Despite showing great potential in lead-free green energy, tin-based perovskite materials still face challenges such as inherent material instability and energy level misalignment with the hole transport layer (HTL), which limits the advancement of tin-based perovskite solar cells (Sn-PSCs). In this work, a natural antioxidant organic small molecule, thiolactic acid (TA), is used to modify the interface between PEDOT:PSS and the tin-based perovskite film. The TA molecule can cross-link to form a network polymer and regulate the microstructure and photoelectrical characteristics of PEDOT:PSS. Meanwhile, TA contains C═O and C─S groups, which can interact with Sn to inhibit its oxidation. Moreover, the introduction of TA interfacial modification effectively improves the morphology of the perovskite film, suppresses interfacial charge recombination, and promotes carrier transport. Thus, TA-modified Sn-PSCs achieve a champion power conversion efficiency of 9.03%, surpassing 6.92% of the control PSCs. Even after being stored for 1000 h in a nitrogen atmosphere, the unencapsulated devices with TA modification still maintain 95.4% of their original PCE, compared to only 66.5% of the control devices. This study demonstrates the significance of the PEDOT:PSS/tin-perovskite interfacial modification on the efficiency and stability of Sn-PSCs.
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http://dx.doi.org/10.1021/acsami.5c01338 | DOI Listing |
ACS Appl Mater Interfaces
March 2025
Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
Rational design of high-performance catalysts for CO electroreduction is crucial for achieving carbon neutrality, yet effective modification strategies remain scarce. In this study, we present the microwave heating approach to incorporate La ions into Sn-based perovskite oxides, significantly enhancing their electrocatalytic performance for the reduction of CO to formate. Through comprehensive characterization techniques, including X-ray photoelectron spectroscopy, synchrotron radiation X-ray absorption spectroscopy, electrochemical measurements (Tafel analysis and impedance spectroscopy), and density functional theory calculations, we demonstrate that La substitution effectively modulates the Sn-O bond distance in BaSnO.
View Article and Find Full Text PDFSmall
February 2025
School of Microelectronics, University of Science and Technology of China, No. 96, Jinzhai Road, Hefei, Anhui, 230026, China.
Tin halide perovskite (THP) has emerged as a promising lead-free material for high-performance solar cells, attracting significant attention for their potential use for energy conversion. However, the rapid crystallization of THP due to its high Lewis acidity and easy oxidation of Sn leads to poor morphology and rampant defects in the resulting perovskite films. These strongly hamper the advances in efficiency and stability in THP solar cells.
View Article and Find Full Text PDFACS Appl Mater Interfaces
March 2025
Guangdong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, South China Academy of Advanced Optoelectronics, South China Normal University, Guangzhou 510006, China.
Despite showing great potential in lead-free green energy, tin-based perovskite materials still face challenges such as inherent material instability and energy level misalignment with the hole transport layer (HTL), which limits the advancement of tin-based perovskite solar cells (Sn-PSCs). In this work, a natural antioxidant organic small molecule, thiolactic acid (TA), is used to modify the interface between PEDOT:PSS and the tin-based perovskite film. The TA molecule can cross-link to form a network polymer and regulate the microstructure and photoelectrical characteristics of PEDOT:PSS.
View Article and Find Full Text PDFNano Lett
February 2025
Department of Microelectronics, University of Science and Technology of China, Hefei 230026, China.
Continuous breakthroughs have been achieved in the photoelectric conversion efficiency (PCE) of tin-based perovskite solar cells (TPSCs) in recent years. Inspired by performance improvements observed during device storage, we identified beneficial light-induced interface doping (LIID) in the TPSCs. In situ analyses using X-ray photoelectron spectroscopy and ultraviolet photoelectron spectroscopy reveal that ion migration and oxidation at the interface induce beneficial doping effects, enhancing carrier transport and significantly boosting device performance.
View Article and Find Full Text PDFMolecules
February 2025
Ruđer Bošković Institute, Bijenička 54, 10000 Zagreb, Croatia.
Two-dimensional tin halide perovskites are of significant interest for light emitting applications. Here, we investigate the effect of organic cation A on the stability of different Dion-Jacobson tin-based halide perovskites. The ASnBr materials using diammonium cation A with shorter alkyl chains are found to exhibit improved stability, exhibiting dramatic stability difference between the most stable HDASnBr, where HDA denotes 1,6-hexanediammonium, and two materials with 8- and 10-carbon alkyl chain ammonium cations.
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