Relevant bibliographies by topics / Methylammonium

Academic literature on the topic 'Methylammonium'

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Published: 6 September 2023

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Journal articles on the topic "Methylammonium"

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Lees, Rachel J. E., Anthony V. Powell, and Ann M. Chippindale. "Methylammonium antimony sulfide." Acta Crystallographica Section C Crystal Structure Communications 61, no. 12 (November 11, 2005): m516—m518. http://dx.doi.org/10.1107/s0108270105032361.

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Djinović, K., and L. Golič. "Structure of methylammonium hydrogen malonate (I) and methylammonium malonate (II)." Acta Crystallographica Section C Crystal Structure Communications 47, no. 11 (November 15, 1991): 2367–71. http://dx.doi.org/10.1107/s0108270191001014.

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Peng, Chu Xin, Lei Meng, Yi Yang Xu, Tian Tian Xing, Miao Miao Zhao, Peng Ren, and Fei Yen. "Ferroelectricity driven by orbital resonance of protons in CH3NH3Cl and CH3NH3Br." Journal of Materials Chemistry C 10, no. 4 (2022): 1334–38. http://dx.doi.org/10.1039/d1tc04718c.

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Soupene, Eric, Robert M. Ramirez, and Sydney Kustu. "Evidence that Fungal MEP Proteins Mediate Diffusion of the Uncharged Species NH3 across the Cytoplasmic Membrane." Molecular and Cellular Biology 21, no. 17 (September 1, 2001): 5733–41. http://dx.doi.org/10.1128/mcb.21.17.5733-5741.2001.

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ABSTRACT Methylammonium and ammonium (MEP) permeases of Saccharomyces cerevisiae belong to a ubiquitous family of cytoplasmic membrane proteins that transport only ammonium (NH4 + + NH3). Transport and accumulation of the ammonium analog [14C]methylammonium, a weak base, led to the proposal that members of this family were capable of energy-dependent concentration of the ammonium ion, NH4 +. In bacteria, however, ATP-dependent conversion of methylammonium to γ-N-methylglutamine by glutamine synthetase precludes its use in assessing concentrative transport across the cytoplasmic membrane. We have confirmed that methylammonium is not metabolized in the yeast S. cerevisiae and have shown that it is little metabolized in the filamentous fungus Neurospora crassa. However, its accumulation depends on the energy-dependent acidification of vacuoles. A Δvph1 mutant of S. cerevisiae and a Δvma1 mutant, which lack vacuolar H+-ATPase activity, had large (fivefold or greater) defects in the accumulation of methylammonium, with little accompanying defect in the initial rate of transport. A vma-1 mutant ofN. crassa largely metabolized methylammonium to methylglutamine. Thus, in fungi as in bacteria, subsequent energy-dependent utilization of methylammonium precludes its use in assessing active transport across the cytoplasmic membrane. The requirement for a proton gradient to sequester the charged species CH3NH3 + in acidic vacuoles provides evidence that the substrate for MEP proteins is the uncharged species CH3NH2. By inference, their natural substrate is NH3, a gas. We postulate that MEP proteins facilitate diffusion of NH3 across the cytoplasmic membrane and speculate that human Rhesus proteins, which lie in the same domain family as MEP proteins, facilitate diffusion of CO2.
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Bhorde, Ajinkya, Shruthi Nair, Haribhau Borate, Subhash Pandharkar, Rahul Aher, Ashvini Punde, Ashish Waghmare, et al. "Highly stable and Pb-free bismuth-based perovskites for photodetector applications." New Journal of Chemistry 44, no. 26 (2020): 11282–90. http://dx.doi.org/10.1039/d0nj01806f.

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Herein, we report synthesis of highly stable, Pb-free bismuth iodide, stoichiometric methylammonium bismuth iodide and non-stoichiometric methylammonium bismuth iodide perovskite thin films for photodetector applications.
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Tansho, Masataka, Daiyu Nakamura, and Ryuichi Ikeda. "1H NMR and Thermal Studies of CH3NH3Br in a Metastable Solid Phase Newly Found above 483 K." Zeitschrift für Naturforschung A 44, no. 8 (August 1, 1989): 738–40. http://dx.doi.org/10.1515/zna-1989-0810.

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Abstract By differential thermal analysis a new high-temperature solid phase of methylammonium bromide was found between 483 K and its “melting point” (510 K). 1H NMR absorption measurements revealed the presence of rapid 3D translational self-diffusion and overall rotation of methylammonium cations in this phase. These cationic motions are quite analogous to those of methylammonium iodide in its ionic plastic phase. Surprisingly, this plastic-like phase is metastable, the stable phase in the same temperature range being liquid.
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Emmanuel Koné, Klègayéré, Amal Bouich, Donafologo Soro, and Bernabé Marí Soucase. "Effect of mixed iodine and bromine on optical properties in methylammonium lead chlorine (MAPbCl3) spin-coated on the zinc oxide film." E3S Web of Conferences 412 (2023): 01066. http://dx.doi.org/10.1051/e3sconf/202341201066.

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The optical influence of mixing methylammonium lead chlorine (MAPbCl3) with iodine and bromine was studied in this work. The spin coating method deposited three layers of perovskites (MAPbCl3, MAPbCl2I, and MAPbCl2Br) on a layer of zinc oxide (ZnO). The zinc oxide solution was prepared by dissolving dehydrated zinc acetate [Zn(CH3COO)2, 2H2O]> 99.5% purity in ethanol to give a 0.5 M solution. The perovskite solutions were prepared using lead chloride (PbCl2), methylammonium chloride (MACl), methylammonium iodide (MAI), and methylammonium bromide (MABr). The precursor containing iodine was dissolved in N, N-dimethylformamide (DMF) and the others in dimethyl sulphoxide (DMSO 99.9%). The films produced were characterized by UV-Visible. The analysis showed that the sample mixed with iodine has good properties. This sample absorbs the most and has a small band gap of 2 eV. The degradation study reveals that the unmixed sample (MAPbCl3) is the most stable.
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Li, Jinqing, Patrick De Smet, Danny Jans, Jeannine Simaels, and Willy Van Driessche. "Swelling-activated cation-selective channels in A6 epithelia are permeable to large cations." American Journal of Physiology-Cell Physiology 275, no. 2 (August 1, 1998): C358—C366. http://dx.doi.org/10.1152/ajpcell.1998.275.2.c358.

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Effects of basolateral monovalent cation replacements (Na+ by Li+, K+, Cs+, methylammonium, and guanidinium) on permeability to86Rb of volume-sensitive cation channels (VSCC) in the basolateral membrane and on regulatory volume decrease (RVD), elicited by a hyposmotic shock, were studied in A6 epithelia in the absence of apical Na+ uptake. A complete and quick RVD occurred only when the cells were perfused with Na+ or Li+ saline. With both cations, hypotonicity increased basolateral86Rb release ([Formula: see text]), which reached a maximum after 15 min and declined back to control level. When the major cation was K+, Cs+, methylammonium, or guanidinium, the RVD was abolished. Methylammonium induced a biphasic time course of cell thickness (Tc), with an initial decline of Tc followed by a gradual increase. With K+, Cs+, or guanidinium, Tc increased monotonously after the rapid initial rise evoked by the hypotonic challenge. In the presence of K+, Cs+, or methylammonium,[Formula: see text] remained high during most of the hypotonic period, whereas with guanidinium blockage of[Formula: see text] was initiated after 6 min of hypotonicity, suggesting an intracellular location of the site of action. With all cations, 0.5 mM basolateral Gd3+ completely blocked RVD and fully abolished the [Formula: see text] increase induced by the hypotonic shock. The lanthanide also blocked the additional volume increase induced by Cs+, K+, guanidinium, or methylammonium. When pH was lowered from 7.4 to 6.0, RVD and[Formula: see text] were markedly inhibited. This study demonstrates that the VSCCs in the basolateral membrane of A6 cells are permeable to K+, Rb+, Cs+, methylammonium, and guanidinium, whereas a marked inhibitory effect is exerted by Gd3+, protons, and possibly intracellular guanidinium.
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Willett, R. D. "Bis(methylammonium) dibromodichlorocuprate(II)." Acta Crystallographica Section C Crystal Structure Communications 47, no. 5 (May 15, 1991): 1081–82. http://dx.doi.org/10.1107/s0108270190012410.

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Srinivasan, Bikshandarkoil R., Christian Näther, Ashish R. Naik, and Wolfgang Bensch. "Bis(methylammonium) tetrathiomolybdate(VI)." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (June 28, 2006): m1635—m1637. http://dx.doi.org/10.1107/s1600536806022410.

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The structure of the title complex, (CNH6)2[MoS4], consists of tetrahedral tetrathiomolybdate dianions, [MoS4]2−, and two crystallographically independent methylammonium cations, MeNH3 +, all of which are located on mirror planes. The tetrathiomolybdate anions are linked to the organic cations via hydrogen bonding.
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Dissertations / Theses on the topic "Methylammonium"

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Chan, Ka Hin. "Solution processable methylammonium-based transistors with different gate dielectric layers." HKBU Institutional Repository, 2019. https://repository.hkbu.edu.hk/etd_oa/656.

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Hybrid organic-inorganic perovskites has attracted much attention for its diverse optoelectronic applications. Many studies point out that hybrid organic-inorganic perovskites compounds have superior physical properties that can enable these materials to fabricate good performance solar cells. However, there is a lack of repeatable recipe for the fabrication of perovskite transistors with high mobilities. In this work, a detailed investigation has been conducted on the fabrication of Methylammonium-based perovskite compounds transistors on various polymer substrates. A group of methacrylate-based polymers has been chosen as the materials for gate dielectric layers. Generally, we found that the growth of perovskite crystals highly depends on the hydrophobicity of the substrates. More hydrophobic polymer layers yield larger crystal growth, but suppress the adhesion of perovskites crystals. Aromatic groups in methacrylate-based polymers have hydrophobic properties but it still gives better compact perovskite films with larger crystals. Poly(phenyl methacrylate) (PPhMA) enables the growth of the best perovskite films. The best performance of MAPbI3-xClx perovskite transistors was fabricated on PPhMA with an electron mobility µsat = 4.30 cm2 V−1 s−1 at 150 K. Photothermal deflection spectroscopy was used to investigate the subgap optical absorptions of the perovskite films.
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Tombe, Sekai Lana. "Optical and electronic properties of methylammonium lead halide perovskite solar cells." University of the Western Cape, 2017. http://hdl.handle.net/11394/6118.

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Philosophiae Doctor - PhD (Chemistry)
Organic-inorganic hybrid perovskite solar cells have emerged as promising materials for next-generation photovoltaics with certified efficiency of 22.1%. Despite rapid developments, achieving precise control over the morphologies of the perovskite films, enhanced stability and reproducibility of the devices remains challenging. In this work, we employed a low-temperature solution processing technique to attain high efficiency inverted planar heterojunction devices with device architecture ITO/PEDOT:PSS/Perovskite/PCBM/Al (indium doped tin oxide; poly(3,4-ethylenedioxythiophene) polystyrene sulfonate; [6,6]-phenyl-C61-butyric acid methyl ester; aluminium). A perovskite solar cell fabrication technique is developed and opto-electronic characterization of solution-processed planar heterojunction perovskite solar cells based on methylammonium (MA) lead halide derivatives, MAPbI3-xYx (Y = Cl, Br, I) is presented in this thesis work. By employing lead iodide (PbI2) with various amounts of additional methylammonium halides, perovskite precursor solutions were obtained, which were used in the fabrication of four perovskite systems, MAPbI3, MAPbI3-xClx and MAPbI3-xBrx and MAPbBr3. The absorption and photoluminescence (steady state and temperature-dependent) behavior were explored in this compositional space.
2021-08-31
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Sendner, Michael [Verfasser], and Annemarie [Akademischer Betreuer] Pucci. "Infrarotspektroskopische Untersuchungen von Methylammonium-Blei-Halogenid-Perowskiten / Michael Sendner ; Betreuer: Annemarie Pucci." Heidelberg : Universitätsbibliothek Heidelberg, 2017. http://d-nb.info/1179189426/34.

