Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2024An ammonium vanadate/MXene nanocomposite for high-performance ammonium ion storage12citations
  • 2023Ceramic-polyaniline composites for asymmetric supercapacitors2citations
  • 2022Tailoring crystallinity of 2D cobalt phosphate to introduce pseudocapacitive behavior22citations
  • 2022Three-Dimensional Graphene-TiO2-SnO2Ternary Nanocomposites for High-Performance Asymmetric Supercapacitors26citations

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Aberoumand, Sadegh
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Padwal, Chinmayee
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Jagadish, Priyanka
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Wageh, S.
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Co-Authors (by relevance)

  • Aberoumand, Sadegh
  • Padwal, Chinmayee
  • Wang, Xijue
  • Harilal, Midhun
  • Jagadish, Priyanka
  • Wageh, S.
  • Pannipara, Mehboobali
  • Khalid, Mohammad
  • Iqbal, Javed
  • Numan, Arshid
  • Zamiri, Golnoush
  • Haseeb, A. S. Md Abdul
  • Kong, Ing
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article

Tailoring crystallinity of 2D cobalt phosphate to introduce pseudocapacitive behavior

  • Wageh, S.
  • Pannipara, Mehboobali
  • Krishnan, Syam
  • Khalid, Mohammad
  • Iqbal, Javed
  • Jagadish, Priyanka
  • Numan, Arshid
Abstract

<p>The latest technological developments have catalyzed the quest for efficient electrochemical energy storage devices. Tailoring the properties of the electrode materials, such as porosity, crystallinity, electrochemical surface area, etc., can enhance the performance of electrochemical energy devices. Herein, the sonochemical synthesis of cobalt phosphate (Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub>) followed by calcination at various temperatures (at 200, 400, 600, and 800 °C) is reported. The effect phase transformation of Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> at various calcination temperatures on its electrochemical performance is evaluated. The prepared Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> samples were characterized by analytical techniques such as X-ray diffraction spectroscopy (XRD), X-ray Photoelectron Spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), field emission scanning electrons microscopy (FESEM), and energy-dispersive X-ray spectroscopy (EDS). The FESEM results showed morphological changes when Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> is calcined at 200, 400, 600, and 800 °C. XRD pattern revealed the phase transformations from crystalline to amorphous and then again crystalline due to the loss of water molecules from the crystal structure Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub>. The EDS provided the elemental analysis and confirmed the high purity of the samples under investigation. The change in electrochemical behavior of the prepared samples was examined in a three-electrode cell using 1 M potassium hydroxide (KOH) electrolyte using cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. The Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> calcined at 200 °C demonstrated excellent electrochemical performance, giving a specific capacity of 352.00 C·g<sup>−1</sup>, selected for the fabrication of supercapattery. The fabricated supercapattery (Co<sub>3</sub>(PO<sub>4</sub>)<sub>2:</sub>@200 °C//AC) produced 51.95 Wh·kg<sup>−1</sup> energy density corresponding to the power density of 346.00 W·kg<sup>−1</sup> at a current density of 1.0 A g<sup>−1</sup>.</p>

Topics
  • density
  • impedance spectroscopy
  • surface
  • amorphous
  • energy density
  • phase
  • x-ray diffraction
  • x-ray photoelectron spectroscopy
  • Potassium
  • cobalt
  • Energy-dispersive X-ray spectroscopy
  • current density
  • porosity
  • Fourier transform infrared spectroscopy
  • crystallinity
  • cyclic voltammetry
  • elemental analysis
  • microscopy