非阻塞I/O
材料科学
钙钛矿(结构)
结晶度
化学工程
图层(电子)
纳米技术
光电子学
化学
复合材料
催化作用
有机化学
工程类
作者
Fang Cheng,Qianqian Zhao,Fuping Zhao,Fuzhi Huang,Yong Peng,Zhiliang Ku,Yi‐Bing Cheng,Zhengyi Fu
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2022-01-01
卷期号:12 (18): 10863-10869
被引量:11
摘要
Organic-inorganic hybrid perovskite solar cells (PSCs) have attracted enormous research attention due to their high efficiency and low cost. However, most of the PSCs with high efficiencies still need expensive organic materials as their hole-transport layer (HTL). Obviously, the highly expensive materials go against the low-cost concept of advanced PSCs. In this regard, inorganic NiO x was considered as an idea HTL due to its good transmittance in the visible region and outstanding chemical stability. But for most of the PSCs with a NiO x HTL, the hole-extraction efficiency was limited by the unmatched valence band and too many surface defects of the NiO x layer, especially for the vacuum-deposited NiO x and perovskite. Herein, we developed a facile strategy to overcome this issue by using self-assembled glycine molecules to treat the NiO x surface. With glycine on the surface, the NiO x exhibited a deeper valence band maximum and a faster charge-extraction at the NiO x /perovskite interface. What's more, the vacuum-deposited perovskite showed a better crystallinity on the NiO x + glycine substrate. As a result, the PSCs with a glycine interfacial layer achieved a champion PCE of 17.96% with negligible hysteresis. This facile approach is expected to be further developed for fabricating high-efficiency PSCs on textured silicon solar cells.
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