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A dopant-free donor-acceptor type semi-crystalline polymeric hole transporting material for superdurable perovskite solar cells

Cited 9 time in Web of Science Cited 9 time in Scopus
Authors

Kim, Dong Won; Choi, Min-Woo; Yoon, Won Sik; Hong, Seung Hwa; Park, Sungjin; Kwon, Ji Eon; Park, Soo Young

Issue Date
2022-06
Publisher
Royal Society of Chemistry
Citation
Journal of Materials Chemistry A, Vol.10 No.22, pp.12187-12195
Abstract
In this work, the performance of perovskite solar cell (PSC) devices using semi-crystalline polymers (PNTDT-TT, PNTDT-2T, and PNTDT-2F2T) consisting of bis-lactam 1,5-dioctyl-3,7-di(thiophen-2-yl)-1,5-naphthyridine-2,6-dione (NTDT) and different donating units depends on the crystalline nature of the polymer. The N-alkylated NTDT unit endows the final polymer with appropriate solubility without backbone distortion. Therefore, despite having strong intra- and inter-molecular interactions of PNTDT-2F2T, it can be easily processed and show much better film formability at moderate solution temperature compared with typical semi-crystalline polymers. Using fully dopant-free PNTDT-2F2T enables PSCs to achieve very high power conversion efficiencies (PCE) of 20.6% and 22.19% in MAPbI(3)- and Cs(0.05)FA(0.90)MA(0.05)PbI(2.85)Br(0.15)-based perovskites, respectively, owing to the large crystal coherence length and excellent hole mobility. The device retains nearly 90% of its initial PCE after storage at a relative humidity of similar to 90% for 1560 h. The PNTDT-2F2T-based PSCs show consistent performance even after soaking in water because of the dense packing and superior hydrophobicity of the PNTDT-2F2T film. Also, owing to the superior thermal stability, the PSC devices with PNTDT-2F2T retain over 85% of their initial efficiency after continuous thermal aging (80 degrees C) for 1008 h, whereas spiro-OMeTAD-based PSC devices exhibit irreversible severe degradation.
ISSN
2050-7488
URI
https://hdl.handle.net/10371/185816
DOI
https://doi.org/10.1039/d2ta02457h
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