In CHNHPbI-based high efficiency perovskite solar cells (PSCs), tiny amount of PbI impurity was often found with the perovskite crystal. However, for two-step solution process-based perovskite films, most of findings have been based on the films having different morphologies between with and without PbI. This was mainly due to the inferior morphology of pure perovskite film without PbI, inevitably produced when the remaining PbI forced to be converted to perovskite, so advantages of pure perovskite photoactive layer without PbI impurity have been overlooked. In this work, we designed a printing-based two-step process, which could not only generate pure perovskite crystal without PbI, but also provide uniform and full surface coverage perovskite film, of which nanoscale morphology was comparable to that prepared by conventional two-step solution process having residual PbI. Our results showed that, in two-step solution process-based PSC, pure perovskite had better photon absorption and longer carrier lifetime, leading to superior photocurrent generation with higher power conversion efficiency. Furthermore, this process was further applicable to prepare mixed phase pure perovskite crystal without PbI impurity, and we showed that the additional merits such as extended absorption to longer wavelength, increased carrier lifetime and reduced carrier recombination could be secured.
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http://dx.doi.org/10.1038/srep35994 | DOI Listing |
Nat Commun
January 2025
College of Materials Science and Engineering & Engineering Research Center of Alternative Energy Materials & Devices, Ministry of Education, Sichuan University, Chengdu, China.
Self-assembled monolayers (SAMs) have displayed unpredictable potential in efficient perovskite solar cells (PSCs). Yet most of SAMs are largely suitable for pure Pb-based devices, precisely developing promising hole-selective contacts (HSCs) for Sn-based PSCs and exploring the underlying general mechanism are fundamentally desired. Here, based on the prototypical donor-acceptor SAM MPA-BT-BA (BT), oligoether side chains with different length (i.
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 PDFJ Am Chem Soc
December 2024
Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning 116023, China.
In recent years, perovskite solar cells (PSCs) have garnered considerable attention as a prime candidate for next-generation photovoltaic technology. Ensuring the structural stability of perovskites is crucial to the operational reliability of these devices. However, the nonphotoactive yellow phase (δ-FAPbI) of formamidine (FA)-based perovskites is more favorable in thermodynamics, making it challenging to achieve pure α phase in crystallization.
View Article and Find Full Text PDFLangmuir
December 2024
Key Laboratory of Photonic Materials and Devices Physics for Oceanic Applications, Ministry of Industry and Information Technology of China, College of Physics and Optoelectronic Engineering, Harbin Engineering University, Harbin 150001, China.
Due to intrinsic defects in blue-light-emitting perovskite materials, the charge carriers are prone to being trapped by the trap states. Therefore, the preparation of efficient blue-light-emitting perovskite materials remains a significant challenge. Herein, CsPb(Cl/Br) nanocrystal (NCs)@SiO structures were fabricated through hydrolyzing (3-aminopropyl)-triethoxysilane (APTS).
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Univ Rennes, ENSCR, CNRS, ISCR-UMR6226, Université de Rennes, Rennes 35042, France.
Metal halide perovskites, including some of their related perovskitoid structures, form a semiconductor class of their own, which is arousing ever-growing interest from the scientific community. With halides being involved in the various structural arrangements, namely, pure corner-sharing MX (M is metal and X is halide) octahedra, for perovskite networks, or alternatively a combination of corner-, edge-, and/or face-sharing for related perovskitoids, they represent the ideal probe for characterizing the way octahedra are linked together. Well known for their inherently large quadrupolar constants, which is detrimental to the resolution of nuclear magnetic resonance spectroscopy, most abundant halide isotopes (Cl, Br, I) are in turn attractive for magnetic field-free nuclear quadrupolar resonance (NQR) spectroscopy.
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