Rutuja U. Amate

Developing multifunctional electrodes for simultaneous energy storage and conversion is essential for sustainable energy technologies. Herein, we report Cu ₂ O coating on niobium phosphate creates a heterogeneous interface that promotes charge separation, reduces interfacial resistance, and stabilizes redox‐active Cu sites. Niobium phosphate acts as a chemically robust, ion‐friendly scaffold, while the Cu ₂ O couple provides a dynamically active surface accelerating electron transfer and intermediate adsorption. The intimate NbP@Cu ₂ O heterointerface induces interfacial charge redistribution and strong electronic coupling, enabling rapid charge transfer, accelerated ion diffusion, and enhanced electrochemical kinetics for improved reaction performance. Consequently, the NbP@Cu ₂ O electrode delivers a high specific capacity of 23.40 F/cm ² at 5 mA/cm ² , approximately 2.4 times higher than pristine NbP, together with excellent rate capability and coulombic efficiency. The assembled device achieves a specific capacitance of 410 mF/cm ² , an energy density of 128 μWh/cm ² at a power density of 760 μW/cm ² and demonstrated robust endurance over an extended 100000‐cycle test (65% retention; 0.00035% loss per cycle). Furthermore, the heterostructure exhibits outstanding OER activity with a low overpotential of 275.2 mV at 100 mA/cm ² , a Tafel slope of 48.2 mV/dec, and stable operation for 120 h. These findings demonstrate the potential of phosphate‐oxide heterointerface engineering for advanced bifunctional energy storage and conversion applications. image

The rational design of electrode architectures is essential for advancing high-performance supercapacitors. In this study, Nd₂O₃ electrodes with controlled structural features were developed via a polyacrylic acid (PAA)-assisted hydrothermal approach. By systematically tuning PAA concentration, the growth mechanism of Nd₂O₃ was effectively regulated, leading to a distinct morphological transition from compact agglomerates to well-defined hierarchical structures. The optimized Nd₂O₃-P2 electrode exhibits a porous and interconnected architecture, providing enhanced electrolyte accessibility and shortened ion diffusion pathways. This structural optimization significantly improves electrochemical performance, delivering a high areal capacitance of 26.889 F/cm² at 10 mA/cm², along with excellent rate capability and reduced internal resistance. Kinetic analysis reveals that charge storage is predominantly governed by diffusion-controlled Faradaic processes, with the optimized structure facilitating rapid ion transport and efficient redox activity. Additionally, the electrode demonstrates excellent cycling durability, retaining 87.08% capacitance over 12,000 cycles. An asymmetric supercapacitor assembled using Nd₂O₃-P2 and activated carbon achieves stable operation up to 1.5 V, delivering good capacitance retention (81.2%) after 7000 cycles. This work highlights the effectiveness of PAA-induced structural tuning and provides a practical strategy for developing advanced rare earth oxide-based electrodes for energy storage applications.

In this study, a systematic investigation was undertaken to elucidate the influence of polymeric surfactants such as polyvinylpyrrolidone (PVP), polyethylene glycol (PEG), and their hybrid combination (PVP/PEG) on the structural, morphological, and electrochemical evolution of Fe₂O₃ electrodes designed for high-performance supercapacitor applications. Fe₂O₃ nanostructures were synthesized via a controlled hydrothermal route, wherein the surfactant composition was precisely tuned to modulate crystal growth, particle dispersion, and surface active-site density. Detailed physicochemical characterization revealed that hybrid PVP/PEG incorporation induced a hierarchically nanograined morphology with optimized porosity. The optimized PVP/PEG-Fe electrode exhibited the largest CV area, lowest equivalent series resistance (0.33 Ω), and superior areal capacitance of 9.17 F cm⁻² at 8 mA cm⁻², attributed to accelerated redox kinetics and efficient ion diffusion. Long-term cycling demonstrated remarkable structural resilience, with ~85.1% capacitance retention after 12,000 cycles. Furthermore, an asymmetric pouch-type supercapacitor (PVP/PEG-Fe//AC) was assembled to validate practical performance, achieving a wide potential window of 1.5 V, an areal capacitance of 0.260 F cm⁻², energy density of 0.081 mWh cm⁻², and coulombic efficiency of 95.73% after 7000 cycles. This work highlights the critical role of cooperative polymer–metal oxide interactions in achieving structural uniformity, optimized electrochemical kinetics, and long-term durability, offering a versatile strategy for engineering cost-effective, high-performance transition metal oxide electrodes for next-generation flexible energy storage devices.

