Related Experiment Video
Updated: Jul 19, 2025

Flash Infrared Annealing for Perovskite Solar Cell Processing
Published on: February 3, 2021
Trace Doping: Fluorine-Containing Hydrophobic Lewis Acid Enables Stable Perovskite Solar Cells
Junsheng Luo1,2, Fangyan Lin1, Jianxing Xia1
1National Key Laboratory of Electronic Thin Films and Integrated Devices, School of Integrated Circuit Science and Engineering, University of Electronic Science and Technology of China, Chengdu, 610054, P. R. China.
Abstract:
With the rapid development in perovskite solar cell (PSC), high efficiency has been achieved, but the long-term operational stability is still the most important challenges for the commercialization of this emerging photovoltaic technology. So far, bi-dopants lithium bis(trifluoromethylsulfonyl)-imide (Li-TFSI)/4-tert-butylpyridine (t-BP)-doped hole-transporting materials (HTM) have led to state-of-the art efficiency in PSCs. However, such dopants have several drawbacks in terms of stability, including the complex oxidation process, undesirable ion migration and ultra-hygroscopic nature. Herein, a fluorine-containing organic Lewis acid dopant bis(pentafluorophenyl)zinc (Zn-FP) with hydrophobic property and high migration barrier has been employed as a potential alternative to widely employed bi-dopants Li-TFSI/t-BP for poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA). The resulting Zn-FP-based PSCs achieve a maximum PCE of 20.34 % with hysteresis-free current density-voltage (J-V) scans. Specifically, the unencapsulated device exhibits a significantly advanced of operational stability under the International Summit on Organic Photovoltaic Stability protocols (ISOS-L-1), maintaining over 90 % of the original efficiency after operation for 1000 h under continuous 1-sun equivalent illumination in N2 atmosphere in both forward and reverse J-V scan.
Related Concept Videos
Halogens
Alkyl Halides
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Molecular Shape and Polarity
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
ortho–para-Directing Deactivators: Halogens

