4.8 Article

Maximizing and stabilizing luminescence from halide perovskites with potassium passivation

期刊

NATURE
卷 555, 期 7697, 页码 497-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nature25989

关键词

-

资金

  1. Nava Technology Limited
  2. Nyak Technology Limited
  3. Winton Studentship
  4. ICON Studentship from Lloyd's Register Foundation
  5. European Union [PIOF-GA-2013-622630]
  6. European Research Council (ERC) under European Union [756962]
  7. Royal Society
  8. Tata Group [UF150033]
  9. Engineering and Physical Sciences Research Council (EPSRC)
  10. EPSRC
  11. ERC [25961976]
  12. Ministry of Presidential Affairs
  13. Swedish research council [20146019]
  14. Swedish foundation for strategic research
  15. Netherlands Organization for Scientific Research under Echo grant [712.014.007]

向作者/读者索取更多资源

Metal halide perovskites are of great interest for various high-performance optoelectronic applications(1). The ability to tune the perovskite bandgap continuously by modifying the chemical composition opens up applications for perovskites as coloured emitters, in building-integrated photovoltaics, and as components of tandem photovoltaics to increase the power conversion efficiency(2-4). Nevertheless, performance is limited by non-radiative losses, with luminescence yields in state-of-the-art perovskite solar cells still far from 100 per cent under standard solar illumination conditions(5-7). Furthermore, in mixed halide perovskite systems designed for continuous bandgap tunability(2) (bandgaps of approximately 1.7 to 1.9 electronvolts), photoinduced ion segregation leads to bandgap instabilities(8,9). Here we demonstrate substantial mitigation of both non-radiative losses and photoinduced ion migration in perovskite films and interfaces by decorating the surfaces and grain boundaries with passivating potassium halide layers. We demonstrate external photoluminescence quantum yields of 66 per cent, which translate to internal yields that exceed 95 per cent. The high luminescence yields are achieved while maintaining high mobilities of more than 40 square centimetres per volt per second, providing the elusive combination of both high luminescence and excellent charge transport(10). When interfaced with electrodes in a solar cell device stack, the external luminescence yielda quantity that must be maximized to obtain high efficiencyremains as high as 15 per cent, indicating very clean interfaces. We also demonstrate the inhibition of transient photoinduced ion-migration processes across a wide range of mixed halide perovskite bandgaps in materials that exhibit bandgap instabilities when unpassivated. We validate these results in fully operating solar cells. Our work represents an important advance in the construction of tunable metal halide perovskite films and interfaces that can approach the efficiency limits in tandem solar cells, coloured-light-emitting diodes and other optoelectronic applications.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据