Publications
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A high-entropy manganite in an ordered nanocomposite for long-term application in solid oxide cells
Baiutti F., Chiabrera F., Acosta M., Diercks D., Parfitt D., Santiso J., Wang X., Cavallaro A., Morata A., Wang H., Chroneos A., MacManus-Driscoll J., Tarancon A. Nature Communications; 12 (1, 2660) 2021. 10.1038/s41467-021-22916-4. IF: 14.919
The implementation of nano-engineered composite oxides opens up the way towards the development of a novel class of functional materials with enhanced electrochemical properties. Here we report on the realization of vertically aligned nanocomposites of lanthanum strontium manganite and doped ceria with straight applicability as functional layers in high-temperature energy conversion devices. By a detailed analysis using complementary state-of-the-art techniques, which include atom-probe tomography combined with oxygen isotopic exchange, we assess the local structural and electrochemical functionalities and we allow direct observation of local fast oxygen diffusion pathways. The resulting ordered mesostructure, which is characterized by a coherent, dense array of vertical interfaces, shows high electrochemically activity and suppressed dopant segregation. The latter is ascribed to spontaneous cationic intermixing enabling lattice stabilization, according to density functional theory calculations. This work highlights the relevance of local disorder and long-range arrangements for functional oxides nano-engineering and introduces an advanced method for the local analysis of mass transport phenomena. © 2021, The Author(s).
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Back-to-Basics tutorial: X-ray diffraction of thin films
Harrington G.F., Santiso J. Journal of Electroceramics; 2021. 10.1007/s10832-021-00263-6. IF: 1.785
X-ray diffraction (XRD) is an indispensable tool for characterising thin films of electroceramic materials. For the beginner, however, it can be a daunting technique at first due to the number of operation modes and measurements types, as well as the interpretation of the resultant patterns and scans. In this tutorial article, we provide a foundation for the thin-film engineer/scientist conducting their first measurements using XRD. We give a brief introduction of the principle of diffraction and description of the instrument, detailing the relevant operation modes. Next, we introduce five types of measurements essential for thin film characterisation: 2 θ/ ω scans, grazing-incidence scans, rocking curves, pole figures, and azimuth scans (or ϕ scans). Practical guidelines for selecting the appropriate optics, mounting and aligning the sample, and selecting scan conditions are given. Finally, we discuss some of the basics of data analysis, and give recommendations on the presentation of data. The aim of this article is to ultimately lower the barrier for researchers to perform meaningful XRD analysis, and, building on this foundation, find the existing literature more accessible, enabling more advanced XRD investigations. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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Carbon Incorporation in MOCVD of MoS2Thin Films Grown from an Organosulfide Precursor
Schaefer C.M., Caicedo Roque J.M., Sauthier G., Bousquet J., Hébert C., Sperling J.R., Pérez-Tomás A., Santiso J., Del Corro E., Garrido J.A. Chemistry of Materials; 33 (12): 4474 - 4487. 2021. 10.1021/acs.chemmater.1c00646. IF: 9.811
With the rise of two-dimensional (2D) transition-metal dichalcogenide (TMD) semiconductors and their prospective use in commercial (opto)electronic applications, it has become key to develop scalable and reliable TMD synthesis methods with well-monitored and controlled levels of impurities. While metal-organic chemical vapor deposition (MOCVD) has emerged as the method of choice for large-scale TMD fabrication, carbon (C) incorporation arising during MOCVD growth of TMDs has been a persistent concern-especially in instances where organic chalcogen precursors are desired as a less hazardous alternative to more toxic chalcogen hydrides. However, the underlying mechanisms of such unintentional C incorporation and the effects on film growth and properties are still elusive. Here, we report on the role of C-containing side products of organosulfur precursor pyrolysis in MoS2 thin films grown from molybdenum hexacarbonyl Mo(CO)6 and diethyl sulfide (CH3CH2)2S (DES). By combining in situ gas-phase monitoring with ex situ microscopy and spectroscopy analyses, we systematically investigate the effect of temperature and Mo(CO)6/DES/H2 gas mixture ratios on film morphology, chemical composition, and stoichiometry. Aiming at high-quality TMD growth that typically requires elevated growth temperatures and high DES/Mo(CO)6 precursor ratios, we observed that temperatures above DES pyrolysis onset (â 600 °C) and excessive DES flow result in the formation of nanographitic carbon, competing with MoS2 growth. We found that by introducing H2 gas to the process, DES pyrolysis is significantly hindered, which reduces carbon incorporation. The C content in the MoS2 films is shown to quench the MoS2 photoluminescence and influence the trion-To-exciton ratio via charge transfer. This finding is fundamental for understanding process-induced C impurity doping in MOCVD-grown 2D semiconductors and might have important implications for the functionality and performance of (opto)electronic devices. ©
