Chemical and Biological Engineering, University of Colorado, Boulder, CO 80309, USA.
National Renewable Energy Laboratory, Golden, CO 80401, USA.
Science. 2020 Mar 6;367(6482):1097-1104. doi: 10.1126/science.aaz5074.
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.
宽带隙卤化物钙钛矿是与硅配对的有前途的半导体,用于串联太阳能电池,以实现低成本下超过 30%的功率转换效率 (PCE)。然而,宽带隙钙钛矿太阳能电池受到光致相分离和开路电压低的根本限制。我们报告了使用三卤化物合金(氯、溴、碘)制造高效的 1.67 电子伏特宽带隙钙钛矿顶电池,以调整带隙并在光照下稳定半导体。我们发现,通过用溴取代部分碘来提高氯的溶解度,从而缩小晶格参数,可以将光生载流子寿命和电荷载流子迁移率提高一倍。我们观察到,即使在 100 倍太阳光强度下照射,薄膜中的光诱导相分离也得到了抑制,在 60°C 下进行 1000 小时最大功率点 (MPP) 操作后,半透明顶电池的降解不到 4%。通过将这些顶电池与硅底电池集成,我们在面积为 1 平方厘米的 2 端单片叠层中实现了 27%的 PCE。