Type-inversion as a working mechanism of high voltage MAPbBr3(Cl)-based halide perovskite solar cells

Nir Kedem, Michael Kulbak, Thomas M. Brenner, Gary Hodes, David Cahen

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Using several metals with different work functions as solar cell back contact we identify majority carrier type inversion in methylammonium lead bromide (MAPbBr3, without intentional doping) as the basis for the formation of a p-n junction. MAPbBr3 films deposited on TiO2 are slightly n-type, whereas in a full device they are strongly p-type. The charge transfer between the metal electrode and the halide perovskite (HaP) film is shown to determine the dominant charge carrier type of the HaP and, thus, also of the final cells. Usage of Pt, Au and Pb as metal electrodes shows the effects of metal work function on minority carrier diffusion length and majority carrier concentration in the HaP, as well as on built-in voltage, band bending, and open circuit voltage (VOC) within a solar cell. VOC > 1.5 V is demonstrated. The higher the metal WF, the higher the carrier concentration induced in the HaP, as indicated by a narrower space charge region and a smaller minority carrier diffusion length. From the analysis of bias-dependent electron beam-induced currents, the HaP carrier concentrations are estimated to be ∼ 1 × 1017 cm-3 with Au and 2-3 × 1018 cm-3 with Pt. A model in which type-inversion stretches across the entire film width implies formation of the p-n junction away from the interface, near the back-contact metal electrode. This work highlights the importance of the contact metal on device performance in that contact engineering can also serve to control the carrier concentration in HaP.

Original languageEnglish
Pages (from-to)5753-5762
Number of pages10
JournalPhysical Chemistry Chemical Physics
Volume19
Issue number8
DOIs
StatePublished - 22 Feb 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© the Owner Societies 2017.

Funding

The authors thank Drs Alex Yoffe and Tatyana Bendikov of the Chemical Research Support (CRS) department for the development of the soft Pt evaporation procedure and for UPS measurements, respectively. We also thank Dr Ifat Kaplan-Ashiri and Mr Ofer Dudovitch of the CRS' Electron Microscopy Unit for their help in constructing and installing the EBIC apparatus on the SEM system. This work was supported by the Israel Ministry of Science via its Tashtyoth and Israel-China programs and by the Israel National Nano-Initiative. This research is made possible in part by the historic generosity of the Harold Perlman Family. T. M. B. thanks the WIS for an Alternative Sustainable Energy Research Initiative (AERI) postdoctoral fellowship. D. C. holds the Sylvia and Rowland Schaefer Chair in Energy Research.

FundersFunder number
Israel National Nano-Initiative
WIS
Archival Education and Research Institute
Ministry of science and technology, Israel

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