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Grossman, Shau. "Methylammonium Formate as a Mobile Phase Modifier for Reversed Phase Liquid Chromatography." Miami University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=miami1217890628.

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Leguy, Aurélien. "Fundamental properties, disorder and stability of methylammonium lead halide perovskites for solar cells." Thesis, Imperial College London, 2016. http://hdl.handle.net/10044/1/50307.

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Hybrid perovskite semiconductors from the MAPbX3 family (MA= CH3NH3; X = I, Br, Cl) can be used to make efficient ( > 22 %) solar cells despite disorder introduced by solution processing. Much remains to be understood about these materials. Optical constants of MAPbX3 single crystals derived from ellipsometry measurements are assigned to inter-band transitions from electronic structure calculations. These are used to simulate the contributions from different optical transitions to a typical transient absorption spectrum. The ellipsometry measurements are further used to show the reversible formation of CH3NH3PbI2·H2O and/or (CH3NH3)4PbI6·2H2O in single crystals thin films and devices upon exposure of MAPbI3 to water vapour, which is an important degradation pathway. Quasi-elastic neutron measurements allowed the dynamics of MA cations to be probed in the material. The dipolar MA+ reorientate between preferred alignments with a room temperature residence time of ~14 ps. Collective realignment of MA+ to screen a device’s built-in potential could reduce photovoltaic performance. However, the timescale for a domain wall to traverse a typical device is roughly estimated to be ~0.1 – 1 ms, faster than most observed hysteresis in MAPbI3 solar cells. Temperature dependent Raman and terahertz spectroscopy measurements indicate that MA+ reorientations are crucial to the transport properties of the material. Most of the vibrational features in MAPbX3 observed between 50 and 3500 cm-1 are assigned to calculated vibrational modes. The presence of additional peaks in the experimental spectra might be due to mode splitting caused by dynamic effects. The spectral linewidths of MAPbX3 indicate unusually short phonon lifetimes, linked to its low lattice thermal conductivity. This suggests that optical rather than acoustic phonon scattering prevails at room temperature in these materials, limiting charge mobility. These findings highlight the central role of disorder and heterogeneity to the optoelectronic properties of MAPbX3 and its impact on device behaviour and stability.
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Miller, David. "The Defect Structure and Performance of Methylammonium Lead Trihalide Thin-film Based Photovoltaics." Thesis, University of Oregon, 2017. http://hdl.handle.net/1794/22662.

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In order to limit global warming to 1.5-2 °C deployed solar photovoltaic (PV) power must increase from today's 0.228 terawatts to 2-10 terawatts installed by 2030, depending on demand. These goals require increasing manufacturing capacity, which, in turn, requires lowering the cost of electricity produced by PV. However, high demand scenarios will require greater cost reductions in order to make PV generated electricity as competitive as it needs to be to enable this growth. It is unclear whether established PV technologies — silicon, CdTe, GaAs, or CuInxGa1-xSe2 — can achieve the necessary breakthroughs in efficiency and price. A newer technology known as the 'perovskite solar cell' (PSC) has recently emerged as promising contender.
     In the last seven years the efficiency of PSCs increased by the same amount covered by established technologies in the last thirty. However, PSCs suffer from chemical instability under operating conditions and hysteresis in current-voltage measurements used to characterize power output. Characterizing the defect structures formed by this material and how they interact with device performance and degradation may allow stabilization of PSCs. To that end, this work investigates defects in perovskite solar cells, the impact of these defects on performance, and the effect of alloying and degradation on the electronically active defect structure. Chapter I gives a brief introduction, motivating research in solar cells generally and perovskites in particular as well as introducing some challenges the technology faces. Chapter II gives some background in semiconductors and the device physics of solar cells. Chapter III introduces the performance and defect characterization methods employed. Chapter IV discusses results of these measurements on methylammonium lead triiodide cells correlating defects with device performance. Chapter V applies the some of the same techniques to a series of CH3NH3Pb(I1-xBrx)3 based perovskites aged for up to 2400 hours to explore the impact of alloying and aging on the defect structure. Chapter VI discusses implications for perovskite development and directions for future research.
     This dissertation includes previously published co-authored material.
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Giesbrecht, Nadja [Verfasser], and Thomas [Akademischer Betreuer] Bein. "Methylammonium lead halide thin film crystallization for optoelectronic applications / Nadja Giesbrecht ; Betreuer: Thomas Bein." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1189585057/34.

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Song, Zhaoning. "Solution Processed High Efficiency Thin Film Solar Cells: from Copper Indium Chalcogenides to Methylammonium Lead Halides." University of Toledo / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1470403462.

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Shrestha, Shreetu [Verfasser], Christoph J. [Akademischer Betreuer] Brabec, and Rainer [Gutachter] Hock. "Methylammonium Lead Iodide Perovskite for Direct X-ray Detection / Shreetu Shrestha ; Gutachter: Rainer Hock ; Betreuer: Christoph J. Brabec." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2018. http://d-nb.info/1172972362/34.

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Dachauer, Ralph [Verfasser], Wolfram [Akademischer Betreuer] Jaegermann, and Oliver [Akademischer Betreuer] Clemens. "Fabrication of methylammonium lead iodide thin films via sequential closed space sublimation / Ralph Dachauer ; Wolfram Jaegermann, Oliver Clemens." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2019. http://d-nb.info/1201482259/34.

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Book chapters on the topic "Methylammonium"

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Holze, Rudolf. "Ionic conductivities of methylammonium formate." In Electrochemistry, 839. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_749.

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Holze, Rudolf. "Ionic conductivities of methylammonium formate." In Electrochemistry, 973. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_875.

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Koh, Teck M., Biplab Ghosh, Padinhare C. Harikesh, Subodh Mhaisalkar, and Nripan Mathews. "Beyond Methylammonium Lead Iodide Perovskite." In Halide Perovskites, 155–81. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527800766.ch2_04.

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Holze, Rudolf. "Ionic conductance of methylammonium picrate." In Electrochemistry, 560. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_527.

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Zhang, Suojiang, Qing Zhou, Xingmei Lu, Yuting Song, and Xinxin Wang. "Properties of tris(2-hydroxyethyl)methylammonium methylsulfate mixtures." In Physicochemical Properties of Ionic Liquid Mixtures, 1245–50. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-017-7573-1_167.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetrakis(methylammonium)-hexachloroferrate(III) chloride." In Magnetic Properties of Paramagnetic Compounds, 70–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_31.

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Holze, Rudolf. "Ionic conductivities of N,N,N,-trioctyl-N-methylammonium 2,2,2-trifluoroethylsulfate." In Electrochemistry, 1042. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_944.

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Holze, Rudolf. "Ionic conductivities of N,N,N,-trioctyl-N-methylammonium 2,2,3,3,-tetrafluoropropylsulfate." In Electrochemistry, 1043. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_945.

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Holze, Rudolf. "Ionic conductivities of N,n,n,-trioctyl-n-methylammonium 2,2,3,3,4,4,5,5-octafluoropentylsulfate." In Electrochemistry, 1044. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_946.

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Holze, Rudolf. "Ionic conductivities of diethyl-(2-methoxy-ethyl)-methylammonium bis(2,2,2-trifluoroethoxysulfonyl)imid." In Electrochemistry, 1027. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_929.

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Conference papers on the topic "Methylammonium"

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Senocrate, Alessandro, Igor Moudrakovski, Tolga Acartuerk, Gee Yeong Kim, Rotraut Merkle, Ulrich Starke, Michael Graetzel, and Joachim Maier. "Slow methylammonium migration in methylammonium lead iodide in the dark and under illumination." In 11th International Conference on Hybrid and Organic Photovoltaics. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.hopv.2019.078.

