Alkali metal cation incorporated Ag3BiI6absorbers for efficient and stable rudorffite solar cells

5Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Toxic lead and poor stability are the main obstacles of perovskite solar cells. Lead-free silver bismuth iodide (SBI) was first attempted as solar cells photovoltaic materials in 2016. However, the short-circuit current of the SBI rudorffite materials is commonly <10 mA/cm2, limiting the overall photovoltaic performance. Here, we present a chemical composition engineering to enhance the photovoltaic performance. In this study, we incorporated a series of alkali metal cations (Li+, Na+, K+, Rb+ and Cs+) into Ag3BiI6 absorbers to investigate the effects on the photovoltaic performance of rudorffite solar cells. Cs+ doping improved VOC and Na+ doping showed an obvious enhancement in JSC. Therefore, we co-doped Na+ and Cs+ into SBI (Na/Cs-SBI) as the absorber and investigated the crystal structure, surface morphology and optical properties. The photo-Assisted Kelvin probe force microscopy was used to measure surface potential and verified that Na/Cs doping could reduce the electron trapping at the grain boundary and facilitate electron transportation. Na/Cs-SBI reduced the electron-holes pairs recombination and promoted the carrier transport of rudorffite solar cells. Finally, the Na/Cs-SBI rudorffite solar cell not only exhibited a power conversion efficiency (PCE) of 2.50%, a 46% increase to the SBI device (PCE = 1.71%), but also was stable in ambient conditions for >6 months.

Cite

CITATION STYLE

APA

Wu, M. C., Kuo, R. Y., Chang, Y. H., Chen, S. H., Ho, C. M., & Su, W. F. (2021). Alkali metal cation incorporated Ag3BiI6absorbers for efficient and stable rudorffite solar cells. Oxford Open Materials Science, 1(1). https://doi.org/10.1093/oxfmat/itab017

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