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Literatura académica sobre el tema "Manganese perovskites"

Autor: Grafiati

Publicado: 25 de mayo de 2024

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Artículos de revistas sobre el tema "Manganese perovskites"

1

Liu, Wei, Liang Chu, Nanjing Liu, Yuhui Ma, Ruiyuan Hu, Yakui Weng, Hui Li, Jian Zhang, Xing’ao Li y Wei Huang. "Efficient perovskite solar cells fabricated by manganese cations incorporated in hybrid perovskites". Journal of Materials Chemistry C 7, n.º 38 (2019): 11943–52. http://dx.doi.org/10.1039/c9tc03375k.

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Alagheband, Razieh, Sarah Maghsoodi, Amirhossein Shahbazi Kootenaei y Hassan Kianmanesh. "Synthesis and Evaluation of ABO3 Perovskites (A=La and B=Mn, Co) with Stoichiometric and Over-stoichiometric Ratios of B/A for Catalytic Oxidation of Trichloroethylene". Bulletin of Chemical Reaction Engineering & Catalysis 13, n.º 1 (2 de abril de 2018): 47. http://dx.doi.org/10.9767/bcrec.13.1.1188.47-56.

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In this contribution, perovskite catalysts (ABO3) were probed that site A and site B were occupied by lanthanum and transition metals of manganese or cobalt, respectively, with stoichiometric ratios as well as 20 % over-stoichiometric ratios of B/A. The perovskite samples were synthesized using a gel-combustion method and characterized by BET, XRD, SEM and O2-TPD analyses. After mounting in a fixed bed reactor, the catalysts were examined in atmospheric pressure conditions at different temperatures for oxidation of 1000 ppm trichloroethylene in the air. Evaluation of over-stoichiometric catalysts activity showed that the increased ratio of B/A in the catalysts compared to the stoichiometric one led to BET surface area, oxygen mobility, and consequently catalytic performance improvement. The lanthanum manganite perovskite with 20 % excess manganese yielded the best catalytic performance among the probed perovskites. Copyright © 2018 BCREC Group. All rights reservedReceived: 28th April 2017; Revised: 31st July 2017; Accepted: 4th August 2017; Available online: 22nd January 2018; Published regularly: 2nd April 2018How to Cite: Alagheband, R., Maghsoodi, S., Kootenaei, A.S., Kianmanesh, H. (2018). Synthesis and Evaluation of ABO3 Perovskites (A=La and B=Mn, Co) with Stoichiometric and Over-stoichiometric Ratios of B/A for Catalytic Oxidation of Trichloroethylene. Bulletin of Chemical Reaction Engineering & Catalysis, 13 (1): 47-56 (doi:10.9767/bcrec.13.1.1188.47-56)

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3

Karpenko, Boris V., Lyubov D. Falkovskaya y Alexandr V. Kuznetsov. "Magnetization of Manganese Perovskites". Israel Journal of Chemistry 47, n.º 3-4 (diciembre de 2007): 397–400. http://dx.doi.org/10.1560/ijc.47.3-4.397.

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4

ZHANG, NING. "SPIN-POLARIZATION DEPENDENT SMALL POLARON HOPPING IN MANGANESE PEROVSKITES". Modern Physics Letters B 17, n.º 01 (10 de enero de 2003): 25–38. http://dx.doi.org/10.1142/s0217984903004816.

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A model of small polaron hopping being dependent on spin-polarization is suggested to describe the transport and the colossal magnetoresistance behaviors in manganese perovskites R-A-Mn-O (R: rear earth; A: alkali earth or transition metals). Being different from the theory of simple small polarons, the double exchange interaction and some empirical rules related to lattice effect induced by an external magnetic field and changing concentration have been taken into account. Based on this, a simple formula of resistivity versus temperature, concentration and normalized magnetization has been obtained for the hole-doped perovskite. From the formula, most of the transport behaviors including the colossal magnetoresistive observed in the perovskite have been successfully illustrated.

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5

Hueso, L. E., A. Fondado, J. Rivas, F. Rivadulla y M. A. López-Quintela. "Efectos intergranulares en perovskitas de manganeso nanocristalinas". Boletín de la Sociedad Española de Cerámica y Vidrio 39, n.º 3 (30 de junio de 2000): 259–62. http://dx.doi.org/10.3989/cyv.2000.v39.i3.837.

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6

Stefańska, Dagmara. "Effect of Organic Cation on Optical Properties of [A]Mn(H2POO)3 Hybrid Perovskites". Molecules 27, n.º 24 (15 de diciembre de 2022): 8953. http://dx.doi.org/10.3390/molecules27248953.

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Hybrid organic–inorganic compounds crystallizing in a three-dimensional (3D) perovskite-type architecture have attracted considerable attention due to their multifunctional properties. One of the most intriguing groups is perovskites with hypophosphite linkers. Herein, the optical properties of six hybrid hypophosphite perovskites containing manganese ions are presented. The band gaps of these compounds, as well as the luminescence properties of the octahedrally coordinated Mn2+ ions associated with the 4T1g(G) → 6A1g(S) transition are shown to be dependent on the organic cation type and Goldschmidt tolerance factor. Thus, a correlation between essential structural features of Mn-based hybrid hypophosphites and their optical properties was observed. Additionally, the broad infrared luminescence of the studied compounds was examined for potential application in an indoor lighting system for plant growth.

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7

Yang, Zhengqiang, Guanqun Cai, Craig L. Bull, Matthew G. Tucker, Martin T. Dove, Alexandra Friedrich y Anthony E. Phillips. "Hydrogen-bond-mediated structural variation of metal guanidinium formate hybrid perovskites under pressure". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 377, n.º 2149 (27 de mayo de 2019): 20180227. http://dx.doi.org/10.1098/rsta.2018.0227.

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The hybrid perovskites are coordination frameworks with the same topology as the inorganic perovskites, but with properties driven by different chemistry, including host-framework hydrogen bonding. Like the inorganic perovskites, these materials exhibit many different phases, including structures with potentially exploitable functionality. However, their phase transformations under pressure are more complex and less well understood. We have studied the structures of manganese and cobalt guanidinium formate under pressure using single-crystal X-ray and powder neutron diffraction. Under pressure, these materials transform to a rhombohedral phase isostructural to cadmium guanidinium formate. This transformation accommodates the reduced cell volume while preserving the perovskite topology of the framework. Using density-functional theory calculations, we show that this behaviour is a consequence of the hydrogen-bonded network of guanidinium ions, which act as struts protecting the metal formate framework against compression within their plane. Our results demonstrate more generally that identifying suitable host–guest hydrogen-bonding geometries may provide a route to engineering hybrid perovskite phases with desirable crystal structures. This article is part of the theme issue ‘Mineralomimesis: natural and synthetic frameworks in science and technology’.

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8

Millis, A. J. "Lattice effects in magnetoresistive manganese perovskites". Nature 392, n.º 6672 (marzo de 1998): 147–50. http://dx.doi.org/10.1038/32348.

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9

Fontcuberta, J., J. L. Garcı́a-Muñoz, M. Suaaidi, B. Martı́nez, S. Piñol y X. Obradors. "Competing magnetic interactions in manganese perovskites". Journal of Applied Physics 81, n.º 8 (15 de abril de 1997): 5481–83. http://dx.doi.org/10.1063/1.364633.

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10

Ibarra, M. R. y J. M. De Teresa. "Colossal magnetoresistance in manganese oxide perovskites". Journal of Magnetism and Magnetic Materials 177-181 (enero de 1998): 846–49. http://dx.doi.org/10.1016/s0304-8853(97)00801-9.

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Tesis sobre el tema "Manganese perovskites"

1

Parsons, Thomas. "The anion chemistry of manganese perovskites". Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.497068.

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Ovalle, Alejandro. "Manganese titanium perovskites as anodes for solid oxide fuel cells". Thesis, St Andrews, 2008. http://hdl.handle.net/10023/567.

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Williams, Anthony James. "Synthesis and neutron diffraction studies of manganese oxide perovskites". Thesis, University of Cambridge, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.615786.

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Rodríguez-Martínez, Lide Mercedes. "The effects of cation disorder in manganese oxide perovskites". Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624354.

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Silberstein, Hont Markus. "Modeling the Effects of Strain in Multiferroic Manganese Perovskites". Thesis, KTH, Materialfysik, MF, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-169584.

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The effects of strain on the magnetic phases in perovskites are of interest in the highly active research field of multiferroics. A Monte Carlo program is written to investigate the influence of strain on the low– temperature magnetic phase diagram of the manganese perovskites, RMnO3, where R is a cation in the lanthanide series. A Metropolis simulation scheme is implemented together with parallel tempering to perform computations in a two–dimensional geometry using a conventional nearest–neighbor and next–nearest–neighbor Heisenberg Hamiltonian, extended to include spin–lattice couplings and single–ion anisotropies. The latter two are important to account for structural distortions such as octahedral tilting and the Jahn–Teller effect. It is shown that even weak single–ion anisotropies render incommensurability in the otherwise structurally commensurate E–type ordering, and that the Dzyaloshinskii–Moriya interaction, in combination with single–ion anisotropies, is crucial for the stabilization of previously experimentally observed incommensurate spin spirals. Simulations performed to account for strain in the crystallographic ab–plane show that tensile strain may improve stability of E–type ordering for R elements with small atomic radii and that compressive strain drives the magnetic ordering toward the incommensurate spiral states.
Spänningsinverkan på de magnetiska faserna i perovskiter är av intresse inom den just nu högaktiva forskningen om multiferroiska material. Ett Monte Carlo-program har skrivits för att undersöka effekterna av spän- ning på de magnetiska lågtemperaturfaserna i multiferroiska manganitpe- rovskiter, RMnO3, där R är en katjon i lantanoidserien. En kombination av Metropolisalgoritmen och parallelltemperering har använts för att utföra beräkningar i tvådimensionell geometri med en konventionell Heisenberghamiltonian, utökad till att även inkludera spinn–gitterkopplingar och enkeljonsanisotropier. De senare har visats vara viktiga för att ta i beaktande den strukturella distortion i materialet som följer av t.ex. syreoktahederförskjutning och Jahn–Tellereffekten. Det visas att även svaga anisotropier orsakar inkommensurabilitet i den i övrigt kommensurabla E–typsfasen, och att Dzyaloshinskii-Moriyainteraktionen, i kombination med anisotropitermerna, är avgörande för att kunna stabilisera de sedan tidigare experimentellt bekräftade inkommensurabla spinnspiralsfaserna. Simuleringar som modellerar spänning i materialets kristallografiska ab–plan visar att dragspänning kan förbättra stabiliteten hos E–typsfasen för R–atomer med liten radie och att tryckspänning leder den magnetiska ordningen mot inkommensurabla spiraltillstånd.

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6

Kruth, Angela. "Synthesis and characterisation of a novel oxygen- deficient manganese-based perovskite series". Thesis, University of Aberdeen, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310732.

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A family of oxygen-deficient perovskite phases with compositions, Ca₂Mn_2-xNb_xO_γ has been synthesised and characterised using X-ray Powder Diffraction and Thermogravimetry. Property characterisation has included the study of electrical properties by Impedance Spectroscopy and the investigation of magnetic properties for one composition, x = 1.0. Some compositions were tested for possible application as electrode materials in gas sensors. The Ca₂Mn_2-xNb_xO_γ system 0 ≤ x ≤ 1.2, with variable oxygen content, γ, can accommodate up to 20% vacancies at oxygen sites and Mn occurs in valence states ranging from +2 to +4. Depending on the B-cation ratio and oxygen content, two solid solution form: an extensive GdFeO₃-type solid solution over the entire range of cation content, 0 ≤ x ≤ 1.2, with zero or small oxygen deficiencies and a closely-related, grossly oxygen-deficient solid solution over the range 0.3 ≤ x ≤ 0.8 with a simple cubic perovskite structure. Unit cell volume and orthorhombic GdFeO₃-type distortion vary greatly with Mn valency, oxygen content and B-cation content. The orthorhombic GdFeO₃-type structure of composition x = 1.0 was refined by the Rietveld method. Mn and Nb are disordered over the B-sites. Jahn-Teller activity of Mn³⁺ does not result in cooperative distortions of (Mn,Nb)O₆ octahedra, but it was observed to effect the oxygen stoichiometry. The Nb-rich composition, x = 1.0, can accommodate large amounts of Ca-vacancies (up to 10%). Electrical conductivity varies greatly with the composition. Results suggest that t_2g electrons are responsible for a variation of conductivity and activation energy rather than e_g electrons. Conductivities are believed to depend mainly on the degree of π-orbital overlap between Mn and oxygen and hence, on interatomic distances. At low temperatures, the material exhibits spin glass-like behaviour.

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7

Caignaert, Vincent. "Non-stoechiometrie par creation de lacunes anioniques : oxydes mixtes de manganese et de fer, de structure apparentee a la perovskite". Caen, 1986. http://www.theses.fr/1986CAEN2007.

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Etude des possibilites d'ecarts a la stoechiometrie sur le sous reseau anionique des perovskites amn::(1-x) fe::(x)o::(3-y) (a=ca, sr, ba) par diffraction x et neutron, microscopie electronique haute resolution, spectre moessbauer et mesures magnetiques. Caracterisation de plusieurs types d'ordre des lacunes oxygene en fonction du cation a et du taux de mn

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8

MONTEIRO, NATALIA K. "Síntese e caracterização de manganita-cromita de lantânio dopada com rutênio para anodos de células a combustível de óxidos sólidos". reponame:Repositório Institucional do IPEN, 2011. http://repositorio.ipen.br:8080/xmlui/handle/123456789/10041.

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Made available in DSpace on 2014-10-09T12:34:06Z (GMT). No. of bitstreams: 0
Made available in DSpace on 2014-10-09T14:00:10Z (GMT). No. of bitstreams: 0
Dissertação (Mestrado)
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Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

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9

Geck, Jochen. "Spins, charges, and orbitals in perovskite manganites : resonant and hard x-ray scattering studies /". Berlin : Mensch & Buch Verl, 2004. http://www.loc.gov/catdir/toc/fy0804/2007464041.html.

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Maguire, Elaine T. "Rare earth manganite perovskites". Thesis, University of Aberdeen, 1999. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU603199.

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The 'RMnO3': R = La, Nd, Pr, phases have been synthesised and characterised by a combination of electron probe microanalysis (EPMA), H2-reduction thermogravimetry (TG), x-ray (XRD) and neutron diffraction (ND). RMnO3 forms, at" 1400C, over the ranges: NdMn0, 95Oz to Nd0 88MnOz PrMn0.97O2 to Pr0 88MnOz LaMno 0.90Oz to La0.97MnOz Oxygen contents vary in air over the range 700 to 1400 C and can be varied further, either by high pressure Oz treatment or by reduction in H2. The structure of 'RMnO3' R = Nd, Pr is based on the GdFe03 structure with a Jahn-Teller distortion associated with the high proportion of Mn3+ ions present. The oxygen deficient 'LaMnOz' compositions also exhibit this structure consistent with earlier reports. By combining EPMA, TG, XRD and ND results various defect models describing the stoichiometry and structure of Mn-rich and R-rich, R = Nd, Pr compositions have been summarised. Both R = Nd and Pr systems exhibit very varied defect structures; depending on composition and heat treatment, vacancies can form on any one or any two of the three sublattices, R, Mn and O and the overall Mn oxidation state can include 2+, 3+ and 4+ contributions. For 'RMn03': R = La, Nd, Pr, data on their compositional ranges and defect crystal structures are presented in the form of novel phase diagram-defect structure maps from which the principal defect structure for a given stoichiometry can be easily obtained. The majority of the Pr-Sr-Mn-O pseudotemary phase diagram has been determined. EPMA was used to follow the progress of reaction and the conditions to achieve complete reaction established. Several solid solutions were evidenced, some previously unreported (3 - 6): 1) Pr1.xSrxMnO3 0[Special character omitted]x[Special character omitted]1.0 2) Pr1+xSr2.xMn2O7 0 [Special character omitted]x [Special character omitted] 0.4 3) SrxPr1-xO2 0[Special character omitted]x[Special character omitted]0.16 4) Sr1-xPrO3 0[Special character omitted]x[Special character omitted]0.15 5) Sr2.xMnxO4 6) Sr2.xPrxMnO4 The perovskite-like Pr1-xSrxMnO3 solid solution extends from PrMnOz to SrMnOz. The unit cell symmetry changes from orthorhombic to rhombohedral to tetragonal to cubic and finally to hexagonal as the Sr content increases. The limits of the Ruddlesden Popper (RP) n=2 Pr1+xSr2_xMn2O7 solid solution were determined: 0 [Special character omitted] x [Special character omitted] 0.4 and a tetragonal unit cell observed consistent with the literature. Synthesis of the RP compositions by solid state methods requires long heating times (up to 36 days) to produce homogeneous samples; qualitative EPMA of younger samples indicated an inhomogeneous distribution of Pr and Sr. Contrary to EPMA results, XRD of younger samples indicated that complete reaction had occurred and single phase compositions produced. It is suggested that the SrxPr1-.xO2 solid solution extends over the range 0 [Special character omitted] x [Special character omitted] 0.16 where similarly to the polymorphism of praseodymium oxides, compositions 0.03 [Special character omitted] x [Special character omitted]0.16 exhibit the cubic fluorite-type structure of Pr6O11 and x [Special character omitted] 0.03 is a mixture of cubic SrxPr1-xO2 and hexagonal SrxPr2.xO3. Perovskite-like SrPrO3 exhibits variable cation ratios; the Pr-rich boundary is Sr0.85PrOz. The lower Sr-rich boundary is yet to be identified. Similarly to 'RMnO3': R = La, Nd, Pr, the oxygen content of 'SrPrOz' is expected to vary. Therefore, various possible defect structures describing vacancies on the three sublattices, Sr, Pr and O could exist and charge compensation would be an interesting example of ionic and electronic mechanisms where Pr adopts the +4 and +3 oxidation states. Four layer hexagonal SrMnO3 exhibits variable Sr:Mn ratios but the solid solution limits are not yet known. The unreported Sr2-xPrxMnO4 solid solution has been observed but the solid solution limits are not yet known. The K2NiF4-type structure of Sr2Mn04 is retained at x = 0.75 and is expected to contain Mn3+ as Mn4+ is reduced to compensate Sr24 substitution by Pr3+.