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Direct Visualization of Anti-Ferroelectric Switching Dynamics via Electrocaloric Imaging
Vales-Castro P., Vellvehi M., Perpiñà X., Caicedo J.M., Jordà X., Faye R., Roleder K., Kajewski D., Perez-Tomas A., Defay E., Catalan G. Advanced Electronic Materials; 7 (12, 2100380) 2021. 10.1002/aelm.202100380. IF: 7.295
The large electrocaloric coupling in PbZrO3 allows using high-speed infrared imaging for visualizing anti-ferroelectric switching dynamics via the associated temperature change. It is found that in ceramic samples of homogeneous temperature and thickness, switching is fast due to the generation of multiple nucleation sites, with devices responding in the millisecond range. By introducing gradients of thickness, however, it is possible to change the dynamics to propagation limited, whereby a single-phase boundary sweeps across the sample like a cold front, at a speed of ≈20 cm s−1. Additionally, introducing thermostatic temperature differences between two sides of the sample enables the simultaneous generation of a negative electrocaloric effect on one side and a positive one on the other, yielding a Janus-like electrocaloric response. © 2021 Wiley-VCH GmbH
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Metallic Diluted Dimerization in VO2 Tweeds
Sandiumenge F., Rodríguez L., Pruneda M., Magén C., Santiso J., Catalan G. Advanced Materials; 33 (9, 2004374) 2021. 10.1002/adma.202004374. IF: 30.849
The observation of electronic phase separation textures in vanadium dioxide, a prototypical electron-correlated oxide, has recently added new perspectives on the long standing debate about its metal–insulator transition and its applications. Yet, the lack of atomically resolved information on phases accompanying such complex patterns still hinders a comprehensive understanding of the transition and its implementation in practical devices. In this work, atomic resolution imaging and spectroscopy unveils the existence of ferroelastic tweed structures on ≈5 nm length scales, well below the resolution limit of currently used spectroscopic imaging techniques. Moreover, density functional theory calculations show that this pretransitional fine-scale tweed, which on average looks and behaves like the standard metallic rutile phase, is in fact weaved by semi-dimerized chains of vanadium in a new monoclinic phase that represents a structural bridge to the monoclinic insulating ground state. These observations provide a multiscale perspective for the interpretation of existing data, whereby phase coexistence and structural intermixing can occur all the way down to the atomic scale. © 2021 Wiley-VCH GmbH
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Orbital occupancy and hybridization in strained SrV O3 epitaxial films
Mirjolet M., Vasili H.B., Valadkhani A., Santiso J., Borisov V., Gargiani P., Valvidares M., Valentí R., Fontcuberta J. Physical Review Materials; 5 (9, 095002) 2021. 10.1103/PhysRevMaterials.5.095002. IF: 3.989
Oxygen packaging in transition metal oxides determines the metal-oxygen hybridization and electronic occupation at metal orbitals. Strontium vanadate (SrVO3), having a single electron in a 3d orbital, is thought to be the simplest example of strongly correlated metallic oxides. Here, we determine the effects of epitaxial strain on the electronic properties of SrVO3 thin films, where the metal-oxide sublattice is corner connected. Using x-ray absorption and x-ray linear dichroism at the VL2,3 and O K edges, it is observed that tensile or compressive epitaxial strain change the hierarchy of orbitals within the t2g and eg manifolds. Data show a remarkable 2p-3d hybridization, as well as a strain-induced reordering of the V3d(t2g,eg) orbitals. The latter is itself accompanied by a consequent change of hybridization that modulates the hybrid π∗ and σ∗ orbitals and the carrier population at the metal ions, challenging a rigid band picture. © 2021 American Physical Society.
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Origin of large negative electrocaloric effect in antiferroelectric PbZr O3
Vales-Castro P., Faye R., Vellvehi M., Nouchokgwe Y., Perpiñà X., Caicedo J.M., Jordà X., Roleder K., Kajewski D., Perez-Tomas A., Defay E., Catalan G. Physical Review B; 103 (5, 054112) 2021. 10.1103/PhysRevB.103.054112. IF: 4.036
We have studied the electrocaloric response of the archetypal antiferroelectric PbZrO3 as a function of voltage and temperature in the vicinity of its antiferroelectric-paraelectric phase transition. Large electrocaloric effects of opposite signs, ranging from an electrocooling of -3.5 K to an electroheating of +5.5K, were directly measured with an infrared camera. We show by calorimetric and electromechanical measurements that the large negative electrocaloric effect comes from an endothermic antiferroelectric-ferroelectric switching, in contrast to dipole destabilization of the antiparallel lattice, previously proposed as an explanation for the negative electrocaloric effect of antiferroelectrics. © 2021 American Physical Society.