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Shcherbakov, Andrii, Shangpu Liu, Manfred Stemplinger, Jonathan Zerhoch, Stanislav Bodnar, and Felix Deschler. "Inhomogeneities in nanoscale Optical and Electronic Properties of the Methylammonium Lead Trihalide Perovskites." In Frontiers in Optics. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fio.2022.jtu4a.22.

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In this work, we unveil the nanoscale inhomogeneities in films of some Methylammonium Lead Trihalide Perovskites with super-resolution nearfield optical microscopy and how they influence the performance of hybrid perovskites.
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Tsui, Hei Chit Leo, Dumitru Sirbu, Naseem Alsaif, Susana Iglesias-Porras, Yifeng Zhang, Ming Wang, Mingzhen Liu, Anna C. Peacock, Pablo Docampo, and Noel Healy. "A Wide Band-gap Metal-free Perovskite for Nonlinear Optics." In Novel Optical Materials and Applications. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/noma.2022.notu3f.3.

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This paper introduces metal-free perovskite structures for third-order nonlin-ear optical processes. Bench-marked against the lead-based prototypical methylammonium lead iodide materials system, their nonlinear figure of merit can be greater by over an order of magnitude.
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Röhm, Holger, Tobias Leonhard, Alexander D. Schulz, Susanne Wagner, Michael J. Hoffmann, and Alexander Colsmann. "Ferroelectric poling of methylammonium lead iodide thin films." In Organic, Hybrid, and Perovskite Photovoltaics XXI, edited by Kwanghee Lee, Zakya H. Kafafi, Paul A. Lane, Harald W. Ade, and Yueh-Lin (Lynn) Loo. SPIE, 2020. http://dx.doi.org/10.1117/12.2568891.

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Leonhard, Tobias, Holger Röhm, Alexander Schulz, Susanne Wagner, Michael J. Hoffmann, and Alexander Colsmann. "Ferroelectricity in methylammonium lead iodide perovskite solar cells." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.308.

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Leonhard, Tobias, Holger Röhm, Alexander Schulz, Susanne Wagner, Michael J. Hoffmann, and Alexander Colsmann. "Ferroelectricity in methylammonium lead iodide perovskite solar cells." In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.308.

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Ehrler, Bruno. "Ion migration in methylammonium lead halide perovskites (Conference Presentation)." In Physical Chemistry of Semiconductor Materials and Interfaces XVII, edited by Hugo A. Bronstein and Felix Deschler. SPIE, 2018. http://dx.doi.org/10.1117/12.2320259.

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Leonhard, Tobias, Holger Röhm, Alexander Schulz, Susanne Wagner, Fabian Altermann, Wolfgang Rheinheimer, Michael J. Hoffmann, and Alexander Colsmann. "Probing the Microstructure of Methylammonium Lead Iodide Solar Cells." In Optics for Solar Energy. Washington, D.C.: OSA, 2018. http://dx.doi.org/10.1364/ose.2018.om2d.6.

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Bhardwaj, Shubhangi, Ashutosh Mohanty, Ranjan Das, Pallavi Singh, Ankit Singh, Dipankar Das Sarma, and Sushobhan Avasthi. "Dielectric Properties of Acetamidinium Substituted Methylammonium Lead Iodide Perovskite." In 2022 IEEE International Conference on Emerging Electronics (ICEE). IEEE, 2022. http://dx.doi.org/10.1109/icee56203.2022.10118156.

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Charest, Jessica, Ryan Tan, Bogdan Dryzhakov, Kate Higgins, Christopher Busch, Bin Hu, Mahshid Ahmadi, and Eric Lukosi. "Dual Gamma/Neutron Sensing with Methylammonium Lead Tribromide Perovskite." In 2020 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC). IEEE, 2020. http://dx.doi.org/10.1109/nss/mic42677.2020.9507877.

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