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A.F. Lahiji, F., Paul, B., Le Febvrier, A. & Eklund, P. (2024). Conventional epitaxy of NiO thin films on muscovite mica and c-Al2O3 substrates. Thin Solid Films, 808, Article ID 140566.
Open this publication in new window or tab >>Conventional epitaxy of NiO thin films on muscovite mica and c-Al2O3 substrates
2024 (English)In: Thin Solid Films, ISSN 0040-6090, E-ISSN 1879-2731, Vol. 808, article id 140566Article in journal (Refereed) Published
Abstract [en]

Fiber-textured and epitaxial NiO thin films were deposited on Si(100), c-Al2O3, and muscovite mica(001) sub-strates using reactive magnetron sputtering at substrate temperatures of 300 °C and 400 °C, to investigate theeffect of film thickness and substrate temperature on epitaxial growth of NiO films. The as-deposited filmsexhibited a face-centered cubic structure with a larger lattice constant, attributed to strain induced during thesputtering process. With an increase in substrate temperature to 400 °C, the d-spacing decreased due to strainrelease, approaching the NiO bulk value for the thickest film. The NiO film grown on Si(100) displayed fibertexture. On c-plane sapphire, NiO thin films exhibited twin domains and three-fold symmetry, consistent withexpected crystallographic orientation relationship for NaCl-structured materials onsapphire: (111)NiO ‖ (0001)Al2O3 and [011]NiO ‖ [1010]Al2O3, [011]NiO ‖[1010]Al2O3. On muscovite mica(001)substrates, the observed epitaxial shows that the mechanism is conventional epitaxy, rather than van der Waalsepitaxy, consistent with the epitaxial growth of the non-layered non-van-der-Waals compound NiO. The epitaxialrelationship was identified as of (111)NiO‖(001)Mica and [011]NiO ‖[010]Mica, [011]NiO ‖[010]Mica.

Place, publisher, year, edition, pages
ELSEVIER SCIENCE SA, 2024
Keywords
Nickel oxide, Thin films, Magnetron sputtering, Mica, Epitaxy
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:liu:diva-209978 (URN)10.1016/j.tsf.2024.140566 (DOI)001359556300001 ()2-s2.0-85208976850 (Scopus ID)
Note

Funding agencies: The Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linköping University (Faculty Grant SFO-Mat-LiU No. 2009 00971), the Knut and Alice Wallenberg foundation through the Wallenberg Academy Fellows program (KAW-2020.0196), the Swedish Research Council (VR) under Project No. 2021-03826, and the Swedish Energy Agency under project 52740-1.

Available from: 2024-11-22 Created: 2024-11-22 Last updated: 2025-05-01Bibliographically approved
Ekström, E., Elsukova, A., Grasland, J., Palisaitis, J., Ramanath, G., Persson, P., . . . Eklund, P. (2022). Epitaxial Growth of CaMnO3-y Films on LaAlO3 (112 over bar 0) by Pulsed Direct Current Reactive Magnetron Sputtering. Physica Status Solidi. Rapid Research Letters, 16(4), Article ID 2100504.
Open this publication in new window or tab >>Epitaxial Growth of CaMnO3-y Films on LaAlO3 (112 over bar 0) by Pulsed Direct Current Reactive Magnetron Sputtering
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2022 (English)In: Physica Status Solidi. Rapid Research Letters, ISSN 1862-6254, E-ISSN 1862-6270, Vol. 16, no 4, article id 2100504Article in journal (Refereed) Published
Abstract [en]

CaMnO3 is a perovskite with attractive magnetic and thermoelectric properties. CaMnO3 films are usually grown by pulsed laser deposition or radio frequency magnetron sputtering from ceramic targets. Herein, epitaxial growth of CaMnO3-y (002) films on a (112 over bar 0)-oriented LaAlO3 substrate using pulsed direct current reactive magnetron sputtering is demonstrated, which is more suitable for industrial scale depositions. The CaMnO3-y shows growth with a small in-plane tilt of <approximate to 0.2 degrees toward the (200) plane of CaMnO3-y and the (1 over bar 104) with respect to the LaAlO3 (112 over bar 0) substrate. X-ray photoelectron spectroscopy of the electronic core levels shows an oxygen deficiency described by CaMnO2.58 that yields a lower Seebeck coefficient and a higher electrical resistivity when compared to stoichiometric CaMnO3. The LaAlO3 (112 over bar 0) substrate promotes tensile-strained growth of single crystals. Scanning transmission electron microscopy and electron energy loss spectroscopy reveal antiphase boundaries composed of Ca on Mn sites along and , forming stacking faults.

