Perovskite Plasticity: Exploiting Instability for Self‐Optimized Performance
Erik Garnett a
a Center for Nanophotonics, AMOLF, Science Park 104, 1098 XG Amsterdam, The Netherlands
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV24)
València, Spain, 2024 May 12th - 15th
Organizer: Bruno Ehrler
Invited Speaker Session, Erik Garnett, presentation 009
DOI: https://doi.org/10.29363/nanoge.hopv.2024.009
Publication date: 6th February 2024

Halide perovskites display outstanding photoluminescence quantum yield, tunable emission and simple deposition, which make them attractive for optoelectronics. At the same time, their facile ion migration and transformation under optical, electrical and chemical stress are seen as a major limitation. Mixed halide perovskites are particularly problematic since optical excitation can cause changes in the bandgap that are detrimental for solar cell and light-emitting diode efficiency and stability. Instead of preventing such changes, in this work I will discuss how we are exploiting photo-induced halide segregation in perovskites to enable responsive, reconfigurable and self-optimizing materials. First, I will detail how we can train a mixed halide perovskite film to give directional light emission using a nanophotonic microlens: through a self-optimized process of halide photosegregation, the system mimics the training stimulus.[1] Longer training leads to more highly directional emission, while different halide migration kinetics in the light (fast training) and dark (slow forgetting) allow for material memory. This self-optimized material performs significantly better than lithographically aligned quantum dots, because it eliminates lens-emitter misalignment and automatically corrects for lens aberrations. The system shows a combination of mimicking, improving over time, and memory, which comprise the basic requirements for learning, and give the intriguing prospect of intelligent optoelectronic materials. Second, I will show how we are trying to use this phenomenon to make self-tracking solar concentrators that can utilize diffuse light, including optical and full device simulations benchmarked by absorption and luminescence measurements.[2] I will conclude by discussing some surprising results we find in the time-dependence of photoluminescence quantum yield, which vary dramatically with slight changes in material composition and interfacial passivation layer. 

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