Roddatis, Vladimir V.

[["dc.bibliographiccitation.firstpage","1700109"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Advanced sustainable systems"],["dc.bibliographiccitation.volume","1"],["dc.contributor.author","Mierwaldt, Daniel"],["dc.contributor.author","Roddatis, Vladimir"],["dc.contributor.author","Risch, Marcel"],["dc.contributor.author","Scholz, Julius"],["dc.contributor.author","Geppert, Janis"],["dc.contributor.author","Abrishami, Majid Ebrahimizadeh"],["dc.contributor.author","Jooss, Christian"],["dc.date.accessioned","2020-12-10T14:06:44Z"],["dc.date.available","2020-12-10T14:06:44Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1002/adsu.201700109"],["dc.identifier.issn","2366-7486"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/70006"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C | C02 In situ hochauflösende Untersuchung des aktiven Zustands bei der photo- und elektrochemischen Wasserspaltung"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","CC BY-NC 4.0"],["dc.title","Environmental TEM Investigation of Electrochemical Stability of Perovskite and Ruddlesden-Popper Type Manganite Oxygen Evolution Catalysts"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Physical review materials"],["dc.bibliographiccitation.volume","4"],["dc.contributor.author","Rieger, F."],["dc.contributor.author","Roddatis, V."],["dc.contributor.author","Kaiser, K."],["dc.contributor.author","Bendt, G."],["dc.contributor.author","Schulz, S."],["dc.contributor.author","Jooss, C."],["dc.date.accessioned","2020-12-10T18:25:53Z"],["dc.date.available","2020-12-10T18:25:53Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1103/PhysRevMaterials.4.025402"],["dc.identifier.eissn","2475-9953"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/75866"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.title","Transition into a phonon glass in crystalline thermoelectric ( S b 1 − x B i x ) 2 T e 3 films"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","012009"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Journal of Physics: Conference Series"],["dc.bibliographiccitation.volume","1190"],["dc.contributor.affiliation","Meyer, T;"],["dc.contributor.affiliation","Kressdorf, B;"],["dc.contributor.affiliation","Lindner, J;"],["dc.contributor.affiliation","Peretzki, P;"],["dc.contributor.affiliation","Roddatis, V;"],["dc.contributor.affiliation","Jooss, C;"],["dc.contributor.affiliation","Seibt, M;"],["dc.contributor.author","Meyer, T."],["dc.contributor.author","Kressdorf, B."],["dc.contributor.author","Lindner, J."],["dc.contributor.author","Peretzki, P."],["dc.contributor.author","Roddatis, V."],["dc.contributor.author","Jooss, Christian"],["dc.contributor.author","Seibt, Michael"],["dc.date.accessioned","2020-12-10T18:15:51Z"],["dc.date.available","2020-12-10T18:15:51Z"],["dc.date.issued","2019"],["dc.date.updated","2022-04-07T11:26:58Z"],["dc.description.abstract","Abstract Fundamental losses of photovoltaic energy conversion are transmission of sub band gap photons and thermalisation which are the underlying physics of the Shockley-Queisser limit defining maximum conversion efficiency of single-junction solar cells. Strongly correlated materials such as perovskites are promising candidates to exceed this limit by exploiting (i) long wavelength light absorption and (ii) the existence of long-living intraband excitations indicating that harvesting hot excess carriers might be feasible in such systems. In this work, we study pn-heterojunctions produced from Pr1-xCaxMnO3 on SrTi1-yNbyO3 by means of microscopic techniques. Such systems exhibit relevant quantities such as space charge layer width, screening lengths and excess carrier diffusion lengths in the 1-10 nm range which makes the use of standard methods such as electron beam induced current a challenging task. We report scanning transmission electron beam induced current experiments of misfit dislocations at the heterojunction. The dislocation-induced reduction of the charge collection is studied with nanometer spatial resolution. Effects of surface recombination and the heterojunction electric field are discussed."],["dc.identifier.doi","10.1088/1742-6596/1190/1/012009"],["dc.identifier.eissn","1742-6596"],["dc.identifier.issn","1742-6588"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16699"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/74976"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area B | B02 Photonen-getriebener Energietransfer über Grenzflächen zwischen Materialien mit starken Korrelationen"],["dc.relation","SFB 1073 | Topical Area Z | Z02 Hochauflösende Charakterisierung von Grenzflächen"],["dc.relation.eissn","1742-6596"],["dc.relation.issn","1742-6588"],["dc.relation.orgunit","Fakultät für Physik"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","CC BY 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/3.0/"],["dc.title","High-resolution Scanning Transmission EBIC Analysis of Misfit Dislocations at Perovskite pn-Heterojunctions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","063046"],["dc.bibliographiccitation.journal","New