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Dipole interlayer molecules have been incorporated into perovskite solar cells (PSCs) to enhance the energy level alignment between the perovskite and charge transport layers, improving charge extraction and device performance. However, the conventional dipole interlayer with a singular functionality is inadequate for high-efficiency PSCs with excellent long-term stability. Here, we design a functionalized dipole interlayer (FDI) between perovskite and electron transport layers that integrates multiple functionalities onto a novel dipole molecule. The FDI not only realizes the field-effect function of the conventional dipole interlayer for tuning energy level matching but also extends the function of the dipole interlayer for diminishing defects, fortifying the perovskite's resistance to moisture, and impeding the migration of I ions within the perovskite layer across perovskite interface. Consequently, FDI proves to be beneficial to air-processed PSCs under a high relative humidity of 45%, yielding enhanced power conversion efficiencies from 19.44 to 21.13%. Furthermore, unencapsulated devices exhibit excellent humidity stability and thermal stability under the standardized International Summit on Organic Photovoltaic Stability (ISOS) protocols for over 1000 h (ISOS-D-1) and 700 h (ISOS-D-2I), respectively. This work extends new functions for dipole interlayers and offers a convenient and effective approach for enhancing the performance of PSCs prepared in air environments.
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http://dx.doi.org/10.1021/acsami.5c09592 | DOI Listing |
ACS Nano
September 2025
Department of Physics, National University of Singapore, Singapore 117551, Singapore.
Two-dimensional ferroelectrics with large out-of-plane polarization (OOP) are promising for the design of low-power memory and logic devices, but their experimental realization remains limited due to the scarcity of homobilayers and the complexity of heterobilayers. Here, we perform high-throughput screening of 24,960 configurations and identify 43 semiconducting heterobilayer ferroelectrics with an OOP exceeding the experimentally reported value in MoS/WS while maintaining sliding barriers below 100 meV/f.u.
View Article and Find Full Text PDFChemSusChem
August 2025
School of Chemistry and Chemical Engineering, Yangzhou University, 180 Si-Wang-Ting Road, Yangzhou, 225002, P. R. China.
In recent years, p-type CuFeO delafossite has attracted considerable interest as a cost-effective H evolution photocatalyst. However, the intrinsic alternating CuO/FeO layered architecture creates a high energy barrier for interlayer charge transfer, which causes rapid bulk recombination of photogenerated electron-hole pairs, severely limiting their photocatalytic reactivity. In this study, CuFeO nanosheets are designed with electron-rich Co sites, which induced enhancement of dipole moment and thereby built-in electric field driving charge separation efficiently.
View Article and Find Full Text PDFSci Rep
August 2025
Department of Physics, Soongsil University, Seoul, 06978, Korea.
The structural asymmetry of Janus transition metal dichalcogenides gives rise to physical properties distinct from those of their symmetric counterparts. When Janus transition metal dichalcogenides are vertically stacked, their resulting heterostructure exhibits novel and enhanced electronic properties due to interactions between interfacial atoms, changes in electric dipole moments, and van der Waals interlayer interactions. In this study, we employ first-principles calculations based on density functional theory using the Vienna Ab initio Simulation Package to investigate the electronic properties of MoSSe-WSSe vertical Janus transition metal dichalcogenides heterostructures.
View Article and Find Full Text PDFACS Nano
September 2025
School of Materials Science and Engineering, Harbin Institute of Technology, Harbin 150001, China.
As an efficient two-dimensional nonlinear optical crystal, 3R-MoS exhibits intrinsic bulk second-order nonlinearity with substantial second harmonic generation (SHG) due to the interfacial charge transfer induced interlayer dipole and intralayer intrinsic asymmetric dipole. However, how these dipoles determine the SHG emission dipole orientation and intensity in 3R-MoS has not been clearly resolved. Here, we accurately determine the coexistence of in-plane and out-of-plane SHG emission dipoles in few-layer 3R-MoS through radial-/azimuthal-polarization excitation SHG measurements and back focal plane (BFP) imaging combined with numerical simulations, where the SHG emission dipole orientation () in real space for 3L, 4L, 5L, and 6L 3R-MoS is determined to be ∼8°, ∼16°, ∼20°, and ∼32°, respectively.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States.
Interfacial charge transfer at electrocatalyst/semiconductor (EC/SC) junctions is central to the performance of photo(electro)catalysts, yet the influence of the reactive environment on these processes remains poorly understood. This is particularly the case for unburied EC/SC junctions, such as EC nanoparticles anchored on a SC (np-EC/SC), where reacting molecules readily access the EC surface sites and the np-EC/SC interfaces. Herein, we uncover a dynamic, chemically driven mechanism by which the local reaction environment modulates charge transfer at Pt/p-Si interfaces under solar water splitting conditions.
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