Publications by authors named "Madhu Ragunath"

Viologen-based covalent organic networks represent a burgeoning class of materials distinguished by their captivating properties. Here, supramolecular chemistry is harnessed to fabricate polyrotaxanated ionic covalent organic polymers (iCOP) through a Schiff-base condensation reaction under solvothermal conditions. The reaction between 1,1'-bis(4-aminophenyl)-[4,4'-bipyridine]-1,1'-diium dichloride (DPV-NH) and 1,3,5-triformylphloroglucinol (TPG) in various solvents yields an iCOP-1 and iCOP-2.

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The development of low-cost, efficient catalysts for electrocatalytic water splitting to generate green hydrogen is a hot topic among researchers. Herein, we have developed a highly efficient heterostructure of CoCr-LDH on NiO on nickel foam (NF) for the first time. The preparation strategy follows the simple annealing of a cleaned NF without using any Ni salt precursor, followed by the growth of CoCr-LDH nanosheets over the surface-oxidized NF.

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Article Synopsis
  • - Electrocatalytic water splitting using the LaFeO perovskite structure shows promise for producing clean hydrogen, but its efficiency is hindered by slow reaction rates.
  • - To enhance performance, gold nanoparticles (Au NPs) are added to the LaFeO surface, which improves the reaction kinetics and increases active sites for water splitting.
  • - The resulting Au@LaFeO catalyst demonstrates significantly better electrocatalytic activity than pure LaFeO, requiring lower overpotentials for effective hydrogen production, making it a strong candidate for renewable energy applications.
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Water electrolysis is considered as one of the alternative potential approaches for producing renewable energy. Due to the sluggish kinetic nature of oxygen evolution reaction (OER), it encounters a significant overpotential to achieve water electrolysis. Hence, the advancement of cost-effective transition metal-based catalysts toward water splitting has gained global attention in recent years.

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Exploiting an affordable, durable, and high-performance electrocatalyst for the oxygen evolution reaction (OER) under lower pH condition (acidic) is highly challengeable and much attractive toward the hydrogen-based energy technologies. A spinel CoCrO is observed as a potential noble-metal-free candidate for OER in alkaline medium. The presence of Cr further leads to electronic structure modulation of CoO and thereby greatly increases the corrosive resistance toward OER in acidic environment.

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Water electrolysis encounters a challenging problem in designing a highly efficient, long durable, non-noble metal-free electrocatalyst for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Here, in our work, a two-step hydrothermal reaction was performed to construct a hierarchal NiFe-layer double hydroxide (LDH)/CuS over copper foam for the overall water splitting reaction. While employed the same as an anode material, the designed heterostructure electrode NiFe-LDH/CuS/Cu exhibits excellent OER performance and it demands 249 mV overpotential to reach a current density of 50 mA cm with a lower Tafel slope value of 81.

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To generate green hydrogen by water electrolysis, it is vital to develop highly efficient electrocatalysts for the oxygen evolution reaction (OER). The utilization of various 3d transition metal-based layered double hydroxides (LDHs), especially NiFe-LDH, has gained vast attention for OER under alkaline conditions. However, the lack of a proper electronic structure of the NiFe-LDH and low stability under high-pH conditions limit its large-scale application.

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Article Synopsis
  • - The study investigates a new bimetallic zeolite imidazolate framework (ZIF) made of cobalt and manganese to enhance electrocatalytic oxygen evolution reactions (OER) through electrospinning.
  • - The resulting nanofibers exhibited a reduced overpotential of 302 mV at 10 mA/cm² in alkaline conditions, with a Tafel slope of 125 mV/dec and a charge-transfer resistance of 4 Ω, indicating efficient kinetics in the OER process.
  • - It was found that manganese acts as the primary active center in the ZIF-67 nanofibers, while the presence of cobalt affects the Jahn-Teller distortion and overall performance, supported by
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The development of efficient electrocatalysts for the water splitting process and understanding their fundamental catalytic mechanisms are highly essential to achieving high performance in energy conversion technologies. Herein, we have synthesised spinel nickel ferrite nanofibers (NiFeO-NFs) an electrospinning (ES) method followed by a carbonization process. The resultant fiber was subjected to electrocatalytic water splitting reactions in alkaline medium.

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Internal Ni-vacancy-enriched spherical AuNi nanoalloys (AuNi-T) have been prepared via a noble electrochemical etching method. AuNi-T showed the highest oxygen evolution reaction (OER) activity compared to bare AuNi, and it demands only 239 mV overpotential, which was 134 mV lesser than the overpotential required by commercial RuO at 10 mA cm current density in a 1 M KOH solution (pH = 14). The calculated turnover frequency (TOF) value for AuNi-T (0.

