| Literature DB >> 32139537 |
Jixian Xu1,2,3, Caleb C Boyd2,4, Zhengshan J Yu5, Axel F Palmstrom2, Daniel J Witter6,2, Bryon W Larson2, Ryan M France2, Jérémie Werner6,2, Steven P Harvey2, Eli J Wolf2,4, William Weigand5, Salman Manzoor5, Maikel F A M van Hest2, Joseph J Berry2, Joseph M Luther2, Zachary C Holman5, Michael D McGehee1,2,7.
Abstract
Wide-band gap metal halide perovskites are promising semiconductors to pair with silicon in tandem solar cells to pursue the goal of achieving power conversion efficiency (PCE) greater than 30% at low cost. However, wide-band gap perovskite solar cells have been fundamentally limited by photoinduced phase segregation and low open-circuit voltage. We report efficient 1.67-electron volt wide-band gap perovskite top cells using triple-halide alloys (chlorine, bromine, iodine) to tailor the band gap and stabilize the semiconductor under illumination. We show a factor of 2 increase in photocarrier lifetime and charge-carrier mobility that resulted from enhancing the solubility of chlorine by replacing some of the iodine with bromine to shrink the lattice parameter. We observed a suppression of light-induced phase segregation in films even at 100-sun illumination intensity and less than 4% degradation in semitransparent top cells after 1000 hours of maximum power point (MPP) operation at 60°C. By integrating these top cells with silicon bottom cells, we achieved a PCE of 27% in two-terminal monolithic tandems with an area of 1 square centimeter.Entities:
Year: 2020 PMID: 32139537 DOI: 10.1126/science.aaz5074
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728