Apr 23, 2024
5:00pm - 7:00pm
Flex Hall C, Level 2, Summit
Tessa Tucker1,Zongmin Yang1,David Bugallo1,Steven May1
Drexel University1
Tessa Tucker1,Zongmin Yang1,David Bugallo1,Steven May1
Drexel University1
Transition metal oxides (TMOs) are attractive in materials science for their structural versatility and property tunability. This tunability can be further expanded by incorporating a second anion, such as F or N, to alter the metal-anion bond ionicity or the metal charge density. In this work, we report on vapor-based fluorination of epitaxial SrCoO<sub>2.5</sub> films. The films are grown by oxygen-assisted molecular beam epitaxy (MBE) under conditions that result in the brownmillerite structure. Topochemical fluorination was conducted on the as-grown films at 200°C using a quartz tube furnace under Ar gas flow with poly(vinylidene fluoride) (PVDF) as the fluorine source. Fluorination reactions were performed on SrCoO<sub>2.5</sub> films synthesized on STO, LAO, LSAT and GSO substrates to understand the impact of substrate-induced strain on fluorine incorporation. Fluorine incorporation was confirmed via depth-dependent elemental analysis performed with X-ray photoelectron spectroscopy (XPS). Fluorine incorporation results in an expansion of the <i>c</i>-axis parameter as determined by X-ray diffraction. Optical absorption spectra, obtained through spectroscopic ellipsometry, reveals a blue-shift of the low-energy absorption edge by 0.1 - 0.3 eV depending on the substrate. This result is attributed to a widening of the band gap due to the increased ionicity of the Co-anion bonds.<br/><br/>This work was supported by the National Science Foundation under grant CMMI-2001888.