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Vapor-deposited inverted perovskite solar cells utilizing self-assembled monolayer (SAM) as hole transport material have gained significant attention for their high efficiencies and compatibility with silicon/perovskite monolithic tandem devices. However, as a small molecule, the SAM layer suffers low thermal tolerance in comparison with other metal oxide or polymers, rendering poor efficiency in solar device with high-temperature (> 160 °C) fabricating procedures. In this study, a dual modification approach involving AlO and F-doped phenyltrimethylammonium bromide (F-PTABr) layers is introduced to enhance the buried interface. The AlO dielectric layer improves the interface contact and prevents the upward diffusion of SAM molecules during the vapor-solid reaction at 170 °C, while the F-PTABr layer regulates crystal growth and reduces the interfacial defects. As a result, the AlO/F-PTABr-treated perovskite film exhibits a homogeneous, pinhole-free morphology with improved crystal quality compared to the control films. This leads to a champion power conversion efficiency of 21.53% for the inverted perovskite solar cells. Moreover, the encapsulated devices maintained 90% of the initial efficiency after 600 h of ageing at 85 °C in air, demonstrating promising potential for silicon/perovskite tandem application.
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http://dx.doi.org/10.1002/smtd.202401339 | DOI Listing |
Nanomicro Lett
September 2025
College of New Materials and New Energies, Shenzhen Technology University, Lantian Road 3002, Pingshan, 518118, Shenzhen, People's Republic of China.
The introduction of two-dimensional (2D) perovskite layers on top of three-dimensional (3D) perovskite films enhances the performance and stability of perovskite solar cells (PSCs). However, the electronic effect of the spacer cation and the quality of the 2D capping layer are critical factors in achieving the required results. In this study, we compared two fluorinated salts: 4-(trifluoromethyl) benzamidine hydrochloride (4TF-BA·HCl) and 4-fluorobenzamidine hydrochloride (4F-BA·HCl) to engineer the 3D/2D perovskite films.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Physical Science and Technology, College of Energy, School of Optoelectronic Science and Engineering, Soochow University, Suzhou, 215000, P. R. China.
Polymer additives exhibit unique advantages in suppressing lead leaching from perovskite solar cells (PSCs). However, polymers tend to excessively aggregate in the perovskite film, which hinders comprehensive encapsulation and disrupts charge transport efficiency, degrading lead leakage inhibition and device performance. Herein, a polymer dynamic soft encapsulation strategy driven by molecular extrusion is introduced to mitigate lead leakage in PSCs, achieved through the incorporation of poly(propylene adipate) (PPA) as a multifunctional additive in the perovskite formulation.
View Article and Find Full Text PDFAdv Mater
September 2025
Guangdong Provincial Key Laboratory of Optical Information Materials and Technology & Institute of Electronic Paper Displays, South China Academy of Advanced Optoelectronics, South China Normal University, Guangzhou, 510006, P. R. China.
Establishing a low-resistance perovskite/ITO contact using self-assembled molecules (SAMs) is crucial for efficient hole transport in perovskite solar cells (PSCs) without a pre-deposited hole-transporting layer. However, SAMs at the buried interface often encounter issues like nonuniform distribution and molecular aggregation during the extrusion process, leading to significant energy loss. Herein, a molecular hybrid bridging strategy by incorporating a novel small molecule is proposed, (2-aminothiazole-4-yl)acetic acid (ATAA), featuring a thiazole ring and carboxylic acid group, along with the commonly used SAM, 4-(2,7-dibromo-9,9-dimethylacridin-10(9H)-yl)butyl)phosphonic acid (DMAcPA), into the perovskite precursor to synergistically optimize the buried interface.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Advanced Photovoltaics Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
NiO is a p-type semiconductor widely used as a hole transport material in perovskite solar cells (PSCs), yet the impact of fabrication methods on its interfacial properties and the underlying mechanisms remains unclear. This study investigates how the fabrication process─nanoparticle precursor (NP NiO) and sputtering deposition (SP NiO)─and interfacial space charge effects influence charge transport and device performance in NiO/perovskite systems. SP NiO exhibits a higher Ni/Ni ratio and greater conductivity but induces significant hole depletion and band bending at the interface, leading to reduced open-circuit voltage and efficiency.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Research Group of Optical Properties of Materials (GPOM), Centro de Investigaciones en Óptica, León, Guanajuato 37150, Mexico.
This study presents a systematic analysis of the impact of polymer hole transport layers (HTLs) in inverted MAPbI perovskite solar cells (PSCs). Devices were fully fabricated under regular atmospheric conditions (≈40% humidity) and low temperature (100 °C) by using Field's Metal (FM) as an alternative top electrode. The widely known π-conjugated polymers P3HT, PTB7-Th, PBDB-T, and MEH-PPV were used as HTLs, and all of them show suitable energy alignment to MAPbI, offering good moisture stability, solution processability, low cost, and attractiveness for large area and flexible PSCs.
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