Achieving long-term stable perovskite solar cells via ion neutralization

被引:278
作者
Back, Hyungcheol [1 ,2 ]
Kim, Geunjin [1 ,2 ]
Kim, Junghwan [1 ,2 ]
Kong, Jaemin [1 ,2 ]
Kim, Tae Kyun [1 ,2 ]
Kang, Hongkyu [1 ,2 ]
Kim, Heejoo [1 ,2 ]
Lee, Jinho [3 ]
Lee, Seongyu [3 ]
Lee, Kwanghee [1 ,2 ,3 ]
机构
[1] Gwangju Inst Sci & Technol, Heeger Ctr Adv Mat, Gwangju 61005, South Korea
[2] Gwangju Inst Sci & Technol, Res Inst Solar & Sustainable Energies, Gwangju 61005, South Korea
[3] Gwangju Inst Sci & Technol, Sch Mat Sci & Engn, Gwangju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
METHYLAMMONIUM LEAD IODIDE; HYSTERESIS; EFFICIENT; PHOTOCURRENT; TRIHALIDE;
D O I
10.1039/c6ee00612d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite recent reports of high power conversion efficiency (PCE) values of over 20%, the instability of perovskite solar cells (PSCs) has been considered the most serious obstacle toward their commercialization. By rigorously exploring the self-degradation process of planar-type PSCs using typical metal electrodes (Ag or Al), we found that the corrosion of the metal electrodes by inherent ionic defects in the perovskite layers is a major origin of intrinsic device degradation even under inert conditions. In this work, we have developed a new concept of a chemical inhibition in PSCs using amine-mediated metal oxide systems and succeeded in chemically neutralizing mobile ionic defects through mutual ionic interaction. As a consequence, we realized planar-type PSCs with long-term stability that maintain nearly 80% of their initial PCEs even after 1 year (9000 h) of storage under nitrogen and 80% of their initial PCEs after 200 h in ambient conditions without any encapsulation.
引用
收藏
页码:1258 / 1263
页数:6
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