Rare-earth oxides possess distinctive electronic configurations, tunable oxidation states, and inherent structural robustness, making them highly attractive for advanced energy storage applications. Among these, neodymium oxide (Nd₂O₃) stands out due to its high surface redox activity, structural stability, and favorable band alignment, enabling efficient charge storage in electrochemical devices. In this study, Nd₂O₃ electrodes were synthesized via a sol–gel method with systematically varied precursor concentrations (1 mM, 3 mM, and 5 mM) to elucidate the impact of synthesis on crystallinity, morphology, and electrochemical performance. X-ray diffraction (XRD) confirmed the formation of the hexagonal Nd₂O₃ phase, with the 3 mM sample (Nd-2) exhibiting the sharpest reflections, indicative of enhanced crystallinity and reduced lattice defects. X-ray photoelectron spectroscopy (XPS) revealed trivalent Nd species and both lattice and surface oxygen, providing abundant redox-active sites. Field Emission Scanning Electron Microscope (FE-SEM) showed Nd-2 possessed a hierarchically interconnected fibrous network decorated with fine granules, maximizing active surface area and facilitating rapid ion diffusion. Electrochemical testing demonstrated that Nd-2 achieved an areal capacitance of 20 F cm⁻², a diffusion-controlled pseudocapacitive contribution of ~84.9%, and retained 86.3% capacitance over 12,000 cycles. An asymmetric supercapacitor with Nd-2 and activated carbon delivered an energy density of 0.132 mWh cm⁻², power density of 1.8 mW/cm², and 81.1% capacitance retention over 7000 cycles. These results highlight the critical role of precursor concentration in tailoring structure and electrochemical performance, establishing Nd₂O₃ as a promising electrode for high-performance energy storage devices.

The rational design of transition metal oxides with tailored electronic structures and defect chemistries is critical for advancing high-performance supercapacitors. Herein, we report the engineering of cobalt oxide (Co₃O₄) gels through controlled sol–gel synthesis and rare earth (RE) incorporation using neodymium (Nd), gadolinium (Gd), and dual neodymium/gadolinium (Nd/Gd) doping. X-ray diffraction (XRD) confirmed the preservation of the cubic spinel structure with systematic peak shifts and broadening, evidencing lattice strain, oxygen vacancy generation, and defect enrichment. Field-emission scanning electron microscopy (FE-SEM) analyses revealed distinct morphological evolution from compact nanoparticle assemblies in pristine Co₃O₄ to highly porous, interconnected frameworks in Nd/Gd–Co₃O₄ (Nd/Gd-Co). X-ray photoelectron spectroscopy (XPS) verified the stable incorporation of RE ions, accompanied by electronic interaction with the Co–O matrix and enhanced oxygen defect states. Electrochemical measurements demonstrated that the Nd/Gd–Co electrode achieved a remarkable areal capacitance of 25 F/cm² at 8 mA/cm², superior ionic diffusion coefficients, and the lowest equivalent series resistance (0.26 Ω) among all samples. Long-term cycling confirmed 84.35% capacitance retention with 94.46% coulombic efficiency after 12,000 cycles. Furthermore, the asymmetric pouch-type supercapacitor (APSD) constructed with Nd/Gd–Co as the positive electrode and activated carbon as the negative electrode delivered a wide operational window of 1.5 V, an areal capacitance of 140 mF/cm², an energy density of 0.044 mWh/cm², and 89.44% retention after 7000 cycles. These findings establish Nd/Gd-Co gels as robust and scalable electrode materials and demonstrate that RE co-doping is an effective strategy for bridging high energy density with long-term electrochemical stability in asymmetric supercapacitors.

