Synthesis and characterization of TiO2–ZnO core–shell nanograss hetero-structure and its application in dye-sensitized solar cell (DSSC)
TiO 2 –ZnO core–shell nanograss (NG) hetero-structure comprising of small nanobranches with sharp edge multiple arms was synthesized via two-step synthesis techniques. Liquid phase deposition and dip-coating technique were employed to prepare the TiO 2 core and ZnO shell, respectively. The effect of...
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Published in | Journal of materials science. Materials in electronics Vol. 26; no. 7; pp. 4936 - 4943 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.07.2015
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | TiO
2
–ZnO core–shell nanograss (NG) hetero-structure comprising of small nanobranches with sharp edge multiple arms was synthesized via two-step synthesis techniques. Liquid phase deposition and dip-coating technique were employed to prepare the TiO
2
core and ZnO shell, respectively. The effect of the annealing temperature on the properties of TiO
2
–ZnO core–shell and the performance of the DSSC has been investigated. The FESEM characterization reveals that at the temperature above 450 °C, NG started to transform into nanoparticle and the particles size increases with temperature. Annealing temperature of 350 °C shows the perfect structure of the TiO
2
–ZnO NG. The phase transformation from amorphous to wurzite in the TiO
2
–ZnO core–shell occurs at 350 °C. Above 400 °C, the crystallinity degree of the ZnO shell decreases with the temperature. The optical absorption of the sample increases with temperature up to 450 °C and decreases due to the decrease in the thickness of the sample. The device utilizing the sample annealed at 350 °C performs the best
J
sc
and
η
of 1.04 mA cm
−2
and 0.204 %, respectively. Annealing temperature of above 350 °C caused the decrease in
η
and
J
sc
and it might due to the transformation of NG to nanoparticles and the existence of cracked-structure film. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-015-3005-4 |