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Centrifugally Spun Binder-Free N, S-Doped Ge@PCNF Anodes for Li-Ion and Na-Ion Batteries
[Image: see text] 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 critical...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193401/ https://www.ncbi.nlm.nih.gov/pubmed/37214696 http://dx.doi.org/10.1021/acsomega.3c00990 |
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author | Yanilmaz, Meltem Cihanbeyoğlu, Göktuğ Kim, Juran |
author_facet | Yanilmaz, Meltem Cihanbeyoğlu, Göktuğ Kim, Juran |
author_sort | Yanilmaz, Meltem |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-10193401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101934012023-05-19 Centrifugally Spun Binder-Free N, S-Doped Ge@PCNF Anodes for Li-Ion and Na-Ion Batteries Yanilmaz, Meltem Cihanbeyoğlu, Göktuğ Kim, Juran ACS Omega [Image: see text] 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. American Chemical Society 2023-05-03 /pmc/articles/PMC10193401/ /pubmed/37214696 http://dx.doi.org/10.1021/acsomega.3c00990 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Yanilmaz, Meltem Cihanbeyoğlu, Göktuğ Kim, Juran Centrifugally Spun Binder-Free N, S-Doped Ge@PCNF Anodes for Li-Ion and Na-Ion Batteries |
title | Centrifugally Spun
Binder-Free N, S-Doped Ge@PCNF
Anodes for Li-Ion and Na-Ion Batteries |
title_full | Centrifugally Spun
Binder-Free N, S-Doped Ge@PCNF
Anodes for Li-Ion and Na-Ion Batteries |
title_fullStr | Centrifugally Spun
Binder-Free N, S-Doped Ge@PCNF
Anodes for Li-Ion and Na-Ion Batteries |
title_full_unstemmed | Centrifugally Spun
Binder-Free N, S-Doped Ge@PCNF
Anodes for Li-Ion and Na-Ion Batteries |
title_short | Centrifugally Spun
Binder-Free N, S-Doped Ge@PCNF
Anodes for Li-Ion and Na-Ion Batteries |
title_sort | centrifugally spun
binder-free n, s-doped ge@pcnf
anodes for li-ion and na-ion batteries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193401/ https://www.ncbi.nlm.nih.gov/pubmed/37214696 http://dx.doi.org/10.1021/acsomega.3c00990 |
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