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Centrifugally Spun Binder-Free N, S-Doped Ge@PCNF Anodes for Li-Ion and Na-Ion Batteries

  • Meltem Yanilmaz*
  • , Göktuğ Cihanbeyoğlu
  • , Juran Kim*
  • *Corresponding author for this work
  • Istanbul Technical University
  • Korea Institute of Industrial Technology

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Germanium has a high theoretical capacity as an anode material for sodium-ion batteries. However, germanium suffers from large capacity losses during cycling because of the large volume change and loss of electronic conductivity. A facile way to prepare germanium anodes is critically needed for next-generation electrode materials. Herein, centrifugally spun binder-free N, S-doped germanium@ porous carbon nanofiber (N, S-doped Ge@ PCNFs) anodes first were synthesized using a fast, safe, and scalable centrifugal spinning followed by heat treatment and N, S doping. The morphology and structure of the resultant N, S-doped Ge@ PCNFs were investigated by scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray mapping, Raman spectroscopy, and X-ray diffraction, while electrochemical performance of N, S-doped Ge@ PCNFs was studied using galvanostatic charge-discharge tests. The results demonstrate that a nanostructured Ge homogeneously distributed on tubular structured porous carbon nanofibers. Moreover, N, S doping via thiourea treatment is beneficial for lithium- and sodium-ion kinetics. While interconnected PCNFs buffered volume change and provided fast diffusion channels for Li ions and Na ions, N, S-doped PCNFs further improved electronic conductivity and thus led to higher reversible capacity with better cycling performance. When investigated as an anode for lithium-ion and sodium-ion batteries, high reversible capacities of 636 and 443 mAhg-1, respectively, were obtained in 200 cycles with good cycling stability. Centrifugally spun binder-free N, S-doped Ge@ PCNFs delivered a capacity of 300 mAhg-1 at a high current density of 1 A g-1, indicating their great potential as an anode material for high-performance sodium-ion batteries.

Original languageEnglish
Pages (from-to)16987-16995
Number of pages9
JournalACS Omega
Volume8
Issue number19
DOIs
Publication statusPublished - 16 May 2023

Bibliographical note

Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society

Funding

This research was supported by the ITU BAP (MYL-2021-43302) and the Korea Institute of Industrial Technology (PEM23020).

FundersFunder number
Korea Institute of Industrial TechnologyPEM23020
Bilimsel Araştırma Projeleri Birimi, İstanbul Teknik ÜniversitesiMYL-2021-43302

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 7 - Affordable and Clean Energy
      SDG 7 Affordable and Clean Energy

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