Browsing by Author "Hegde, A.P."

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Ag2Cu2O3 Nanorods as Electrocatalysts for Hydrogen Production and Overall Water Splitting
(American Chemical Society, 2025) Kumar, A.; Hegde, A.P.; Puttur, M.; Gangadharappa, L.S.; Hosakoppa, N.S.
In this research, a series of Ag2Cu2O3 nanorods as electrocatalysts were prepared with three different drying temperatures (namely, W - 50, W - 80, and W - 120), utilizing a regular coprecipitation approach. These nanorods’ surface morphology and structural attributes were thoroughly characterized using Field Emission Scanning Electron Microscopy and High-Resolution Transmission Electron Microscopy, while X-ray diffraction provided insight into their crystal structures. The compositional analysis was accomplished via X-ray photoelectron spectroscopy and Raman spectroscopy. The W - 50 catalyst exhibited the most promising electrochemical response among the synthesized samples. In the solution of 1 M KOH, at a current density of 10 mA cm-2, it demonstrated modest overpotential values and Tafel slopes of 81 and 97 mV dec-1 for the hydrogen evolution reaction (HER), whereas 409 and 140 mV dec-1 for the oxygen evolution reaction (OER). When tested with a two-electrode electrolyzer, W - 50 serving as together the anode and cathode, a trivial cell voltage of 1.9842 V was required to accomplish a current density of 100 mA cm-2, with surprising stability over 50 h of continuous operation at 200 mA cm-2 for overall water splitting. Additionally, W - 50 displayed excellent performance for HER; it necessitated an overpotential of 337 mV to accomplish an extreme current density of 800 mA cm-2. This inquiry provides precious perceptions into the importance of confined spaces within transition metal oxide-based catalysts, advancing their application in electrocatalysis. © 2025 American Chemical Society.
Cerium doping of FeS2 for the effective hydrogen evolution reaction (HER) electrocatalysis
(Taylor and Francis Ltd., 2025) Hegde, A.P.; Gonde, A.; Kumawat, A.; Mukesh, P.; Lakshmisagar, G.; Kumar, A.; Nagaraja, H.S.
Crafting and developing nanostructured electrocatalyst materials that are both active and stable plays a pivotal role in the shift toward economically viable hydrogen production through electrochemical water splitting, paving the way for the future replacement of fossil fuels. Such materials need to be cost-effective, simple to produce, and durable. In this context, the current research delves into improving the hydrogen evolution reaction (HER) electrocatalytic performance by incorporating cerium (Ce) into iron disulfide (FeS2) catalysts, using an uncomplicated hydrothermal fabrication approach. The study systematically examines the effects of various Ce doping levels on electrocatalytic activity. Notably, the catalyst with 15% Ce doping demonstrated exceptional efficiency, reducing the overpotential to 369 mV at 100 mA cm?2 current density. This enhanced performance can be attributed to the reduction in total charge-transfer resistance and a significant increase in the electrochemical active surface area (ECSA). Furthermore, the durability assessment of the 15% Ce-doped sample revealed its ability to sustain its catalytic activity for over 100 h under a continuous HER operation at 300 mA cm-2, with low performance-falloff. These results highlight the potential of Ce-dopping of FeS2 catalysts as a formidable choice for achieving efficient and long lasting HER electrocatalysis. © 2025 Taylor & Francis Group, LLC.
Dual storage mechanism of Bi2O3/Co3O4/MWCNT composite as an anode for lithium-ion battery and lithium-ion capacitor
(Elsevier B.V., 2024) Lakshmi Sagar, G.; Brijesh, K.; Mukesh, P.; Hegde, A.P.; Kumar, A.; Kumar, A.; Bhat, K.S.; Nagaraja, H.S.