Journal of Physics"],["dc.bibliographiccitation.volume","19"],["dc.contributor.author","Ifland, Benedikt"],["dc.contributor.author","Hoffmann, Joerg"],["dc.contributor.author","Kressdorf, Birte"],["dc.contributor.author","Roddatis, Vladimir"],["dc.contributor.author","Seibt, Michael"],["dc.contributor.author","Jooss, Christian"],["dc.date.accessioned","2018-11-07T10:22:28Z"],["dc.date.available","2018-11-07T10:22:28Z"],["dc.date.issued","2017"],["dc.description.abstract","The effect of correlation effects on photovoltaic energy conversion at manganite/titanite heterojunctions is investigated. As a model system we choose a heterostructure consisting of the small polaron absorber Pr0.66Ca0.34MnO3 (PCMO) epitaxially grown on single-crystalline Nb-doped SrTi0.998Nb0.002O3 (STNO) substrates. The high structural and chemical quality of the interfaces is proved by detailed characterization using high-resolution transmission electron microscopy (TEM) and electron energy loss spectroscopy (EELS) studies. Spectrally resolved and temperature-dependent photovoltaic measurements show pronounced contributions of both the Jahn-Teller (JT) excitations and the charge transfer (CT) transitions to the photovoltaic effect at different photon energies. A linear temperature dependence of the open-circuit voltage for an excitation in the PCMO manganite is only observed below the charge-ordering temperature, indicating that the diffusion length of the photocarrier exceeds the size of the space charge region. The photovoltaic response is compared to that of a heterojunction of lightly doped Pr0.05Ca0.95MnO3 (CMO)/STNO, where the JT transition is absent. Here, significant contributions of the CT transition to the photovoltaic effect set in below the Neel temperature. We conclude that polaronic correlations and ordering effects are essentials for photovoltaic energy conversion in manganites."],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft (DFG) [SFB1073]"],["dc.description.sponsorship","Open-Access-Publikationsfonds 2017"],["dc.identifier.doi","10.1088/1367-2630/aa6c22"],["dc.identifier.isi","000404761900009"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14592"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42283"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area B | B02 Photonen-getriebener Energietransfer über Grenzflächen zwischen Materialien mit starken Korrelationen"],["dc.relation.issn","1367-2630"],["dc.relation.orgunit","Fakultät für Physik"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","CC BY 4.0"],["dc.title","Contribution of Jahn-Teller and charge transfer excitations to the photovoltaic effect of manganite/titanite heterojunctions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2002049"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Advanced Materials Interfaces"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Hoffmann-Urlaub, Sarah"],["dc.contributor.author","Ross, Ulrich"],["dc.contributor.author","Hoffmann, Jörg"],["dc.contributor.author","Belenchuk, Alexandr"],["dc.contributor.author","Shapoval, Oleg"],["dc.contributor.author","Roddatis, Vladimir"],["dc.contributor.author","Ma, Qian"],["dc.contributor.author","Kressdorf, Birte"],["dc.contributor.author","Moshnyaga, Vasily"],["dc.contributor.author","Jooss, Christian"],["dc.date.accessioned","2021-04-14T08:29:32Z"],["dc.date.available","2021-04-14T08:29:32Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract Interest in layered Ruddlesden–Popper (RP) strongly correlated manganites of Pr0.5Ca1.5MnO4 as well as in their thin film polymorphs is motivated by the high temperature of charge orbital ordering above room temperature. The c‐axis orientation in epitaxial films is tailored by different SrTiO3 (STO) substrate orientations and CaMnO3 (CMO) buffer layers. Films on STO(110) show in‐plane alignment of the c‐axis parallel to the [100] direction. On STO(100), two possible directions of the in‐plane c‐axis lead to a mosaic like, quasi 2D nanostructure, consisting of RP, rock‐salt, and perovskite blocks. With the CMO buffer layer, Pr0.5Ca1.5MnO4 epitaxial films with c‐axis out‐of‐plane are realized. Different physical vapor deposition techniques as ion beam sputtering, pulsed laser deposition and metalorganic aerosol deposition are applied in order to distinguish effects of growth conditions from intrinsic epitaxial properties. Despite their very different growth conditions, surface morphology, crystal structure, and orientation of the thin films reveal a high level of similarity as verified by X‐ray diffraction, scanning, and high resolution transmission electron microscopy. For different epitaxial relations stress in the films is relaxed by means of modified interface chemistry. The charge ordering in the films occurs at a temperature close to that expected in bulk material."],["dc.description.abstract","The growth direction of a Ruddlesden–Popper Pr0.5Ca1.5MnO4 thin film is governed by its strain state. For different SrTiO3 substrate orientations the unit cells of the film are aligned in parallel