Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.
DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.
Incorporating low band gap bulky π-conjugated organic spacers into layered 2D lead halide perovskites can enable tunable, high-performance optoelectronic materials but has been limited to a few examples due to challenges integrating bulky cations into the layered structure. Here we present a general strategy employing a secondary small organic spacer to assist formation of layered perovskites containing bulky cations. Using naphthalene diimide hexyldiammonium (NDI-dH 2+) as a model, we show that an assisting spacer, phenylethylammonium, even at >100 mol % loading, surprisingly does not primarily form its own perovskite phase but instead significantly improves crystallinity of (NDI-dH)PbI 4 and charge transport. Carrier transport increases up to an order of magnitude, with out-of-plane mobility reaching 8.6 × 10 −3 cm 2 V −1 s −1. This approach also enables incorporation of divalent 5bromoisoindigo hexyldiammonium (5BrISO-dH 2+), which otherwise degrades during iodide formation, suggesting a valuable route for integrating novel bulky π-conjugated spacers into perovskites for next-generation tunable optoelectronics.