al. Effect of annealing temperature on morphologies of metal organic framework derived NiFe2O4 for supercapacitor application. J. Energy Storage 40, 102821. https://doi.org/10.1016/j.est.2021.102821 (2021).

Article Google Scholar

Samuel, E., Aldalbahi, A., El-newehy, M., El-hamshary, H. & Yoon, S. S. Nickel ferrite beehive-like nanosheets for binder-free and high- energy-storage supercapacitor electrodes. J. Alloys Compd. 852, 156929. https://doi.org/10.1016/j.jallcom.2020.156929 (2021).

Article CAS Google Scholar

Wongpratat, U., Tipsawat, P. & Khajonrit, J. Effects of Nickel and Magnesium on electrochemical performances of partial substitution in spinel ferrite. J. Alloys Compd. 831, 154718. https://doi.org/10.1016/j.jallcom.2020.154718 (2020).

Article CAS Google Scholar

Fu, M., Chen, W., Zhu, X. & Liu, Q. One-step preparation of one dimensional nickel ferrites/ graphene composites for supercapacitor electrode with excellent cycling stability. J. Power Sour. 396, 41–48. https://doi.org/10.1016/j.jpowsour.2018.06.019 (2018).

Article ADS CAS Google Scholar

Ain, N. et al. Electrical, magnetic and photoelectrochemical activity of rGO / MgFe2O4 nanocomposites under visible light irradiation. Ceram. Int. 42, 12401–12408. https://doi.org/10.1016/j.ceramint.2016.04.179 (2016).

Article CAS Google Scholar

Askari, M. B. & Salarizadeh, P. Binary nickel ferrite oxide (NiFe2O4) nanoparticles coated on reduced graphene oxide as stable and high-performance asymmetric supercapacitor electrode material. Int. J. Hydrog. Energy 45, 27482–27491. https://doi.org/10.1016/j.ijhydene.2020.07.063 (2020).

Article CAS Google Scholar

Sivakumar, M. et al. Facile synthesis of NiFe2O4 nanoparticle with carbon nanotube composite electrodes for high-performance asymmetric supercapacitor. Colloids Surfaces A Physicochem. Eng. Asp. 648, 129188. https://doi.org/10.1016/J.COLSURFA.2022.129188 (2022).

Article CAS Google Scholar

Bhujun, B., Tan, M. T. T. & Shanmugam, A. S. Study of mixed ternary transition metal ferrites as potential electrodes for supercapacitor applications. Results Phys. 7, 345–353. https://doi.org/10.1016/j.rinp.2016.04.010 (2017).

Article ADS Google Scholar

Chu, D. et al. A novel dual-tasking hollow cube NiFe2O4-NiCo-LDH@rGO hierarchical material for high preformance supercapacitor and glucose sensor. J. Colloid Interface Sci. 568, 130–138. https://doi.org/10.1016/j.jcis.2020.02.012 (2020).

Article ADS CAS PubMed Google Scholar

Zhang, X. et al. A facile one-step hydrothermal approach to synthesize hierarchical core-shell NiFe2O4@NiFe2O4 nanosheet arrays on Ni foam with large specific capacitance for supercapacitors. RSC Adv. 8, 15222–15228. https://doi.org/10.1039/c8ra02559b (2018).

Article ADS CAS PubMed PubMed Central Google Scholar

Bazhan, Z., Ghodsi, F. E. & Mazloom, J. Modified voltammetric, impedimetric and optical behavior of polymer- assisted sol-gel MgFe2O4 nanostructured thin films. Electrochim. Acta. 250, 143–151. https://doi.org/10.1016/j.electacta.2017.08.026 (2017).

Article CAS Google Scholar

Liang, J. et al. Recent advances in electrospun nanofibers for supercapacitors. J. Mater. Chem. A. 8, 16747–16789. https://doi.org/10.1039/d0ta05100d (2020).

