OUR RESEARCH

Inverted perovskite solar cells are promising candidates in photovoltaic fields due to their low-temperature processing, simplified fabrication, and enhanced stability when compared with the conventional configuration. However, the significant non-radiative recombination losses and energy alignment mismatch at the perovskite/C₆₀ interface limit the device's performance and long-term stability. To overcome this drawback, we introduced trifluoromethoxy-functionalized phenethylammonium iodide salts with high polarity between the perovskite and C₆₀ electron transporting layer. This bifunctional interlayer not only effectively passivates the perovskite surface and interface but also reduces the minority carriers through the band rearrangement at this interface, thus significantly suppressing the deteriorating interfacial non-radiative recombination. The modified interlayer also facilitates electron extraction by reducing the offset between the perovskite and C₆₀, contributing to an improved photocurrent and fill factor. The resultant inverted perovskite solar cell based on a Cs_0.05FA_0.85MA_0.10Pb(I_0.95Br_0.05)₃ composition reveals a power conversion efficiency of 24.7% at the reverse scan and shows negligible efficiency loss after 600 hours of maximum power point tracking under one-sun illumination. Overall, this feasible deposition of ammonium-based interlayer establishes a successful demonstration of efficient and stable inverted devices to accelerate the commercialization of perovskite photovoltaics.

Figure 1. Characterization of perovskite films.

Figure 2. Photovoltaic performance and long-term stability of inverted perovskite solar cells.

Source:

Regulating the perovskite/C60 interface via a bifunctional interlayer for efficient inverted perovskite solar cells.

https://doi.org/10.1016/j.cej.2024.151403