Publication date: 22nd July 2026
All-perovskite multijunction solar cells promise to deliver power conversion efficiencies (PCEs) beyond the theoretical limit of single-junction devices at low fabrication costs. However, the sub-par performance of wide-bandgap perovskite subcells remains a key bottleneck limiting the efficiency gains of tandem architectures.
In this presentation, I will discuss how initial morphological and compositional disorder in as-deposited Br-rich, wide-bandgap perovskite films can be the primary cause of VOC losses and stability issues in high-bandgap perovskite solar cells. I will then present our latest mitigation strategies based on templated growth of Br-rich perovskites, which improve halide homogeneity and suppress energetic losses, achieving open-circuit voltages approaching 90% of the theoretical limit across photovoltaic bandgaps ranging from 1.8 to 2.3 eV.
Building on these advances, we demonstrate efficient monolithic all-perovskite double-junction, triple-junction, and quadruple-junction solar cells with PCEs beyond 27% at a 1 cm² device area.
