17 results on '"Philipp Rieder"'
Search Results
2. Seed crystal free growth of high-quality double cation – double halide perovskite single crystals for optoelectronic applications
- Author
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Melina Armer, Philipp Rieder, Sebastian Hammer, Mathias Fischer, Mehmet Ozcan, Vladimir Dyakonov, Benedikt Bichler, Julian Höcker, Volker Drach, Jens Pflaum, and Bert Nickel
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Materials science ,business.industry ,Band gap ,Trihalide ,General Chemistry ,law.invention ,Semiconductor ,Formamidinium ,law ,Materials Chemistry ,Optoelectronics ,Crystallization ,business ,Single crystal ,Seed crystal ,Perovskite (structure) - Abstract
Organo-lead trihalide perovskites (OLTPs) form a highly interesting class of semiconductors, which might play an important role in future photovoltaics and optoelectronics. Particularly, formamidinium lead triiodide – methylammonium lead tribromide mixed perovskite (FAPbI3)0.9(MAPbBr3)0.1 is one of the most important representatives of this material class. In order to estimate the full optoelectronic potential of this perovskite system and thus to foster its future technological use, it is essential to investigate high-quality single crystals with the lowest structural as well as chemical defect density and with a stoichiometry relevant for their thin-film counterparts. However, the liquid growth of perovskite crystals without seed crystals is usually challenging and becomes even more demanding in the case of mixed cation–mixed halide single crystals, making it difficult to access their inherent properties. Here, we introduce a new efficient seed crystal free re-fill crystallization method (RFCM) based on inverse temperature crystallization (ITC) to grow large-sized single crystals. We performed qualitative and quantitative analyses, which confirmed the targeted elemental composition and the exact stoichiometry of the grown crystals. By means of polychromatic and monochromatic X-ray diffraction (XRD), we have demonstrated the high single crystal quality of the RFCM crystals, superior to crystals obtained by the seed crystal method. Steady-state photoluminescence (PL), absorption and temperature-dependent electrical measurements completed the investigation and enabled the determination of the optical band gap, relative permittivity and electrical conductivity of the grown single crystals. The conductivity clearly exhibits an ionic contribution and is therefore relevant for photovoltaic and optoelectronic implementation of this perovskite system.
- Published
- 2020
3. Efficient Solution Processed CH3NH3PbI3 Perovskite Solar Cells with PolyTPD Hole Transport Layer
- Author
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Kristofer Tvingstedt, Philipp Rieder, Andreas Baumann, David Kiermasch, Vladimir Dyakonov, and Julian Höcker
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Materials science ,business.industry ,General Physics and Astronomy ,Hole transport layer ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Solution processed ,Optoelectronics ,Physical and Theoretical Chemistry ,0210 nano-technology ,business ,Mathematical Physics ,Perovskite (structure) - Abstract
The organic and hydrophobic polymer poly[N, N′-bis(4-butilphenyl)-N, N′-bis(phenyl)-benzidine] (polyTPD) represents a promising hole transport layer (HTL) for perovskite photovoltaics due to its suitable energy levels, whereby its highest occupied molecular orbital level matches well with the valence band level of methylammonium lead triiodide (CH3NH3PbI3, MAPbI3) perovskite. However, processing a perovskite layer from the solution on the surface of this organic material, is found to be difficult due to the surface properties of the latter. In this study, we evaluate efficient p-i-n type MAPbI3 perovskite solar cells employing differently processed polyTPD layers. We found that the surface coverage of the MAPbI3 perovskite layer strongly depends on the preparation method of the underlying polyTPD layer. By varying the solvents for the polyTPD precursor, its concentration, and by applying an optimised two-step perovskite deposition technique we increased both the surface coverage of the perovskite layer as well as the power conversion efficiency (PCE) of the corresponding solar cell devices. Our simple solvent-engineering approach demonstrates that no further interface modifications are needed for a successful preparation of efficient planar photovoltaic devices with PCEs in the range of 15 %–16 %.
