Abstract

Perovskite solar cells represent a highly promising third-generation photovoltaic technology. However, their practical implementation is hindered by low device operational stability, mostly related to facile degradation of the absorber materials under exposure to light and elevated temperatures. Improving the intrinsic stability of complex lead halides is a big scientific challenge, which might be addressed using various “molecular modifiers”. These modifiers are usually represented by some additives undergoing strong interactions with the perovskite absorber material, resulting in enhanced solar cell efficiency and/or operational stability. Herein, we present a derivative of 1,4,6,10-tetraazaadamantane, NAdCl, as a promising molecular modifier for lead halide perovskites. NAdCl spectacularly improved both the thermal and photochemical stability of methylammonium lead iodide (MAPbI3) films and, most importantly, prevented the formation of metallic lead Pb0 as a photolysis product. NAdCl improves the electronic quality of perovskite films by healing the traps for charge carriers. Furthermore, it strongly interacts with the perovskite framework and most likely stabilizes undercoordinated Pb2+ ions, which are responsible for Pb0 formation under light exposure. The obtained results feature 1,4,6,10-tetraazaadamantane derivatives as highly promising molecular modifiers that might help to improve the operational lifetime of perovskite solar cells and facilitate the practical implementation of this photovoltaic technology.

Highlights

  • Perovskite solar cells have recently attracted tremendous attention among academic and industry research communities due to their impressive efficiency records, surpassing25.5% and coming close to the performance of the best laboratory samples of crystalline silicon solar cells [1]

  • 2D/3D architectures by introducing additional amounts of ammonium salts, usually with bulky organic cations [26,27,28]. It has been reported in a number of studies that decreasing the dimensionality of the perovskite lattice improves the ambient stability of the absorber materials, as well as the operational stability of perovskite solar cells [29,30,31]

  • Similar electronic effects were observed in X-ray photoelectron spectroscopy (XPS) spectra and were reported previously [52,53] as signatures of strong electronic interactions between the introduced molecular modifier and the entire perovskite framework

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Summary

Introduction

Perovskite solar cells have recently attracted tremendous attention among academic and industry research communities due to their impressive efficiency records, surpassing. 2D/3D architectures by introducing additional amounts of ammonium salts, usually with bulky organic cations [26,27,28] It has been reported in a number of studies that decreasing the dimensionality of the perovskite lattice improves the ambient stability of the absorber materials, as well as the operational stability of perovskite solar cells [29,30,31]. Loading perovskite films with either pristine adamantane or 1-adamantylamine resulted in passivation of the surface defects at the grain boundaries and improvements in the solar cell open-circuit voltage (VOC ) and power conversion efficiency (PCE) [32]. This modification substantially increased the hydrophobicity of perovskite films and improved their ambient stability.

Results
40 I40119
MA39 Pb40 I119 Cl2 films well-defined grain boundaries
O white light with a power of
MA39 Pb40 Iintensity
Discussion
Materials
Synthesis and Characterization of solution
Preparation of the MAPbI3 and NAd2 MA39 Pb40 I119 Cl2 Films
Aging Experiments
Characterization Techniques
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