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Lukas Schmidt-Mende

Publications and source records attributed to Lukas Schmidt-Mende.

3 recordsLinked to original sources

Controlled nucleation in methylamine-treated perovskite films by artificial seeding and phase-field simulations

Large perovskite crystals with reduced defect density enable superior charge transport and stability. Therefore, controlling their nucleation and growth is key to advancing high-performance optoelectronic devices based on perovskite semiconductors. Millimeter-scale perovskite crystals can be synthesized as a continuous film through methylamine treatment, with nucleation sites directed by pre-patterned seeds. Nonetheless, certain configurations may lead to unwanted parasitic nucleation. To predict and mitigate this effect, we employ phase-field simulations alongside an analytical model. Their predictive capability is demonstrated across three distinct material-substrate systems, enabling precise control over nucleation and subsequent crystal growth. Notably, the only material-specific input required is the nucleation density (i.e., the number of crystals nucleated per unit area on an unpatterned substrate). This generality makes the models broadly applicable to diverse material systems for achieving controlled two-dimensional crystallization for improved optoelectronic device performance.

cond-mat.mtrl-sci

Chemical Strain Engineering of MAPbI3 Perovskite Films

This study introduces a new chemical method for controlling the strain in methylammonium lead iodide (MAPbI3) perovskite crystals by varying the ratio of Pb(Ac)2 and PbCl2 in the precursor solution. To observe the effect on crystal strain, a combination of piezoresponse force microscopy (PFM) and X-ray diffraction (XRD) is used. The PFM images show an increase in the average size of ferroelastic twin domains upon increasing the PbCl2 content, indicating an increase in crystal strain. The XRD spectra support this observation with strong crystal twinning features that appear in the spectra. This behaviour is caused by a strain gradient during the crystallization due to different evaporation rates of methylammonium acetate and methylammonium chloride as revealed by time-of-flight secondary ion mass spectroscopy (ToF-SIMS) and grazing incidince x-ray diffraction (GIXRD) measurements. Additional time-resolved photoluminescence (TRPL) show an increased carrier lifetime in the MAPbI3 films prepared with higher PbCl2 content, suggesting a decreased trap density in films with larger twin domain structures. The results demonstrate the potential of chemical strain engineering as an easy method for controlling strain-related effects in lead halide perovskites.

cond-mat.mtrl-sci

Quantification of Ion Migration in CH3NH3PbI3 Perovskite Solar Cells by Transient Capacitance Measurements

Solar cells based on organic-inorganic metal halide perovskites show efficiencies close to highly-optimized silicon solar cells. However, ion migration in the perovskite films leads to device degradation and impedes large scale commercial applications. We use transient ion-drift measurements to quantify activation energy, diffusion coefficient, and concentration of mobile ions in methylammonium lead triiodide (MAPbI3) perovskite solar cells, and find that their properties change close to the tetragonal-to-orthorhombic phase transition temperature. We identify three migrating ion species which we attribute to the migration of iodide (I-) and methylammonium (MA+). We find that the concentration of mobile MA+ ions is one order of magnitude higher than the one of mobile I- ions, and that the diffusion coefficient of mobile MA+ ions is three orders of magnitude lower than the one for mobile I- ions. We furthermore observe that the activation energy of mobile I- ions (0.29 eV) is highly reproducible for different devices, while the activation energy of mobile MA+ depends strongly on device fabrication. This quantification of mobile ions in MAPbI3 will lead to a better understanding of ion migration and its role in operation and degradation of perovskite solar cells.

cond-mat.mtrl-sci