- Published
- 2019
4. Mechanism and Impact of Cation Polarization in Methylammonium Lead Iodide
- Author
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Susanne T. Birkhold, Pius T. Höger, Andreas Baumann, Hao Hu, Lukas Schmidt-Mende, Ka Kan Wong, and Philipp Rieder
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chemistry.chemical_classification ,Phase transition ,Materials science ,Iodide ,Halide ,02 engineering and technology ,Crystal structure ,Atmospheric temperature range ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Surfaces, Coatings and Films ,Electronic, Optical and Magnetic Materials ,Condensed Matter::Materials Science ,General Energy ,chemistry ,Chemical physics ,Polarizability ,Orthorhombic crystal system ,Physical and Theoretical Chemistry ,0210 nano-technology ,Polarization (electrochemistry) - Abstract
Despite the intense research effort on metal halide perovskites, the fundamental correlation between the crystal structure and optoelectronic properties remains unclear. As many intriguing phenomena are expected to be based on the dipolar character of the rotating organic cations, an improved understanding of the material’s polarizability is of high relevance. Here, we study the orthorhombic–tetragonal phase transition of methylammonium lead iodide to gain insight into the polarization mechanism at low temperatures and the resulting effects on solar cell performances. Using thermally stimulated current measurements, we detect polarization currents when cooling or heating across the phase transition. These (de)polarization currents are found to correlate with a sudden change in rotational freedom of the organic cations, with a temperature range of 20 K separating polarizing and depolarizing processes. The nature of this cation polarization within the orthorhombic phase is investigated with respect to its i...
- Published
- 2018
5. Influence of Fermi Level Alignment with Tin Oxide on the Hysteresis of Perovskite Solar Cells
- Author
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Meltem F. Aygüler, Thomas Bein, Wolfram Jaegermann, Michiel L. Petrus, Alexander G. Hufnagel, Andreas Baumann, Pablo Docampo, Vladimir Dyakonov, Philipp Rieder, and Michael Wussler
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Electron transport layer ,Materials science ,Condensed matter physics ,Fermi level ,Charge (physics) ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Tin oxide ,01 natural sciences ,0104 chemical sciences ,Hysteresis ,symbols.namesake ,symbols ,General Materials Science ,0210 nano-technology ,Conduction band ,Recombination ,Perovskite (structure) - Abstract
We tune the Fermi level alignment between the SnOx electron transport layer (ETL) and Cs0.05(FA0.83MA0.17)0.95Pb(I0.83Br0.17)3 and highlight that this parameter is interlinked with current–voltage hysteresis in perovskite solar cells (PSCs). Furthermore, thermally stimulated current measurements reveal that the depth of trap states in the ETL or at the ETL–perovskite interface correlates with Fermi level positions, ultimately linking it to the energy difference between the Fermi level and conduction band minimum. In the presence of deep trap states, charge accumulation and recombination at the interface are promoted, affecting the charge collection efficiency adversely, which increases the hysteresis of PSCs.
- Published
- 2018
6. Single-crystal-like optoelectronic-properties of MAPbI3 perovskite polycrystalline thin films
- Author
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Peter Müller-Buschbaum, Thomas Bein, Achim Hartschuh, Johannes Schlipf, Irene Grill, Nadja Giesbrecht, Vladimir Dyakonov, Pablo Docampo, and Philipp Rieder
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Materials science ,Renewable Energy, Sustainability and the Environment ,business.industry ,02 engineering and technology ,General Chemistry ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Grain size ,0104 chemical sciences ,Crystal ,Crystallinity ,Optoelectronics ,General Materials Science ,Grain boundary ,Crystallite ,0210 nano-technology ,business ,High-resolution transmission electron microscopy ,Single crystal ,Perovskite (structure) - Abstract
Our understanding of the crystallization process of hybrid halide perovskites has propelled the efficiency of state-of-the-art photovoltaic devices to over 22%. Further improvements to the performance will likely arise from reducing the number of grain boundaries. Here, current methods lead to grain sizes in the 1 micrometer range and the resulting optoelectronic properties suffer as compared to single-crystal materials. In this work, we introduce a new synthesis procedure with MAPbI3 leading to crystal sizes in the tens of microns range. This approach is based on the pre-crystallization of an intermediate phase (IP) based on the solid-state reaction of a lead-acetate trihydrate precursor mixture in a highly polar solvent. Beyond large grain sizes, the crystal orientation is also tightly controlled, leading to perovskite crystallites which remain perfectly aligned with the c-axis of the tetragonal structure parallel to the substrate as evidenced by grazing incidence wide angle X-ray scattering (GIWAXS). Furthermore, we demonstrate the high crystallinity and large grain size of the developed films via high-resolution transmission electron microscopy (HRTEM). The charge carrier mobilities are significantly improved with larger grain size and approach mobility values of about 40 cm2 V−1 s−1, moving toward the values observed for single crystals. We capitalize on the enhanced optoelectronic properties of the developed films by incorporating them into planar heterojunction solar cells which reach power conversion efficiencies of 18.5%, higher than MAPbI3-based device prepared from standard methods in a like-to-like comparison.