Place, publisher, year, edition, pages
Wiley-V C H Verlag GMBH, 2022
Keywords
CaMnO3; epitaxy; perovskites; PVD
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:liu:diva-182501 (URN)10.1002/pssr.202100504 (DOI)000741329200001 ()
Note

Funding Agencies|Swedish Research Council (VR)Swedish Research Council [2016-03365]; Knut and Alice Wallenberg Foundation through the Wallenberg Academy Fellows program [KAW 2020.0196]; Electron Microscopy Laboratory at Linkoping University; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009 00971]; Swedish Energy AgencySwedish Energy AgencyMaterials & Energy Research Center (MERC) [46519-1]; Swedish Foundation for Strategic Research (SSF)Swedish Foundation for Strategic Research [RIF 14-0074]

Available from: 2022-01-26 Created: 2022-01-26 Last updated: 2023-05-09Bibliographically approved
Xin, B., Le Febvrier, A., Lu, J., Paul, B. & Eklund, P. (2022). Synthesis of textured discontinuous-nanoisland Ca3Co4O9 thin films. Nanoscale Advances, 4, 3318-3322
Open this publication in new window or tab >>Synthesis of textured discontinuous-nanoisland Ca3Co4O9 thin films
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2022 (English)In: Nanoscale Advances, E-ISSN 2516-0230, Vol. 4, p. 3318-3322Article in journal (Refereed) Published
Abstract [en]

Controllable engineering of the nanoporosity in layered Ca3Co4O9 remains a challenge. Here, we show the synthesis of discontinuous films with islands of highly textured Ca3Co4O9, effectively constituting distributed nanoparticles with controlled porosity and morphology. These discontinuously dispersed textured Ca3Co4O9 nanoparticles may be a candidate for hybrid thermoelectrics.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2022
National Category
Polymer Chemistry
Identifiers
urn:nbn:se:liu:diva-187438 (URN)10.1039/d2na00373b (DOI)000823803700001 ()
Available from: 2022-08-23 Created: 2022-08-23 Last updated: 2023-08-17Bibliographically approved
Magnusson, R., Paul, B., Eklund, P., Greczynski, G., Birch, J., Jonsson, B. & Ali, S. (2021). Preparation and tunable optical properties of amorphous AlSiO thin films. Vacuum, 187, Article ID 110074.
Open this publication in new window or tab >>Preparation and tunable optical properties of amorphous AlSiO thin films
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2021 (English)In: Vacuum, ISSN 0042-207X, E-ISSN 1879-2715, Vol. 187, article id 110074Article in journal (Refereed) Published
Abstract [en]

Thin films in the aluminosilicate (AlSiO) system containing up to 31 at. % Al and 23 at. % Si were prepared by reactive RF magnetron co-sputtering in order to investigate the dependence of film formation and optical properties on substrate temperature and Si and Al contents. The obtained films were amorphous with smooth microstructure. The growth rate at different substrate temperatures ranged from 1.2 to 3.3 nm/min and increase with increasing the Si target power. The roughness decreases and thickness increases with increasing Si content. The thickness of the films grown at a deposition temperature of 100 °C is found to be higher than the films deposited at 300 and 500 °C. The AlSiO-coated glasses have a higher transmission in the visible region than the uncoated glass. The spectroscopic ellipsometry analysis reveals that the refractive index value decreased with decreasing the Al content, having extinction coefficient values of zero in the measured spectral region and band gap values ≥ 3.4 eV. The obtained thin films have over 90% transmittance in the visible range and no systematic variation of transmittance was observed with substrate temperature. The results suggest that glass substrate coated with AlSiO thin films have improved optical properties.

