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Enhanced long-term stability of perovskite solar cells by passivating grain boundary with polydimethylsiloxane (PDMS)

Authors
Kim, WoochulPark, Jong BaeKim, HyeonghunKim, KihyeunPark, JiyoonCho, SungjunLee, HeonPak, YusinJung, Gun Young
Issue Date
28-Sep-2019
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.7, no.36, pp.20832 - 20839
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MATERIALS CHEMISTRY A
Volume
7
Number
36
Start Page
20832
End Page
20839
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/62827
DOI
10.1039/c9ta06688h
ISSN
2050-7488
Abstract
Organic-inorganic hybrid perovskite solar cells (PSCs) have attracted considerable attention due to their superior power conversion efficiency (PCE), which has recently exceeded 22%. However, some issues remain regarding their use in real-life environments, with the most pressing matter being their long-term stability under humid conditions. Hybrid perovskites are naturally vulnerable to water molecules, which can induce the decomposition of perovskite photoactive chemicals such as MAPbI(3) and FAPbI(3). Therefore, to achieve commercial-level long-term PSC stability, the adsorption and infiltration of water into the perovskite films must be minimized. Herein, it is demonstrated that polydimethylsiloxane (PDMS) introduced simultaneously during perovskite spin-coating is highly beneficial to passivate the perovskite grains and adjacent grain boundaries (GBs). This not only promotes the formation of lead oxide (PbO) bonds that prevent a water-perovskite reaction, but also contributes to reducing the Pb defect density related to trap-assisted recombination. The photovoltaic performance of the prepared PDMS-passivated PSC is notably enhanced compared to a reference PSC (without PDMS), and surprisingly, more than 90% of the initial PCE (similar to 15%) is sustained after laboratory storage for 5000 h under 70% relative humidity. These results will pave the way for developing commercial perovskite optoelectronic devices.
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