Carbon as amorphous shell and interstitial dopant in mesoporous rutile TiO2: Bio-template assisted sol-gel synthesis and photocatalytic activity
Creators
- 1. Faculty of Chemical and Energy Engineering, Universiti Teknologi Malaysia, 81310, Skudai, Johor Bahru (Malaysia)
- 2. Advanced Membrane Technology Research Centre, Universiti Teknologi Malaysia, 81310, Skudai, Johor Bahru (Malaysia)
- 3. Department of Frontier Materials, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan)
- 4. Department of Chemistry, Faculty of Science and Mathematics, Universiti Pendidikan Sultan Idris, 35900, Tanjung Malim, Perak (Malaysia)
- 5. Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 Serdang, Selangor (Malaysia)
Description
Highlights: • RCM as bio-template and in-situ carbon shell and interstitial carbon doping. • Photo-sensitizers by carbonaceous layer grafted onto the surface of TiO2. • Visible light response could be tailored depending on the annealing temperature. • Photocatalytic properties and charge carrier transfer mechanism was proposed. - Abstract: Regenerated cellulose membrane was used as bio-template nanoreactor for the formation of rutile TiO2 mesoporous, as well as in-situ carbon dopant in acidified sol-gel system. The effects of calcination temperature on the physicochemical characteristic of core-shell nanostructured of bio-templated C-doped mesoporous TiO2 are highlighted in this study. By varying the calcination temperature, the thickness of the carbon shell coating on TiO2, crystallinity, surface area, and optical properties could be tuned as confirmed by HRTEM, nitrogen adsorption/desorption measurement, XRD and UV–vis-NIR spectroscopy. The results suggested that increment in the calcination temperature would lead to the band gap narrowing from 2.95 to 2.80 eV and the thickness of carbon shell increased from 0.40 to 1.20 nm. The x-ray photoelectron spectroscopy showed that the visible light absorption capability was mainly due to the incorporation of carbon dopant at interstitial position in the TiO2 to form O−Ti−C or Ti−O−C bond. In addition, the formation of the carbon core-shell nanostructured was due to carbonaceous layer grafted onto the surface of TiO2 via Ti−O−C and Ti−OCO bonds. The result indicated that bio-templated C-doped core-shell mesoporous TiO2 prepared at 300 °C exhibited the highest photocatalytic activity. It is worthy to note that, the calcination temperature provided a huge impact towards improving the physicochemical and photocatalytic properties of the prepared bio-templated C-doped core-shell mesoporous TiO2.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2016.09.145Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2016.09.145;
- PII
- S0169-4332(16)32026-8;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 393
- Journal Page Range
- p. 46-59
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48077713
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ADSORPTION; AMORPHOUS STATE; ANNEALING; CARBON; CARBON ADDITIONS; COATINGS; DESORPTION; DOPED MATERIALS; LAYERS; NANOSTRUCTURES; OPTICAL PROPERTIES; PHOTOCATALYSIS; POROUS MATERIALS; RUTILE; SHELLS; SOL-GEL PROCESS; TITANIUM OXIDES; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALLOYS; CATALYSIS; CHALCOGENIDES; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; HEAT TREATMENTS; MATERIALS; MICROSCOPY; MINERALS; NONMETALS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; PHYSICAL PROPERTIES; RADIOACTIVE MATERIALS; RADIOACTIVE MINERALS; SCATTERING; SORPTION; SPECTROSCOPY; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.