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Vast attention from researchers is being given to the development of suitable oxygen evolution reaction (OER) electrocatalysts water electrolysis. Being highly abundant, the use of transition-metal-based OER catalysts has been attractive more recently. Among the various transition-metal-based electrocatalysts, the use of layered double hydroxides (LDHs) has gained special attention from researchers owing to their high stability under OER conditions.

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The generation of pure H from a neutral electrolyte solution represents a transformative route with low cost and environmentally friendly nature. However, the complex kinetics of hydrogen evolution reaction (HER) via water electrolysis make its practical application to be difficult. Herein, we have reported Ru-doping-induced formation of VS nanostructures with a rich S vacancy for neutral HER in a 0.

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Electrocatalytic water splitting has gained vast attention in recent decades for its role in catalyzing hydrogen production effectively as an alternative to fossil fuels. Moreover, the designing of highly efficient oxygen evolution reaction (OER) electrocatalysts across the universal pH conditions was more challengeable as in harsh anodic potentials, it questions the activity and stability of the concerned catalyst. Generally, geometrical engineering and electronic structural modulation of the catalyst can effectively boost the OER activity.

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Development of a low-cost transition metal-based catalyst for water splitting is of prime importance for generating green hydrogen on an industrial scale. Recently, various transition metal-based oxides, hydroxides, sulfides, and other chalcogenide-based materials have been synthesized for developing a suitable anode material for the oxygen evolution reaction (OER). Among the various transition metal-based catalysts, their oxides have received much consideration for OER, especially in lower pH condition, and MnO is one of the oxides that have widely been used for the same.

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The replacement of noble metals with alternative electrocatalysts is highly demanded for water splitting. From the exploration of 3D -transition metal based heterostructures, engineering at the nano-level brought more enhancements in active sites with reduced overpotentials for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). However, recent developments in 3D transition metal based heterostructures like direct growth on external substrates (Ni foam, Cu foam) gave highly impressive activities and stabilities.

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The development of a highly efficient electrocatalyst for the oxygen evolution reaction (OER) with a lower overpotential and high intrinsic activity is highly challenging owing to its sluggish kinetic behavior. As an alternative to the state-of-the-art OER catalyst, recently, transition-metal-based hydroxide materials have been shown to play important roles for the same. Owing to the high earth abundance of various Ni-based hydroxide and its derivatives, these are known to be highly studied materials for the OER.

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Developing non-noble, earth-ample, and stable electrocatalysts are highly anticipated in oxygen-evolution reaction (OER) and hydrogen-evolution reaction (HER) at unique pH conditions. Herein, we have synthesized bimetallic (nickel and iron) zeolite imidazolate framework (ZIF)-based nanofibrous materials via a simple electrospinning (ES) process. The structural stability of the fibrous material is subjected to various calcination conditions.

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Metal-organic framework (MOF)-based materials have attracted attention in recent times owing to their remarkable properties such as regulatable pore size, high specific surface area, and elasticity in their network topology, geometry, dimension, and chemical functionality. It is believed that the incorporation of a MOF network into a fibrous matrix results in the improvement of the electrocatalytic properties of the material. Herein, we have synthesized a Co-incorporated MOF-5-based fibrous material by a simple wet-chemical method, followed by an electrospinning (ES) process.

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The use of nanomaterials (NMs) in various applications via multidisciplinary approaches is highly necessary in this era. In this line, the impact of noble metals in organic media for both catalysis and surface-enhanced Raman spectroscopic (SERS) studies is most interesting and also has a wider scope in various fields. Nonetheless, the catalytic reduction of aromatic nitro compounds is difficult with poor solubility in aqueous media, and reduction also is less feasible in the absence of noble metal-based catalysts.

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Surface Enhanced Raman Scattering (SERS) is a field of research that has shown promising application in the analysis of various substrate molecules by means of rough metallic surfaces. In directing the enhancement of substrate molecules in micro and nano-molar concentrations, plasmonic coupling of metal nanoparticles (NPs), morphology of metal NPs and the closely arrangement of rough metal surfaces that produces 'hot spots' can effectively increase the so-called enhancement factor (EF) that will be applicable in various fields. As the mechanistic aspects are still not clear, research has been triggered all over the world for the past two decades to have a clear understanding in chemical and electromagnetic effects.

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Out of various available methods, generation of hydrogen by electrocatalytic water splitting is the most accepted one which consists of two half-cell reactions, , oxygen evolution reaction (OER) at the anode and hydrogen evolution reaction at the cathode. OER is a complex four-electron transfer process, and to sustain the spontaneous generation of hydrogen at the cathode, it is urgent to develop some earth-abundant, low-cost electrode materials. Recently, use of cobalt-based hydroxide as the electrode substrate has taken much consideration and has been fabricated over various substrates.

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