Issue 28, 2015

Study on hole-transport-material-free planar TiO2/CH3NH3PbI3 heterojunction solar cells: the simplest configuration of a working perovskite solar cell

Abstract

Perovskite solar cells have been widely investigated owing to their high efficiency and low production cost. The working principle of perovskite solar cells is also a hot research topic. Investigations show that either the microporous oxide layer or the hole transport material could be omitted (planar configuration vs. hole-transport-material-free configuration). However, it is not known if the configuration of perovskite solar cells could be further simplified. In this work, we report on a simple hole-transport-material-free planar heterojunction perovskite solar cell with the structure FTO/hole blocking layer (compact TiO2 film)/CH3NH3PbI3/Au. We achieved a power conversion efficiency of 10.04% under one sun illumination for this simple configuration of perovskite solar cells using high-quality planar CH3NH3PbI3 films grown by a well reproducible method. Capacitance–voltage measurements show that a built-in field aiding in taking out the photocurrent to the external circuit and suppressing the back reaction of electrons from the TiO2 to the CH3NH3PbI3 film was formed in the TiO2/CH3NH3PbI3 interface depletion region. Impedance spectroscopy measurements show that a transport resistance Rtr originating from the perovskite active layer was suppressed by a large number of photo-generated currents produced at the CH3NH3PbI3 layer under light illumination.

Graphical abstract: Study on hole-transport-material-free planar TiO2/CH3NH3PbI3 heterojunction solar cells: the simplest configuration of a working perovskite solar cell

Supplementary files

Article information

Article type
Paper
Submitted
21 May 2015
Accepted
08 Jun 2015
First published
10 Jun 2015

J. Mater. Chem. A, 2015,3, 14902-14909

Study on hole-transport-material-free planar TiO2/CH3NH3PbI3 heterojunction solar cells: the simplest configuration of a working perovskite solar cell

Y. Liu, S. Ji, S. Li, W. He, K. Wang, H. Hu and C. Ye, J. Mater. Chem. A, 2015, 3, 14902 DOI: 10.1039/C5TA03693C

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