or in a perpendicular configuration—forming a mosaic like microstructure. With a CaMnO3 buffer layer the c‐axis can even be tilted to the out‐of‐plane direction. image"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659"],["dc.identifier.doi","10.1002/admi.202002049"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82926"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area A | A02 Verständnis und Manipulation von Dissipationskanälen des Energietransports"],["dc.relation","SFB 1073 | Topical Area B | B02 Photonen-getriebener Energietransfer über Grenzflächen zwischen Materialien mit starken Korrelationen"],["dc.relation","SFB 1073 | Topical Area Z | Z02 Hochauflösende Charakterisierung von Grenzflächen"],["dc.relation.eissn","2196-7350"],["dc.relation.issn","2196-7350"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made."],["dc.title","Tailoring c-axis orientation in epitaxial Ruddlesden-Popper Pr0.5Ca1.5MnO4 films"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","175108"],["dc.bibliographiccitation.issue","17"],["dc.bibliographiccitation.journal","Journal of Applied Physics"],["dc.bibliographiccitation.volume","123"],["dc.contributor.author","Rieger, F."],["dc.contributor.author","Kaiser, K."],["dc.contributor.author","Bendt, G."],["dc.contributor.author","Roddatis, V."],["dc.contributor.author","Thiessen, P."],["dc.contributor.author","Schulz, S."],["dc.contributor.author","Jooss, C."],["dc.date.accessioned","2020-12-10T18:12:40Z"],["dc.date.available","2020-12-10T18:12:40Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1063/1.5025491"],["dc.identifier.eissn","1089-7550"],["dc.identifier.issn","0021-8979"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/74452"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.title","Low intrinsic c-axis thermal conductivity in PVD grown epitaxial Sb 2 Te 3 films"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","751"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Catalysts"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Roddatis, Vladimir"],["dc.contributor.author","Lole, Gaurav"],["dc.contributor.author","Jooss, Christian"],["dc.date.accessioned","2019-09-24T07:57:53Z"],["dc.date.available","2019-09-24T07:57:53Z"],["dc.date.issued","2019"],["dc.description.abstract","The study of changes in the atomic structure of a catalyst under chemical reaction conditions is extremely important for understanding the mechanism of their operation. For in situ environmental transmission electron microscopy (ETEM) studies, this requires preparation of electron transparent ultrathin TEM lamella without surface damage. Here, thin films of Pr1-xCaxMnO3 (PCMO, x = 0.1, 0.33) and La1-xSrxMnO3 (LSMO, x = 0.4) perovskites are used to demonstrate a cross-section specimen preparation method, comprised of two steps. The first step is based on optimized focused ion beam cutting procedures using a photoresist protection layer, finally being removed by plasma-etching. The second step is applicable for materials susceptible to surface amorphization, where in situ recrystallization back to perovskite structure is achieved by using electron beam driven chemistry in gases. This requires reduction of residual water vapor in a TEM column. Depending on the gas environment, long crystalline facets having di erent atomic terminations and Mn-valence state, can be prepared."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2019"],["dc.identifier.doi","10.3390/catal9090751"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16391"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/62448"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C | C02 In situ hochauflösende Untersuchung des aktiven Zustands bei der photo- und elektrochemischen Wasserspaltung"],["dc.relation","SFB 1073 | Topical Area Z | Z02 Hochauflösende Charakterisierung von Grenzflächen"],["dc.relation.issn","2073-4344"],["dc.relation.orgunit","Fakultät für Physik"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0/"],["dc.title","In Situ Preparation of Pr1-xCaxMnO3 and La1-xSrxMnO3 Catalysts Surface for High-Resolution Environmental Transmission Electron Microscopy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2170042"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Small Methods"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Meyer, Tobias"],["dc.contributor.author","Kressdorf, Birte"],["dc.contributor.author","Roddatis, Vladimir"],["dc.contributor.author","Hoffmann, Jörg"],["dc.contributor.author","Jooss, Christian"],["dc.contributor.author","Seibt, Michael"],["dc.date.accessioned","2021-12-08T12:27:17Z"],["dc.date.available","2021-12-08T12:27:17Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1002/smtd.202170042"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/95308"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-476"],["dc.relation.eissn","2366-9608"],["dc.relation.issn","2366-9608"],["dc.title","Phase Transitions in a Perovskite Thin Film Studied by Environmental In Situ Heating Nano‐Beam Electron Diffraction (Small Methods 