The continuous increase in global energy demand necessitates the development of sustainable, clean, and highly efficient methods of energy generation. Electrochemical water splitting, comprising hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), represents a promising strategy but remains hindered by sluggish reaction kinetics and limited availability of highly active electrocatalysts especially under alkaline conditions. Addressing this challenge, we successfully synthesized a rGO-VO₂/W₅O₁₄ (rG-VO₂/W₅O₁₄) hydrogel electrocatalyst through a facile hydrothermal approach. The prepared composite distinctly reveals an advantageous hierarchical microstructure characterized by VO₂ nanoflakes uniformly distributed on the surface of rGO nanosheets, intricately integrated with W₅O₁₄ nanorods. Evaluated in a 1.0 M KOH electrolyte, the optimized rG-VO₂/W₅O₁₄-2 catalyst demonstrates remarkable electrocatalytic performance towards OER, achieving a low overpotential of 265.8 mV and a reduced Tafel slope of 81.9 mV dec⁻¹. Furthermore, the catalyst maintains robust stability with minimal performance degradation, exhibiting an overpotential of only 273.0 mV after 5000 cyclic stability tests. The superior catalytic activity and durability are attributed to the synergistic combination of enriched chemical composition, effective electron transfer, and abundant catalytic active sites inherent in the well-optimized rG-VO₂/W₅O₁₄-2 composite.

Electrochemical water splitting represents a sustainable approach for hydrogen production, yet efficient hydrogen evolution reaction (HER) catalysts operating in alkaline environments remain critically needed. Herein, we report the fabrication of Co₃O₄–NiS₂ nanocomposites synthesized through a facile coprecipitation and subsequent thermal treatment method. Detailed characterization via physicochemical techniques confirmed the successful formation of a hybrid Co₃O₄–NiS₂ heterostructure with tunable compositional and morphological characteristics. Among the synthesized catalysts (Co–Ni–1, Co–Ni–2, and Co–Ni–3), the Co–Ni–2 sample demonstrated optimal structural integration, displaying interconnected nanosheet morphologies and balanced elemental distribution. Remarkably, Co–Ni–2 achieved exceptional HER performance in 1 M KOH electrolyte, requiring an ultralow overpotential of only 84 mV at 10 mA cm⁻² and exhibiting a favorable Tafel slope of 67.5 mV dec⁻¹. Electrochemical impedance spectroscopy and electrochemical surface area measurements further substantiated the superior electrocatalytic kinetics, rapid charge transport, and abundant active site accessibility in the optimized Co–Ni–2 composite. Additionally, Co–Ni–2 demonstrated outstanding durability with negligible activity decay over 5000 cycles. This study not only highlights the strategic synthesis of Co₃O₄–NiS₂ nanostructures but also provides valuable insights for designing advanced, stable, and efficient non-noble electrocatalysts for sustainable hydrogen generation.

Designing advanced electrode architectures with tailored morphology and redox synergy is essential for achieving high-performance supercapacitive energy storage. In this study, a PVP-assisted hydrothermal approach was employed to synthesize binder-free NiCo₂O₄ nanostructured electrodes directly on nickel foam substrates. By modulating the PVP concentration (0.5–2 wt%), hierarchical flower-like nanosheets were engineered, with the NiCo-P₁ sample (1 wt% PVP) exhibiting an optimized structure, superior electroactive surface area, and enhanced ion accessibility. Comprehensive electrochemical analysis revealed that NiCo-P₁ delivered an outstanding areal capacitance of 36.5 F/cm² at 10 mA/cm², along with excellent cycling stability over 15,000 cycles with 80.97% retention. Kinetic studies confirmed dominant diffusion-controlled redox behavior with high OH⁻ diffusion coefficients and minimal polarization. An asymmetric pouch-type supercapacitor device (NiCo-P₁//AC) exhibited a wide operating window of 1.5 V, achieving a remarkable areal capacitance of 187 mF/cm², energy density of 0.058 mWh/cm², and capacitive retention of 78.78% after 5000 cycles. The superior performance is attributed to the synergistic integration of mixed-valence Ni and Co species, engineered nanosheet morphology, and low interfacial resistance. This work underscores the significance of surfactant-directed design in advancing cost-effective, high-performance electrodes for next-generation flexible energy storage technologies.