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Träfflista för sökning "WFRF:(Shargaieva Oleksandra) "

Sökning: WFRF:(Shargaieva Oleksandra)

  • Resultat 1-6 av 6
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1.
  • Li, Jinzhao, et al. (författare)
  • 20.8% Slot-Die Coated MAPbI3 Perovskite Solar Cells by Optimal DMSO-Content and Age of 2-ME Based Precursor Inks
  • 2021
  • Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6832 .- 1614-6840. ; 11:10
  • Tidskriftsartikel (refereegranskat)abstract
    • Solar cells incorporating metal-halide perovskite (MHP) semiconductors are continuing to break efficiency records for solution-processed solar cell devices. Scaling MHP-based devices to larger area prototypes requires the development and optimization of scalable process technology and ink formulations that enable reproducible coating results. It is demonstrated that the power conversion efficiency (PCE) of small-area methylammonium lead iodide (MAPbI3) devices, slot-die coated from a 2-methoxy-ethanol (2-ME) based ink with dimethyl-sulfoxide (DMSO) used as an additive depends on the amount of DMSO and age of the ink formulation. When adding 12 mol% of DMSO, small-area devices of high performance (20.8%) are achieved. The effect of DMSO content and age on the thin film morphology and device performance through in situ X-ray diffraction and small-angle X-ray scattering experiments is rationalized. Adding a limited amount of DMSO prevents the formation of a crystalline intermediate phase related to MAPbI3 and 2-ME (MAPbI3-2-ME) and induces the formation of the MAPbI3 perovskite phase. Higher DMSO content leads to the precipitation of the (DMSO)2MA2Pb3I8 intermediate phase that negatively affects the thin-film morphology. These results demonstrate that rational insights into the ink composition and process control are critical to enable reproducible large-scale manufacturing of MHP-based devices for commercial applications.
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2.
  • Näsström, Hampus, et al. (författare)
  • Combinatorial inkjet printing for compositional tuning of metal-halide perovskite thin films
  • 2022
  • Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 10:9, s. 4906-4914
  • Tidskriftsartikel (refereegranskat)abstract
    • To accelerate the materials discovery and development process for a sustainable technology advancement it is imperative to explore and develop combined high-throughput material synthesis and analysis workflows. In this work, we investigate a method of combinatorial inkjet-printing to tune the composition of the inorganic cesium lead mixed halide perovskite solid solution, CsPb(BrxI1-x)3. The compositional variation is achieved by simultaneous printing of different precursor inks with multiple printheads and controlled by varying the number of droplets printed by each printhead throughout the sample. The droplet placement is optimised through an algorithm that allows maximum mixing of the combined inks. The local compositional homogeneity of thin-film samples was investigated as a function of the printing resolution by micrometer-resolution X-ray fluorescence and synchrotron-based grazing-incidence wide-angle X-ray scattering. We show that a combinatorial library of ten compositions between CsPbI3 and CsPbBr2I, printed using the developed algorithm, is locally homogeneous for the optimised printing parameters. An implementation of the algorithm in the high-level programming language Python is provided for easy use in other systems.
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3.
  • Shargaieva, Oleksandra, et al. (författare)
  • Hybrid perovskite crystallization from binary solvent mixtures: interplay of evaporation rate and binding strength of solvents
  • 2020
  • Ingår i: Materials Advances. - : Royal Society of Chemistry (RSC). - 2633-5409. ; 1:9, s. 3314-3321
  • Tidskriftsartikel (refereegranskat)abstract
    • In this work, we rationalize the chemical pathways and kinetics of the crystallization of methylammonium lead iodide hybrid perovskite. Our approach includes a combination of analysis of solvent coordination, the structure of intermediate solvate phases, and modeling evaporation rates of precursor solutions. The evolution of solution species via intermediate solvate phases and into perovskite thin films during drying was monitored by in situ grazing-incidence wide-angle X-ray scattering (GIWAXS). All studied precursor solutions exhibited the formation of intermediate solvate phases including a previously unreported GBL phase. In single-solvent solutions, crystallization kinetics are determined by the solvent evaporation rate and saturation concentration required for nucleation. In binary solvent mixtures, the evaporation rate of solutions is dominated by the most volatile solvent which leads to unequal evaporation of the components of the mixture. The structure of the intermediate phases in such systems strongly depends on the coordination strength and the availability of solvents upon nucleation. The combined approach described in this work allows predicting the kinetics and the chemical pathways of crystallization of hybrid perovskites in complex solvent mixtures. This insight is of great importance for future perovskite ink design.
