4.7 Article

Highly porous TiO2 nanofibers by humid-electrospinning with enhanced photocatalytic properties

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 790, 期 -, 页码 257-265

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2019.03.175

关键词

TiO2 nanofibers; Electrospinning; Highly porous nanofibers; Photocatalytic activity

资金

  1. Research Affairs Division at Amirkabir University of Technology [40/1080]
  2. Flagship Leap 3 research grant of Universiti Malaysia Pahang [RDU 172201]

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Development of porous TiO2 nanostructures with high surface area and porosity is an active area of research due to their versatile properties for diverse applications. Owing to the large aspect ratio of nanofibers (NFs) and their impressive properties, electrospinning has been a widely adopted technology for developing TiO2 nanofibers. Conventionally, porous electrospun ceramic nanostructures are produced by using sacrificial materials and post-sintering secondary chemical treatments. In this work, we demonstrate that porous TiO2 nanofibers (NFs) could be synthesized by optimizing the humidity in the electrospinning chamber without any post-sintering treatments and the porous TiO2 nanofibers thereby produced show high catalytic activities. Three other TiO2 structures are used as benchmark materials in this work: (i) solid TiO2 NFs, (ii) TiO2 NFs obtained by the removal of glycerin and (iii) TiO2 NFs obtained by etching TiO2/ZnO composite nanofibers. The BET surface area of the materials (ii) and (iii) did not differ much (similar to 60-63 m(2)/g); however, the porous TiO2 NFs produced in high humidity nearly thrice surface area (similar to 128 m(2)/g) than (i). To demonstrate the variation of properties of the four types of TiO2 NFs, photocatalytic degradation of methylene blue (MB) is demonstrated. Over 70% of the MB could be degraded by the materials produced by high humidity in 30 min whereas it was 30% for the benchmark materials. The strategy presented here could be adopted for synthesizing highly porous TiO2 NFs for a range of applications. (C) 2019 Elsevier B.V. All rights reserved.

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