TY - JOUR A1 - Steigert, Alexander A1 - Kojda, Sandrino Danny A1 - Ibaceta-Jaña, Josefa Fernanda A1 - Abou-Ras, Daniel A1 - Gunder, René A1 - Alktash, Nivin A1 - Habicht, Klaus A1 - Wagner, Markus Raphael A1 - Klenk, Reiner A1 - Raoux, Simone A1 - Szyszka, Bernd A1 - Lauermann, Iver A1 - Muydinov, Ruslan T1 - Water-assisted crystallization of amorphous indium zinc oxide films JF - Materials today. Communications N2 - Transparent conductive materials based on indium oxide remain yet irreplaceable in various optoelectronic applications. Amorphous oxides appear especially attractive for technology as they are isotropic, demonstrate relatively high electron mobility and can be processed at low temperatures. Among them is indium zinc oxide (IZO) with a large zinc content that is crucial for keeping the amorphous state but redundant for the doping. In this work we investigated water-free and water containing IZO films obtained by radio frequency sputtering. The correlation between temperature driven changes of the chemical state, the optical and electrical properties as well as the progression of crystallization was in focus. Such characterization methods as: scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, temperature dependent Hall-effect measurements and others were applied. Temperature dependent electrical properties of amorphous IZO and IZO:H2O films were found to evolve similarly. Based on our experience in In2O3:H2O (In2O3:H or IOH) we proposed an explanation for the changes observed. Water admixture was found to decrease crystallization temperature of IZO significantly from similar to 550 degrees C to similar to 280 degrees C. Herewith, the presence and concentration of water and/or hydroxyls was found to determine Zn distribution in the film. In particular, Zn enrichment was detected at the film's surface respective to the high water and/or hydroxyl amount. Raman spectra revealed a two-dimensional crystallization of w-ZnO which precedes regardless water presence an extensive In2O3 crystallization. An abrupt loss of electron mobility as a result of crystallization was attributed to the formation of ZnO interlayer on grain boundaries. KW - IZO KW - Thin films KW - TCOs KW - Crystallization KW - Water-assisted crystallization Y1 - 2022 U6 - https://doi.org/10.1016/j.mtcomm.2022.103213 SN - 2352-4928 VL - 31 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Panchal, Gyanendra A1 - Kojda, Sandrino Danny A1 - Sahoo, Sophia A1 - Bagri, Anita A1 - Kunwar, Hemant Singh A1 - Bocklage, Lars A1 - Panchwanee, Anjali A1 - Sathe, Vasant G. A1 - Fritsch, Katharina A1 - Habicht, Klaus A1 - Choudhary, Ram Janay A1 - Phase, Deodutta M. T1 - Strain and electric field control of magnetic and electrical transport properties in a magnetoelastically coupled Fe3O4/BaTiO3 (001) heterostructure JF - Physical review : B, Condensed matter and materials physics N2 - We present a study of the control of electric field induced strain on the magnetic and electrical transport properties in a magnetoelastically coupled artificial multiferroic Fe3O4/BaTiO3 heterostructure. In this Fe3O4/BaTiO3 heterostructure, the Fe3O4 thin film is epitaxially grown in the form of bilateral domains, analogous to a-c stripe domains of the underlying BaTiO3(001) substrate. By in situ electric field dependent magnetization measurements, we demonstrate the extrinsic control of the magnetic anisotropy and the characteristic Verwey metal-insulator transition of the epitaxial Fe3O4 thin film in a wide temperature range between 20-300 K, via strain mediated converse magnetoelectric coupling. In addition, we observe strain induced modulations in the magnetic and electrical transport properties of the Fe3O4 thin film across the thermally driven intrinsic ferroelectric and structural phase transitions of the BaTiO3 substrate. In situ electric field dependent Raman measurements reveal that the electric field does not significantly modify the antiphase boundary defects in the Fe3O4 thin film once it is thermodynamically stable after deposition and that the modification of the magnetic properties is mainly caused by strain induced lattice distortions and magnetic anisotropy. These results provide a framework to realize electrical control of the magnetization in a classical highly correlated transition metal oxide. Y1 - 2022 U6 - https://doi.org/10.1103/PhysRevB.105.224419 SN - 2469-9950 SN - 2469-9969 VL - 105 IS - 22 PB - The American Institute of Physics CY - Woodbury, NY ER - TY - GEN A1 - Mazzio, Katherine A. A1 - Thulasimani, Monika Raja A1 - Ryll, Britta A1 - Kojda, Sandrino Danny A1 - Habicht, Klaus A1 - Raoux, Simone T1 - Synthetic manipulation of hybrid thermoelectric materials T2 - Abstracts of papers : joint conference / The Chemical Institute of Cananda, CIC, American Chemical Society, ACS Y1 - 2018 SN - 0065-7727 VL - 255 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Mazzio, Katherine A. A1 - Kojda, Sandrino Danny A1 - Rubio-Govea, Rodrigo A1 - Niederhausen, Jens A1 - Ryll, Britta A1 - Raja-Thulasimani, Monika A1 - Habicht, Klaus A1 - Raoux, Simone T1 - P-type-to-n-type transition in hybrid AgxTe/PEDOT:PSS thermoelectric materials via stoichiometric control during solution-based synthesis JF - ACS applied energy materials N2 - This work demonstrates the production of high-performing p- type and n-type hybrid AgxTe/poly(3,4-ethylenedioxythiopene):polystyrene sulfonic acid (PE-DOT:PSS) thermoelectric materials from the same Te/PEDOT:PSS parent structure during aqueous-based synthesis. All samples were solution-processed and analyzed in thin- film architectures. We were able to demonstrate a power factor of 44 mu W m(-1) K-2 for our highest-performing n-type material. In addition, we were also able to realize a 68% improvement in the power factor of our p-type compositions relative to the parent structure through manipulation of the inorganic nanostructure composition. We demonstrate control over the thermoelectric properties by varying the stoichiometry of AgxTe nanoparticles in AgxTe/PEDOT:PSS hybrid materials via a topotactic chemical transformation process at room temperature. This process offers a simple, low-temperature, and cost-effective route toward the production of both efficient n-type and p-type hybrid thermoelectric materials. KW - thermoelectrics KW - hybrid material KW - PEDOT:PSS KW - tellurium KW - silver KW - telluride KW - hybrid synthesis Y1 - 2020 U6 - https://doi.org/10.1021/acsaem.0c01774 SN - 2574-0962 VL - 3 IS - 11 SP - 10734 EP - 10743 PB - ACS Publications CY - Washington, DC ER - TY - JOUR A1 - Crovetto, Andrea A1 - Hempel, Hannes A1 - Rusu, Marin A1 - Choubrac, Leo A1 - Kojda, Sandrino Danny A1 - Habicht, Klaus A1 - Unold, Thomas T1 - Water adsorption enhances electrical conductivity in transparent p-type CuI JF - ACS applied materials & interfaces N2 - CuI has been recently rediscovered as a p-type transparent conductor with a high figure of merit. Even though many metal iodides are hygroscopic, the effect of moisture on the electrical properties of CuI has not been clarified. In this work, we observe a 2-fold increase in the conductivity of CuI after exposure to ambient humidity for 5 h, followed by slight long-term degradation. Simultaneously, the work function of CuI decreases by almost 1 eV, which can explain the large spread in the previously reported work function values. The conductivity increase is partially reversible and is maximized at intermediate humidity levels. On the basis of the large intragrain mobility measured by THz spectroscopy, we suggest that hydration of grain boundaries may be beneficial for the overall hole mobility. KW - transparent conductors KW - CuI KW - copper iodide KW - conductivity KW - humidity KW - p-type KW - work function Y1 - 2020 U6 - https://doi.org/10.1021/acsami.0c11040 SN - 1944-8244 SN - 1944-8252 VL - 12 IS - 43 SP - 48741 EP - 48747 PB - American Chemical Society CY - Washington, DC ER -