Spontaneous crystal coalescence enables highly efficient perovskite solar cells

被引:66
作者
Roose, Bart [1 ]
Ummadisingu, Amita [2 ]
Correa-Baena, Juan-Pablo [3 ]
Saliba, Michael [2 ]
Hagfeldt, Anders [3 ]
Graetzel, Michael [2 ]
Steiner, Ullrich [1 ]
Abate, Antonio [1 ,4 ]
机构
[1] Adolphe Merkle Inst, Chemin Verdiers 4, CH-1700 Fribourg, Switzerland
[2] Ecole Polytech Fed Lausanne, Swiss Fed Inst Technol, Lab Photon & Interfaces, Stn 6, CH-1015 Lausanne, Switzerland
[3] Ecole Polytech Fed Lausanne, Swiss Fed Inst Technol, Lab Photomol Sci, Stn 6, CH-1015 Lausanne, Switzerland
[4] Helmholtz Zentrum Berlin Mat & Energie, Kekulestr 5, D-12489 Berlin, Germany
基金
瑞士国家科学基金会;
关键词
Perovskite solar cell; Photovoltaics; Coalescence; Aging; Ion migration; Hysteresis; FILM MORPHOLOGY; PHOTOLUMINESCENCE; CRYSTALLIZATION; PERFORMANCE; IMPACT; DYE;
D O I
10.1016/j.nanoen.2017.06.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Perovskite solar cells have recently reached staggering efficiencies, through efforts focused on reducing grain boundaries, by enlarging the size of the crystalline domains that constitute the perovskite films. Here, we demonstrate that smaller crystallites within perovskite films spontaneously coalesce into larger ones, even when complete devices are stored in the dark at room temperature. We show that crystal coalescence greatly improves the performance of state-of-the-art perovskite solar cells. Our results reveal the dynamic nature of the morphology of perovskite films and highlight the crucial role that coalescence plays in producing highly efficient devices.
引用
收藏
页码:24 / 29
页数:6
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