Article CAS Google Scholar

Zhou, H. et al. Microwave-enhanced catalytic degradation of p-nitrophenol in soil using MgFe2O4. Chem. Eng. J. 284, 54–60. https://doi.org/10.1016/j.cej.2015.08.103 (2016).

Article CAS Google Scholar

Ikram, M. et al. Synthesis of Al/starch co-doped in CaO nanoparticles for enhanced catalytic and antimicrobial activities: experimental and DFT approaches. RSC Adv. 12, 32142–32155. https://doi.org/10.1039/d2ra06340a (2022).

Article ADS CAS PubMed PubMed Central Google Scholar

Zak, A. K., Majid, W. A., Abrishami, M. E. & Yousefi, R. X-ray analysis of ZnO nanoparticles by Williamson-Hall and size–strain plot methods. Solid State Sci. 13(1), 251–256 (2011).

Article ADS Google Scholar

Bharadwaj, P. S. J., Prasad, K., Sai, V. & Dandamudi, B. Study of magneto-supercapacitance properties of nickel cobalt ferrite-activated carbon composite. J. Energy Storage 36, 102444. https://doi.org/10.1016/j.est.2021.102444 (2021).

Article Google Scholar

Udhaya, P. A., Meena, M. & Queen, M. A. J. Green synthesis of MgFe2O4 nanoparticles using albumen as fuel and their physicochemical properties. Int. J. Sci. Res. Phys. Appl. Sci 7, 71–74. https://doi.org/10.26438/ijsrpas/v7i2.7174 (2019).

Article Google Scholar

Zhao, X. & Liu, X. A novel magnetic NiFe2O4@graphene–Pd multifunctional nanocomposite for practical catalytic application. RSC Adv. 5, 79548–79555. https://doi.org/10.1039/C5RA12720C (2015).

Article ADS CAS Google Scholar

Maensiri, S., Sangmanee, M. & Wiengmoon, A. Magnesium ferrite (MgFe2O4) nanostructures fabricated by electrospinning. Nanoscale Res. Lett. https://doi.org/10.1007/s11671-008-9229-y (2009).

Article PubMed PubMed Central Google Scholar

Shahzadi, I. et al. Formation of biocompatible MgO/cellulose grafted hydrogel for efficient bactericidal and controlled release of doxorubicin. Int. J. Biol. Macromol. 220, 1277–1286. https://doi.org/10.1016/j.ijbiomac.2022.08.142 (2022).

Article CAS PubMed Google Scholar

Reddy, M. P., Shakoor, R. A., Mohamed, A. M. A., Gupta, M. & Huang, Q. Effect of sintering temperature on the structural and magnetic properties of MgFe2O4 ceramics prepared by spark plasma sintering. Ceram. Int. 42, 4221–4227. https://doi.org/10.1016/j.ceramint.2015.11.097 (2015).

Article CAS Google Scholar

He, Z. et al. Tailored electrospinning of WO3 nanobelts as efficient ultraviolet photodetectors with photo-dark current ratios up to 1000. ACS Appl. Mater. Interfaces 7(20), 10878–10885. https://doi.org/10.1021/acsami.5b02020 (2015).

Article CAS PubMed Google Scholar

Wei, S., Zhou, M. & Du, W. Improved acetone sensing properties of ZnO hollow nanofibers by single capillary electrospinning. Sens. Actuators B. Chem. 160, 753–759. https://doi.org/10.1016/j.snb.2011.08.059 (2011).

Article CAS Google Scholar

Peng, S. & Li, L. Electrospun CuFe2O4 nanotubes as anodes for high-performance lithium-ion batteries. J. Energy Chem. 23, 301–307. https://doi.org/10.1016/S2095-4956(14)60151-0 (2014).