- Published
- 2018
7. How far does the defect tolerance of lead-halide perovskites range? The example of Bi impurities introducing efficient recombination centers
- Author
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Kristofer Tvingstedt, Tonio Buonassisi, Juan-Pablo Correa-Baena, Alessio Filippetti, Heidi A. Schwartz, Selina Olthof, Simone Meloni, Zishuai Wang, Firouzeh Ebadi, Terry Chien-Jen Yang, Shijing Sun, Wolfgang Tress, Wallace C. H. Choy, Thomas Dittrich, Bjoern Niesen, Javier Durantini, Philipp Rieder, Zaiwei Wang, and Mozhgan Yavari
- Subjects
Photoluminescence ,Materials science ,PEROVSKITE ,Surface photovoltage ,Físico-Química, Ciencia de los Polímeros, Electroquímica ,Perovskite solar cell ,chemistry.chemical_element ,02 engineering and technology ,7. Clean energy ,Bismuth ,NO ,purl.org/becyt/ford/1 [https] ,Impurity ,hybrid perovskites photovoltaics ,evolution ,ch3nh3pbi3 perovskite ,purl.org/becyt/ford/1.4 [https] ,General Materials Science ,Perovskite (structure) ,hole-transport layers ,Renewable Energy, Sustainability and the Environment ,Ciencias Químicas ,IMPURITIES ,SOLAR CELLS ,General Chemistry ,p-i-n ,BISMUTH ,021001 nanoscience & nanotechnology ,Crystallographic defect ,solar-cells ,chemistry ,open-circuit voltage ,highly efficient ,Chemical physics ,lifetimes ,Charge carrier ,iodide ,0210 nano-technology ,CIENCIAS NATURALES Y EXACTAS ,grain-boundaries - Abstract
One of the key properties of lead-halide perovskites employed in solar cells is the defect tolerance of the materials, in particular regarding intrinsic point defects, which mainly form shallow traps. Considering that high luminescence yields and photovoltaic performance are obtained by simple solution processing from commercial chemicals, it is commonly anticipated that the defect tolerance-at least to a considerable degree-extends to grain boundaries and extrinsic defects, i.e. impurities, as well. However, the effect of impurities has hardly been investigated. Here, we intentionally introduce small quantities of bismuth (10 ppm to 2%) in solution to be incorporated in the perovskite films based on mixed cation mixed anion compositions. We observe that Bi impurities in the %-regime reduce charge carrier collection efficiency and, more importantly, that the open-circuit voltage decreases systematically with impurity concentration even in the ppm regime. This strong defect intolerance against Bi impurities comes along with reduced electroluminescence yields and charge carrier lifetimes obtained from transient photoluminescence experiments. Calculations based on molecular dynamics and density functional theory predict delocalized (≈0.16 eV) and localized deep (≈0.51 eV) trap states dependent on the structural arrangement of the surrounding atoms. Structural characterization supports the idea of Bi being present as a homogeneously spread point defect, which substitutes the Pb2+ by Bi3+ as seen from XPS and a reduction of the lattice parameter in XRD. Sensitive measurements of the photocurrent (by FTPS) and surface photovoltage (SPV) confirm the presence of tail states. Photoelectron spectroscopy measurements show evidence of a deep state. These results are consistent with the common idea of shallow traps being responsible for the reduced charge collection efficiency and the decreased fill factor, and deeper traps causing a substantial reduction of the open-circuit voltage. As Bi is only one potential impurity in the precursor salts used in perovskite solar cell fabrication, our findings open-up a research direction focusing on identifying