In order to study the photoelectric properties of the adsorption of different metal atoms on a two-dimensional (2D) perovskite surface, in this article, we built many models of Ag, Au, and Bi atoms adsorbed on 2D perovskite. We studied the rules influencing 2D perovskite adsorbing metal atoms with different values (the value is the number of inorganic layers of 2D perovskite; here = 1, 2, and 3). Based on = 2 2D perovskite, we successively used Ag, Au, and Bi metal atoms to adsorb on the 2D perovskite surface. Firstly, we calculated their adsorption energies. Based on the lowest energy principle, we found that Bi atom adsorption on the 2D perovskite surface gave the most stable structure among the three metal adsorptions because the energy of the Bi adsorption system was the smallest. Secondly, the electron transport process takes place from the s to the p orbital when Au and Ag atoms adsorb on the 2D perovskite surface, but in the Bi atom adsorption, the electron transport process takes place from the p to the p orbital, because the p-p orbital transport energy is lower than that of the s-p orbital. Therefore, Bi atom adsorption on the 2D perovskite surface can improve charge carrier transfer. Thirdly, we calculated the bond angles and bond energies of different metal adsorptions on 2D perovskite. Bi adsorption has greater interaction with the surface atoms of 2D perovskite than Ag or Au atom adsorption, which effectively enhances the surface polarization effects, and enhances the photoelectric properties of 2D perovskite. The light absorption spectrum further confirms that Bi atom adsorption has a greater impact on the 2D perovskite than the action of Ag or Au adsorption. Finally, in an experiment, we fabricated a 2D perovskite solar cell with an ITO/PEDOT:PSS/2D perovskite/PEI/Ag (Au, Bi) structure. The Bi electrode solar cell achieves the highest photoelectric conversion efficiency (PCE) of 15.16% among the three cells with forward scanning, which is consistent with the theoretical analysis. We believe that the adsorption of metals like Bi on a 2D perovskite surface as an electrode is conducive to improving the charge transport performance.
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http://dx.doi.org/10.1039/d1ra04557a | DOI Listing |
Adv Mater
January 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, P. R. China.
Effective modifications for the buried interface between self-assembled monolayers (SAMs) and perovskites are vital for the development of efficient, stable inverted perovskite solar cells (PSCs) and their tandem photovoltaics. Herein, an ionic-liquid-SAM hybrid strategy is developed to synergistically optimize the uniformity of SAMs and the crystallization of perovskites above. Specifically, an ionic liquid of 1-butyl-3-methyl-1H-imidazol-3-iumbis((trifluoromethyl)sulfonyl)amide (BMIMTFSI) is incorporated into the SAM solution, enabling reduced surface roughness, improved wettability, and a more evenly distributed surface potential of the SAM film.
View Article and Find Full Text PDFLight Sci Appl
January 2025
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, China.
Perovskite quantum dots (PQDs) show promise in light-emitting diodes (LEDs). However, near-infrared (NIR) LEDs employing PQDs exhibit inferior external quantum efficiency related to the PQD emitting in the visible range. One fundamental issue arises from the PQDs dynamic surface: the ligand loss and ions migration to the interfacial sites serve as quenching centers, resulting in trap-assisted recombination and carrier loss.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London E1 4NS, U.K.
Halide perovskites have attracted recent attention as thermoelectric materials due to their low thermal conductivity combined with good charge transport characteristics. The tin halide perovskites hold the highest within metal halide perovskites and offer lower toxicity than lead-containing perovskites that are well-known for photovoltaics. In this study, we partially substitute Sn (II) with Ge (II) to form mixed metal CsSnGeI perovskite thin films that have substantially improved stability, remaining in the black orthorhombic phase after hours of ambient air exposure.
View Article and Find Full Text PDFSmall
January 2025
Dalian National Laboratory for Clean Energy, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, P. R. China.
Organic-inorganic formamidinium lead triiodide (FAPbI) hybrid perovskite quantum dots (QDs) have garnered considerable attention in the photovoltaic field due to their narrow bandgap, exceptional environmental stability, and prolonged carrier lifetime. Unfortunately, their insulating ligands and surface vacancy defects pose significant obstacles to efficient charge transfer across device interfaces. In this work, an electrostatic harmonization strategy at the interface using a donor-acceptor dipole molecular attachment to achieve enhanced charge separation capabilities on the QD surface is ventured.
View Article and Find Full Text PDFSmall
January 2025
Department of Physics, Pukyong National University, Busan, 48513, Republic of Korea.
Improving the interface characteristics between the hole-transport layer (HTL) and perovskite absorber layer is crucial for achieving maximum efficiency in inverted perovskite solar cells (PSCs). This paper presents an effective functional compensation layer (FCL) composed of benzothiophene derivatives, particularly 5-(trifluoromethyl)-1-benzothiophene-2-carboxylic acid (TFMBTA); this layer is introduced between the MeO-2PACz HTL and perovskite absorber layer to improve the interfacial characteristics between them. This FCL improves charge transfer, hole extraction, and perovskite deposition by improving the surface morphology of the HTL and optimizing the energy level alignment.
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