Bismuth oxide(Bi2O3) and cobalt oxide(Co3O4) are promising owing to their unique properties, high storage capacity, low cost, and eco-friendliness, making them ideal for lithium-ion batteries(LIBs) and lithium-ion capacitors(LICs) anodes. This study presents the synthesis and thorough characterization of Bi2O3/Co3O4 and Bi2O3/Co3O4/MWCNT composites as potential LIB and LIC anode materials. The materials are synthesized using a hydrothermal process succeeded by annealing. Structural, morphological, and compositional studies were analyzed. Various tests evaluated electrochemical performance, including cyclic voltammetry(CV), confirming a dual storage mechanism like alloying and conversion reaction involved for better energy storage. Specific discharge capacities of 834 mAh/g and 1184 mAh/g were recorded for Bi2O3/Co3O4 and Bi2O3/Co3O4/MWCNT composite electrodes at a current density of 100 mA/g, respectively. The composite material exhibited notably enhanced rate capability, with 31 % and 51 % discharge capacities for Bi2O3/Co3O4 and Bi2O3/Co3O4/MWCNT, respectively. The cyclic stability assessment revealed that Bi2O3/Co3O4 and Bi2O3/Co3O4/MWCNT maintained a high coulombic efficiency of around 99 % over 250 charge–discharge cycles at a high current density of 1 A/g. The capacity retention was approximately 253 mAh/g for Bi2O3/Co3O4 and 439 mAh/g for the Bi2O3/Co3O4/MWCNT composite, indicating excellent cyclic stability and minimal energy loss during cycling. Moreover, the LICs assembly of Bi2O3/Co3O4/MWCNT//CB was investigated, revealing a power density of 200 W kg?1 alongside an energy density of 8.64 Wh kg?1. The cyclic stability assessment over 10,000 cycles exhibits a capacity retention of approximately 45 % under a high current density of 2 A/g. © 2024 Elsevier B.V.
Enhancing conductivity of Bi2O3 through ‘Fe3+’ doping for pseudocapacitor application
(Springer Science and Business Media Deutschland GmbH, 2025) G, L.S.; Bhat, K.S.; Mukesh, P.; Hegde, A.P.; Kumar, A.; Brijesh, K.; Nagaraja, H.S.
Binary metal oxides have emerged as pSromising materials for advanced electrochemical energy storage systems due to their superior performance characteristics. In this study, we focus on bismuth oxide (Bi?O?), a material renowned for its high theoretical capacity, wide potential range, and exceptional power density, as a potential candidate for supercapacitors. Iron doping was employed as a strategy to enhance its electrochemical performance and modulate the band gap, thereby improving conductivity and charge storage efficiency. Fe-doped bismuth oxide (Fe-Bi?O?) was synthesized via a solvothermal method with varying iron concentrations (2%, 4%, and 6%), followed by annealing. The pure and iron-doped bismuth oxide samples revealed a combination of monoclinic and cubic phases and a prominent micro-sheet architecture. The introduction of iron doping led to a noticeable reduction in the band gap, highlighting its role in fine-tuning the electronic properties for enhanced energy storage capabilities. The electrochemical evaluation highlighted the 4% Fe-Bi?O? sample as the optimal composition, achieving a remarkable specific capacity of 904 F g?1, a substantial improvement over 101 F g?1 for pristine Bi?O?, at 1 A g?1 in a 2 M KOH electrolyte. Moreover, this sample exhibited outstanding cyclic stability, retaining 104 F g?1 after 2000 cycles at 10 A g?1. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2025.
Melamine – Ni-MIL-88A blend derived Trevorite/C-g-C3N4 for stable and efficient overall electrocatalytic water splitting applications
(Elsevier Ltd, 2025) Hegde, A.P.; P, M.; G, L.; Kumar, A.; Nagaraja, H.S.
