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Thematische Bibliographien / Spectroscopie Mössbauer in situ / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Spectroscopie Mössbauer in situ“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 4. Mai 2024

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1

Fleischer, Iris, Göstar Klingelhöfer, Richard V. Morris, Christian Schröder, Daniel Rodionov, and Paulo A. de Souza. "In-situ Mössbauer spectroscopy with MIMOS II." Hyperfine Interactions 207, no. 1-3 (2011): 97–105. http://dx.doi.org/10.1007/s10751-011-0437-y.

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2

BIBICU, ION. "Nanomaterials characterization by Mössbauer spectroscopy." Journal of Engineering Sciences and Innovation 3, no. 3 (2018): 239–50. http://dx.doi.org/10.56958/jesi.2018.3.3.239.

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Mössbauer spectroscopy has one of its most important features the ability to undertake bulk of varying thickness using the secondary radiation emitted after resonant absorption of a gamma ray. Using emitted electrons it is possible to characterize the nanomaterials. It is a non-destructive technique that can be applied in situ investigations. A short description of the technique is given. The author presents the detectors achieved for these studies and the principal results in nanomaterial characterization. Few results are described more detailed.

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3

Loup, Joachim, Tobias Parchomyk, Stefan Lülf, et al. "Mössbauer and mass spectrometry support for iron(ii) catalysts in enantioselective C–H activation." Dalton Transactions 48, no. 16 (2019): 5135–39. http://dx.doi.org/10.1039/c9dt00705a.

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A combination of electrospray-ionization mass spectrometry and Mössbauer spectroscopy was used to investigate the species generated in situ in highly enantioselective Fe/NHC-catalyzed C–H alkylations.

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4

Dräger, Christoph, Florian Sigel, Ralf Witte, et al. "Observation of electrochemically active Fe3+/Fe4+ in LiCo0.8Fe0.2MnO4 by in situ Mössbauer spectroscopy and X-ray absorption spectroscopy." Physical Chemistry Chemical Physics 21, no. 1 (2019): 89–95. http://dx.doi.org/10.1039/c8cp06177g.

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5

Clausen, Bjerne S., and Henrik TopsØe. "In-situ studies of catalysts by XAFS and Mössbauer spectroscopy." Hyperfine Interactions 47-48, no. 1-4 (1989): 203–17. http://dx.doi.org/10.1007/bf02351608.

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6

Fournes, L., J.-C. Grenier, C. Chanson, P. Bezdicka, A. Wattiaux, and M. Pouchard. "Use of in situ Mössbauer spectroscopy for electrochemical reactions involving57Fe." Hyperfine Interactions 57, no. 1-4 (1990): 1829–32. http://dx.doi.org/10.1007/bf02405729.

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7

Dézsi, I., and Cs Fetzer. "In situ study of electrodeposited thin layers by Mössbauer spectroscopy." Electrochemistry Communications 9, no. 7 (2007): 1846–49. http://dx.doi.org/10.1016/j.elecom.2007.04.007.

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8

Aldon, Laurent, and Alexis Perea. "2D-correlation analysis applied to in situ and operando Mössbauer spectroscopy." Journal of Power Sources 196, no. 3 (2011): 1342–48. http://dx.doi.org/10.1016/j.jpowsour.2010.08.013.

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9

Fleischer, I., G. Klingelhöfer, F. Rull, et al. "In-situ Mössbauer Spectroscopy with MIMOS II at Rio Tinto, Spain." Journal of Physics: Conference Series 217 (March 1, 2010): 012062. http://dx.doi.org/10.1088/1742-6596/217/1/012062.

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10

Ksenofontov, V., S. Reiman, M. Waldeck, R. Niewa, R. Kniep, and P. Gütlich. "In situ— High Temperature Mössbauer Spectroscopy of Iron Nitrides and Nitridoferrates." Zeitschrift für anorganische und allgemeine Chemie 629, no. 10 (2003): 1787–94. http://dx.doi.org/10.1002/zaac.200300135.

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11

Aboulaich, Abdelmaula, Florent Robert, Pierre Emmanuel Lippens, et al. "In situ 119Sn Mössbauer spectroscopy study of Sn-based electrode materials." Hyperfine Interactions 167, no. 1-3 (2006): 733–38. http://dx.doi.org/10.1007/s10751-006-9358-6.

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12

Marras, Giulia, Gabriele Carnevale, Antonio Caracausi, Silvio Giuseppe Rotolo, and Vincenzo Stagno. "First measurements of the Fe oxidation state of spinel inclusions in olivine single crystals from Vulture (Italy) with the in situ synchrotron micro-Mössbauer technique." European Journal of Mineralogy 35, no. 4 (2023): 665–78. http://dx.doi.org/10.5194/ejm-35-665-2023.

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Abstract. The redox state of the Earth's upper mantle (i.e., oxygen fugacity, fO2) is a key variable that influences numerous processes occurring at depth like the mobility of volatile species, partial melting, and metasomatism. It is linked to the oxidation state of peridotite rocks, which is normally determined through the available oxythermobarometers after measuring the chemical composition of equilibrated rock-forming minerals and the Fe3+ in redox-sensitive minerals like spinel or garnet. To date, accurate measurements of Fe3+ / ∑Fe in peridotites have been limited to those peridotites (

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13

Berry, Frank J., Lin Liwu, Du Hongzhang, et al. "An in situ Mössbauer spectroscopic investigation of titania-supported iron–ruthenium catalysts." Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases 83, no. 8 (1987): 2573. http://dx.doi.org/10.1039/f19878302573.

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14

BARTELS, O., K. BECKER, E. BUCHER та W. SITTE. "In-situ Mössbauer spectroscopy and thermogravimetry of La0.2Sr0.8FeO3−Δ and La0.4Sr0.6FeO3−Δ". Solid State Ionics 177, № 19-25 (2006): 1677–80. http://dx.doi.org/10.1016/j.ssi.2006.03.042.

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15

Bødker, F., I. Chorkendorff та S. Mørup. "Nitrogen chemisorption on α -Fe nanoparticles studied by in situ Mössbauer spectroscopy". Zeitschrift f�r Physik D Atoms, Molecules and Clusters 40, № 1-4 (1997): 152–54. http://dx.doi.org/10.1007/s004600050181.

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16

Peña Rodrı́guez, V. A., J. Flores Regalado, E. Baggio-Saitovitch, and E. C. Passamani. "Nanocrystallization process in Finemet-type alloys followed by in situ Mössbauer spectroscopy." Journal of Alloys and Compounds 379, no. 1-2 (2004): 23–27. http://dx.doi.org/10.1016/j.jallcom.2004.02.023.

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17

Lázár, K., A. M. Szeleczky, N. K. Mal, and A. V. Ramaswamy. "In situ 119Sn-Mössbauer spectroscopic study on MR, MEL, and MTW tin silicalites." Zeolites 19, no. 2-3 (1997): 123–27. http://dx.doi.org/10.1016/s0144-2449(97)00056-0.

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18

Mitov, I., S. Asenov, T. Tomov, and A. Andreev. "In situ Mössbauer spectroscopic investigation of iron-oxide based water-gas shift catalysts." Reaction Kinetics & Catalysis Letters 50, no. 1-2 (1993): 145–50. http://dx.doi.org/10.1007/bf02062201.

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19

David, B., N. Pizúrová, O. Schneeweiss, T. Hoder, V. Kudrle, and J. Janča. "Iron-Based Nanocomposite Synthesised by Microwave Plasma Decomposition of Iron Pentacarbonyl." Defect and Diffusion Forum 263 (March 2007): 147–52. http://dx.doi.org/10.4028/www.scientific.net/ddf.263.147.

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A nanocrystalline iron-based powder has been prepared by microwave plasma method: Fe(CO)5 vapor was introduced into an argon discharge at ~1 kPa. A microwave 2.45 GHz generator was operated at 430 W. The reaction took place inside a quartz tube passing through a microwave waveguide. The microwave discharge (without and with Fe(CO)5) was characterized by optical emission spectroscopy. The synthesized nanopowder was passivated in situ with air. The asprepared nanopowder was characterized by TEM, XRD, Raman and Mössbauer spectroscopies. The nanopowder included α-Fe, α-Fe2O3, and Fe3O4 phases. The

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20

Aldon, L., C. M. Ionica, P. E. Lippens, et al. "In situ 119Sn Mössbauer spectroscopy used to study lithium insertion in c-Mg2Sn." Hyperfine Interactions 167, no. 1-3 (2006): 729–32. http://dx.doi.org/10.1007/s10751-006-9366-6.

