Enhancing Surface Modification and Carrier Extraction in Inverted Perovskite Solar Cells via Self-Assembled Monolayers
Gisung Kim,
Hyojung Kim,
Mijoung Kim,
Jaegwan Sin,
Moonhoe Kim,
Jaeho Kim,
Haoran Zhou,
Sung Ho Kang,
Hye Min Oh,
JungYup Yang
Affiliations
Gisung Kim
Korea Institute of Fusion Energy (KFE), Daejeon 34133, Republic of Korea
Hyojung Kim
The Institute of Basic Science, Kunsan National University, Gunsan 54150, Republic of Korea
Mijoung Kim
Department of Physics, Kunsan National University, Gunsan 54150, Republic of Korea
Jaegwan Sin
Department of Physics, Kunsan National University, Gunsan 54150, Republic of Korea
Moonhoe Kim
Department of Physics, Kunsan National University, Gunsan 54150, Republic of Korea
Jaeho Kim
Department of Physics, Kunsan National University, Gunsan 54150, Republic of Korea
Haoran Zhou
Renewable Energy Materials Laboratory (REML), Advanced Institute of Convergence Technology (AICT), Seoul National University, Suwon 16229, Republic of Korea
Sung Ho Kang
Renewable Energy Materials Laboratory (REML), Advanced Institute of Convergence Technology (AICT), Seoul National University, Suwon 16229, Republic of Korea
Hye Min Oh
Department of Physics, Kunsan National University, Gunsan 54150, Republic of Korea
JungYup Yang
Department of Physics, Kunsan National University, Gunsan 54150, Republic of Korea
Perovskite solar cells (PSCs) have been significantly improved by utilizing an inorganic hole-transporting layer (HTL), such as nickel oxide. Despite the promising properties, there are still limitations due to defects. Recently, research on self-assembled monolayers (SAMs) is being actively conducted, which shows promise in reducing defects and enhancing device performance. In this study, we successfully engineered a p-i-n perovskite solar cell structure utilizing HC-A1 and HC-A4 molecules. These SAM molecules were found to enhance the grain morphology and uniformity of the perovskite film, which are critical factors in determining optical properties and device performance. Notably, HC-A4 demonstrated superior performance due to its distinct hydrophilic properties with a contact angle of 50.3°, attributable to its unique functional groups. Overall, the HC-A4-applied film exhibited efficient carrier extraction properties, attaining a carrier lifetime of 117.33 ns. Furthermore, HC-A4 contributed to superior device performance, achieving the highest device efficiency of 20% and demonstrating outstanding thermal stability over 300 h.