| Literature DB >> 30697836 |
Bao Tu1,2, Yangfan Shao2,3, Wei Chen1,4, Yinghui Wu1, Xin Li1,5, Yanling He1,3, Jiaxing Li1,3, Fangzhou Liu4, Zheng Zhang1, Yi Lin1, Xiaoqi Lan1, Leiming Xu1, Xingqiang Shi3, Alan Man Ching Ng3, Haifeng Li2, Lung Wa Chung5, Aleksandra B Djurišić4, Zhubing He1.
Abstract
Molecular doping of inorganic semiconductors is a rising topic in the field of organic/inorganic hybrid electronics. However, it is difficult to find dopant molecules which simultaneously exhibit strong reducibility and stability in ambient atmosphere, which are needed for n-type doping of oxide semiconductors. Herein, successful n-type doping of SnO2 is demonstrated by a simple, air-robust, and cost-effective triphenylphosphine oxide molecule. Strikingly, it is discovered that electrons are transferred from the R3P+ O- σ-bond to the peripheral tin atoms other than the directly interacted ones at the surface. That means those electrons are delocalized. The course is verified by multi-photophysical characterizations. This doping effect accounts for the enhancement of conductivity and the decline of work function of SnO2 , which enlarges the built-in field from 0.01 to 0.07 eV and decreases the energy barrier from 0.55 to 0.39 eV at the SnO2 /perovskite interface enabling an increase in the conversion efficiency of perovskite solar cells from 19.01% to 20.69%.Entities:
Keywords: SnO2; delocalized electrons; molecular doping; n-type; perovskite solar cells
Year: 2019 PMID: 30697836 DOI: 10.1002/adma.201805944
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849