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21

Korecki, J., and U. Gradmann. "In-situ conversion electron Mössbauer spectroscopy on Fe(110)-surfaces and thin films." Hyperfine Interactions 28, no. 1-4 (1986): 931–34. http://dx.doi.org/10.1007/bf02061597.

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22

Kirsch, Andrea, M. Mangir Murshed, Piotr Gaczynski, Klaus-Dieter Becker, and Thorsten M. Gesing. "Bi2Fe4O9: Structural changes from nano- to micro-crystalline state." Zeitschrift für Naturforschung B 71, no. 5 (2016): 447–55. http://dx.doi.org/10.1515/znb-2015-0227.

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AbstractBi2Fe4O9 was synthesized using a polyol-mediated method. X-ray powder diffraction (XRPD) revealed that the as-synthesized sample is nano-crystalline. During heating, the X-ray amorphous powder transformed into a rhombohedral perovskite-type bismuth ferrate followed by a second transformation into mullite-type Bi2Fe4O9 at higher temperatures. This transformation was studied at in-situ conditions by temperature-dependent XRPD and 57Fe Mössbauer spectroscopy. The 57Fe Mössbauer spectra indicate the existence of two Fe3+ species at two different octahedrally coordinated sites leading to th

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23

de Resende, Valdirene G., Alain Peigney, Eddy De Grave, and Christophe Laurent. "In situ high-temperature Mössbauer spectroscopic study of carbon nanotube–Fe–Al2O3 nanocomposite powder." Thermochimica Acta 494, no. 1-2 (2009): 86–93. http://dx.doi.org/10.1016/j.tca.2009.04.024.

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24

Lázár, K., G. Lejeune, R. K. Ahedi, S. S. Shevade, and A. N. Kotasthane. "Interpreting the Oxidative Catalytic Activity in Iron-Substituted Ferrierites Using in Situ Mössbauer Spectroscopy." Journal of Physical Chemistry B 102, no. 25 (1998): 4865–70. http://dx.doi.org/10.1021/jp9734639.

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25

Hou, Kaipeng, Jonas Börgel, Henry Z. H. Jiang, et al. "Reactive high-spin iron(IV)-oxo sites through dioxygen activation in a metal–organic framework." Science 382, no. 6670 (2023): 547–53. http://dx.doi.org/10.1126/science.add7417.

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In nature, nonheme iron enzymes use dioxygen to generate high-spin iron(IV)=O species for a variety of oxygenation reactions. Although synthetic chemists have long sought to mimic this reactivity, the enzyme-like activation of O 2 to form high-spin iron(IV) = O species remains an unrealized goal. Here, we report a metal–organic framework featuring iron(II) sites with a local structure similar to that in α-ketoglutarate-dependent dioxygenases. The framework reacts with O 2 at low temperatures to form high-spin iron(IV) = O species that are characterized using in situ diffuse reflectance infrare

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26

Luo, Fang, Aaron Roy, Moulay-Tahar Sougrati, et al. "Operando x-Ray Absorption Spectroscopy Investigation of Secondary Metal Doping into Iron-Nitrogen-Carbon Catalysts for Oxygen Electroreduction." ECS Meeting Abstracts MA2023-02, no. 55 (2023): 2676. http://dx.doi.org/10.1149/ma2023-02552676mtgabs.

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Oxygen reduction reaction (ORR) plays a key role in the development of fuel cell technology, and great efforts have been made to reduce the amount of platinum, required to speed up this sluggish reaction, or, even more desirable, to use efficient electrocatalysts based on earth-abundant metals. To date, numerous single-atom catalysts in the form of metal-doped carbon-nitrogen materials (MNC) have proved to be a promising alternative to ORR Pt-based materials. [1-3] In this study we employed advanced spectroscopic techniques, namely Mössbauer spectroscopy and operando X-ray absorption (XAS) spe

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27

Ni, Lingmei, Charlotte Gallenkamp, Markus Kübler, et al. "Operando ⁵⁷ Fe Mössbauer Spectroscopy of Fe-N-C Catalysts during Oxygen Reduction Reaction." ECS Meeting Abstracts MA2022-02, no. 42 (2022): 1596. http://dx.doi.org/10.1149/ma2022-02421596mtgabs.

