Abstract

The major challenge towards the commercialization of perovskite solar cells is to find an alternative stable, low-cost, and solution-processible hole transporting material to unstable and expensive 2,2’,7,7’-tetrakis-(N,N-di-p-methoxyphenylamine)− 9,9’- spirobifluorene. Despite having all prerequisite properties like the ease of synthesis, low cost, tunability of hole conductivity, the conducting polymers such as polypyrrole are hardly being explored extensively as hole-transporting materials because of their insolubility in common organic solvents. Here, a colloidal solution of hydrophobic polypyrrole nanotubes co-doped with sodium dodecylbenzenesulfonate has been developed and explored for the hole transporting layer in methylammonium lead iodide-based perovskite solar cells. The best device has shown a power conversion efficiency of 7.3% at ambient conditions and without sealing. In terms of stability, the unsealed polypyrrole-based devices maintaining 85% of the initial efficiency at relative humidity 75–80 % with over 120 h have outperformed the unencapsulated poly(3-hexylthiophene)- based devices (average power conversion efficiency ∼11 %) fabricated using the same procedure and measured under same conditions. Frequency response analysis and electroluminescent imaging reveal that the photovoltaic performance of the polypyrrole-based cells can further be improved by reducing series resistance arising due to hole transporting layers. These studies show the polypyrrole colloids as a promising low-cost solution for the hole transporting layer in perovskite solar cells.

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