Perovskite solar cells (PSCs) have received high attention in the past few years due to their terrific photovoltaic performance and potentially low production cost. However, the use of hole transport materials (HTMs) with hygroscopic dopants, which cause the inevitable instability of device performance, has hampered commercialization. Herein, a dopant-free polymeric HTM with functional aromatic rings was used to optimize the HTM/perovskite interface and employed in a planar n-i-p configuration. Poly(1,4-(2,5-bis((2-butyloctyloxy)phenylene)-2,7-(5,5,10,10-tetrakis(4-hexylphenyl)-5,10-dihydro-s-indaceno[2,1-b:6,5-b']dithiophene)) (IDTB) co-polymer constructed with indaceno[1,2-b:5,6-b']dithiophene and bis(alkyloxy)benzene units adopts an S⋅⋅⋅O intramolecular bond linked ladder-like planar conjugated polymer backbone. Without any dopant, the hole mobility of IDTB is in the same order of magnitude as a doped 2,2',7,7'-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9'-spirobifluorene (spiro-OMeTAD). Also, the hydrophobic nature of IDTB facilitated the long-term stability of the perovskite underneath. The unencapsulated PSC devices made of IDTB-based HTM achieved a power conversion efficiency of 19.38 % with a high moisture stability, retaining above 80 % of initial power conversion efficiency at 65 % relative humidity for more than 10 days. The superior passivation effect to perovskite surface made a hysteresis of 0.44 % was almost the least reported for regular planar undoped polymer HTM PSCs.
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http://dx.doi.org/10.1002/cssc.202001350 | DOI Listing |
Nano Lett
January 2025
Departments of Chemistry, and Physics and Astronomy, University of Southern California, Los Angeles, California 90089, United States.
A-site cations in ABX metal halide perovskites do not contribute to the frontier electronic states. They influence optoelectronic properties indirectly through interaction with the BX sublattice. By systematically investigating correlated motions of Cs cations and the PbX lattice (X = Cl, Br, I), we demonstrate that the interaction between the two subsystems depends on electronegativity and size of the X-site anion.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Department of Chemistry, College of Science, King Khalid University, Abha 61413, P.O. Box 9004, Saudi Arabia.
Lead-free inorganic halide perovskites, specifically BaPX (X = Cl, F, I, Br) have gained attention in green photovoltaics due to their remarkable mechanical, optical, structural, and electronic properties. Using first-principles calculations, we investigated the mechanical, electronic, and optical characteristics of BaPX, revealing direct band gaps at the -symmetry point, assessed with the PBE and HSE functionals. The charge distribution analysis shows strong ionic bonding between Ba and halides and covalent bonding between P and halides.
View Article and Find Full Text PDFSmall
January 2025
School of Materials Science and Engineering, Wuhan University of Technology, Wuhan, 430070, China.
2D perovskite has demonstrated great potential for application in photovoltaic devices due to the tunable energy bands, suppressed ion migration, and high stability. However, 2D perovskite solar cells (PSCs) display suboptimal efficiency in comparison to 3D perovskite solar cells, which can be attributed to the quantum confinement and dielectric confinement effects resulting from the intercalation of organic spacer cations into the perovskite lattice. This review starts with the fundamental structural characteristics, optoelectronic properties, and carrier transport dynamics of 2D PSCs, followed by the discussion of approaches to improve the photovoltaic performance of 2D PSCs, including the manipulation of crystal orientation, phase distribution, pure phase, organic layer, and device engineering.
View Article and Find Full Text PDFACS Omega
December 2024
Department of Material Science and Engineering, Drexel University, Philadelphia 19104, Pennsylvania, United States.
The optimization of nonradiative recombination losses through interface engineering is key to the development of efficient, stable, and hysteresis-free perovskite solar cells (PSCs). In this study, for the first time in solar cell technology, we present a novel approach to interface modification by employing one-dimensional lepidocrocite (henceforth referred to as 1DL) TiO-based nanofilaments, NFs, between the mesoporous TiO (mp TiO) and halide perovskite film in PSCs to improve both the efficiency and stability of the devices. The 1DLs can be easily produced on the kilogram scale starting with cheap and earth-abundant precursor powders, such as TiC, TiN, TiB, etc.
View Article and Find Full Text PDFLight Sci Appl
January 2025
Executive Management College of CHN ENERGY, No.7 Binhe Avenue, North District of Future Science City, Changping District, Beijing, 102211, China.
In 2012, Prof. Henry Snaith demonstrated the first solid-state perovskite solar cell (PSC) with an efficiency of 10.9%, igniting a surge of interest and research into perovskite materials for their potential to revolutionize the photovoltaic (PV) industry.
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