Maximizing and stabilizing luminescence from halide perovskites with potassium passivation

被引:1507
作者
Abdi-Jalebi, Mojtaba [1 ]
Andaji-Garmaroudi, Zahra [1 ]
Cacovich, Stefania [2 ]
Stavrakas, Camille [1 ]
Philippe, Bertrand [3 ]
Richter, Johannes M. [1 ]
Alsari, Mejd [1 ]
Booker, Edward P. [1 ]
Hutter, Eline M. [4 ]
Pearson, Andrew J. [1 ]
Lilliu, Samuele [5 ,6 ]
Savenije, Tom J. [4 ]
Rensmo, Hakan [3 ]
Divitini, Giorgio [2 ]
Ducati, Caterina [2 ]
Friend, Richard H. [1 ]
Stranks, Samuel D. [1 ]
机构
[1] Univ Cambridge, Dept Phys, Cavendish Lab, JJ Thomson Ave, Cambridge CB3 0HE, England
[2] Univ Cambridge, Dept Mat Sci & Met, 27 Charles Babbage Rd, Cambridge CB3 0FS, England
[3] Uppsala Univ, Dept Phys & Astron, Box 516, S-75120 Uppsala, Sweden
[4] Delft Univ Technol, Dept Chem Engn, van der Maasweg 9, NL-2629 HZ Delft, Netherlands
[5] Univ Sheffield, Dept Phys & Astron, Sheffield S3 7RH, S Yorkshire, England
[6] UAE Ctr Crystallog, Abu Dhabi, U Arab Emirates
基金
瑞典研究理事会; 欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
LEAD IODIDE PEROVSKITE; SOLAR-CELLS; THIN-FILMS; PERFORMANCE; SEGREGATION; EFFICIENCY; ABSORBER; CARRIERS; DEFECTS;
D O I
10.1038/nature25989
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:497 / +
页数:19
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