and eliminating impurities that act as recombination centers-a topic that has so far not been fully considered in device optimization studies. Fil: Yavari, M.. École Polytechnique Fédérale de Lausanne; Suiza Fil: Ebadi, Firouzeh. École Polytechnique Fédérale de Lausanne; Suiza Fil: Meloni, Simone. Università di Roma; Italia Fil: Wang, Zishuai. École Polytechnique Fédérale de Lausanne; Suiza Fil: Yang, Terry Chien-Jen. École Polytechnique Fédérale de Lausanne; Suiza Fil: Sun, Shijing. Massachusetts Institute Of Technology; Estados Unidos Fil: Schwartz, Heidi. University Of Cologne; Alemania Fil: Wang, Zaiwei. École Polytechnique Fédérale de Lausanne; Suiza Fil: Niesen, Bjoern. École Polytechnique Fédérale de Lausanne; Suiza Fil: Durantini, Javier Esteban. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados; Argentina Fil: Rieder, Philipp. Julius Maximilian University Of Würzburg; Alemania Fil: Tvingstedt, Kristofer. Julius Maximilian University Of Würzburg; Alemania Fil: Buonassisi, Tonio. Massachusetts Institute Of Technology; Estados Unidos Fil: Choy, Wallace C.H.. The University Of Hong Kong; Hong Kong Fil: Filippetti, Alessio. Università Di Cagliari; Italia Fil: Dittrich, Thomas. Helmholtz Center Berlin For Materials And Energy; Alemania Fil: Olthof, Selina. University Of Cologne; Alemania Fil: Correa Baena, Juan Pablo. Massachusetts Institute Of Technology; Estados Unidos Fil: Tress, Wolfgang. École Polytechnique Fédérale de Lausanne; Suiza
- Published
- 2019
8. Removing Leakage and Surface Recombination in Planar Perovskite Solar Cells
- Author
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Michele Sessolo, Cristina Momblona, David Kiermasch, Lidón Gil-Escrig, Vladimir Dyakonov, Kristofer Tvingstedt, Philipp Rieder, Andreas Baumann, and Henk J. Bolink
- Subjects
Iodide ,FOS: Physical sciences ,Energy Engineering and Power Technology ,Hole transport layer ,Applied Physics (physics.app-ph) ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Planar ,PEDOT:PSS ,Materials Chemistry ,Leakage (electronics) ,chemistry.chemical_classification ,Renewable Energy, Sustainability and the Environment ,business.industry ,Physics - Applied Physics ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Fuel Technology ,chemistry ,Chemistry (miscellaneous) ,Optoelectronics ,0210 nano-technology ,business ,Shunt (electrical) ,Recombination ,Voltage - Abstract
Thin-film solar cells suffer from various types of recombination, of which leakage current usually dominates at lower voltages. Herein, we demonstrate first a three-order reduction of the shunt loss mechanism in planar methylammonium lead iodide perovskite solar cells by replacing the commonly used hole transport layer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) with a better hole-selective polyarylamine. As a result, these cells exhibit superior operation under reduced light conditions, which we demonstrate for the extreme case of moonlight irradiance, at which open-circuit voltages of 530 mV can still be obtained. By the shunt removal we also observe the VOC to drop to zero after as long as 2 h after the light has been switched off. Second, at higher illumination intensities the dominant losses in the PEDOT:PSS-based cell are ascribed to surface recombination and are also proven to be substantially minimized by instead employing the polyarylamine. We attribute the reduced shunt and surface recombination to the far better suited semiconductor character of the polyarylamine, compared to that of PEDOT:PSS, efficiently blocking electrons from recombining at this electrode.
