材料科学
串联
钙钛矿(结构)
带隙
硒化铜铟镓太阳电池
光电子学
光伏
钝化
能量转换效率
异质结
光伏系统
纳米技术
太阳能电池
电气工程
结晶学
化学
图层(电子)
复合材料
工程类
作者
Saba Gharibzadeh,Ihteaz M. Hossain,Paul Faßl,Bahram Abdollahi Nejand,Tobias Abzieher,Moritz Schultes,Erik Ahlswede,Philip Jackson,Michael Powalla,Sören Schäfer,Michael Rienäcker,Tobias Wietler,Robby Peibst,Uli Lemmer,Bryce S. Richards,Ulrich W. Paetzold
标识
DOI:10.1002/adfm.201909919
摘要
Abstract Wide‐bandgap perovskite solar cells (PSCs) with optimal bandgap ( E g ) and high power conversion efficiency (PCE) are key to high‐performance perovskite‐based tandem photovoltaics. A 2D/3D perovskite heterostructure passivation is employed for double‐cation wide‐bandgap PSCs with engineered bandgap (1.65 eV ≤ E g ≤ 1.85 eV), which results in improved stabilized PCEs and a strong enhancement in open‐circuit voltages of around 45 mV compared to reference devices for all investigated bandgaps. Making use of this strategy, semitransparent PSCs with engineered bandgap are developed, which show stabilized PCEs of up to 25.7% and 25.0% in four‐terminal perovskite/c‐Si and perovskite/CIGS tandem solar cells, respectively. Moreover, comparable tandem PCEs are observed for a broad range of perovskite bandgaps. For the first time, the robustness of the four‐terminal tandem configuration with respect to variations in the perovskite bandgap for two state‐of‐the‐art bottom solar cells is experimentally validated.
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