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Oxidation processes at the surface of BaTiO3 thin films under environmental conditions
Spasojevic I., Sauthier G., Caicedo J.M., Verdaguer A., Domingo N. Applied Surface Science; 565 (150288) 2021. 10.1016/j.apsusc.2021.150288. IF: 6.707
Dissociation and adsorption of water on ferroelectric oxide surfaces play important role in the processes of screening and switching dynamics of ferroelectric polarization, as well as in catalytic processes which can be additionally coupled with light, temperature or vibration stimuli. In this work, we present XPS study of ferroelectric BaTiO3thin films and determine the entanglement between surface chemistry, polarization direction and stability, by observing changes upon time exposure to environmental conditions, heating in O2atmosphere and irradiation in vacuum. We devote special attention to Ba 3d spectral region and identify two different oxidation states of O atoms in the compounds of Ba. While this second specie was generally attributed to Ba in surface compounds where it has different oxygen coordination than in the bulk, based on the XPS results of oxygen annealed thin films, we demonstrate that this so far neglected component, corresponds to barium peroxide (BaO2) and identify it as important active specie for the study of screening mechanisms closely related with catalytic activity present in this ferroelectric material. Finally, we report on chemically assisted polarization switching in thin films induced by heating in vacuum or exposure to X-Ray radiation due to the formation of positive surface electric field created by oxygen or electron vacancies, respectively. © 2021 The Authors
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Pulsed laser deposition of epitaxial non-doped PbTiO3 thin films from Pbo-TiO2 mosaic targets
Sakai J., Roque J.M.C., Vales-Castro P., Padilla-Pantoja J., Sauthier G., Santiso J. Coatings; 11 (6, 662) 2021. 10.3390/coatings11060662. IF: 2.881
PbTiO3 (PTO) suffers from difficulty in preparing high-density robust bulk ceramics, which in turn has been a bottleneck in thin films growth with physical vapor deposition (PVD) methods. In the present work, we prepared non-doped PTO thin films by a pulsed laser deposition (PLD) method with either a single PTO target or a mosaic target consisting of PbO and TiO2 pie-shaped pieces. On the PTO single target, laser irradiation caused selective ablation of Pb, resulting in Tirich cone-shaped pillar structure on the surface, whereas the irradiated surface of PbO and TiO2 pieces was smoother. Epitaxial PTO films deposited on SrTiO3 (001) substrates from the pie-chart targets with PbO:TiO2 areal ratio from 3:5 to 5:3 resulted in composition, crystallinity, flatness, and ferroelectric properties almost independent of the areal ratio. The averaged composition of each film was close to stoichiometric, suggesting a compositional self-control mechanism. For growing epitaxial and high-quality non-doped PTO films, a PbO-TiO2 pie-chart target is advantageous in easiness of handling and stable surface structure. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
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Strong strain gradients and phase coexistence at the metal-insulator transition in VO2 epitaxial films
Rodríguez L., Sandiumenge F., Frontera C., Caicedo J.M., Padilla J., Catalán G., Santiso J. Acta Materialia; 220 (117336) 2021. 10.1016/j.actamat.2021.117336. IF: 8.203
The proximity of a thermodynamic triple point and the formation of transient metastable phases may result in complex phase and microstructural trajectories across the metal-insulator transition in strained VO2 films. A detailed analysis using in-situ synchrotron X-ray diffraction unveils subtle fingerprints of this complexity in the structure of epitaxial films. During phase transition the low-temperature monoclinic M1 phase is constrained along the {111}R planes by the coexisting high-temperature R phase domains, which remain epitaxially clamped to the substrate. This geometrical constraint induces counteracting local stresses that result in a combined tilt and uniaxial in-plane compression of M1 domains, and a concomitant anomalous cR-axis elongation. This mechanism progressively transforms the M1 phase into the transitional triclinic phase (T), and ultimately into the monoclinic M2 phase, generating strong strain and tilt gradients that remain frozen after the complete transformation of the R phase upon cooling to RT. The transformation path of VO2 films, the complex competition between stable and metastable VO2 polymorphs and its impact on the structure of the low temperature monoclinic state, provide essential insights for understanding the electronic and mechanical properties of the films at the nanoscale, as well as to control their use in functional devices. © 2021
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The effect of Ni and Fe on the decomposition of yttrium doped barium zirconate thin films
Jennings D., Ricote S., Caicedo J.M., Santiso J., Reimanis I. Scripta Materialia; 201 (113948) 2021. 10.1016/j.scriptamat.2021.113948. IF: 5.611
Transition metal dopants like Ni and Fe are known to influence the densification and microstructure evolution of yttrium doped barium zirconate (BZY), and understanding their behavior impacts the use of BZY in applications like protonic ceramic fuel cells and catalysts. This work investigates the effects of Ni and Fe on the evolution of BZY thin films in high temperature (1175°C), reducing environments, where BZY faceting and decomposition is observed. It is shown that the addition of Ni promotes film decomposition, whereas Fe prevents decomposition. The effects of the dopants on film decomposition are consistent with thermodynamic predictions that indicate the addition of Fe to the B-site of the perovskite structure diminishes the Gibbs free energy change for decomposition. © 2021
