Issue 41, 2017

Enhanced electronic transport in Fe3+-doped TiO2 for high efficiency perovskite solar cells

Abstract

Oxygen vacancies in non-stoichiometric TiO2 electron transport layers can capture injected electrons and act as recombination centers. In this study, the compact TiO2 electron transport layers of perovskite solar cells (PSCs) are doped with different molar ratios of Fe3+ in order to passivate such defects and improve their electron transport properties. The electrical conductivity, absorption, crystal structure, and the performance of the PSCs are systematically studied. It shows that Fe3+-doping improves the conductivity of TiO2 compact layers compared with the pristine TiO2, boosting the photovoltaic performance of PSCs. The reduced trap-filled limit voltage (VTFL) of the Fe3+-doped TiO2 compact layers suggests that trap density in the Fe3+-TiO2 films is much lower than that of a pristine TiO2 film. With the optimized doping concentration (1 mol%) of Fe3+, the best power conversion efficiency of PSCs is improved from 16.02% to 18.60%.

Graphical abstract: Enhanced electronic transport in Fe3+-doped TiO2 for high efficiency perovskite solar cells

Supplementary files

Article information

Article type
Paper
Submitted
23 Aug 2017
Accepted
15 Sep 2017
First published
18 Sep 2017

J. Mater. Chem. C, 2017,5, 10754-10760

Enhanced electronic transport in Fe3+-doped TiO2 for high efficiency perovskite solar cells

X. Gu, Y. Wang, T. Zhang, D. Liu, R. Zhang, P. Zhang, J. Wu, Z. D. Chen and S. Li, J. Mater. Chem. C, 2017, 5, 10754 DOI: 10.1039/C7TC03845C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements