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具有抑制相分离的三卤化物宽带隙钙钛矿,用于高效串联结构。

Triple-halide wide-band gap perovskites with suppressed phase segregation for efficient tandems.

机构信息

Chemical and Biological Engineering, University of Colorado, Boulder, CO 80309, USA.

National Renewable Energy Laboratory, Golden, CO 80401, USA.

出版信息

Science. 2020 Mar 6;367(6482):1097-1104. doi: 10.1126/science.aaz5074.

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.

摘要

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。

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