journal article·2008-10

Adsorption and photocatalytic decomposition of organic molecules on carbon-coated TiO2

Tae-Won Kim, Min-Joo Lee, Wang-Geun Shim, Jae-Wook Lee, Tae-Young Kim, Dae-Haeng Lee, Hee Moon

Journal of Materials Science· Volume 43· Issue 19
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Abstract

Carbon-coated anatase TiO2 samples were prepared from the mixture of poly vinyl alcohol (PVA) and commercial TiO2 (P-25) with different mass ratios and heating temperatures. The samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), energy dispersive spectrometer (EDX), transmission electron microscope (TEM), and nitrogen adsorption analyses. The adsorption properties and photocatalytic activity of commercial and carbon-coated TiO2 catalysts were compared for the oxidation of methylene blue (MB) and bisphenol-A (BPA). It was interesting to find that the transition from anatase to rutile was suppressed by carbon coating of TiO2 at high temperature up to 800 °C. The carbon-coated TiO2 samples have a higher surface area and a greater adsorption amount than commercial P-25 because of the thin layer of carbon that covered TiO2. It was also observed that the photodecomposition efficiency was dependent on the crystallinity of the carbon-coated sample.
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Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Catalytic Processes in Materials Science

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (20)

Show source-provided references
1. Ohko Y, Ando I, Niwa C, Tatsuma T, Yamamura T, Nakamura T et al (2002) Environ Sci Technol 35:2365. doi: https://doi.org/10.1021/es001757t10.1021/es001757t ↗
2. Lee JM, Kim MS, Kim BW (2004) Water Res 38:3605. doi: https://doi.org/10.1016/j.watres.2004.05.01510.1016/j.watres.2004.05.015 ↗
3. Tryba B, Morawski AW, Tsumura T, Toyoda M, Inagaki M (2004) J Photoch Photobiol Chem (Kyoto) 167:12710.1016/j.jphotochem.2004.04.011 ↗
4. Tsumura T, Kojutani N, Umemura H, Toyoda M, Inagaki M (2002) Appl Surf Sci 196:429. doi: https://doi.org/10.1016/S0169-4332(02)00081-810.1016/S0169-4332(02)00081-8 ↗
5. Li Y, Zhang S, Yu O, Yin W (2007) Appl Surf Sci 253:9254. doi: https://doi.org/10.1016/j.apsusc.2007.05.05710.1016/j.apsusc.2007.05.057 ↗
6. Tsumura T, Kojitan N, Izumi I, Iwashita N, Toyoda M, Inagaki M (2002) J Mater Chem 12:1391. doi: https://doi.org/10.1039/b201942f10.1039/b201942f ↗
7. Tsumura T, Kojitan N, Umemura H, Toyoda M, Inagaki M (2002) Appl Surf Sci 196:429. doi: https://doi.org/10.1016/S0169-4332(02)00081-810.1016/S0169-4332(02)00081-8 ↗
8. Torimoto T, Okawa Y, Takeda N, Yoneyama H (1997) J Photoch Photobiol Chem (Kyoto) 103:15310.1016/S1010-6030(96)04503-0 ↗
9. Inagaki M, Kojin F, Tryba B, Toyoda M (2005) Carbon 43:1652. doi: https://doi.org/10.1016/j.carbon.2005.01.04310.1016/j.carbon.2005.01.043 ↗
10. Zhang X, Zhou M, Lei L (2006) Carbon 44:325. doi: https://doi.org/10.1016/j.carbon.2005.07.03310.1016/j.carbon.2005.07.033 ↗
11. Inagaki M, Imai T, Yoshikawa T, Tryba B (2004) Appl Catal B Environ 51:247. doi: https://doi.org/10.1016/j.apcatb.2004.02.01710.1016/j.apcatb.2004.02.017 ↗
12. Inagaki M, Hirose Y, Matsunaga T, Tsumura T, Toyoda M (2003) Carbon 41:2619. doi: https://doi.org/10.1016/S0008-6223(03)00340-310.1016/S0008-6223(03)00340-3 ↗
13. Li Y, Zhang S, Yu O, Yin W (2007) Appl Surf Sci 253:9254. doi: https://doi.org/10.1016/j.apsusc.2007.05.05710.1016/j.apsusc.2007.05.057 ↗
14. Fiona L, Brian R, Heather M (2002) J Photoch Photobiol Chem (Kyoto) 148:13710.1016/S1010-6030(02)00083-7 ↗
15. Jaroniec M, Madey R, Choma J, Piotrowska J (1988) J Colloid Interface Sci 125(2):561. doi: https://doi.org/10.1016/0021-9797(88)90022-710.1016/0021-9797(88)90022-7 ↗
16. Podko′scielny P, Nieszporek K, Szabelski P (2006) Colloid Surf A Physicochem Eng Aspects 277:5210.1016/j.colsurfa.2005.10.078 ↗
17. Konstantinou IK, Albanis TA (2004) Appl Catal B Environ 49:1. doi: https://doi.org/10.1016/j.apcatb.2003.11.01010.1016/j.apcatb.2003.11.010 ↗
18. Hoffman M, Martin S, Choi W, Bahnemann D (1995) Chem Rev 95:69. doi: https://doi.org/10.1021/cr00033a00410.1021/cr00033a004 ↗
19. Peral J, Domenech X, Ollis D (1997) J Chem Technol Biotechnol 70:117. doi:10.1002/(SICI)1097-4660(199710)70:2<117::AID-JCTB746>3.0.CO;2-F10.1002/(SICI)1097-4660(199710)70:2<117::AID-JCTB746>3.0.CO;2-F ↗
20. Poulios I, Aetopoulou I (1999) J Chem Technol Biotechnol 74:357. doi:10.1002/(SICI)1097-4660(199904)74:4<349::AID-JCTB5>3.0.CO;2-7