Hostname: page-component-cd9895bd7-gbm5v Total loading time: 0 Render date: 2024-12-29T15:43:44.222Z Has data issue: false hasContentIssue false
  • English
  • Français

Effect of the Nature of the Metal Co-Catalyst on CO2 Photoreduction Using Fast-Grown Periodically Modulated Titanium Dioxide Nanotube Arrays (PMTiNTs)

Published online by Cambridge University Press:  28 June 2013

Babak Amirsolaimani ,
Xiaojiang Zhang ,
Fei Han ,
Samira Farsinezhad ,
Arash Mohammadpour ,
Greg Dechaine  and
Karthik Shankar
Babak Amirsolaimani
Affiliation:
Department of Electrical & Computer Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4.
Xiaojiang Zhang
Affiliation:
Department of Electrical & Computer Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4. Department of Chemical & Materials Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4.
Fei Han
Affiliation:
Department of Chemical & Materials Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4.
Samira Farsinezhad
Affiliation:
Department of Electrical & Computer Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4.
Arash Mohammadpour
Affiliation:
Department of Electrical & Computer Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4.
Greg Dechaine
Affiliation:
Department of Chemical & Materials Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4.
Karthik Shankar
Affiliation:
Department of Electrical & Computer Engineering, University of Alberta, 9107 - 116 St, Edmonton, AB T6G 2V4. National Institute for Nanotechnology, National Research Council, 11421 Saskatchewan Drive, Edmonton, AB, T6G 2M9, Canada.
Get access

Abstract

Anodically formed TiO2 nanotube arrays composed of the anatase phase with periodically modulated diameters (PMTiNTs) are excellent photocatalysts for the sunlight-driven transformation of carbon dioxide into hydrocarbons. Exploiting the full potential of this nanoarchitecture for CO2 photoreduction requires integration with metal nanoparticles that function as catalytic promoters for multistep electron transfer reactions. We studied the effect of different metallic and bimetallic nanoparticles on the rate of generation of light hydrocarbons by the photoreduction of CO2. All the metal nanoparticles were loaded on to the TiO2nanotubes using the technique of photodeposition, which standardized the coating process and enabled examination purely of the effect of different metals. Photodeposition was used not only due to its simplicity but also because it enabled us to engineer very fine coatings possessing excellent uniformity and depth penetration into the nanotubes. The best performing co-catalysts were found to be CuPt (atomic ratio of 0.33:0.67), Pt and NiPt (1:2), which when loaded onto the PMTiNTs yielded total hydrocarbon generation rates of 3.5, 0.85 and 0.8 mL g-1 hr-1 respectively. The time required to form PMTiNTs was reduced by a factor of 160 by using a recently reported recipe based on fluoride ion bearing electrolyte containing lactic acid. PMTiNTs formed using the ultrafast growth lactic acid-based electrolytes exhibited similar photocatalytic properties to samples obtained more slowly using conventional ethylene glycol-based electrolytes.

Keywords

photochemicalnanostructureelectrochemical synthesis
Type
Articles
Information
MRS Online Proceedings Library (OPL) , Volume 1578: Symposium YY – Titanium Dioxide—Fundamentals and Applications , 2013 , mrss13-1578-yy05-08
Copyright
Copyright © Materials Research Society 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Inoue, T.; Fujishima, A.; Konishi, S.; Honda, K. Nature 1979, 277, (5698), 637–638.CrossRefGoogle Scholar
Deinega, A.; John, S. Journal of Applied Physics 2012, 112, (7), 074327–7.CrossRefGoogle Scholar
Ouchani, N.; Bria, D.; Djafari-Rouhani, B.; Nougaoui, A. Journal of Applied Physics 2009, 106, (11), 113107–8.CrossRefGoogle Scholar
Yip, C. T.; Huang, H. T.; Zhou, L. M.; Xie, K. Y.; Wang, Y.; Feng, T. H.; Li, J. S.; Tam, W. Y. Adv. Mater. 2011, 23, (47), 5624–+.CrossRefGoogle Scholar
Zhang, X.; Han, F.; Shi, B.; Farsinezhad, S.; Dechaine, G. P.; Shankar, K. Angewandte Chemie International Edition 2012, 51, (51), 12732–12735.CrossRefGoogle Scholar
Solymosi, F.; Tombácz, I. Catal Lett 1994, 27, (1-2), 61–65.CrossRefGoogle Scholar
Varghese, O. K.; Paulose, M.; LaTempa, T. J.; Grimes, C. A. Nano Lett. 2009, 9, (2), 731–737.CrossRefGoogle Scholar
Kumar, B.; Llorente, M.; Froehlich, J.; Dang, T.; Sathrum, A.; Kubiak, C. P. Annual Review of Physical Chemistry 2012, 63, (1), 541–569.CrossRefGoogle Scholar
Hou, W.; Hung, W. H.; Pavaskar, P.; Goeppert, A.; Aykol, M.; Cronin, S. B. ACS Catalysis 2011, 1, (8), 929–936.CrossRefGoogle Scholar
Vijayakumar, K. M.; Lichtin, N. N. Journal Name: J. Catal.; (United States); Journal Volume: 90:1 1984, Medium: X; Size: Pages: 173–177.Google Scholar
Indrakanti, V. P.; Kubicki, J. D.; Schobert, H. H. Energy & Environmental Science 2009, 2, (7), 745–758.CrossRefGoogle Scholar
Wang, W.-N.; An, W.-J.; Ramalingam, B.; Mukherjee, S.; Niedzwiedzki, D. M.; Gangopadhyay, S.; Biswas, P. Journal of the American Chemical Society 2012.Google Scholar
Irie, H.; Miura, S.; Kamiya, K.; Hashimoto, K. Chem. Phys. Lett. 2008, 457, (1-3), 202–205.CrossRefGoogle Scholar
Kamiya, K.; Miura, S.; Hashimoto, K.; Irie, H. Electrochemistry 2011, 79, (10), 793–796.CrossRefGoogle Scholar
Nakajima, A.; Akiyama, Y.; Yanagida, S.; Koike, T.; Isobe, T.; Kameshima, Y.; Okada, K. Mater. Lett. 2009, 63, (20), 1699–1701.CrossRefGoogle Scholar
Pakizeh, T. The Journal of Physical Chemistry C 2011, 115, (44), 21826–21831 CrossRefGoogle Scholar