Abstract

Commercialization of lead halide perovskite-based devices is hindered by their instability towards environmental conditions. In particular, water promotes fast decomposition, leading to a drastic decrease in device performance. Integrating water-splitting active species within ancillary layers to the perovskite absorber might be a solution to this, as they could convert incoming water into oxygen and hydrogen, preserving device performance. Here, we suggest that a CuSCN nanoplatelete/p-type semiconducting polymer composite, combining hole extraction and transport properties with water oxidation activity, transforms incoming water molecules and triggers the in situ p-doping of the conjugated polymer, improving transport of photocharges. Insertion of the nanocomposite into a lead perovskite solar cell with a direct photovoltaic architecture causes stable device performance for 28 days in high-moisture conditions. Our findings demonstrate that the engineering of a hole extraction layer with possible water-splitting additives could be a viable strategy to reduce the impact of moisture in perovskite devices.

Highlights

  • Commercialization of lead halide perovskite-based devices is hindered by their instability towards environmental conditions

  • We demonstrate that CuSCN@P3HT could work as a WS-active combination for preventing the moisturemediated degradation of a perovskite solar cell (PSC) and for the concomitant in situ p-doping of the P3HT hole-transporting material (HTM) phase, that further affects favorably the figures of merit of the direct architecture PSC in which it is integrated

  • The synthesis of surfactant-free CuSCN-NP was performed by continuous flow hydrothermal synthesis (CFHS), as reported in detail in the “Methods” section and schematized in Supplementary Fig. 1

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Summary

Introduction

Commercialization of lead halide perovskite-based devices is hindered by their instability towards environmental conditions.

Results
Conclusion
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