Place, publisher, year, edition, pages
Elsevier, 2021
National Category
Inorganic Chemistry
Identifiers
urn:nbn:se:liu:diva-174575 (URN)10.1016/j.vacuum.2021.110074 (DOI)000635485100001 ()
Note

Fulltext published with Attribution 4.0 International (CC BY 4.0) license.

https://creativecommons.org/licenses/by/4.0/

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Funding: VinnovaVinnova [2015-04809]; AForsk foundation [14-457]; Knut and Alice Wallenberg Foundation through the Wallenberg Academy Fellows program; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009 00971]

Available from: 2021-03-24 Created: 2021-03-24 Last updated: 2021-12-29Bibliographically approved
Paul, B., Björk, E. M., Kumar, A., Lu, J. & Eklund, P. (2018). Nanoporous Ca3Co4O9 Thin Films for Transferable Thermoelectrics. ACS Applied Energy Materials, 1(5), 2261-2268
Open this publication in new window or tab >>Nanoporous Ca3Co4O9 Thin Films for Transferable Thermoelectrics
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2018 (English)In: ACS Applied Energy Materials, E-ISSN 2574-0962, Vol. 1, no 5, p. 2261-2268Article in journal (Refereed) Published
Abstract [en]

The development of high-performance and transferable thin-film thermoelectric materials is important for low-power applications, e.g., to power wearable electronics, and for on-chip cooling. Nanoporous films offer an opportunity to improve thermoelectric performance by selectively scattering phonons without affecting electronic transport. Here, we report the growth of nanoporous Ca3Co4O9 thin films by a sequential sputtering-annealing method. Ca3Co4O9 is promising for its high Seebeck coefficient and good electrical conductivity and important for its nontoxicity, low cost, and abundance of its constituent raw materials. To grow nanoporous films, multilayered CaO/CoO films were deposited on sapphire and mica substrates by rf-magnetron reactive sputtering from elemental Ca and Co targets, followed by annealing at 700 C to form the final phase of Ca3Co4O9. This phase transformation is accompanied by a volume contraction causing formation of nanopores in the film. The thermoelectric propoperties of the nanoporous Ca3Co4O9 films can be altered by controlling the porosity. The lowest electrical resistivity is ~7 mO cm, yielding a power factor of 2.32 × 10-4 Wm-1K-2 near room temperature. Furthermore, the films are transferable from the primary mica substrates to other arbitrary polymer platforms by simple dry transfer, which opens an opportunity of low-temperature use these materials.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2018
Keywords
Ca3Co4O9; nanoporous; thermoelectrics; thin film; transferable
National Category
Inorganic Chemistry
Identifiers
urn:nbn:se:liu:diva-155845 (URN)10.1021/acsaem.8b00333 (DOI)000458705500058 ()29905306 (PubMedID)
Available from: 2019-03-29 Created: 2019-03-29 Last updated: 2020-12-15Bibliographically approved
Rawat, P. K. & Paul, B. (2016). Simple design for Seebeck measurement of bulk sample by 2-probe method concurrently with electrical resistivity by 4-probe method in the temperature range 300-1000 K. Measurement, 91, 613-619
Open this publication in new window or tab >>Simple design for Seebeck measurement of bulk sample by 2-probe method concurrently with electrical resistivity by 4-probe method in the temperature range 300-1000 K
2016 (English)In: Measurement, ISSN 0263-2241, E-ISSN 1873-412X, Vol. 91, p. 613-619Article in journal (Refereed) Published
Abstract [en]

The 4-probe method has so far been the most popular method for concurrent measurement of Seebeck coefficient and electrical resistivity of bulk samples. However, for Seebeck measurement with higher accuracy, the 2-probe method is becoming preferred over 4-probe method. The problem with the previous apparatus designs is that they do not allow 2-probe arrangement for Seebeck measurement simultaneously with linear 4-probe arrangement for electrical resistivity measurement. So, the challenge is find a design where two different probe arrangements become possible at the same time in a single measurement run. Here, we report design and fabrication of an apparatus that allows Seebeck measurement by 2-probe method concurrently with electrical resistivity by 4-probe method of bar and disc samples in the temperature range from 300 to 1000 K. The uniqueness of the present design is that it does not require heating the entire sample chamber for temperature dependent measurements. This is because a small cylindrical furnace inside the sample chamber is used to control the sample background temperature. This internal furnace arrangement results in readily achievable set temperature with desired uniformity. Thus, it allows faster thermoelectric evaluation of samples. The design includes several preventive steps to negate the effect of off-axial heat flows on the measurement accuracy. The measurement error in Seebeck coefficient and electrical resistivity of PbTe sample is estimated to be smaller than 5%. (C) 2016 Elsevier Ltd. All rights reserved.