- Published
- 2019
9. Understanding the role of Cesium and Rubidium additives in perovskite solar cells: trap states, charge transport, and recombination
- Author
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Philipp Rieder, Achim Hartschuh, Vladimir Dyakonov, Tom J. Savenije, Eline M. Hutter, Kristofer Tvingstedt, Jonas Hanisch, Thomas Bein, Andreas Baumann, Meltem F. Aygüler, Irene Grill, Michiel L. Petrus, Matthias Handloser, Pablo Docampo, Alexander G. Hufnagel, and Yinghong Hu
- Subjects
Work (thermodynamics) ,Materials science ,Renewable Energy, Sustainability and the Environment ,Halide ,chemistry.chemical_element ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Rubidium ,law.invention ,Hysteresis ,chemistry ,Chemical physics ,law ,Caesium ,Solar cell ,General Materials Science ,0210 nano-technology ,Voltage ,Perovskite (structure) - Abstract
Adding cesium (Cs) and rubidium (Rb) cations to FA(0.83)MA(0.17)Pb(I0.83Br0.17)(3) hybrid lead halide perovskites results in a remarkable improvement in solar cell performance, but the origin of the enhancement has not been fully understood yet. In this work, time-of-flight, time-resolved microwave conductivity, and thermally stimulated current measurements are performed to elucidate the impact of the inorganic cation additives on the trap landscape and charge transport properties within perovskite solar cells. These complementary techniques allow for the assessment of both local features within the perovskite crystals and macroscopic properties of films and full devices. Strikingly, Csincorporation is shown to reduce the trap density and charge recombination rates in the perovskite layer. This is consistent with the significant improvements in the open-circuit voltage and fill factor of Cs-containing devices. By comparison, Rb-addition results in an increased charge carrier mobility, which is accompanied by a minor increase in device efficiency and reduced currentvoltage hysteresis. By mixing Cs and Rb in quadruple cation (Cs-Rb-FA-MA) perovskites, the advantages of both inorganic cations can be combined. This study provides valuable insights into the role of these additives in multiplecation perovskite solar cells, which are essential for the design of high-performance devices.
- Published
- 2018
10. The Influence of Fermi Level Alignment with Tin Oxide on the Hysteresis of Perovskite Solar Cells
- Author
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Philipp Rieder, Vladimir Dyakonov, Pablo Docampo, Michiel L. Petrus, Andreas Baumann, Thomas Bein, Meltem F. Aygüler, Michael Wussler, Wolfram Jaegermann, and Alexander G. Hufnagel
- Subjects
symbols.namesake ,Hysteresis ,Materials science ,Condensed matter physics ,Fermi level ,symbols ,Tin oxide ,Perovskite (structure) - Published
- 2018
11. Understanding the Role of Cesium and Rubidium Additives in Perovskite Solar Cells: Trap States and Charge Carrier Mobility
- Author
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Philipp Rieder, Pablo Docampo, Michiel L. Petrus, Meltem F. Aygüler, Kristofer Tvingstedt, Thomas Bein, Irene Grill, Eline M. Hutter, Andreas Baumann, Yinghong Hu, Alexander G. Hufnagel, Achim Hartschuh, Matthias Handloser, Jonas Hanisch, Vladimir Dyakonov, and Tom J. Savenije
- Subjects
Trap (computing) ,Materials science ,chemistry ,Charge carrier mobility ,Chemical physics ,Caesium ,chemistry.chemical_element ,Perovskite (structure) ,Rubidium - Published
- 2018
12. Efficient Monolithic Perovskite/Perovskite Tandem Solar Cells
- Author
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Andreas Baumann, Kristofer Tvingstedt, David Kiermasch, Vladimir Dyakonov, Philipp Rieder, Henk J. Bolink, Cristina Momblona, Michele Sessolo, and Lidón Gil-Escrig
- Subjects
charge recombination layer ,Materials science ,doping ,02 engineering and technology ,Electron ,010402 general chemistry ,01 natural sciences ,Planar ,PEDOT:PSS ,General Materials Science ,vacuum deposition ,Materials ,perovskite ,Cèl·lules fotoelèctriques ,Leakage (electronics) ,Renewable Energy, Sustainability and the Environment ,business.industry ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Semiconductor ,Electrode ,Optoelectronics ,tandem solar cells ,0210 nano-technology ,business ,Recombination ,Voltage - Abstract
Thin-film solar cells suffer from various types of recombination, of which leakage current usually dominates at lower voltages. Herein, we demonstrate first a three-order reduction of the shunt loss mechanism in planar methylammonium lead iodide perovskite solar cells by replacing the commonly used hole transport layer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) with a better hole-selective polyarylamine. As a result, these cells exhibit superior operation under reduced light conditions, which we demonstrate for the extreme case of moonlight irradiance, at which open-circuit voltages of 530 mV can still be obtained. By the shunt removal we also observe the VOC to drop to zero after as long as 2 h after the light has been switched off. Second, at higher illumination intensities the dominant losses in the PEDOT:PSS-based cell are ascribed to surface recombination and are also proven to be substantially minimized by instead employing the polyarylamine. We attribute the reduced shunt and surface recombination to the far better suited semiconductor character of the polyarylamine, compared to that of PEDOT:PSS, efficiently blocking electrons from recombining at this electrode.
