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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Shahzad, Rana Faisal

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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
2 / 4 shared
Quddus, Khadija Abdul
1 / 1 shared
Tariq, Hanan Abdurehman
1 / 1 shared
Shakoor, R. A.
1 / 4 shared
Qureshi, Zawar Alam
1 / 1 shared
Rasul, Shahid
7 / 18 shared
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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Zia, Abdul Wasy
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Shakoor, Rana Abdul
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Lukose, Cecil Cherian
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Brewis, Ian
1 / 1 shared
Gayara, R. A. Harindi
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Ahmed, Abdul Moiz
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Moossa, Buzaina
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Abraham, Jeffin James
1 / 1 shared
Al-Qaradawi, Siham
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2024
2023

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

document

Advancing Lithium-Ion Battery Anodes: Novel Sn and Hard Carbon Architectures for Long-Term Stability and High Capacity

  • Rasul, Shahid
  • Zia, Abdul Wasy
  • Shakoor, Rana Abdul
  • Shahzad, Rana Faisal
Abstract

Tin (Sn) is a promising candidate for lithium-ion batteries (LIBs) because of its high theoretical capacity, abundance, and low cost. However, Sn suffers from large volumetric expansion during charging and discharging causing cracking and degradation of the electrode material. Thus, development of new Sn based interfaces and architectures is crucial that can accommodate the volume changes and improve cyclic performance. In this study, we present the development of a novel Sn and hard carbon (h-carbon) architectures for LIB anodes, with a focus on improving their long-term stability and high capacity. The composite architectures is achieved through nano Physical Vapor Deposition (nano-PVD) technique by depositing Sn and hard carbon on Copper substrate at the room temperature and a high temperature (470 oC). Our results show that the Sn and h-carbon architectures exhibit significantly improved long-term cycling stability (> 94% coulombic efficiency after 25 cycles) and higher capacities reaching upto 915 mAh g-1 at 2nd cycle after SEI formation. The resultant microstructures especially at 400 oC created a multi-layer interface with Cu-Sn and h-carbon. The newly developed, so called soft (Cu-Sn) and a hard interface (h-Carbon) provides a cushion against volumetric expansion of Sn microstructures. These findings demonstrate the potential of Sn and hard carbon as promising anode materials for advancing the performance of LIBs.

Topics
  • impedance spectroscopy
  • microstructure
  • Carbon
  • physical vapor deposition
  • composite
  • copper
  • Lithium
  • tin