Place, publisher, year, edition, pages
ELSEVIER SCI LTD, 2016
Keywords
Measurement; Seebeck coefficient; 2-probe method; Electrical resistivity; 4-probe method
National Category
Other Engineering and Technologies
Identifiers
urn:nbn:se:liu:diva-130366 (URN)10.1016/j.measurement.2016.05.104 (DOI)000379507400068 ()
Note

Funding Agencies|University Grant Commission (UGC) of India through UGC (NET); Council of Scientific and Industrial Research (CSIR) India through CSIR (NET); Eurostars project [E!8892 T-to-Power]; European Research Council under the European Communitys Seventh Framework Programme/ERC - Belgium [335383]

Available from: 2016-08-15 Created: 2016-08-05 Last updated: 2025-02-10
Paul, B., Schroeder, J. L., Kerdsongpanya, S., van Nong, N., Schell, N., Ostach, D., . . . Eklund, P. (2015). Mechanism of Formation of the Thermoelectric Layered Cobaltate Ca3Co4O9 by Annealing of CaO-CoO Thin Films. Advanced Electronic Materials, 1(3), Article ID 1400022.
Open this publication in new window or tab >>Mechanism of Formation of the Thermoelectric Layered Cobaltate Ca3Co4O9 by Annealing of CaO-CoO Thin Films
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2015 (English)In: Advanced Electronic Materials, E-ISSN 2199-160X, Vol. 1, no 3, article id 1400022Article in journal (Refereed) Published
Abstract [en]

The layered cobaltate Ca3Co4O9 is of interest for energy-harvesting and heat-conversion applications because of its good thermoelectric properties and the fact that the raw materials Ca and Co are nontoxic, abundantly available, and inexpensive. While single-crystalline Ca3Co4O9 exhibits high Seebeck coefficient and low resistivity, its widespread use is hampered by the fact that single crystals are too small and expensive. A promising alternative approach is the growth of highly textured and/or epitaxial Ca3Co4O9 thin films with correspondingly anisotropic properties. Here, we present a two-step sputtering/annealing method for the formation of highly textured virtually phase-pure Ca3Co4O9 thin films by reactive cosputtering from Ca and Co targets followed by an annealing process at 730 °C under O2-gas flow. The thermally induced phase transformation mechanism is investigated by in situ time-resolved annealing experiments using synchrotron-based 2D X-ray diffraction (XRD) as well as ex situ annealing experiments and standard lab-based XRD. By tuning the proportion of initial CaO and CoO phases during film deposition, the method enables synthesis of Ca3Co4O9 thin films as well as CaxCoO2. With this method, we demonstrate production of epitaxial Ca3Co4O9 thin films with in-plane electrical resistivity of 6.44 mΩ cm and a Seebeck coefficient of 118 μV K−1 at 300 K.

Place, publisher, year, edition, pages
Wiley-Blackwell, 2015
Keywords
Thermoelectrics, Ca3Co4O9, thin film, sputtering, phase transformation
National Category
Condensed Matter Physics Other Materials Engineering Nano Technology
Identifiers
urn:nbn:se:liu:diva-117610 (URN)10.1002/aelm.201400022 (DOI)000357653900004 ()
Funder
EU, European Research Council, 335383Swedish Research Council, 2012-4430Swedish Research Council, 2011-6505Swedish Foundation for Strategic Research , Future Research Leaders 5
Available from: 2015-05-06 Created: 2015-05-06 Last updated: 2021-12-29Bibliographically approved
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0003-0858-3792

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