Shell-in-Shell TiO2 hollow microspheres and optimized application in light-trapping perovskite solar cells

The shell-in-shell structured TiO2 hollow microspheres with enhanced light scattering ability were synthesized via a facile one step hydrothermal process. The diameter of the microsphere is about 1.5 μm, the core of the unique shell-in-shell structure is composed of TiO2 nanoparticles with a diamete...

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Veröffentlicht in:Solid state sciences 2015-02, Vol.40, p.60-66
Hauptverfasser: Sun, Hongxia, Ruan, Peng, Bao, Zhongqiu, Chen, Lei, Zhou, Xingfu
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Sprache:eng
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Zusammenfassung:The shell-in-shell structured TiO2 hollow microspheres with enhanced light scattering ability were synthesized via a facile one step hydrothermal process. The diameter of the microsphere is about 1.5 μm, the core of the unique shell-in-shell structure is composed of TiO2 nanoparticles with a diameter of about 15 nm, while the shell is constructed with ∼50 nm TiO2 nanocubes. The hollow space between the outer shell and the inner shell is about 230 nm. The formation mechanism of the unique shell-in-shell structure is interpreted. The design and the optimized application of shell-in-shell structured TiO2 hollow microspheres in the light-trapping perovskite solar cells are also investigated. Owing to the light scattering properties of the shell-in-shell structure of the hollow microsphere, the optimized photoelectrode exhibits an enhanced photoelectric conversion efficiency of 4.29% using perovskite CH3NH3PbI3 as the sensitizer. The shell-in-shell hollow TiO2 microsphere shows a 21.2% increase in conversion efficiency when compared with P25 nanoparticels photoanode. The conversion efficiency enhancement is mainly attributed to the increase of short-current density induced by the light scattering effect. [Display omitted] •Shell-in-shell structured TiO2 hollow microspheres were synthesized.•The growth mechanism of the unique structure was interpreted.•Four types of light-trapping structures were designed and optimized.•Enhanced light scattering ability increase the photoelectric conversion efficiency.
ISSN:1293-2558
1873-3085
DOI:10.1016/j.solidstatesciences.2014.12.015