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4.
  • Shargaieva, Oleksandra, et al. (författare)
  • Temperature-Dependent Crystallization Mechanisms of Methylammonium Lead Iodide Perovskite From Different Solvents
  • 2021
  • Ingår i: Frontiers in Energy Research. - : Frontiers Media SA. - 2296-598X. ; 9
  • Tidskriftsartikel (refereegranskat)abstract
    • Hybrid perovskites are a novel type of semiconductors that show great potential for solution-processed optoelectronic devices. For all applications, the device performance is determined by the quality of the solution-processed perovskite thin films. During solution processing, the interaction of solvent with precursor molecules often leads to the formation of solvate intermediate phases that may diverge the crystallization pathway from simple solvent evaporation to a multi-step formation process. We here investigate the crystallization of methylammonium lead iodide (MAPbI3) from a range of commonly utilized solvents, namely dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF), N-methylpyrrolidone (NMP), and gamma-butyrolactone (GBL) at different temperatures ranging from 40°C to >100°C by in-situ grazing-incidence wide-angle X-ray scattering (GIWAXS) measurements. For all solvents but GBL, we clearly observe the formation of solvate-intermediate phases at moderate processing temperatures. With increasing temperatures, an increasing fraction of the MAPbI3 perovskite phase is observed to form directly. From the temperature-dependence of the phase-formation and phase-decomposition rates, the activation energy to form the MAPbI3 perovskite phase from the solvate-phases are determined as a quantitative metric for the binding strength of the solvent within the solvate-intermediate phases and we observe a trend of DMSO > DMF > NMP > GBL. These results enable prediction of processing temperatures at which solvent molecules can be effectively removed.
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5.
  • Shen, Xinyi, et al. (författare)
  • Chloride-Based Additive Engineering for Efficient and Stable Wide-Bandgap Perovskite Solar Cells
  • 2023
  • Ingår i: Advanced Materials. - 0935-9648. ; 35:30
  • Tidskriftsartikel (refereegranskat)abstract
    • Metal halide perovskite based tandem solar cells are promising to achieve power conversion efficiency beyond the theoretical limit of their single-junction counterparts. However, overcoming the significant open-circuit voltage deficit present in wide-bandgap perovskite solar cells remains a major hurdle for realizing efficient and stable perovskite tandem cells. Here, a holistic approach to overcoming challenges in 1.8 eV perovskite solar cells is reported by engineering the perovskite crystallization pathway by means of chloride additives. In conjunction with employing a self-assembled monolayer as the hole-transport layer, an open-circuit voltage of 1.25 V and a power conversion efficiency of 17.0% are achieved. The key role of methylammonium chloride addition is elucidated in facilitating the growth of a chloride-rich intermediate phase that directs crystallization of the desired cubic perovskite phase and induces more effective halide homogenization. The as-formed 1.8 eV perovskite demonstrates suppressed halide segregation and improved optoelectronic properties.
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6.
  • Valencia, Ana M., et al. (författare)
  • Optical Fingerprints of Polynuclear Complexes in Lead Halide Perovskite Precursor Solutions
  • 2021
  • Ingår i: Journal of Physical Chemistry Letters. - : American Chemical Society (ACS). - 1948-7185. ; 12:9, s. 2299-2305
  • Tidskriftsartikel (refereegranskat)abstract
    • Solvent-solute interactions in precursor solutions of lead halide perovskites (LHPs) critically impact the quality of solution-processed materials, as they lead to the formation of a variety of poly-iodoplumbates that act as building blocks for LHPs. The formation of [PbI2+n]n- complexes is often expected in diluted solutions, while coordination occurring at high concentrations is not yet well understood. In a combined ab initio and experimental work, we demonstrate that the optical spectra of the quasi-one-dimensional iodoplumbate complexes PbI2(DMSO)4, Pb2I4(DMSO)6, and Pb3I6(DMSO)8 formed in dimethyl sulfoxide solutions are compatible with the spectral fingerprints measured at high lead iodide concentrations. This finding suggests that the interpretation of optical spectra of LHP precursor solutions should account for the formation of polynuclear lead halide complexes.
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  • Resultat 1-6 av 6

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