Nanosheet-like MoO3 and conductive PANI electrodeposited on flexible carbon cloth for self-supported solid-state supercapacitor electrode

In this paper, uniformly transition metal oxide (MoO₃) nanosheets were electrochemically deposited on flexible carbon cloth (CC), and then conductive polyaniline (PANI) was orderly wrapped around their surface by electrochemical polymerization. The morphology and structure of as-obtained self-supported PANI/MoO₃/CC electrode were investigated by FTIR, X-ray diffraction, Raman, scanning electron microscope (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy measurements in detail. Among all PANI/MoO₃/CC electrode, the self-supported PMC-3 (deposition time of 300 s) has high specific capacitance of 841.6 F g⁻¹ at current density of 0.5 A g⁻¹ in the three-electrode system, having specific capacitance of 595.7 F g⁻¹ even at 10 A g⁻¹. Novelty, the as-assembled symmetrical capacitor is flexible and convenient with power density of 199.93 W kg⁻¹ at the energy density of 9.69 Wh kg⁻¹ and the energy density of 3.88 Wh kg⁻¹ at power density of 4000 W kg⁻¹. Thus, the electrochemical properties of the self-supported PANI/MoO₃/CC electrode were significantly improved, and the self-supported electrodes are more competitive than other materials in practical application of clean energy storage systems.     

Anode electrodeposition of 3D mesoporous Fe2O3 nanosheets on carbon fabric for flexible solid-state asymmetric supercapacitor

Novel nanostructured Fe₂O₃ with a network of 3D mesoporous nanosheets was synthesized by depositing on carbon fabric (Fe₂O₃@CF) for use as an anode using a potentially low-cost electrodeposition technique. The electrode with freestanding binder-free Fe₂O₃@CF of high surface area displayed an exceptional specific capacitance of 394.2?F?g^?1. Moreover, a flexible solid-state asymmetric supercapacitor (ASC) was fabricated with a negative electrode based on Fe₂O₃@CF and a positive electrode based on MnO₂@CF in the presence of PVA-LiCl as gel electrolyte. The above ASC exhibited a high operating potential up to 1.8?V, a favorable specific capacitance of 93.5?F?g^?1 (2.92?F?cm^?3), long-term stability (91.3% retention of initial value over 5000 cycles), and remarkable mechanical stability and flexibility, suggesting its potential application for wearable electronics.     

Synthesis of cross-linked graphene aerogel/Fe2O3 nanocomposite with enhanced supercapacitive performance

In this work, cross-linked graphene aerogel (CL-GA) and its composite with Fe₂O₃ nanoparticles (NPs) were synthesized through a one-step hydrothermal procedure by using p-phenylenediamine (PPD). Structural characterizations revealed that in the preparation of the composite PPD acts as a cross-liker and provides high surface area by decreasing restacking of graphene sheets and functions as nitrogen source simultaneously. The electrochemical characteristics of the nanocomposite were investigated by cyclic voltammetry (CV), galvanostatic charge/discharge, electrochemical impedance spectroscopy (EIS) and Fast Fourier transform continues cyclic voltammetry (FFTCCV). The results show that cross-linked graphene aerogel/Fe₂O₃ (CL-GA/Fe₂O₃) nanocomposite displays enhanced supercapacitive performance, where it has capacitance of 445 at 1 A g⁻¹, high energy density of 63 W h Kg⁻¹, and 89% capacitance retention after 5000 cycles in 3 M KOH. Presence of PPD considerably improved supercapacitive performance of nanocomposite as a result it could be promising material in synthesis of efficient graphene/metal oxide-based electrode material for high performance supercapacitors.     

Hydrothermal synthesis and characterization studies of α-Fe2O3/MnO2 nanocomposites for energy storage supercapacitor application