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Proton exchange fuel cells (PEFCs) are a clean technology for efficient conversion of chemical into electrical energy and are specifically promising for the decarbonization of heavy duty vehicles [1]. Currently, the drawback of PEFCs is the high cost of Pt-based catalysts used for cathode and anode, which hinders their commercialization. [2] The rapid development of FeNCs holds promise for replacing Pt-based catalysts for the oxygen reduction reaction (ORR). The nature and characterization of the FeNC active sites is a challenging subject of research, and the exact structure of intrinsic activ

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28

Buelens, Lukas C., Antoon Van Alboom, Hilde Poelman, Christophe Detavernier, Guy B. Marin, and Vladimir V. Galvita. "Fe2O3–MgAl2O4 for CO Production from CO2: Mössbauer Spectroscopy and in Situ X-ray Diffraction." ACS Sustainable Chemistry & Engineering 7, no. 10 (2019): 9553–65. http://dx.doi.org/10.1021/acssuschemeng.9b01036.

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29

Bødker, F., and S. Mørup. "In situ cell for Mössbauer spectroscopy between 5 and 800 K in applied magnetic fields." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 108, no. 4 (1996): 413–16. http://dx.doi.org/10.1016/0168-583x(95)01154-4.

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30

Jumas, Jean-Claude, Manfred Womes, Ricardo Alcántara, Pedro Lavela, and José L. Tirado. "A 57Fe Mössbauer spectroscopy study of iron nanoparticles obtained in situ in conversion ferrite electrodes." Hyperfine Interactions 183, no. 1-3 (2008): 1–5. http://dx.doi.org/10.1007/s10751-008-9728-3.

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31

Benaichouba, B. "In-situ Mössbauer spectroscopic study of iron site evolution in iron and cobalt molybdates catalysts in propene oxidation reaction conditions." Applied Catalysis A: General 130, no. 1 (1995): 31–45. http://dx.doi.org/10.1016/0926-860x(95)00112-3.

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32

Bouda, S., and K. P. Isaac. "Influence of soil redox conditions on oxidation of biotite." Clay Minerals 21, no. 2 (1986): 149–57. http://dx.doi.org/10.1180/claymin.1986.021.2.04.

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AbstractBiotites from three peaty gleyed podzol soil profiles on ranite bedrock were examined to investigate the oxidation of the octahedral Fe during weathering. Oxidation of these biotites as determined by Mössbauer spectroscopy shows a good correlation with the in situ measured soil Eh values of the sampled horizons. In every soil profile the highest Eh measured is in the A horizon and the lowest in the C horizon. Similarly, biotites from the A horizons are the most oxidized compared with those from the lower horizons. In most of the samples the oxidation is accompanied by loss of K+ from t

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33

Ahmed, Ayman H. "Zeolite-encapsulated transition metal chelates: synthesis and characterization." Reviews in Inorganic Chemistry 34, no. 3 (2014): 153–75. http://dx.doi.org/10.1515/revic-2013-0013.

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AbstractThis article reviews some important recent works on the synthesis and characterization of zeolite-encapsulated transition metal complexes containing different organic ligands. Distinct methodologies of preparation, including the in situ one-pot template (IOPT) and flexible ligand methods (FLM) are described. The mode of bonding, composition, overall geometry and surface characteristics have been inferred by various physicochemical characterization techniques. Chemical analysis, spectroscopic methods [Fourier transform infrared spectroscopy (FT-IR), diffuse reflectance spectroscopy (DRS

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34

Berry, Frank J., Xu Changhai, and Simon Jobson. "An in situ Mössbauer spectroscopic investigation of the hydrogen pretreatment of titania-supported iron-iridium catalysts." Hyperfine Interactions 57, no. 1-4 (1990): 1759–63. http://dx.doi.org/10.1007/bf02405718.

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35

Biryukov, Yaroslav P., Almaz L. Zinnatullin, Rimma S. Bubnova, et al. "Investigation of thermal behavior of mixed-valent iron borates vonsenite and hulsite containing [OM 4] n + and [OM 5] n + oxocentred polyhedra by in situ high-temperature Mössbauer spectroscopy, X-ray diffraction and thermal analysis." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 4 (2020): 543–53. http://dx.doi.org/10.1107/s2052520620006538.

