Proceedings of International Conference on Perovskite Thin Film Photovoltaics and Perovskite Photonics and Optoelectronics (NIPHO24)
Publication date: 25th April 2024
Colloidal tin-based perovskite nanocrystals have gaining attention for their excellent optoelectronic properties and reduced or negligible toxicity, showing promise for various commercial applications. However, the isolation and purification of the as-synthesized all-inorganic tin-based perovskite nanocrystals remain a challenge, as they rapidly undergo decomposition in common antisolvents and an open atmosphere.[1] Here we mitigate such instabilities and endow strong resistance to antisolvent by introducing an organometallic compound (zinc diethyldithiocarbamate [Zn(DDTC)2]) during the solution-based synthesis of CsSnI3 nanocrystals. Thiourea and H2S are shown to be generated through the thermal-driven conversion of Zn(DDTC)2 during synthesis, which bind to un-passivated Sn sites on the nanocrystal surface and shields it from irreversible oxidation reactions.[2] The CsSnI3 nanocrystals resurfaced with thiourea shown great stability after two antisolvent washing cycles using methyl acetate (MeOAc), without any change in morphology, phase, and optical properties. These findings deliver an effective in-situ modification pathway during the synthesis of stable tin-based perovskites and viable platform to explore all-inorganic tin-based nanocrystals optoelectronics.
This work was supported by the Australian Research Council (ARC) Laureate Fellowship (FL190100139), Discovery Project (DP200101900), and Discovery Early Career Researcher Award (DE230100173). H. C. acknowledges financial support from the Australian Government through the Research Training Program Scholarship.