In this present study, semiconductor magnetic α-Fe₂O₃/MnO₂ nanocomposites (NCs) were prepared by a facile hydrothermal (HT) method. The crystallographic structure, morphology, chemical configuration and magnetic features were analysed by X-ray powder diffraction (XRD), high resolution scanning electron microscope (HR-SEM), energy dispersive X-ray analysis (EDX), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and vibrating sample magnetometer (VSM) analyses. The as-prepared NCs were used as an electrode in energy storing supercapacitor was systematically examined. The electrochemical deeds of α-Fe₂O₃/MnO₂ NCs was analysed by cyclic voltammetry (C–V) and galvanostatic charge–discharge (GCD) tests. The CV analysis of the NCs electrode showed a distinctive pseudocapacitive behaviour in 1 M KOH solution. The NCs electrode reveals enhanced specific capacitance compared to plain α-Fe₂O₃ and MnO₂ nanoparticles (NPs) and generates high specific capacitance of 216.35 Fg⁻¹. Pseudocapacitor obtains of energy density 135.42 Wh kg⁻¹ at power density of 6.399 kW kg⁻¹, indicating the as-prepared α-Fe₂O₃/MnO₂ NCs shows noteworthy high-energy, specific capacitance, power densities and long-standing cyclic stability with 89.2% of preliminary capacitance reserved at 1A g⁻¹ after 10000 cycles in judgement with the pure α-Fe₂O₃ and MnO₂ NPs electrode. The α-Fe₂O₃/MnO₂ NCs electrode having noteworthy electrochemical characteristics performance renders promising applications in energy storing systems.     

Promising electrode material of Fe3O4 nanoparticles decorated on V2O5 nanobelts for high-performance symmetric supercapacitors

Bundled V₂O₅ nanobelts decorated with Fe₃O₄ nanoparticles (F3V nanostructures) were successfully synthesized to develop a low-cost electrode material for energy storage applications. The synthesized samples were subjected to structural, morphological and electrochemical studies. The Fe₃O₄ nanoparticles decorated over bundled V₂O₅ nanobelts exhibited better electrochemical properties than the pristine Fe₃O₄ nanoparticles and V₂O₅ nanobelts. The electrochemical behavior of the fabricated electrodes was investigated in an electrolyte of 3 M KOH, demonstrated an exceptional specific capacity values of 750.1, 660.3, and 1519 F g^–1 for V₂O₅, Fe₃O₄, and F3V respectively at a current density of 15 A g^–1. The assembled F3V symmetric supercapacitor (SSC) device exhibited an excellent specific capacitance of 93 F g^–1 at a current density of 0.5 A g^–1, delivering energy and power densities of 13 Wh.kg^–1 and 1530 W kg^–1, respectively, and superior long-term cycling stability of ～84% capacity retention over 5000 galvanostatic charge–discharge cycles. These findings demonstrate the extraordinary electrochemical characteristics of the F3V nanostructures, indicating their potential use in energy storage applications.     

High‐Energy Pollen‐Like Porous Fe2O3/Al Thermite: Synthesis and Properties

A pollen‐like porous Fe₂O₃/Al thermite was prepared by a templated method, with aluminium nanoparticles (Al‐NPs) embedded in the porous channels. The thermite prepared by reduced pressure released the largest exothermic heat during DSC testing period compared with Fe₂O₃/Al thermites prepared by ultrasonic mixing and physical mixing. The exothermic heats in the range of 773 K to 1273 K are 3742.3 J g⁻¹, 2279.0 J g⁻¹, 1981.1 J g⁻¹, and 2621.0 J g⁻¹ for pollen‐like Fe₂O₃/Al by reduced pressure, pollen‐like Fe₂O₃/Al by ultrasonic mixing, pollen‐like Fe₂O₃/Al by physical mixing, and commercial Fe₂O₃/Al by ultrasonic mixing, respectively. The reactivity between Fe₂O₃ and Al‐NPs was efficiently improved, corresponding to its enlarged contact surface area between Al‐NPs and the porous pollen‐like Fe₂O₃, and the reduced pre‐combustion sintering. Furthermore, pollen‐like Fe₂O₃/Al has good compatibility with both RDX and HMX and it is not compatible with Cl‐20 and GAP.     

Anchoring mesoporous Fe3O4 nanospheres onto N-doped carbon nanotubes toward high-performance composite electrodes for supercapacitors

Fe-based oxide electrodes for practical applications in supercapacitors (SCs) suffer from low conductivity and poor structural stability. To settle these issues, we report on the design and synthesis of Fe₃O₄/carbon nanocomposites via firmly anchoring mesoporous Fe₃O₄ nanospheres onto N-doped carbon nanotubes (N-CNTs) via C–O–Fe bonds. Mesoporous Fe₃O₄ nanospheres are featured by rich electroactive sites and short ion diffusion pathways. The N-CNTs, on the other hand, serve as the scaffolds, which not only provide conductive networks but also suppress the accumulation between mesoporous Fe₃O₄ nanospheres as well as alleviate volume changes during charge/discharge cycles. Accordingly, the constructed Fe₃O₄/N-CNTs nanocomposite electrode demonstrates improved specific capacity values of up to 314 C g⁻¹ at 1 A g⁻¹, with 92% retention of the initial capacity after 5000 cycles at 10 A g⁻¹. In addition, the assembled Fe₃O₄/N-CNTs//active carbon (AC) asymmetric supercapacitor (ASC) device possesses an energy density of 25.3 Wh kg⁻¹, suggesting that the prepared Fe₃O₄/N-CNTs nanocomposites are promising electrode materials for use in SCs.     

