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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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 (7/7 displayed)

  • 2024Enhancing lithium-ion battery anode performance via heterogeneous nucleation of silver within Ti3C2-MXene frameworks4citations
  • 2024Innovative Tin and hard carbon architecture for enhanced stability in lithium-ion battery anodes3citations
  • 2024Sputtered Hard Carbon for High-Performance Energy Storage Batteriescitations
  • 2024Designing Molybdenum Trioxide and Hard Carbon Architecture for Stable Lithium‐Ion Battery Anodes2citations
  • 2023Multi-layered Sn and Hard Carbon Architectures for Long-Term Stability and High-Capacity Lithium-Ion Battery Anodescitations
  • 2023Advancing Lithium-Ion Battery Anodes: Novel Sn and Hard Carbon Architectures for Long-Term Stability and High Capacitycitations
  • 2023Molybdenum Incorporated O3‐type Sodium Layered Oxide Cathodes for High‐Performance Sodium‐Ion Batteries8citations

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Kahraman, Ramazan
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Quddus, Khadija Abdul
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Tariq, Hanan Abdurehman
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Shakoor, R. A.
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Qureshi, Zawar Alam
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Rasul, Shahid
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Alqaradawi, Siham
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Bensalah, Nasr
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Cherian Lukose, Cecil
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Mamlouk, Mohamed
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Shakoor, Rana Abdul
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Lukose, Cecil Cherian
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Brewis, Ian
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Gayara, R. A. Harindi
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Ahmed, Abdul Moiz
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Moossa, Buzaina
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Abraham, Jeffin James
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Al-Qaradawi, Siham
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Co-Authors (by relevance)

  • Kahraman, Ramazan
  • Quddus, Khadija Abdul
  • Tariq, Hanan Abdurehman
  • Shakoor, R. A.
  • Qureshi, Zawar Alam
  • Rasul, Shahid
  • Alqaradawi, Siham
  • Bensalah, Nasr
  • Cherian Lukose, Cecil
  • Mamlouk, Mohamed
  • Zia, Abdul Wasy
  • Shakoor, Rana Abdul
  • Lukose, Cecil Cherian
  • Brewis, Ian
  • Gayara, R. A. Harindi
  • Ahmed, Abdul Moiz
  • Moossa, Buzaina
  • Abraham, Jeffin James
  • Al-Qaradawi, Siham
OrganizationsLocationPeople

article

Enhancing lithium-ion battery anode performance via heterogeneous nucleation of silver within Ti3C2-MXene frameworks

  • Kahraman, Ramazan
  • Quddus, Khadija Abdul
  • Tariq, Hanan Abdurehman
  • Shakoor, R. A.
  • Qureshi, Zawar Alam
  • Rasul, Shahid
  • Alqaradawi, Siham
  • Bensalah, Nasr
  • Shahzad, Rana Faisal
Abstract

<p>Silver (Ag) nanoparticles are strategically integrated with 2D MXene material to engineer a high-capacity anode material suitable for lithium-ion batteries (LIBs). MXenes, renowned for their exceptional structural, mechanical, and chemical attributes, have emerged as promising candidates for advanced LIB electrode materials. However, the inherently narrow interlayer spacing within MXene poses challenges for efficient loading or modification with metal oxide nanoparticles, necessitating intricate and time-consuming processes. In this study, exfoliated MXene layers are subjected to an in-situ decoration process with Ag nanoparticles to augment interlayer spacing and enhance MXene conductivity. This augmentation is achieved through a direct reduction approach followed by a meticulously controlled two-step heat treatment process. Characterization analyses of the synthesized Ag-MXene nanoparticles unveil a uniform and homogeneous dispersion of nanoparticles, each measuring &lt;50 nm. X-ray diffraction (XRD) confirms successful MXene formation from the MAX phase, accompanied by pure Ag nanoparticles affixed onto Ti<sub>3</sub>C<sub>2</sub> layers, as evidenced by sharp peaks indicative of crystalline structure. Fourier-transform infrared spectroscopy (FTIR) further confirms the low amount of terminal functional groups (-OH and -F) on the MXene layers. Thermal gravimetric analysis (TGA) highlights an enhancement in the thermal stability of Ti<sub>3</sub>C<sub>2</sub> upon Ag incorporation. Electrochemical performance evaluations demonstrate the exceptional cyclic stability of the Ag-Ti<sub>3</sub>C<sub>2</sub> nanocomposite, showcasing a highly reversible potential of approximately 544 mAhg<sup>−1</sup> after 100 cycles at a current rate of 0.1 C. Moreover, the rate capability is substantially improved, reaching up to 193 mAhg<sup>−1</sup> at 10 C, a significant enhancement compared to the mere 20 mAhg<sup>−1</sup> exhibited by pristine Ti<sub>3</sub>C<sub>2</sub>. Notably, the performance of Ag-Ti<sub>3</sub>C<sub>2</sub> as an anode material surpasses that of pristine Ti<sub>3</sub>C<sub>2</sub> across all evaluated metrics, attributed to the enhanced electrochemical kinetics facilitated by Ag's high electronic conductivity. These superior properties, stemming from the tailored material's unique morphology, effectively mitigate MXene layer restacking, rendering it highly advantageous for next-generation LIBs.</p>

Topics
  • nanoparticle
  • nanocomposite
  • impedance spectroscopy
  • dispersion
  • silver
  • phase
  • x-ray diffraction
  • thermogravimetry
  • Lithium
  • infrared spectroscopy
  • gravimetric analysis