- Published
- 2017
13. Improved charge carrier lifetime in planar perovskite solar cells by bromine doping
- Author
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David Kiermasch, Philipp Rieder, Kristofer Tvingstedt, Andreas Baumann, and Vladimir Dyakonov
- Subjects
integumentary system ,ddc:621 ,Article - Abstract
The charge carrier lifetime is an important parameter in solar cells as it defines, together with the mobility, the diffusion length of the charge carriers, thus directly determining the optimal active layer thickness of a device. Herein, we report on charge carrier lifetime values in bromine doped planar methylammonium lead iodide (MAPbI\(_3\)) solar cells determined by transient photovoltage. The corresponding charge carrier density has been derived from charge carrier extraction. We found increased lifetime values in solar cells incorporating bromine compared to pure MAPbI\(_3\) by a factor of ~2.75 at an illumination intensity corresponding to 1 sun. In the bromine containing solar cells we additionally observe an anomalously high value of extracted charge, which we deduce to originate from mobile ions.
- Published
- 2016
14. Perovskite Solar Cells: Understanding the Role of Cesium and Rubidium Additives in Perovskite Solar Cells: Trap States, Charge Transport, and Recombination (Adv. Energy Mater. 16/2018)
- Author
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Pablo Docampo, Yinghong Hu, Achim Hartschuh, Kristofer Tvingstedt, Meltem F. Aygüler, Matthias Handloser, Jonas Hanisch, Vladimir Dyakonov, Tom J. Savenije, Andreas Baumann, Michiel L. Petrus, Irene Grill, Philipp Rieder, Thomas Bein, Eline M. Hutter, and Alexander G. Hufnagel
- Subjects
Materials science ,Renewable Energy, Sustainability and the Environment ,Charge carrier mobility ,chemistry.chemical_element ,Charge (physics) ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Rubidium ,Trap (computing) ,chemistry ,Chemical physics ,Caesium ,Trap density ,General Materials Science ,0210 nano-technology ,Recombination ,Perovskite (structure) - Published
- 2018
15. Positive inotropic effects of epigallocatechin-3-gallate (EGCG) involve activation of Na+/H+and Na+/Ca2+exchangers
- Author
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Alexander Staudt, Christiane Trimpert, Philipp Rieder, Stephan B. Felix, Verena Stangl, Karl Stangl, Hans-Tilmann Kinkel, Mario Lorenz, Niels Hellige, and Gert Baumann
- Subjects
Male ,medicine.medical_specialty ,Cardiotonic Agents ,Sodium-Hydrogen Exchangers ,Gallopamil ,Lusitropy ,complex mixtures ,Catechin ,Sodium-Calcium Exchanger ,Calcium in biology ,Contractility ,Nifedipine ,Internal medicine ,medicine ,Animals ,Myocytes, Cardiac ,heterocyclic compounds ,Rats, Wistar ,business.industry ,Myocardium ,food and beverages ,Myocardial Contraction ,Rats ,Phospholamban ,Amiloride ,Endocrinology ,sense organs ,Cardiology and Cardiovascular Medicine ,business ,Intracellular ,Signal Transduction ,medicine.drug - Abstract
Background: There is evidence that the tea catechin epigallocatechin-3-gallate (EGCG) modulates myocardial contractility. However, the underlying mechanisms remain to be determined. Aims: To study potential signalling pathways involved in EGCG-induced contractile parameters. Methods and results: EGCG increased fractional shortening in rat cardiac myocytes and enhanced intracellular systolic Ca2+ concentrations. In isolated rat hearts, perfusion with EGCG resulted in significant, dose-dependent increase in peak systolic left ventricular pressure, as well as in contraction and relaxation velocities. Heart rate did not change. Inhibition of the β1-receptor with metoprolol had no influence on the contractile effects of EGCG. Furthermore, levels of cAMP and phosphorylation of phospholamban did not change with EGCG, indicating that the beta-receptor pathway is not involved. The L-type Ca2+ channel inhibitors, nifedipine and gallopamil, failed to modulate EGCG-induced increase in contractility. However, the myocardial effects and intracellular calcium transients stimulated by EGCG were significantly reduced by the antagonist of the Na+/H+ exchanger (NHE) methyl-N-isobutyl amiloride (MIA), and by blocking of the reverse mode of the Na+/Ca2+ exchanger (NCX) by KB-R7943. Conclusion: These results indicate that Ca2+-dependent positive inotropic and lusitropic effects of EGCG are mediated in part via activation of the Na+/H+ exchanger and the reverse mode of the Na+/Ca2+ exchanger in the rat myocardium.
