Decoupling the effects of defects on efficiency and stability through phosphonates in stable halide perovskite solar cells
Loading...
Date
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier BV
https://doi.org/10.1016/j.joule.2021.04.003
https://doi.org/10.1016/j.joule.2021.04.003
Abstract
Description
The understanding of defects is of paramount importance for the development of stable halide
perovskite solar cells (PSCs). However, isolating their distinctive effects on the device efficiency and
stability is currently a challenge. Here, we report that adding the organic molecule 3-
phosphonopropionic acid (H3pp) to the halide perovskite precursor solution results in unchanged
overall optoelectronic performance while having a tremendous impact on the stability of the halide
perovskite by means of ion immobilization. As a result, we obtained PSCs with ~21 % efficiency and
outstanding operational stability, retaining nearly 100 % of the initial efficiency after 1000 h at the
maximum power point under simulated AM1.5 illumination. The strong interaction between the
perovskite and the H3pp molecule through two types of hydrogen bonds (H…
I and O…H) from the
phosphonate group allows immobilization of ions that leads to remarkable device stability. This
binding mode results in shallow point defect passivation that has a significant impact on the device
stability but not on the nonradiative recombination and device efficiency. We expect that
decoupling the effect of defects on the efficiency and stability will have important implications for
the current understanding and advancement of operational PSCs.