Unraveling the Positive Effects of Glycine Hydrochloride on the Performance of Pb–Sn-Based Perovskite Solar Cells

Journal article (2024)

Authors

Lana M. Kessels Eindhoven University of Technology
Willemijn H.M. Remmerswaal Eindhoven University of Technology
L.M. van der Poll ChemE/Opto-electronic Materials - AS
Laura Bellini Eindhoven University of Technology
L.J. Bannenberg RID/TS/Instrumenten groep
Martijn M. Wienk Eindhoven University of Technology
T.J. Savenije ChemE/Opto-electronic Materials - AS
René A.J. Janssen DIFFER – Dutch Institute for Fundamental Energy Research, Eindhoven University of Technology
Research Group
ChemE/Opto-electronic Materials (AS) (TU Delft)
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Published Date

2024

Language

English

Faculty

Applied Sciences

Department

ChemE/Chemical Engineering

Research Group

ChemE/Opto-electronic Materials

Abstract

Additives are commonly used to increase the performance of metal-halide perovskite solar cells, but detailed information on the origin of the beneficial outcome is often lacking. Herein, the effect of glycine hydrochloride is investigated when used as an additive during solution processing of narrow-bandgap mixed Pb–Sn perovskites. By combining the characterization of the photovoltaic performance and stability under illumination, with determining the quasi-Fermi level splitting, time-resolved microwave conductivity (TRMC), and morphological and elemental analysis a comprehensive insight is obtained. Glycine hydrochloride is able to retard the oxidation of Sn2+ in the precursor solution, and at low concentrations (1–2 mol%) it improves the grain size distribution and crystallization of the perovskite, causing a smoother and more compact layer, reducing non-radiative recombination, and enhancing the lifetime of photogenerated charges. These improve the photovoltaic performance and have a positive effect on stability. By determining the quasi-Fermi level splitting on perovskite layers without and with charge transport layers it is found that glycine hydrochloride primarily improves the bulk of the perovskite layer and does not contribute significantly to passivation of the interfaces of the perovskite with either the hole or electron transport layer (ETL).