posted on 2017-08-30, 00:00authored byYinghong Hu, Meltem F. Aygüler, Michiel L. Petrus, Thomas Bein, Pablo Docampo
Rubidium and cesium cations have
been recently identified as enhancers
for perovskite solar cell performance. However, the impact of these
inorganic cations on the stability of the (FA<sub>0.83</sub>MA<sub>0.17</sub>)Pb(I<sub>0.83</sub>Br<sub>0.17</sub>)<sub>3</sub> perovskite
crystal lattice has not been fully understood yet. Here, we show via
in situ X-ray diffraction and energy-dispersive X-ray spectrometry
measurements that the unsuitably small ionic radius of Rb<sup>+</sup> can lead to several nonphotoactive side-products. During the perovskite
film synthesis, RbPb(I<sub>1–<i>x</i></sub>Br<sub><i>x</i></sub>)<sub>3</sub> is formed, while exposure to
humid air leads to the rapid formation of another hitherto unreported
side phase (RbPb<sub>2</sub>I<sub>4</sub>Br). The formation of the
Rb-rich side phases not only results in a loss of light absorption
but also extracts bromide ions from the photoactive perovskite phase,
thereby reducing its band gap. In comparison, the moisture-assisted
formation of a CsPb<sub>2</sub>I<sub>4</sub>Br phase upon Cs-addition
occurs on a significantly longer time scale than its Rb analog. While
the incorporation of Cs<sup>+</sup> remains attractive for high-performance
solar cells, the severe moisture-sensitivity of Rb-containing mixed-halide
perovskites may create additional engineering challenges.