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Cited 25 time in webofscience Cited 27 time in scopus
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Vapor-Assisted Ex-Situ Doping of Carbon Nanotube towards Efficient and Stable Perovskite Solar Cells

Authors
Lee, Jin-WookJeon, IlLin, Hao-ShengSeo, SeungjuHan, Tae HeeAnisimov, AntonKauppinen, Esko I.Matsuo, YutakaMaruyama, ShigeoYang, Yang
Issue Date
Apr-2019
Publisher
AMER CHEMICAL SOC
Keywords
Perovskite; carbon nanotube; doping; stability; electrode
Citation
NANO LETTERS, v.19, no.4, pp.2223 - 2230
Indexed
SCIE
SCOPUS
Journal Title
NANO LETTERS
Volume
19
Number
4
Start Page
2223
End Page
2230
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/14215
DOI
10.1021/acs.nanolett.8b04190
ISSN
1530-6984
Abstract
Single-walled carbon nanotubes (CNTs) has been considered as a promising material for a top electrode of perovskite solar cells owing to its hydrophobic nature, earth-abundance, and mechanical robustness. However, its poor conductivity, a shallow work function, and nonreflective nature have limited further enhancement in power conversion efficiency (PCE) of top CNT electrode-based perovskite solar cells. Here, we introduced a simple and scalable method to address these issues by utilizing an ex-situ vapor-assisted doping method. Trifluoromethane-sulfonic acid (TFMS) vapor doping of the free-standing CNT sheet enabled tuning of conductivity and work function of the CNT electrode without damaging underneath layers. The sheet resistance of the CNT sheet was decreased by 21.3% with an increase in work function from 4.75 to 4.96 eV upon doping of TFMS. In addition, recently developed 2D perovskite-protected Cs-containing formamidium lead iodide (FACsPbI(3)) technology was employed to maximize the absorption. Because of the lowered resistance, better energy alignment, and improved absorption, the CNT electrode-based PSCs produced a PCE of 17.6% with a J(SC) of 24.21 mA/cm(2), V-OC of 1.005 V, and FF of 0.72. Furthermore, the resulting TFMS-doped CNT-PSCs demonstrated higher thermal and operational stability than bare CNT and metal electrode-based devices.
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