The electrocatalytic splitting of water into hydrogen and oxygen plays a pivotal role in addressing the energy demands associated with expanding anthropogenic activities. The design of economically feasible and effective electrocatalytic materials for water electrolysis is imperative for the sustainable production of hydrogen and oxygen. In this context, this study introduces an electrocatalyst design comprising graphitic carbon nitride (g-C3N4) and Trevorite (Ni(Ni, Fe)2O4) synthesized through the pyrolysis of a mixture Ni-substituted metal–organic framework (MOF) MIL-88A and of melamine. The synthesized material was evaluated as an electrocatalyst for both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER). The nickel foam coated with this electrocatalyst exhibits a performance characterized by lower overpotentials of 121 mV for HER and 231 mV for OER at a current density of 10 mA cm-2 in an alkaline medium of 1 M KOH. Furthermore, the composite demonstrated an excellent overall water splitting capacity, maintaining a high current density of 500 mA cm-2 for more than 50 h of continuous electrolysis in 1 M KOH solution with a minimal voltage increase of approximately 0.025 V. © 2025
Novel Ag2Cu2O3 nanorods as stable anode material for lithium-ion battery
(Elsevier B.V., 2025) Kumar, A.; Sagar G, L.; P, M.; Hegde, A.P.; Nagaraja, H.S.
In this research novel Ag2Cu2O3 nanorods was prepared, for lithium-ion battery as anode, using facile co-precipitation method with four different stirring time and correspondingly Ag2Cu2O3 named ACO – 30 M, ACO – 12 H, ACO – 24 H, and ACO – 36 H. Field Emission Scanning Electron Microscopy (FESEM) and High-Resolution Transmission Electron Microscopy (HRTEM) analyze surface and morphology, while X-ray Diffraction (XRD) examines structural properties. Compositional analysis is carried out using X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. The electrochemical analysis is evaluated by cyclic stability, rate capability, discharge/charge capacity, electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). The ACO – 24 H nanomaterial demonstrates an initial discharge capacity of 943 mAh g?1 at a current density of 50 mA g?1. Among the four materials tested, ACO – 24 H shows superior cycling performance, with a discharge capacity of 174 mAh g?1 at 200 mA g?1 after 1003 cycles. In comparison, ACO – 30 M, ACO – 12 H, and ACO – 36 H exhibit capacities of 134 mAh g?1, 91 mAh g?1, and 43 mAh g?1, respectively, under the same conditions. This study suggests that ACO – 24 H is a promising anode material for lithium-ion battery applications. © 2025 Elsevier B.V.
Reinforcing NiO microsphere structural stability via amorphous carbon sheets obtained from waste milk for lithium-ion capacitor application
(Springer Science and Business Media B.V., 2025) Lakshmi Sagar, G.; Brijesh, K.; Mukesh, P.; Hegde, A.P.; Kumar, A.; Paliwal, A.; Bhat, K.S.; Nagaraja, H.S.
In the pursuit of sustainable chemistry and environmentally friendly energy storage, the study addressed the limitations of nickel oxide utilized as the active material for the anode in lithium-ion capacitors. Despite its abundance and favorable environmental properties, NiO suffered from significant volumetric expansion and slow electrochemical kinetics compared to carbon materials. To overcome these issues, amorphous carbon was extracted from spoiled waste milk through a simple combustion process, effectively converting biomass waste into renewable resources. The engineered NiO/amorphous carbon composite, synthesized through hydrothermal and annealing processes, mitigated the limitations of NiO. Field Emission Scanning Electron Microscopy confirmed the deposition of amorphous carbon sheets encasing NiO microspheres, which preserved structural integrity during electrochemical cycling. The amorphous carbon acted as a stabilizing matrix, encapsulating NiO microspheres to mitigate volumetric expansion and enhance lithium-ion transport kinetics. Electrochemical tests demonstrated a specific discharge capacity of 1230 mAh g?1 at a current density of 100 mA g?1, retaining 401 mAh g?1 after 1000 cycles at 1 A g?1, nearly doubling the retention performance of pristine NiO. Furthermore, the NiO/AC//AC lithium-ion capacitor achieved an energy density of 25.4 Wh kg?1 at a power density of 1991 W kg?1, maintaining 96% capacity after 3500 cycles. This study highlighted the potential of waste-derived carbon in developing high-performance, sustainable energy storage systems. © The Author(s), under exclusive licence to Springer Nature B.V. 2025.