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  5. Ga<sup>3+</sup> and Y<sup>3+</sup> Cationic Substitution in Mesoporous TiO<sub>2</sub> Photoanodes for Photovoltaic Applications

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Article
en
2011

Ga<sup>3+</sup> and Y<sup>3+</sup> Cationic Substitution in Mesoporous TiO<sub>2</sub> Photoanodes for Photovoltaic Applications

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en
2011
Vol 115 (18)
Vol. 115
DOI: 10.1021/jp1121068

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Michael Graetzel
Michael Graetzel

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Aravind Kumar Chandiran
Frédéric Sauvage
Lioz Etgar
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Abstract

The optoelectronic properties of transparent nanocrystalline TiO2 films were modified by the incorporation of a low level of Ga3+ or Y3+ cations. After optimizing their relative concentration level, we were able to increase in a noticeable manner the power conversion efficiency from 7.4% to 8.1% for gallium and even to 9.0% in the case of yttrium where all three photovoltaic (PV) performance parameters were improved simultaneously. The beneficial effect of gallium and yttrium on the PV characteristics is attributed to a lower electrical resistance and longer electron lifetime enhancing the charge collection efficiency in the transparent layer. We also herein demonstrate that the substitution of the titanium site by a trivalent element in the benchmark TiO2 enables the disposal of the “magic” TiCl4(aq) post-treatment. The potential of this approach was also confirmed in solid-state PbS quantum-dot (QD) solar cells. In particular, a gallium-containing TiO2 anatase photoanode generated twice as much short-circuit photocurrent density as the standard electrode. A 1.9% power conversion efficiency has been achieved by using a solid-state heterojunction of the doped TiO2 with a 100 nm of PbS QD overlayer and using a gold back contact.

How to cite this publication

Aravind Kumar Chandiran, Frédéric Sauvage, Lioz Etgar, Michael Graetzel (2011). Ga<sup>3+</sup> and Y<sup>3+</sup> Cationic Substitution in Mesoporous TiO<sub>2</sub> Photoanodes for Photovoltaic Applications. , 115(18), DOI: https://doi.org/10.1021/jp1121068.

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Publication Details

Type

Article

Year

2011

Authors

4

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1021/jp1121068

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