Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-26T14:13:48.979Z Has data issue: false hasContentIssue false
  • English
  • Français

Bandgap narrowing of iron oxide nanotubes upon doping with zinc and their spectral sensitivity used as photoelectrode

Published online by Cambridge University Press:  23 December 2015

Y. Kosugi ,
T. Tomiyasu  and
S. Bandow
Y. Kosugi
Affiliation:
Department of Materials Science and Engineering, Meijo University, 1-501 Shiogamaguchi, Tenpaku, Nagoya, Aichi 468-8502, Japan
T. Tomiyasu
Affiliation:
Department of Materials Science and Engineering, Meijo University, 1-501 Shiogamaguchi, Tenpaku, Nagoya, Aichi 468-8502, Japan
S. Bandow*
Affiliation:
Department of Applied Chemistry, Meijo University, 1-501 Shiogamaguchi, Tenpaku, Nagoya, Aichi 468-8502, Japan
*
*(Email: [email protected])
Get access

Abstract

Iron oxide nanotubes (NTs) and zinc doped iron oxide NTs were prepared by sol-gel method. Obtained NTs have spinel structure represented by ZnδFe3-δO4. Iron oxide NTs indicated a spectral sensitivity maximum at the wavelength of 500-550 nm and a long tail toward red light. These features were explained by a typical bandgap of iron oxide NTs to be ∼2.3 eV and bandgap narrowing for a small diameter NT. Organometal perovskite solar cell was constructed by using these NTs and evaluated by measuring the spectral sensitivity between the wavelength of 390 and 710 nm. For the present perovskite solar cell, drastic increase of the spectral sensitivity was obtained when we adjusted penetration depth of organometal perovskite into the porous layer of NTs. However, deep penetration worsened the spectral sensitivity. A similar trend was obtained for the cell using Zn doped iron oxide NTs, but the magnitude of incident power conversion efficiency (IPCE) became almost a half. This was explained by worsening the electrical conductivity, even the bandgap became narrower by Zn dope.

Keywords

photovoltaicoxidenanoscale
Type
Articles
Information
MRS Advances , Volume 1 , Issue 59: Energy and Sustainability , 2016 , pp. 3891 - 3896
Copyright
Copyright © Materials Research Society 2015 

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

Ikeda, N., Ohsumi, H., Ohwada, K., Ishii, K., Inami, T., Kakurai, K., Murakami, Y., Yoshii, K., Mori, S., Horibe, Y. and Kito, H., Nature 436, 1136 (2005).CrossRefGoogle Scholar
Zeng, Q., Bai, J., Li, J., Xia, L., Huang, K., Li, X. and Zhou, B., J. Mater. Chem. A3, 4345 (2015).CrossRefGoogle Scholar
Gilbert, B., Katz, J.E., Huse, N., Zhang, X., Frandsen, C., Falcone, R.W. and Waychunas, G.A., Phys. Chem. Chem. Phys. 15, 17303 (2013).CrossRefGoogle Scholar
Zheng, J.Y., Son, S.L., Van, T.K. and Kang, Y.S., RSC Adv. 5, 36307 (2015).CrossRefGoogle Scholar
Jung, H.S. and Park, N.-G., Small 11, 10 (2015).CrossRefGoogle Scholar
Shinde, S.S., Bansode, R.A., Bhosale, C.H. and Rajpure, K.Y., J. Semicond. 32, 013001 (2011).CrossRefGoogle Scholar
Seki, M., Takahashi, M., Ohshima, T., Yamada, H and Tabata, H., Jpn. J. Appl. Phys. 53, 05FA07 (2014).CrossRefGoogle Scholar
Kosugi, Y. and Bandow, S., J. Inorg. Organomet. Polym. 24, 933 (2014).CrossRefGoogle Scholar
Bandow, S. and Shiraki, Y., Mater. Res. Soc. Symp. Proc. 1659 (2014), doi: 10.1557/opl.2014.133.CrossRefGoogle Scholar