Design and synthesis of interconnected hierarchically porous anatase titanium dioxide nanofibers as high-rate and long-cycle-life anodes for lithium-ion batteries

Min Su Jo, Gi Dae Park, Yun Chan Kang, Jung Sang Cho

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

We suggest an efficient and simple synthetic strategy to prepare interconnected hierarchically porous anatase TiO2 (IHP-A-TiO2) nanofibers by two synergetic effects: phase separation between polymers and relative humidity control during electrospinning. The macro channels formed by polystyrene decomposition were interconnected by numerous mesopores that were formed by evaporation of infiltrated water vapor in the structure. The resulting IHP-A-TiO2 nanofibers showed better Li+ ion storage performances than the TiO2 materials reported in the literature. The discharge capacity of IHP-A-TiO2 nanofibers for the 3000th cycle at 1.0 A g-1 and corresponding coulombic efficiency from the 20th cycle onward were 142 mA h g-1 and >99.0%, respectively. Well-interconnected, ultrafine TiO2 nanocrystals within the nanofiber showed structural stability during cycling and facilitated facile charge transfer at the electrode-electrolyte interface.

Original languageEnglish
Pages (from-to)13539-13547
Number of pages9
JournalNanoscale
Volume10
Issue number28
DOIs
Publication statusPublished - 2018 Jul 28

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Nanofibers
Titanium dioxide
Life cycle
Anodes
Humidity control
Polystyrenes
Steam
Electrospinning
Phase separation
Nanocrystals
Water vapor
Electrolytes
Macros
Charge transfer
Atmospheric humidity
Polymers
Evaporation
Ions
Decomposition
Electrodes

ASJC Scopus subject areas

  • Materials Science(all)

Cite this

Design and synthesis of interconnected hierarchically porous anatase titanium dioxide nanofibers as high-rate and long-cycle-life anodes for lithium-ion batteries. / Jo, Min Su; Park, Gi Dae; Kang, Yun Chan; Cho, Jung Sang.

In: Nanoscale, Vol. 10, No. 28, 28.07.2018, p. 13539-13547.

Research output: Contribution to journalArticle

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