Publications by authors named "Sankalpita Chakrabarty"

Rechargeable Mg-ion Batteries (RMB) containing a Mg metal anode offer the promise of higher specific volumetric capacity, energy density, safety, and economic viability than lithium-ion battery technology, but their realization is challenging. The limited availability of suitable inorganic cathodes compatible with electrolytes relevant to Mg metal anode restricts the development of RMBs. Despite the promising capability of some oxides to reversibly intercalate Mg ions at high potential, its lack of stability in chloride-containing ethereal electrolytes, relevant to Mg metal anode hinders the realization of a full practical RMB.

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Article Synopsis
  • The development of all-solid-state lithium batteries (ASSLBs) faces challenges in lowering fabrication costs without losing performance.* -
  • A new sulfide ASSLB features a Co-free LiNiO cathode with a unique LiAlZnO protective layer that enhances stability and reduces undesirable reactions at the electrolyte interface.* -
  • This innovative approach results in impressive performance metrics, including high capacity, cycling stability, and insights on avoiding the use of costly materials while maintaining energy efficiency.*
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Sodium-ion batteries have recently emerged as a promising alternative to lithium-based batteries, driven by an ever-growing demand for electricity storage systems. The present workproposes a cobalt-free high-capacity cathode for sodium-ion batteries, synthesized using a high-entropy approach. The high-entropy approach entails mixing more than five elements in a single phase; hence, obtaining the desired properties is a challenge since this involves the interplay between different elements.

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To achieve sustainable production of H at ambient temperature, highly active and stable electrocatalysts are the key to water splitting technology commercialization for hydrogen and oxygen production to replace Pt and IrO catalysts. Herein, a modified interface of palladium (Pd) and reduced graphene oxide (RGO)-supported molybdenum disulfide (MoS) prepared by the solvothermal followed by chemical reduction method is established, in which abundant interfaces are formed. The phase structure, composition, chemical coupling, and morphology of the two-dimensional nanostructures are established by X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy, respectively.

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Reduced graphene oxide (RGO)-supported bismuth ferrite (BiFeO) (RGO-BFO) nanocomposite is synthesized via a two-step chemical route for photoelectrochemical (PEC) water splitting and photocatalytic dye degradation. The detailed structural analysis, chemical coupling, and morphology of BFO- and RGO-supported BFO are established through X-ray diffraction, Raman and X-ray photoelectron spectroscopy, and high-resolution transmission electron microscopy studies. The modified band structure in RGO-BFO is obtained from the UV-vis spectroscopy study and supported by density functional theory (DFT).

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We report, herein, the results of an in depth study and concomitant analysis of the AC conduction [σ'(ω): f=20 Hz to 2 MHz] mechanism in a reduced graphene oxide-zinc sulfide (RGO-ZnS) composite. The magnitude of the real part of the complex impedance decreases with increase in both frequency and temperature, whereas the imaginary part shows an asymptotic maximum that shifts to higher frequencies with increasing temperature. On the other hand, the conductivity isotherm reveals a frequency-independent conductivity at lower frequencies subsequent to a dispersive conductivity at higher frequencies, which follows a power law [σ'(ω)∝ω(s) ] within a temperature range of 297 to 393 K.

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