ZIF-derived wrinkled Co3O4 polyhedra supported on 3D macroporous carbon sponge for supercapacitor electrode

Co₃O₄/melamine-derived carbon sponge (MCS) nanocomposite in which wrinkled ball-in-dodecahedral Co₃O₄ nanoparticles derived from ZIF-67 were homogeneously dispersed on the interconnected MSC was fabricated via a simple immersion and thermolysis route. As-prepared ultralight Co₃O₄/MCS possessed mechanically robust characteristic and unique 3D macroporous framework anchored with corrugated Co₃O₄ dodecahedra. Utilized as a pseudocapacitor electrode, Co₃O₄/MCS hybrid exhibited a great specific capacitance of 1409.5 F g⁻¹ at the current density of 0.5 A g⁻¹ and excellent long-term cycling stability of 93.2% after 1000 charge/discharge cycles, which might be ascribed to the synergistic effect of the inherent high redox activity from Co₃O₄ polyhedra combined with excellent electrical conductivity of MCS. This work demonstrates that tunable structure design and rational morphology control are efficient approaches for manufacturing novel electrode materials with extraordinary electrochemical performance.     

Polyaniline grafted chitosan/GO-CNT/Fe3O4 nanocomposite as a superior electrode material for supercapacitor application

Developing appropriate stable electroactive electrode materials for supercapacitor application is the challenging issue, which attracts enormous attention in recent decades. In this regard, Fe₃O₄ nanoparticles are firstly synthesized on chitosan/graphene oxide-multiwall carbon nanotubes (CS/GM/Fe₃O₄). Then, polyaniline (PANI) is grafted on it via in situ chemical polymerization and named as CS/GM/Fe₃O₄/PANI. The as-prepared nanocomposites are characterized by Field emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and energy dispersive X-ray spectroscopy. The capacitive properties of the electrodes are investigated in a three electrode configuration in 0.5 M Na₂SO₄ electrolyte by various electrochemical techniques. The specific capacitance of CS/GM/Fe₃O₄/PANI electrode is 1513.4 Fg⁻¹ at 4 Ag⁻¹ which is 1.9 times higher than that of CS/GM/Fe₃O₄ (800 Fg⁻¹). Meanwhile, the electrodes exhibit appropriate cycle life along with 99.8% and 93.95% specific capacitance at 100 Ag⁻¹ for chitosan/GO-CNT/Fe₃O₄ and polyaniline grafted chitosan/GO-CNT/Fe₃O₄, respectively.     

MWCNTs-GONRs/Co3O4 electrode with needle-like arrays for outstanding supercapacitors

Multiwalled carbon nanotubes-graphene oxide nanoribbons (MWCNTs-GONRs) exhibit high specific surface area and good electroconductivity because of their unique three-dimensional cross-linking structure with the properties of both CNTs and GONRs. In this study, a hydrothermal method was employed to anchor MWCNTs–GONRs onto a Ni foam (NF) to obtain a precursor substrate. Subsequently, Co₃O₄ arrays were grown on the NF substrate to synthesize a MWCNTs–GONR/Co₃O₄ electrode. The electrode showed a capacitance of 846.2 F g⁻¹ at 1 A g⁻¹ and a capacitance retention of 90.1% after 3000 cycles. Furthermore, MWCNTs–GONRs/Co₃O₄ and active carbon (AC) were used as the positive and negative electrodes, respectively, to assemble a supercapacitor, which delivered a maximum energy density of 38.23 W h kg⁻¹ and a high power density of 6.80 kW kg⁻¹. In addition, the specific capacitance of the device reached a maximum of 91.5% after 9000 cycles. Thus, the MWCNTs–GONRs/Co₃O₄ electrode showed huge potential for supercapacitor applications.     