- Published
- 2008
16. Identification of Trap States in Perovskite Solar Cells
- Author
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Andreas Baumann, Kristofer Tvingstedt, Vladimir Dyakonov, Michael C. Heiber, Philipp Rieder, and Stefan Väth
- Subjects
chemistry.chemical_classification ,Phase transition ,Chemistry ,Bilayer ,Iodide ,Analytical chemistry ,Nanotechnology ,Atmospheric temperature range ,Electron transport chain ,law.invention ,Trap (computing) ,law ,Solar cell ,General Materials Science ,Physical and Theoretical Chemistry ,Perovskite (structure) - Abstract
Thermally stimulated current (TSC) measurements are used to characterize electronic trap states in methylammonium lead iodide perovsite solar cells. Several TSC peaks were observed over the temperature range from 20 K to room temperature. To elucidate the origins of these peaks, devices with various organic charge transport layers and devices without transport layers were tested. Two peaks appear at very low temperatures, indicating shallow trap states that are mainly attributed to the PCBM/C60 electron transport bilayer. However, two additional peaks appear at higher temperatures, that is, they are deeper in energy, and are assigned to the perovskite layer. At around T = 163 K, a sharp peak, also present in the dark TSC measurements, is assigned to the orthorhombic-tetragonal phase transition in the perovskite. However, a peak at around T = 191 K is assigned to trap states with activation energies of around 500 meV but with a rather low concentration of 1 × 10(21) m(-3).
- Published
- 2015
17. Impact of Interfaces and Laser Repetition Rate on Photocarrier Dynamics in Lead Halide Perovskites
- Author
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G. V. Astakhov, Kristofer Tvingstedt, Philipp Rieder, Andreas Baumann, Marshall Campbell, David Kiermasch, Vladimir Dyakonov, and Liudmila G. Kudriashova
- Subjects
Photoluminescence ,Materials science ,business.industry ,Halide ,02 engineering and technology ,Electron ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Laser ,01 natural sciences ,0104 chemical sciences ,law.invention ,law ,Pulse wave ,Optoelectronics ,General Materials Science ,Charge carrier ,Physical and Theoretical Chemistry ,0210 nano-technology ,business ,Excitation ,Perovskite (structure) - Abstract
We studied charge carrier recombination in methylammonium lead iodide (MAPbI3) perovskite and the impact of interfaces on the charge carrier lifetime using time-resolved photoluminescence. Pristine films and those covered with organic electron and hole transport materials (TM) were investigated at various laser repetition rates ranging from 10 kHz to 10 MHz in order to separate the bulk and interface-affected recombination. We revealed two different components in the PL decay. The fast component (shorter than 300ns) is assigned to interfacial processes, and the slow one to bulk recombination. A high repetition pulse train was shown to shorten PL decay in pristine perovskite, while significantly prolonging the photocarrier lifetime in MAPbI3covered by TMs. This effect can be qualitatively explained with kinetic model taking interface traps into account. We demonstrate a significant influence of excitation repetition rate on photocarrier lifetime, which should be considered when studying charge carrier dynamics in perovskites.
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