Article CAS Google Scholar

Sharma, R., Thakur, P., Sharma, P. & Sharma, V. Ferrimagnetic Ni2+ doped Mg-Zn spinel ferrite nanoparticles for high density information storage. J. Alloys Compd. 704, 7–17. https://doi.org/10.1016/j.jallcom.2017.02.021 (2017).

Article CAS Google Scholar

Ikram, M. et al. Assessment of catalytic, antimicrobial and molecular docking analysis of starch-grafted polyacrylic acid doped BaO nanostructures. Int. J. Biol. Macromol. 230, 123190. https://doi.org/10.1016/j.ijbiomac.2023.123190 (2023).

Article CAS PubMed Google Scholar

Sing, K. S. W. Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity. Pure Appl. Chem. 57, 603–619. https://doi.org/10.1351/pac198557040603 (1985).

Article CAS Google Scholar

Safari, M. & Mazloom, J. Outstanding energy storage performance in Co–Fe bimetallic metal-organic framework spindles via decorating with reduced graphene oxide nanosheets. Journal of Energy Storage 58, 106390. https://doi.org/10.1016/j.est.2022.106390 (2023).

Article Google Scholar

Tauc, J., Optical properties of non-crystalline solids, optical properties of solids. 277–313 (1972).

Chavan, P. & Naik, L. R. Investigation of energy band gap and conduction mechanism of magnesium substituted nickel ferrite nanoparticles. Phys. Status Solidi Appl. Mater. Sci. 214, 1700077. https://doi.org/10.1002/pssa.201700077 (2017).

Article ADS CAS Google Scholar

Aslibeiki, B., Varvaro, G., Peddis, D. & Kameli, P. Particle size, spin wave and surface effects on magnetic properties of MgFe2O nanoparticles. J. Magn. Magn. Mater. 422, 7–12. https://doi.org/10.1016/j.jmmm.2016.08.057 (2017).

Article ADS CAS Google Scholar

Wang, Z. et al. Preparation of ferrite MFe2O4 (M = Co, Ni) ribbons with nanoporous structure and their magnetic properties. J. Phys. Chem. B. 112, 11292–11297. https://doi.org/10.1021/jp804178w (2008).

Article CAS PubMed Google Scholar

Ali, R. et al. Impacts of Ni–Co substitution on the structural, magnetic and dielectric properties of magnesium nano-ferrites fabricated by micro-emulsion method. J. Alloys Compd. 584, 363–368. https://doi.org/10.1016/j.jallcom.2013.08.114 (2014).

Article CAS Google Scholar

Safartoobi, A., Mazloom, J. & Ghodsi, F. E. Electrochemical and optical properties of magnetic CuFe2O4 nanofibers grown by PVP and PVA-assisted sol–gel electrospinning. Appl. Phys. A. 128, 1–15. https://doi.org/10.1007/s00339-021-05162-9 (2022).

Article CAS Google Scholar

Sivakumar, N., Narayanasamy, A., Greneche, J., Murugaraj, R. & Lee, Y. S. Electrical and magnetic behaviour of nanostructured MgFe2O4 spinel ferrite. J. Alloys Compd. 504, 395–402. https://doi.org/10.1016/j.jallcom.2010.05.125 (2010).

Article CAS Google Scholar

Manohar, A., Vijayakanth, V., Pallavolu, M. R. & Kim, K. H. Effects of Ni - substitution on structural, magnetic hyperthermia, photocatalytic and cytotoxicity study of MgFe2O4 nanoparticles. J. Alloys Compd. 879, 160515. https://doi.org/10.1016/j.jallcom.2021.160515 (2021).

Article CAS Google Scholar

Lynda, I. J. C., Dinesh, M. D. A., Jaganathan, A. M. S. K., Baykal, A. & Antony, S. A. Enhanced magneto-optical and photocatalytic properties of ferromagnetic Mg1−y NiyFe2O4 (0.0 ≤ y ≤ 1.0) spinel nano-ferrites. J. Superconduct. Novel Magn. 4, 3637–3647 (2018).

