Nanotechnology

Energy conversion efficiency

Formamidinium

Photovoltaics

Crystallography

Biology

Perovskite (structure)

Luminescence

Band gap

Halide

Inorganic chemistry

Chemistry

Ecology

Materials science

Layer (electronics)

Photovoltaic system

Photoluminescence

Passivation

Optoelectronics

Nature

Modifying the surfaces and grain boundaries of perovskites with passivating potassium halide layers can mitigate non-radiative losses and photoinduced ion migration, increasing luminescence yields and improving charge transport and interfaces with device electrodes. Metal halide perovskites have excellent optoelectronic properties and are cheap and easy to manufacture, making them potential rivals for leading optoelectronic technologies. Solar cells are one promising direction, with efficiencies greater than 20% already achieved within just a few years. Despite this, luminescence yields in state-of-the-art perovskite solar cells are still far below 100%, so there is room for improvement. Samuel Stranks and colleagues decorate the surfaces and grain boundaries of perovksites with passivating potassium halide layers. This reduced parasitic non-radiative losses and photo-induced ion migration—two key causes of low luminescence yields. They applied this approach to a wide range of mixed halide perovskites, which not only yielded luminescence approaching the efficiency limits, but also improved the charge transport and interfaces with device electrodes. Metal halide perovskites are of great interest for various high-performance optoelectronic applications1. The ability to tune the perovskite bandgap continuously by modifying the chemical composition opens up applications for perovskites as coloured emitters, in building-integrated photovoltaics, and as components of tandem photovoltaics to increase the power conversion efficiency2,3,4. Nevertheless, performance is limited by non-radiative losses, with luminescence yields in state-of-the-art perovskite solar cells still far from 100 per cent under standard solar illumination conditions5,6,7. Furthermore, in mixed halide perovskite systems designed for continuous bandgap tunability2 (bandgaps of approximately 1.7 to 1.9 electronvolts), photoinduced ion segregation leads to bandgap instabilities8,9. Here we demonstrate substantial mitigation of both non-radiative losses and photoinduced ion migration in perovskite films and interfaces by decorating the surfaces and grain boundaries with passivating potassium halide layers. We demonstrate external photoluminescence quantum yields of 66 per cent, which translate to internal yields that exceed 95 per cent. The high luminescence yields are achieved while maintaining high mobilities of more than 40 square centimetres per volt per second, providing the elusive combination of both high luminescence and excellent charge transport10. When interfaced with electrodes in a solar cell device stack, the external luminescence yield—a quantity that must be maximized to obtain high efficiency—remains as high as 15 per cent, indicating very clean interfaces. We also demonstrate the inhibition of transient photoinduced ion-migration processes across a wide range of mixed halide perovskite bandgaps in materials that exhibit bandgap instabilities when unpassivated. We validate these results in fully operating solar cells. Our work represents an important advance in the construction of tunable metal halide perovskite films and interfaces that can approach the efficiency limits in tandem solar cells, coloured-light-emitting diodes and other optoelectronic applications.

Maximizing and stabilizing luminescence from halide perovskites with potassium passivation