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Libros sobre el tema "Manganese perovskites"

1

Hezareh, Talayeh. Study on the properties of piezoelectric materials and manganese-based oxide perovskites. St. Catharines, Ont: Brock University, Dept. of Physics, 2005.

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Gillie, Lisa Jane. Structural and magnetic studies of manganese perovskite-related materials. Birmingham: University of Birmingham, 2002.

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3

Geck, Jochen. Spins, charges, and orbitals in perovskite manganites: Resonant and hard X-ray scattering studies. Berlin: Mensch & Buch, 2004.

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Capítulos de libros sobre el tema "Manganese perovskites"

1

Dabrowski, B., X. Xiong, O. Chmaissem, Z. Bukowski y J. D. Jorgensen. "Structure- Properties Relationships For Manganese Perovskites". En Supermaterials, 27–36. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-010-0912-6_3.

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Jaenicke, S., G. K. Chuah y J. Y. Lee. "Catalytic CO Oxidation Over Manganese-Containing Perovskites". En Fourth Symposium on our Environment, 131–38. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-2664-9_13.

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Fontcuberta, J., Ll Balcells, B. Martínez y X. Obradors. "Magnetoresistance at Interfaces in Submicrometric Manganese Perovskites Ceramics". En Nano-Crystalline and Thin Film Magnetic Oxides, 105–18. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4493-3_7.

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Zhou, J. S. y J. B. Goodenough. "Orbital Ordering and Vibronic States in Manganese Perovskites". En Vibronic Interactions: Jahn-Teller Effect in Crystals and Molecules, 15–22. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0985-0_3.

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Raveau, B. "Metallic Conductivity and Magnetism: The Great Potential of Manganese and Cobalt Perovskites". En Mixed Ionic Electronic Conducting Perovskites for Advanced Energy Systems, 27–38. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/978-1-4020-2349-1_3.

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Panagiotopoulos, I., M. Pissas, C. Christides, G. Kallias, V. Psycharis, N. Moutis y D. Niarchos. "Colossal Magnetoresistance in Manganese Perovskite Films and Multilayers". En Nano-Crystalline and Thin Film Magnetic Oxides, 119–32. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4493-3_8.

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Solovyev, I. y K. Terakura. "Orbital Degeneracy and Magnetism of Perovskite Manganese Oxides". En Electronic Structure and Magnetism of Complex Materials, 253–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05310-2_6.

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Masrour, Rachid. "Magnetocaloric and Magnetic Properties of Bilayer Manganite". En Magnetoelectronic, Optical, and Thermoelectric Properties of Perovskite Materials, 87–94. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-48967-9_6.

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Pardasani, R. T. y P. Pardasani. "Magnetic properties of double perovskite of lanthanum, gallium and manganese". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1, 44–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_12.

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Masrour, Rachid. "Magnetocaloric Effect, Electronic and Magnetic Properties in Manganite Perovskites". En Magnetoelectronic, Optical, and Thermoelectric Properties of Perovskite Materials, 17–38. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-48967-9_2.