Article Google Scholar

Farooq, N. et al. Au@GO@g-C3N4 and Fe2O3 nanocomposite for efficient photocatalytic and electrochemical applications. Surf. Interfaces. 26, 101399. https://doi.org/10.1016/j.surfin.2021.101399 (2021).

Article CAS Google Scholar

Safari, M. & Mazloom, J. Electrochemical performance of spindle-like Fe2Co-MOF and derived magnetic yolk-shell CoFe2O4 microspheres for supercapacitor applications. J. Solid State Electrochem. 25, 2189–2200. https://doi.org/10.1007/s10008-021-04989-9 (2021).

Article CAS Google Scholar

Rajapriya, A., Keerthana, S. & Ponpandian, N. Chalcogenides based nano composites for supercapacitors. In Nanostructured Materials for Supercapacitors (eds Thomas, S. et al.) (Springer, 2022).

Google Scholar

Choubari, M. S., Mazloom, J. & Ghodsi, F. E. Supercapacitive properties, optical band gap, and photoluminescence of CeO2–ZnO nanocomposites prepared by eco-friendly green and citrate sol-gel methods : A comparative study. Ceram. Int. 48, 21344–21354. https://doi.org/10.1016/j.ceramint.2022.04.100 (2022).

Article CAS Google Scholar

Xie, L., Wu, J., Chen, C., Zhang, C. & Wan, L. A novel asymmetric supercapacitor with an activated carbon cathode and a reduced graphene oxide e cobalt oxide nanocomposite anode. J. Power Sources. 242, 148–156. https://doi.org/10.1016/j.jpowsour.2013.05.081 (2013).

Article ADS CAS Google Scholar

Nabi, G. et al. Role of cerium-doping in CoFe2O4 electrodes for high performance supercapacitors. J. Energy Storage 29, 101452. https://doi.org/10.1016/j.est.2020.101452 (2020).

Article Google Scholar

Shannon, R. D. Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides. Acta Crystallogr. Sect. A. 32, 751–767. https://doi.org/10.1107/S0567739476001551 (1976).

Article ADS Google Scholar

El-Fadl, A. A., Hassan, A. M. & Kassem, M. A. Structural and spectroscopic studies of nanocrystalline Ni1-xMgxFe2O4 ferrites synthesized by a microwave-assisted combustion route. Phys. Scr. 95, 055813. https://doi.org/10.1088/1402-4896/ab7a39 (2020).

Article ADS CAS Google Scholar

Khairy, M., El-shaarawy, M. G. & Mousa, M. A. Characterization and super-capacitive properties of nanocrystalline copper ferrite prepared via green and chemical methods. Mater. Sci. Eng. B. 263, 114812. https://doi.org/10.1016/j.mseb.2020.114812 (2021).

Article CAS Google Scholar

Zhang, H. et al. Flexible supercapacitors with high areal capacitance based on hierarchical carbon tubular nanostructures. J. Power Sour. 331, 332–339. https://doi.org/10.1016/j.jpowsour.2016.09.064 (2016).

Article ADS CAS Google Scholar

Ghasemi, A., Kheirmand, M. & Heli, H. Synthesis of novel NiFe2O4 nanospheres for high performance pseudocapacitor applications. Russ. J. Electrochem. 55, 206–214. https://doi.org/10.1134/S1023193519020022 (2019).

Article CAS Google Scholar

Fu, M. et al. Multifunctional pompon flower-like nickel ferrites as novel pseudocapacitive electrode materials and advanced absorbing materials. Ceram. Int. 46, 850–856. https://doi.org/10.1016/j.ceramint.2019.09.042 (2019).

Article CAS Google Scholar

Aparna, M. L., Grace, A. N., Sathyanarayanan, P. & Sahu, N. K. A comparative study on the supercapacitive behaviour of solvothermally prepared metal ferrite (MFe2O4, M = Fe Co, Ni, Mn, Cu, Zn) nanoassemblies. J. Alloys Compd. 745, 385–395. https://doi.org/10.1016/j.jallcom.2018.02.127 (2018).