Tunable oxygen vacancies in MoO3 lattice with improved electrochemical performance for Li-ion battery thin film cathode

MoO₃ is a kind of promising cathode material for lithium-ion batteries (LIBs), owing to its high specific capacity (279 mA h g⁻¹) and layered structure. However, low electrical conductivity and sluggish reaction kinetics results in poor rate and Li-ions storage capability. The introduction of oxygen vacancies (OVs) can promote Li⁺ diffusion, and produce great electrical conductivity. Here, we report a strategy to synergize the merits of OVs by pulsed laser deposition (PLD) by adjusting oxygen partial pressures (2～20 Pa). The appropriate OVs concentration not only significantly approves electrochemical performance but also increases pseudocapacitance contribution. The Li-ion diffusion coefficient of MoO_3−x is remarkably improved by one or two orders of magnitude compared with that of MoO₃. Therefore, this facile and efficient strategy on OVs could afford a reference for other metal oxides for high-performance electrode materials.     

Electrophoretic co-deposition of Bi2O3–multiwalled carbon nanotubes coating as supercapacitor electrode

Nafion is suggested as an efficient assistant in preparing supercapacitor by employing nanoparticles. In this work, using a bi-additive of 0.10-mM NaOH + 0.10 g L⁻¹ Nafion, Nafion-assisted electrophoretic co-deposition of Bi₂O₃–multiwalled carbon nanotubes (MWCNTs) coating is successfully realized in ethanol solvent. The capacitance performances of the electrophoretic coatings in 6.0-M KOH electrolyte are investigated by cyclic voltammetry and galvanostatic charge–discharge techniques. Comparing with Bi₂O₃ coating prepared with electrophoretic deposition (EPD) by employing other additive (such as polyethyleneimine), the Bi₂O₃ coating prepared by Nafion-assisted EPD shows a better capacitance performance. Benefiting from the improvement in coating conductivity caused by MWCNTs, with a small additional amount of 4.0 wt.%, the Bi₂O₃–MWCNTs coating exhibits an amazing 164% increase of mass-specific capacitance (473 F g⁻¹ at the current density of 1.0 A g⁻¹) in comparison with pure Bi₂O₃ coating (179 F g⁻¹ at the current density of 1.0 A g⁻¹). The cyclic stability test exhibits excellent capacitance retention of 88.7% over 3000 cycles at a constant current density of 10.0 A g⁻¹. This work combines the advantages of MWCNTs, Nafion, and EPD to provide a facile route for preparing Bi₂O₃-based coating as a high-performance supercapacitor electrode.     

Enhancing the performance and stability of NiCo2O4 nanoneedle coated on Ni foam electrodes with Ni seed layer for supercapacitor applications

We introduce a facile way to improve the performance of NiCo₂O₄ electrode by including a Ni seed layer. The seed layer deposited on Ni foam electrode (NiCo₂O₄/Ni@NF) shows the superior specific capacity of 1142 C g⁻¹ at 1 A g⁻¹ with the excellent cycle stability of ∼96% even after 5000 cycles at a higher current density of 5 A g⁻¹. These values are about 3.7 times higher than that of the electrode (NiCo₂O₄@NF) without a seed layer, which shows the specific capacity of 305 C g⁻¹@1 A g⁻¹ with cycle stability of 84% even at a lower current density of 1 A g⁻¹. The enhanced performance of the NiCo₂O₄/Ni@NF electrode may be attributed to lower interface resistance, fast redox reversible reaction, and improved surface active sites. Further, the asymmetric solid-state supercapacitor device is fabricated by using the NiCo₂O₄/Ni@NF electrode as a positive and reduced graphene oxide (rGO)-Fe₂O₃ nanograin as a negative electrode with PVA-KOH gel electrolyte, and the NiCo₂O₄/Ni20@NF//rGO-Fe₂O₃@NF asymmetric solid state device delivers an areal capacitance of 446 mF cm⁻² with a low capacitance loss of 18% even after 10000 cycles. Further, the fabricated asymmetric solid state device shows a maximum energy density of 124.3 Wh cm⁻² (at 3.58 kW cm⁻²) and power density of 14.88 kW cm⁻² (at 31.41 Wh cm⁻²).     