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The investigation of elemental composition, crystal structure and thermal behavior of vonsenite and hulsite from the Titovskoe boron deposit in Russia is reported. The structures of the borates are described in terms of cation-centered and oxocentred polyhedra. There are different sequences of double chains and layers consisting of oxocentred [OM 4] n + tetrahedra and [OM 5] n + tetragonal pyramids forming a framework. Elemental composition was determined by energy-dispersive X-ray spectroscopy (EDX). Oxidation states and coordination sites of iron and tin in the oxoborates are determined usin

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36

Lázár, Károly. "Redistribution of iron ions in porous ferrisilicates during redox treatments." Pure and Applied Chemistry 89, no. 4 (2017): 471–79. http://dx.doi.org/10.1515/pac-2016-1026.

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Abstract Relocation of iron ions in microporous Fe-FER, (Al+Fe)-FER, Fe-MFI (FER: ferrierite, MFI: silicalite) and in mesoporous Fe-MCM-41 ferrisilicate (MCM: Mobile Crystalline Material) samples was followed during redox treatments primarily by tool of the in situ Mössbauer spectroscopy. Coexistence of various Fe3+ and Fe2+ species is demonstrated. In microporous Fe-FER and Fe-MFI existence of combined μ-oxo iron dimers, Fe3+FW-O-Fe2+EFW can be proposed. The presence of these dimers can easily be correlated with catalytic effect shown in certain oxidation processes. Structural rearrangement c

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37

Yoshida, Y., S. Horie, K. Niira, K. Fukui, and K. Shirasawa. "In situ observation of iron atoms in multicrystalline silicon at 1273 and 300K by Mössbauer spectroscopy." Physica B: Condensed Matter 376-377 (April 2006): 227–30. http://dx.doi.org/10.1016/j.physb.2005.12.060.

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38

ALIFANTI, M., M. FLOREA, G. FILOTTI, V. KUNCSER, V. CORTESCORBERAN, and V. PARVULESCU. "In situ structural changes during toluene complete oxidation on supported EuCoO3 monitored with 151Eu Mössbauer spectroscopy." Catalysis Today 117, no. 1-3 (2006): 329–36. http://dx.doi.org/10.1016/j.cattod.2006.05.036.

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39

Berry, F. J., and S. Jobson. "In situ characterisation of supported iron-iridium catalysts by iron-57 and iridium-193 Mössbauer spectroscopy." Hyperfine Interactions 46, no. 1-4 (1989): 557–65. http://dx.doi.org/10.1007/bf02398243.

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40

Zhang, Hui-Liang, Jian-yi Shen, and Xin Ge. "A study of in-situ Mössbauer spectroscopy on Fe−Mo oxides for selective oxidation of toluene." Hyperfine Interactions 69, no. 1-4 (1992): 859–62. http://dx.doi.org/10.1007/bf02401962.

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41

Somodi, Ferenc, Irina Borbáth, József L. Margitfalvi, Sándor Stichleutner, and Károly Lázár. "Study of Au/SnO x –Al2O3 catalysts used in CO oxidation by in situ Mössbauer spectroscopy." Hyperfine Interactions 192, no. 1-3 (2009): 13–21. http://dx.doi.org/10.1007/s10751-009-9941-8.

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42

Chmielewski, Tomasz, Marcin Chmielewski, Anna Piątkowska, Agnieszka Grabias, Beata Skowrońska, and Piotr Siwek. "Phase Structure Evolution of the Fe-Al Arc-Sprayed Coating Stimulated by Annealing." Materials 14, no. 12 (2021): 3210. http://dx.doi.org/10.3390/ma14123210.

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The article presents the results of research on the structural evolution of the composite Fe-Al-based coating deposited by arc spray with initial low participation of in situ intermetallic phases. The arc spraying process was carried out by simultaneously melting two different electrode wires, aluminum and low alloy steel (98.6 wt.% of Fe). The aim of the research was to reach protective coatings with a composite structure consisting of a significant participation of FexAly as intermetallic phases reinforcement. Initially, synthesis of intermetallic phases took place in situ during the sprayin

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43

Lázár, K., A. M.-Szeleczky, G. Vorbeck, R. Fricke, A. Vondrova, and J. Cejka. "In situ Mössbauer study of iron containing MFI ferrisilicates: Relations to catalytic properties." Journal of Radioanalytical and Nuclear Chemistry Articles 190, no. 2 (1995): 407–11. http://dx.doi.org/10.1007/bf02040019.

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44

Loiselle, Liane, Michael McCraig, M. Dyar, Richard Léveillé, Sean Shieh, and Gordon Southam. "A Spectral Comparison of Jarosites Using Techniques Relevant to the Robotic Exploration of Biosignatures on Mars." Life 8, no. 4 (2018): 61. http://dx.doi.org/10.3390/life8040061.