Article CAS Google Scholar

Lin, Y., Wang, J., Yang, H., Wang, L. & Cao, M. Increased capacitance of porous Co0.5Ni0.5Fe2O4 for supercapacitor application. Mater. Sci. Eng. B. 228, 103–108. https://doi.org/10.1016/j.mseb.2017.11.013 (2018).

Article CAS Google Scholar

Uke, S. J., Mardikar, S. P., Bambole, D. R., Kumar, Y. & Chaudhari, G. N. Sol-gel citrate synthesized Zn doped MgFe2O4 nanocrystals : A promising supercapacitor electrode material. Mater. Sci. Energy Technol. 3, 446–455. https://doi.org/10.1016/j.mset.2020.02.009 (2020).

Article CAS Google Scholar

Heiba, Z. K., Deyab, M. A., El-naggar, A. M. & Mohamed, M. B. Electrochemical performance of quaternary (1–x)ZnMn2O4/(x)MgFe2O4 solid solution as supercapacitor electrode. Ceram. Int. 47, 7475–7486. https://doi.org/10.1016/j.ceramint.2020.11.088 (2021).

Article CAS Google Scholar

Wang, Q., Gao, H., Qin, X., Dai, J. & Li, W. Fabrication of NiFe2O4@CoFe2O4 core-shell nanofibers for high-performance supercapacitors. Mater. Res. Express. 7, 015020. https://doi.org/10.1088/2053-1591/ab61ba (2019).

Article ADS CAS Google Scholar

Bandgar, S. B. et al. Metal precursor dependent synthesis of NiFe2O4 thin films for high-performance flexible symmetric supercapacitor. ACS Appl. Energy Mater. https://doi.org/10.1021/acsaem.7b00163 (2018).

Article Google Scholar

Liu, W. et al. 3D hierarchical porous N-doped carbon nanosheets/MgFe2O4 composite as anode material with excellent cycling stability and rate performance. Scr. Mater. 189, 36–41. https://doi.org/10.1016/j.scriptamat.2020.07.060 (2020).

Article CAS Google Scholar

Sagadevan, S. et al. Reduced graphene/nanostructured cobalt oxide nanocomposite for enhanced electrochemical performance of supercapacitor applications. J. Colloid Interface Sci. 558, 68–77. https://doi.org/10.1016/j.jcis.2019.09.081 (2020).

Article ADS CAS PubMed Google Scholar

Download references

The authors would like to appreciate the University of Guilan Research Council for supporting this work.

Department of Physics, Faculty of Science, University of Guilan, Namjoo Avenue, P.O. Box 4193833697, Rasht, Iran

Matin Shirzad Choubari, Soghra Rahmani & Jamal Mazloom

You can also search for this author in PubMed Google Scholar

You can also search for this author in PubMed Google Scholar

You can also search for this author in PubMed Google Scholar

M.S.C.: Writing original draft, Data curation, Software, Visualization, Investigation, Formal analysis, Methodology. S.R.: Investigation, Formal analysis, Methodology. J.M.: Conceptualization, Methodology, Writing-review & editing, Validation, Supervision.

Correspondence to Jamal Mazloom.

The authors declare no competing interests.

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

Shirzad Choubari, M., Rahmani, S. & Mazloom, J. Boosted electrochemical performance of magnetic caterpillar-like Mg0.5Ni0.5Fe2O4 nanospinels as a novel pseudocapacitive electrode material. Sci Rep 13, 7822 (2023). https://doi.org/10.1038/s41598-023-35014-w

Download citation

Received: 16 February 2023

Accepted: 11 May 2023

Published: 15 May 2023

DOI: https://doi.org/10.1038/s41598-023-35014-w

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.