In the search for improvements in perovskite solar cells (PSCs), several different aspects are currently being addressed, including an increase in the stability and a reduction in the hysteresis. Both are mainly achieved by improving the cell structure, employing new materials or novel cell arrangements. We introduce a hysteresis-free low-temperature planar PSC, composed of a poly(3-hexylthiophene) (P3HT)/CuSCN bilayer as a hole transport layer (HTL) and a mixed cation perovskite absorber. Proper adjustment of the precursor concentration and thickness of the HTL led to a homogeneous and dense HTL on the perovskite layer. This strategy not only eliminated the hysteresis of the photocurrent, but also permitted power conversion efficiencies exceeding 15.3%. The P3HT/CuSCN bilayer strategy markedly improved the life span and stability of the non-encapsulated PSCs under atmospheric conditions and accelerated thermal stress. The device retained more than 80% of its initial efficiency after 100 h (60% after 500 h) of continuous thermal stress under ambient conditions. The performance and durability of the PSCs employing a polymer/inorganic bilayer as the HTL are improved mainly due to restraining perovskite ions, metals, and halides migration, emphasizing the pivotal role that can be played by the interface in the perovskite-additive hole transport materials (HTM) stack.
Rapid Oxidation of the Hole Transport Layer in Perovskite Solar Cells by A Low-Temperature Plasma
