Facile and fast Na-ion intercalation employing amorphous black TiO^sub 2-x^/C composite nanofiber anodes
Structural and electronic modification of titanium oxide (TiO2) nanomaterials induced by the co-introduction of fully disordered glass phase and oxygen vacancies can lead to remarkable advances in the electrode performance in emerging energy storage systems. We report on the effective co-creation of...
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Published in | Electrochimica acta Vol. 263; p. 417 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Oxford
Elsevier BV
10.02.2018
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Abstract | Structural and electronic modification of titanium oxide (TiO2) nanomaterials induced by the co-introduction of fully disordered glass phase and oxygen vacancies can lead to remarkable advances in the electrode performance in emerging energy storage systems. We report on the effective co-creation of fully amorphous nanofibers (NFs) composed of black TiO2-x and conductive carbons throughout the NF structure, and evaluate the materials as potential anodes in sodium-ion batteries. The black TiO2-x nanofiber is successfully fabricated by electrospinning a precursor solution followed by a two-step sequential thermal treatment in an air and reducing atmosphere. The NF electrode could deliver approximately two-fold higher 2nd discharge capacity and an excellent kinetic performance even under high rates compared to that delivered by anatase-structured white TiO2 NFs used as reference, because of (i) an inherent free volume in the glass phase corresponding to the enlarged Na+ sites, (ii) increased electrical conductivity (low bandgap) resulting from the presence of Ti3+, (iii) introduction of conductive carbon agents around the TiO2-x domain, and (iv) one-dimensional NF feature allowing numerous Na+ reaction sites at the electrochemical interface. We also elucidate the morphological and structural changes in the nanofibers after discharge and charge by ex-situ characterizations. |
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AbstractList | Structural and electronic modification of titanium oxide (TiO2) nanomaterials induced by the co-introduction of fully disordered glass phase and oxygen vacancies can lead to remarkable advances in the electrode performance in emerging energy storage systems. We report on the effective co-creation of fully amorphous nanofibers (NFs) composed of black TiO2-x and conductive carbons throughout the NF structure, and evaluate the materials as potential anodes in sodium-ion batteries. The black TiO2-x nanofiber is successfully fabricated by electrospinning a precursor solution followed by a two-step sequential thermal treatment in an air and reducing atmosphere. The NF electrode could deliver approximately two-fold higher 2nd discharge capacity and an excellent kinetic performance even under high rates compared to that delivered by anatase-structured white TiO2 NFs used as reference, because of (i) an inherent free volume in the glass phase corresponding to the enlarged Na+ sites, (ii) increased electrical conductivity (low bandgap) resulting from the presence of Ti3+, (iii) introduction of conductive carbon agents around the TiO2-x domain, and (iv) one-dimensional NF feature allowing numerous Na+ reaction sites at the electrochemical interface. We also elucidate the morphological and structural changes in the nanofibers after discharge and charge by ex-situ characterizations. |
Author | Lee, Jun-Seo Jang, Hye-Yeon Jung, Ji-Won Kim, Il-Doo Ryu, Won-Hee Lee, Na-Won |
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SubjectTerms | Anatase Anodes Batteries Composite materials Conductivity Electrical resistivity Electrodes Energy storage Heat treatment Nanofibers Nanomaterials Rechargeable batteries Sodium-ion batteries Storage systems System effectiveness Titanium Titanium dioxide Titanium oxides |
Title | Facile and fast Na-ion intercalation employing amorphous black TiO^sub 2-x^/C composite nanofiber anodes |
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