Facile synthesis of pseudocapacitive Mn3O4 nanoparticles for high-performance supercapacitor

In this work, a facile method to produce the ultrafine (4–14 nm) and mixed valence Mn₃O₄ nanoparticles from low-cost MnSiO₃ (manganese silicate) particles were introduced. The best NaOH concentration in hydrothermal treatment has been determined after a series of experiments. Also, the as-synthesized Mn₃O₄ material with good specific capacitance has been investigated attentively at a high mass loading (∼3 mg cm⁻²). The particles size and the pore size distribution is found to be refined and optimized, respectively. This increased the crystallinity and the capacitive contribution in the energy process. Thereby improving the rate capability and cycling stability, which result in significant improvement of specific capacitance (401 F g⁻¹ at 10 mV s⁻¹). The aqueous asymmetric supercapacitor device AC//Mn₃O₄ with a stable working voltage window up to 2.0 V has been fabricated, and it is found to have an energy density of 40.2 W h kg⁻¹ at 500 W kg⁻¹ power density. This could sustain 5000 cycles galvanostatic charge/discharge with 96.9% retention.     

Preparation,sintering and electrochemical performance of novel Fe2N-TiN nanocomposites

Transition metal nitrides (TMNs) hold great promises as electrode materials in energy devices like supercapacitors, lithium ion batteries and solar cells. However, the poor electrochemical stability severely limits their real-life applications. In this study, we prepared electrochemically stable Fe₂N-TiN nanocomposite with varied TiN contents by the nitridation of oxide precursors by ammonia. The formation mechanism consists of the solid reaction between TiO₂ and Fe₂O₃. A protective sintering (PS) technique has been developed for the first time to fabricate pure Fe₂N-TiN nanocomposite ceramics after comparing different sintering methods including spark plasma sintering (SPS). Porous microstructures formed by homogenous distribution of ultrafine TiN nanoparticles within large Fe₂N micro-grains skeleton were obtained after sintering. The electrochemical performances of the Fe₂N-TiN nanocomposites by PS have been investigated in different electrolytes. The mechanism of charge storage is mainly due to the double layer capacitance. The composites with 15 wt% TiN loading show the highest specific capacitance of 58.4 F g⁻¹ in 7.5 M KOH. Furthermore, excellent cycling stability with zero degradation after 1000 cycles was proved for such nanocomposite electrodes, confirming their potential for energy storage.     

3D network-like porous MnCo2O4 by the sucrose-assisted combustion method for high-performance supercapacitors

3D network-like porous MnCo₂O₄ nanostructures have been successfully fabricated through a facile and scalable sucrose-assisted combustion route followed by calcination treatment. Benefiting from its advantages of the unique 3D network-like architectures with large specific surface area (216.15 m² g⁻¹), abundant mesoporosity (2–50 nm) and high electronic conductivity, the as-prepared MnCo₂O₄ electrode displays a high specific capacitance of 647.42 F g⁻¹ at a current density of 1 A g⁻¹, remarkable capacitance retention rate of 70.67% at current density of 10 A g⁻¹ compared with 1 A g⁻¹, and excellent cycle stability (only 6.32% loss after 3000 cycles). The excellent electrochemical performances coupled with facile and cost effective method will render the as-fabricated 3D network-like porous MnCo₂O₄ as a promising electrode material for supercapacitors.     

Electrospinning-derived ZnCo2O4@carbon nanofiber composite for high-performance lithium ion storage

The degradation of the cobalt-zinc oxide structure and its poor conductivity during the charge and discharge limit their further applications for lithium ion storage. Herein, ZnCo₂O₄@carbon nanofiber composite with nano-fibrous structure is obtained by electrospinning, annealing in argon and low-temperature oxidation to effectively overcome the above issue. The active sites of ZnCo₂O₄ are evenly dispersed inside the carbon nanofibers, which can effectively avoid its aggregation and improve electrical conductivity. Additionally, the stable nanofibrous structure can maintain structural stability. The composite exhibits superior lithium ion storage capacity when being served as anode electrode. The ZnCo₂O₄@carbon nanofiber electrode possesses a high capacity of 1071 mA h g⁻¹ at 0.1 A g⁻¹. Besides, the electrode shows an outstanding rate capability of 505 mA h g⁻¹ at 3 A g⁻¹ and maintain 714 mA h g⁻¹ after 250 cycles when current density is adjusted to 0.2 A g⁻¹ again. Additionally, the electrode has an outstanding long-cycle performance, which remains a capacity of 447.165 mA h g⁻¹ at 0.5 A g⁻¹ after 500 cycles and 421.477 mA h g⁻¹ at 1 A g⁻¹ after 518 cycles. This result demonstrates that ZnCo₂O₄@carbon nanofiber composite has potential application prospects in the fields of advanced energy storage.     

