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Analysis of stainless steel 316 as a containment material in the presence of a phase change material (PCM) cycled at high temperature was carried out through a combination of X-ray photoelectron spectroscopy and X-ray diffraction methods. In this work, stainless steel tokens were half-immersed in a chloride carbonate-based PCM, which were then thermally cycled in an air or a nitrogen environment up to 500 times, allowing the PCM to repeatedly transform between solid and liquid phases. Spectroscopy and diffraction methods were applied on the tokens, as well as the cycled PCM, to investigate the extent and nature of corrosion in such steel alloys. With varying sputtering conditions, the oxidation state at different depths of token surfaces was quantified. From the outermost corroded layer through to the bulk, this study shows a gradual change in distribution in both Cr and oxidation of Fe, while Cr was specifically found to have depleted and migrated into the PCM. The oxidation and depletion have been found to increase with increasing exposure time to PCM while sigma-phase structure embrittled in the corrosion layer. Refereed/Peer-reviewed

The formation and mechanism that drive corrosion in stainless steel as a containment material in the presence of phase change materials is of importance in solar thermal energy storage systems. In our work, half-immersed stainless steel 316 tokens in a carbonate-based phase change material (PCM 638) have been investigated. The samples were thermally cycled in air and Nitrogen environment up to 500 times within a high-temperature range, allowing the PCM to transform between solid and liquid states repeatedly. As a consequence of thermal cycling, severe thickness loss on steel token was observed, indicating a degree of oxidation occurring, which depleted the uncorroded steel. Cross-sectional microstructural analysis was carried out to determine the elemental distribution and structural morphology along the corrosion layers. This study shows that thermal cycling of SS 316 in PCM results in active Ni and Cr migration to the surface, leading to a significant depletion of Cr from steel moving into the PCM. Cr and Fe on the surface are found to oxidise with varying degrees, with respect to the exposure time. The depletion of Cr was found to be higher in SS 316 immersed in PCM, while also increasing with exposure time. Refereed/Peer-reviewed

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)., The combination of ultraviolet photoelectron spectroscopy and metastable helium induced electron spectroscopy is used to determine the density of states of the inner and outer coaxial carbon nanotubes. Ultraviolet photoelectron spectroscopy typically measures the density of states across the entire carbon nanotube, while metastable helium induced electron spectroscopy measures the density of states of the outermost layer alone. The use of double-walled carbon nanotubes in electronic devices allows for the outer wall to be functionalised whilst the inner wall remains defect free and the density of states is kept intact for electron transport. Separating the information of the inner and outer walls enables development of double-walled carbon nanotubes to be independent, such that the charge transport of the inner wall is maintained and confirmed whilst the outer wall is modified for functional purposes., This research received no external funding.