Passivating Surface Defects and Reducing Interface Recombination in CuInS2 Solar Cells by a Facile Solution Treatment

11Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Interface recombination at the absorber surface impedes the efficiency of a solar cell with an otherwise excellent absorber. The internal voltage or quasi-Fermi-level splitting (qFLs) measures the quality of the absorber. Interface recombination reduces the open-circuit voltage (VOC) with respect to the qFLs. A facile solution-based sulfur postdeposition treatment (S-PDT) is explored to passivate the interface of CuInS2 grown under Cu-rich conditions, which show excellent qFLs values, but much lower VOCs. The absorbers are treated in S-containing solutions at 80 °C. Absolute calibrated photoluminescence and current–voltage measurements demonstrate a reduction of the deficit between qFLs and VOC by almost one-third compared with the untreated device. Temperature dependence of the open-circuit voltage shows increased activation energy for the dominant recombination path, indicating less interface recombination. In addition, capacitance transients reveal the presence of slow metastable defects in the untreated solar cell. The slow response is considerably reduced by the S-PDT, suggesting passivation of these slow metastable defects. The results demonstrate the effectiveness of solution-based S-treatment in passivating defects, presenting a promising strategy to explore and reduce defect states near the interface of chalcogenide semiconductors.

Cite

CITATION STYLE

APA

Sood, M., Lomuscio, A., Werner, F., Nikolaeva, A., Dale, P. J., Melchiorre, M., … Siebentritt, S. (2021). Passivating Surface Defects and Reducing Interface Recombination in CuInS2 Solar Cells by a Facile Solution Treatment. Solar RRL, 5(4). https://doi.org/10.1002/solr.202100078

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free