journal article·2015-04-15

Simple Ethanol Impregnation Treatment Can Enhance Photocatalytic Activity of TiO2 Nanoparticles under Visible-Light Irradiation

Lina Kong, Zhiqiang Jiang, Changhua Wang, Fangxu Wan, Yingying Li, Liangzhuan Wu, Jin-Fang Zhi, Xintong Zhang, Shijian Chen, Yichun Liu

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Abstract

Doping with impurities as well as introducing oxygen vacancies has been recognized as an important means to enhance photocatalytic activity of TiO2 under visible-light irradiation. Here we report that simple ethanol impregnation followed with mild heat treatment (150-400 °C) can color TiO2 nanoparticles and enhance visible-light photocatalytic activity of the material. The coloration and photocatalytic activity for β-naphthol and rhodamine B (RhB) degradation were observed to be dependent on heat-treatment temperature, and the highest activity as well as the most coloration was obtained at temperatures around 200 to 250 °C. Comprehensive analyses based on X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) investigations as well as first-principle density functional calculation suggest that the simple ethanol impregnation treatment leads to the generation of oxygen vacancy on TiO2 surface which should be responsible for the coloration and enhanced photocatalytic activity.
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Research context

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

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

Affiliations

Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory for UV-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024, China

School of Physics, Chongqing University, Shapingba, Chongqing 401331, China

Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, 29 Zhongguancun East Road, Haidian District, Beijing 100190, China

Funding

State Administration of Foreign Experts Affairs · Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China

References (39)

Show source-provided references
1. Asahi R. · Science · 2001 · 293 · 26910.1126/science.1061051 ↗
2. Di Valentin C. · Chem. Phys. · 2007 · 339 · 4410.1016/j.chemphys.2007.07.020 ↗
3. Di Valentin C. · J. Phys. Chem. C · 2009 · 113 · 2054310.1021/jp9061797 ↗
4. Fu R. · RSC Adv. · 2014 · 4 · 3706110.1039/C4RA06152G ↗
5. Fujishima A. · Surf. Sci. Rep. · 2008 · 63 · 51510.1016/j.surfrep.2008.10.001 ↗
6. Hong X. · Chem. Mater. · 2005 · 17 · 154810.1021/cm047891k ↗
7. Irie H. · J. Phys. Chem. B · 2003 · 107 · 548310.1021/jp030133h ↗
8. Liao W. · Electrochim. Acta · 2014 · 136 · 31010.1016/j.electacta.2014.05.091 ↗
9. Sakthivel S. · Angew. Chem., Int. Ed. · 2003 · 42 · 490810.1002/anie.200351577 ↗
10. Xing M. · Chem. Commun. · 2011 · 47 · 494710.1039/c1cc10537j ↗
11. Yu J. · Appl. Catal. B · 2009 · 90 · 59510.1016/j.apcatb.2009.04.021 ↗
12. Zou Z. · Nature · 2001 · 414 · 62510.1038/414625a ↗
13. Cho I. S. · Nat. Commun. · 2013 · 4 · 172310.1038/ncomms2729 ↗
14. Kong M. · J. Am. Chem. Soc. · 2011 · 133 · 1641410.1021/ja207826q ↗
15. Chang S.-m. · Appl. Catal. B · 2011 · 101 · 33310.1016/j.apcatb.2010.09.035 ↗
16. Chen X. · Science · 2011 · 331 · 74610.1126/science.1200448 ↗
17. Sakthivel S. · J. Phys. Chem. B · 2004 · 108 · 1938410.1021/jp046857q ↗
18. Dong J. · ACS Appl. Mater. Interfaces · 2014 · 6 · 138510.1021/am405549p ↗
19. Naldoni A. · J. Am. Chem. Soc. · 2012 · 134 · 760010.1021/ja3012676 ↗
20. Nakamura I. · J. Mol. Catal. A: Chem. · 2000 · 161 · 20510.1016/S1381-1169(00)00362-9 ↗
21. Tan H. · Nanoscale · 2014 · 6 · 1021610.1039/C4NR02677B ↗
22. Feibelman P. J. · Phys. Rev. B · 1978 · 18 · 653110.1103/PhysRevB.18.6531 ↗
23. Li Y. · ChemCatChem. · 2010 · 2 · 108210.1002/cctc.201000085 ↗
24. Panayotov D. A. · J. Phys. Chem. C · 2009 · 113 · 1568410.1021/jp9036233 ↗
25. Wachs I. E. · Phys. Chem. B · 2005 · 109 · 227510.1021/jp048839e ↗
26. Yang J. K. · Solid State Sci. · 2012 · 14 · 13910.1016/j.solidstatesciences.2011.11.010 ↗
27. He D. · ACS Appl. Mater. Interfaces · 2011 · 3 · 316710.1021/am200664y ↗
28. Kresse G. · Phys. Rev. B · 1993 · 47 · 55810.1103/PhysRevB.47.558 ↗
29. Perdew J. P. · Phys. Rev. B · 1992 · 45 · 1324410.1103/PhysRevB.45.13244 ↗
30. Sen S. K. · Chem. Phys. Lett. · 1976 · 39 · 56010.1016/0009-2614(76)80329-6 ↗
31. Cappelletti G. · Res. Lett. · 2009 · 4 · 97
32. Kumar P. M. · Thin Solid Films · 2000 · 358 · 12210.1016/S0040-6090(99)00722-1 ↗
33. Conesa J. C. · J. Phys. Chem. · 1982 · 86 · 139210.1021/j100397a035 ↗
34. Fu R. · RSC Adv. · 2014 · 4 · 3706110.1039/C4RA06152G ↗
35. Komaguchi K. · J. Phys. Chem. C · 2010 · 114 · 124010.1021/jp909678e ↗
36. Hirakawa T. · Appl. Catal., A · 2007 · 325 · 10510.1016/j.apcata.2007.03.015 ↗
37. Coronado J. M. · Catal. Today · 2007 · 123 · 3710.1016/j.cattod.2007.01.016 ↗
38. Carter E. · J. Phys. Chem. C · 2007 · 111 · 1063010.1021/jp0729516 ↗
39. Mishra V. S. · Ind. Eng. Chem. Res. · 1995 · 34 · 210.1021/ie00040a001 ↗