Microporous Sulfur–Carbon Materials with Extended Sodium Storage Window

Enis Oğuzhan Eren, Cansu Esen, Ernesto Scoppola, Zihan Song, Evgeny Senokos, Hannes Zschiesche, Daniel Cruz, Iver Lauermann, B. Kumru, More Authors

Research output: Contribution to journalArticleScientificpeer-review

21 Downloads (Pure)

Abstract

Developing high-performance carbonaceous anode materials for sodium-ion batteries (SIBs) is still a grand quest for a more sustainable future of energy storage. Introducing sulfur within a carbon framework is one of the most promising attempts toward the development of highly efficient anode materials. Herein, a microporous sulfur-rich carbon anode obtained from a liquid sulfur-containing oligomer is introduced. The sodium storage mechanism shifts from surface-controlled to diffusion-controlled at higher synthesis temperatures. The different storage mechanisms and electrode performances are found to be independent of the bare electrode material's interplanar spacing. Therefore, these differences are attributed to an increased microporosity and a thiophene-rich chemical environment. The combination of these properties enables extending the plateau region to higher potential and achieving reversible overpotential sodium storage. Moreover, in-operando small-angle X-ray scattering (SAXS) reveals reversible electron density variations within the pore structure, in good agreement with the pore-filling sodium storage mechanism occurring in hard carbons (HCs). Eventually, the depicted framework will enable the design of high-performance anode materials for sodium-ion batteries with competitive energy density.

Original languageEnglish
Article number2310196
Number of pages12
JournalAdvanced Science
Volume11
Issue number16
DOIs
Publication statusPublished - 2024

Keywords

  • anode
  • carbon
  • in-operando SAXS
  • sodium-ion battery
  • sulfur

Fingerprint

Dive into the research topics of 'Microporous Sulfur–Carbon Materials with Extended Sodium Storage Window'. Together they form a unique fingerprint.

Cite this