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Actas de conferencias sobre el tema "Manganese perovskites"

1

Kennedy, B. J., Abarrul Ikram, Agus Purwanto, Sutiarso, Anne Zulfia, Sunit Hendrana y Zeily Nurachman. "Powder Diffraction Studies of Phase Transitions in Manganese Perovskites". En NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906095.

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Hetaba, Walid. "HRSTEM-EELS investigation of manganese based perovskites for the oxidative dehydrogenation of propane". En European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.1060.

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Monterrubio-Badillo, C., H. Ageorges, T. Chartier, J. F. Coudert y P. Fauchais. "Chemical Composition Optimization of Perovskite Coatings by Suspension Plasma Spraying for SOFC Cathodes". En ITSC2004, editado por Basil R. Marple y Christian Moreau. ASM International, 2004. http://dx.doi.org/10.31399/asm.cp.itsc2004p0562.

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Abstract The purpose of this work is to optimise the chemical composition of perovskite coatings prepared by injecting a suspension of submicrometric LaMnO3 perovskite particles (d50 =~ 1 µm) in a direct current (d.c.) plasma jet. The perovskite powder composition, the particle size and the plasma parameters were modified in order to diminish the manganese evaporation. The process consists in mechanically injecting a well dispersed stable suspension of submicrometric perovskite particles in a dc plasma jet. In the process, large suspension droplets (~300 µm) are sheared into tiny ones (a few µm) by the plasma jet flow. Then the solvent is evaporated and the particles melt resulting in perovskite droplets of about 1 µm impacting on the substrate, the coating resulting from their layering. Such coatings are to be used as cathodes for the SOFCs (Solid Oxide Fuel Cells). Best results were obtained by injecting a stable suspension containing a 10 mol% MnO2 doped perovskite powder with 3 µm particle size in an Ar plasma forming gas and 300 A of current intensity.

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Matuhina, Anastasia, G. Krishnamurthy Grandhi, Maning Liu, Jan-Henrik Smått, Harri Ali-Löytty y Paola Vivo. "Luminescent all-inorganic manganese halide perovskite nanocrystals". En nanoGe Spring Meeting 2022. València: Fundació Scito, 2022. http://dx.doi.org/10.29363/nanoge.nsm.2022.168.

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Liu, H. L., S. Yoon, S. L. Cooper, S.-W. Cheong y P. D. Han. "Electronic Raman scattering in the perovskite manganese oxides". En High temperature superconductivity. AIP, 1999. http://dx.doi.org/10.1063/1.59603.

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Strashevskyi, A. V., M. K. Khodzitsky y S. I. Tarapov. "Photonic crystals based on manganite-perovskite structure". En 2010 International Kharkov Symposium on Physics and Engineering of Microwaves, Millimeter and Submillimeter Waves (MSMW). IEEE, 2010. http://dx.doi.org/10.1109/msmw.2010.5545955.

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Huang, Yingqun, Xiong Li, Xinglai Che y Hailang Ju. "Preparation and characterization of A-site doped Perovskite-type manganese oxides". En ISPDI 2013 - Fifth International Symposium on Photoelectronic Detection and Imaging, editado por Min Gu, Xiaocong Yuan y Min Qiu. SPIE, 2013. http://dx.doi.org/10.1117/12.2032759.

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Halizan, M. Z. M., Z. Mohamed y A. K. Yahya. "Structural properties of tellurium based double perovskite with small doped of manganese". En PROCEEDINGS OF THE 2ND PHYSICS AND MATERIALS SCIENCE INTERNATIONAL SYMPOSIUM (PhyMaS 2.0). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0057779.

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Tachikawa, Sumitaka, Akira Ohnishi, Yuichi Shimakawa, Atsushi Ochi, Akira Okamoto y Yasuyuki Nakamura. "Development of a Variable Emittance Radiator Based on a Perovskite Manganese Oxide". En 8th AIAA/ASME Joint Thermophysics and Heat Transfer Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2002. http://dx.doi.org/10.2514/6.2002-3017.

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Batdemberel, G., G. Bulgan, R. E. Dinnebier, P. Munkhbaatar, D. Sangaa y Sh Chadraabal. "Rietveld refinement of nanostructural LaMnO3+δ perovskite-type manganite". En 2010 International Forum on Strategic Technology (IFOST). IEEE, 2010. http://dx.doi.org/10.1109/ifost.2010.5668011.

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