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The acidic sulfate-rich waters of the Meridiani Planum region were potentially a habitable environment for iron-oxidizing bacteria on ancient Mars. If life existed in this ancient martian environment, jarosite minerals precipitating in these waters may record evidence of this biological activity. Since the Meridiani jarosite is thermodynamically stable at the martian surface, any biosignatures preserved in the jarosites may be readily available for analysis in the current surface sediments during the ongoing robotic exploration of Mars. However, thermal decomposition experiments indicate that

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45

Aparicio, Claudia, Jan Filip, and Libor Machala. "From Prussian blue to iron carbides: high-temperature XRD monitoring of thermal transformation under inert gases." Powder Diffraction 32, S1 (2017): S207—S212. http://dx.doi.org/10.1017/s0885715617000471.

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The thermal behavior and decomposition reaction of Prussian blue (PB) (Fe43+[Fe2+(CN)6]3·xH2O) was studied under inert atmosphere of argon by simultaneous thermogravimetry and differential scanning calorimetry, from room temperature up to 900 °C, with a heating rate of 5 K min−1. Parallel to the thermogravimetric measurements, the thermal process was monitored by in situ X-ray powder diffraction (XRD) technique under nitrogen atmosphere. The thermogravimetric data show six steps, corresponding to different stages of the decomposition reaction; comparable results are also obtained by in situ XR

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46

Gallenkamp, Charlotte, Lingmei Ni, Vera Krewald, and Ulrike I. Kramm. "Oxygen Reduction Reaction on Fe-N-C Catalysts: A Computational Spectroscopy Study." ECS Meeting Abstracts MA2022-02, no. 42 (2022): 1595. http://dx.doi.org/10.1149/ma2022-02421595mtgabs.

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The oxygen reduction reaction (ORR) plays an important role in proton exchange fuel cells (PEFCs). In PEFCs, ORR is the cathodic half-cell reaction complementary to the oxidation of the fuel, but since ORR has slow kinetics, it requires high amounts of catalyst. State-of-the-art ORR catalysts are based on the expensive metal platinum. Even though the amount of platinum needed for ORR in PEFCs has been reduced significantly over the last decade, it is still the major contributor to the cost of PEFCs, thus hindering the commercialization and accessibility of this technology.[1] Iron and nitrogen

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Ivanova, Tatiana K., Irina P. Kremenetskaya, Andrey I. Novikov, Valentin G. Semenov, Anatoly G. Nikolaev, and Marina V. Slukovskaya. "In Situ Control of Thermal Activation Conditions by Color for Serpentines with a High Iron Content." Materials 14, no. 21 (2021): 6731. http://dx.doi.org/10.3390/ma14216731.

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Serpentine heat treatment at temperatures of 650–750 °C yields magnesium–silicate reagent with high chemical activity. Precise and express control of roasting conditions in laboratory kilns and industrial aggregates is needed to derive thermally activated serpentines on a large scale. Color change in serpentines with a high iron content during roasting might be used to indicate the changes in chemical activity in the technological process. This study gives a scientific basis for the express control of roasting of such serpentines by comparing the colors of the obtained material and the referen

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Guerlou‐Demourgues, L., L. Fournès, and C. Delmas. "In Situ 57Fe Mössbauer Spectroscopy Study of the Electrochemical Behavior of an Iron‐Substituted Nickel Hydroxide Electrode." Journal of The Electrochemical Society 143, no. 10 (1996): 3083–88. http://dx.doi.org/10.1149/1.1837168.

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Berry, Frank J., Du Hongzhang, Simon Jobson, Liang Dongbai, and Lin Liwu. "Oxidation of iron in titania-supported iron–ruthenium under reducing conditions: in situ evidence from57Fe Mössbauer spectroscopy." J. Chem. Soc., Chem. Commun., no. 3 (1987): 186–88. http://dx.doi.org/10.1039/c39870000186.

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Bødker, Franz, Steen Mørup, and J. W. Niemantsverdriet. "In situ Mössbauer spectroscopy of carbon-supported iron catalysts at cryogenic temperatures and in external magnetic fields." Catalysis Letters 13, no. 3 (1992): 195–202. http://dx.doi.org/10.1007/bf00770991.

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