9/2021)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","2100464"],["dc.bibliographiccitation.journal","Small methods"],["dc.contributor.author","Meyer, Tobias"],["dc.contributor.author","Kressdorf, Birte"],["dc.contributor.author","Roddatis, Vladimir V."],["dc.contributor.author","Hoffmann, Jörg"],["dc.contributor.author","Jooss, Christian"],["dc.contributor.author","Seibt, Michael"],["dc.date.accessioned","2021-09-01T06:42:46Z"],["dc.date.available","2021-09-01T06:42:46Z"],["dc.date.issued","2021"],["dc.description.abstract","The rich phase diagram of bulk Pr1−xCaxMnO3 resulting in a high tunability of physical properties gives rise to various studies related to fundamental research as well as prospective applications of the material. Importantly, as a consequence of strong correlation effects, electronic and lattice degrees of freedom are vigorously coupled. Hence, it is debatable whether such bulk phase diagrams can be transferred to inherently strained epitaxial thin films. In this paper, the structural orthorhombic to pseudo-cubic transition for x = 0.1 is studied in ion-beam sputtered thin films and differences to the respective bulk system are pointed out by employing in situ heating nano-beam electron diffraction to follow the temperature dependence of lattice constants. In addition, it is demonstrated that controlling the environment during heating, that is, preventing oxygen loss, is crucial in order to avoid irreversible structural changes, which is expected to be a general problem of compounds containing volatile elements under non-equilibrium conditions."],["dc.identifier.doi","10.1002/smtd.202100464"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/89140"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-455"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area B | B02 Photonen-getriebener Energietransfer über Grenzflächen zwischen Materialien mit starken Korrelationen"],["dc.relation","SFB 1073 | Topical Area Z | Z02 Hochauflösende Charakterisierung von Grenzflächen"],["dc.relation.eissn","2366-9608"],["dc.relation.issn","2366-9608"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","CC BY-NC-ND 4.0"],["dc.title","Phase Transitions in a Perovskite Thin Film Studied by Environmental In Situ Heating Nano‐Beam Electron Diffraction"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5037"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","The Journal of Physical Chemistry C"],["dc.bibliographiccitation.lastpage","5047"],["dc.bibliographiccitation.volume","125"],["dc.contributor.author","Ronge, Emanuel"],["dc.contributor.author","Lindner, Jonas"],["dc.contributor.author","Ross, Ulrich"],["dc.contributor.author","Melder, Jens"],["dc.contributor.author","Ohms, Jonas"],["dc.contributor.author","Roddatis, Vladimir"],["dc.contributor.author","Kurz, Philipp"],["dc.contributor.author","Jooss, Christian"],["dc.date.accessioned","2021-04-14T08:28:43Z"],["dc.date.available","2021-04-14T08:28:43Z"],["dc.date.issued","2021"],["dc.description.abstract","Hydrogen production by electrochemical water splitting is limited by the sluggish oxygen evolution reaction (OER). In order to improve our understanding of the underlying mechanisms, information about the atomic surface structure of the active state of the electrode is required. Here, we present environmental transmission electron microscopy studies of Ca-birnessite (K0.20Ca0.21MnO2.21·1.4H2O) electrodes under conditions close to those of the OER. Remarkably, in H2O vapor, a highly dynamic state of the surface and subsurface develops with a thickness of the formed dynamic layer of up to 0.6 nm, which is absent in O2 and inert gases. Electron beam-induced effects are carefully studied, showing high stability of the material against radiation damage in high vacuum until a dose rate of 42,000 e–/(Å2 s). In contrast, in H2O, the dynamic surface layer develops and forms a stationary state even at low dose rates, down to 5000 e–/(Å2 s). Electron energy-loss spectroscopy reveals an increase in the Mn oxidation state in H2O and in O2 ambient. Our results are interpreted as the formation of a few-angstrom-thick, dynamic, and hydrated surface layer of birnessite in H2O, with an increased Mn valence state. Such a dynamic surface layer with a flexible Mn coordination and valence state might be optimal for oxygen evolution due to the higher effective interaction volume beyond the surface area and a flexible bond coordination of partially hydrated Mn species."],["dc.identifier.doi","10.1021/acs.jpcc.0c09806"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82690"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C | C02 In situ hochauflösende Untersuchung des aktiven Zustands bei der photo- und elektrochemischen Wasserspaltung"],["dc.relation.eissn","1932-7455"],["dc.relation.issn","1932-7447"],["dc.relation.orgunit","Institut für Materialphysik"],["dc.rights","CC BY 4.0"],["dc.title","Atom Surface Dynamics of Manganese Oxide under Oxygen Evolution Reaction-Like Conditions Studied by In Situ Environmental Transmission Electron Microscopy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]