Fe3O4 nanoparticles encapsulated in electrospun porous carbon fibers with a compact shell as high-performance anode for lithium ion batteries

Fe₃O₄ nanoparticles encapsulated in porous carbon fibers (Fe₃O₄@PCFs) as anode materials in lithium ion batteries are fabricated by a facile single-nozzle electrospinning technique followed by heat treatment. A mixed solution of polyacrylonitrile (PAN) and polystyrene (PS) containing Fe₃O₄ nanoparticles is utilized to prepare hybrid precursor fibers of Fe₃O₄@PS/PAN. The resulted porous Fe₃O₄/carbon hybrid fibers composed of compact carbon shell and Fe₃O₄-embeded honeycomb-like carbon core are formed due to the thermal decomposition of PS and PAN. The Fe₃O₄@PCF composite demonstrates an initial reversible capacity of 1015 mAh g⁻¹ with 84.4% capacity retention after 80 cycles at a current density of 0.2 A g⁻¹. This electrode also exhibits superior rate capability with current density increasing from 0.1 to 2.0 A g⁻¹, and capacity retention of 91% after 200 cycles at 2.0 A g⁻¹. The exceptionally high performances are attributed to the high electric conductivity and structural stability of the porous carbon fibers with unique structure, which not only buffers the volume change of Fe₃O₄ with the internal space, but also acts as high-efficient transport pathways for ions and electrons. Furthermore, the compact carbon shell can promote the formation of stable solid electrolyte interphase on the fiber surface.     

MoO3/reduced graphene oxide composites as anode material for sodium ion batteries

MoO₃/reduced graphene oxide (MoO₃/RGO) composites were successfully prepared via a facile one-step hydrothermal method, and evaluated as anode materials for sodium ion batteries (SIBs). The crystal structures, morphologies and electrochemical properties of the as-prepared samples were characterized by X-ray diffraction, field-emission scanning electron microscopy, cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge/discharge tests, respectively. The results show that the introduction of RGO can enhance the electrochemical performances of MoO₃/RGO composites. MoO₃/RGO composite with 6 wt% RGO delivers the highest reversible capacity of ~208 mA h g⁻¹ at 50 mA g⁻¹ after 50 cycles with good cycling stability and excellent rate performance for SIBs. The excellent sodium storage performance of MoO₃/RGO should be attributed to the synergistic effect between MoO₃ and RGO, which offers the increased electrical conductivity, the facilitated electron transfer ability and the buffering of volume expansion.     

Effect of core-shell reversal on the structural,magnetic and adsorptive properties of Fe2O3-GO nanocomposites

Effect of core-shell reversal on the nanocomposites of graphene oxide (GO) and ferric oxide (Fe₂O₃) was studied. Fe₂O₃@GO core-shell nanosheets were synthesized by sonication method, while the GO@Fe₂O₃ core-shell nanospheres by employing N,N′-dicyclohexylcarbodimide as the binding agent for the wrapping of GO sheets on pre-formed Fe₂O₃ nanoparticles (NPs). The phase composition, crystallinity and morphology of the nanocomposites were characterized by FT-IR, TEM, SEM-EDS, VSM, BET surface area study and XRD techniques. The saturation magnetization (M_s) was 1.25 and 0.51 emu g⁻¹ for GO@Fe₂O₃ and Fe₂O₃@GO respectively owing to the dependence of magnetic properties on the reversal of core-shell. BET analysis revealed the surface area of 100.32 m² g⁻¹ and 45.69 m² g⁻¹ for GO@Fe₂O₃ and Fe₂O₃@GO nanocomposites respectively. The fabricated nanocomposites were analyzed as adsorbents for the uptake of Pb (II) ions. The impact of various factors affecting adsorption process such as pH, adsorbent dose, contact time, temperature and metal ion concentration was also investigated. GO@Fe₂O₃ core-shell nanospheres showed a higher adsorption capacity for Pb (II) ions as compared to Fe₂O₃@GO core-shell nanosheet with the maximum adsorption capacities (q_m) of 303.0 and 125.0 mg g⁻¹ respectively. The equilibrium data was estimated by Freundlich, Langmuir, D-R and Temkin isotherm models. Thermodynamic analysis confirmed the spontaneous and exothermic nature of the adsorption process. The adsorption kinetics was significantly fitted to pseudo-second order model. The results confirmed that core-shell reversal can significantly alter the adsorptive properties of Fe₂O₃-GO nanocomposite