High-entropy alloys (HEAs) are a relatively new class of materials that have gained considerable attention from the metallurgical research community over recent years. They are characterised by their unconventional compositions, in that they are not based around a single major component, but rather comprise multiple principal alloying elements. Four core effects have been proposed in HEAs: (1) the entropic stabilisation of solid solutions, (2) the severe distortion of their lattices, (3) sluggish diffusion kinetics and (4) that properties are derived from a cocktail effect. By assessing these claims on the basis of existing experimental evidence in the literature, as well as classical metallurgical understanding, it is concluded that the significance of these effects may not be as great as initially believed. The effect of entropic stabilisation does not appear to be overarching, insufficient evidence exists to establish the strain in the lattices of HEAs, and rapid precipitation observed in some HEAs suggests their diffusion kinetics are not necessarily anomalously slow in comparison to conventional alloys. The meaning and influence of the cocktail effect is also a matter for debate. Nevertheless, it is clear that HEAs represent a stimulating opportunity for the metallurgical research community. The complex nature of their compositions means that the discovery of alloys with unusual and attractive properties is inevitable. It is suggested that future activity regarding these alloys seeks to establish the nature of their physical metallurgy, and develop them for practical applications. Their use as structural materials is one of the most promising and exciting opportunities. To realise this ambition, methods to rapidly predict phase equilibria and select suitable HEA compositions are needed, and this constitutes a significant challenge. However, while this obstacle might be considerable, the rewards associated with its conquest are even more substantial. Similarly, the challenges associated with comprehending the behaviour of alloys with complex compositions are great, but the potential to enhance our fundamental metallurgical understanding is more remarkable. Consequently, HEAs represent one of the most stimulating and promising research fields in materials science at present.

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The macro-scale segregation of alloying elements during the casting continues to afflict the manufacturers of steel ingots, despite many decades of research into its prediction and elimination. Defects such as A-segregates are still commonplace, and components are regularly scrapped due to their presence, leading to increased economic and environmental costs. With the growth of the nuclear power industry, and the increased demands placed on new pressure vessels, it is now more important than ever that today's steel ingots are as chemically homogeneous as possible.This article briefly reviews the development of our current understanding of macrosegregation phenomena during the 20 th century, before going on to assess the latest developments in the field of macrosegregation modelling. The aim of the text is to highlight the shortcomings of applying contemporary macromodels to steel-ingot casting, and to suggest practical alternatives. In addition, the experimental characterisation of macrosegregation is explored, and a review of the various techniques currently available is presented.

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The expanded compositional freedom afforded by high-entropy alloys (HEAs) represents a unique opportunity for the design of alloys for advanced nuclear applications, in particular for applications where current engineering alloys fall short. This review assesses the work done to date in the field of HEAs for nuclear applications, provides critical insight into the conclusions drawn, and highlights possibilities and challenges for future study. It is found that our understanding of the irradiation responses of HEAs remains in its infancy, and much work is needed in order for our knowledge of any single HEA system to match our understanding of conventional alloys such as austenitic steels. A number of studies have suggested that HEAs possess ‘special’ irradiation damage resistance, although some of the proposed mechanisms, such as those based on sluggish diffusion and lattice distortion, remain somewhat unconvincing (certainly in terms of being universally applicable to all HEAs). Nevertheless, there may be some mechanisms and effects that are uniquely different in HEAs when compared to more conventional alloys, such as the effect that their poor thermal conductivities have on the displacement cascade. Furthermore, the opportunity to tune the compositions of HEAs over a large range to optimise particular irradiation responses could be very powerful, even if the design process remains challenging.

High entropy (HE) materials have received significant attention in recent years, due to their intrinsically high levels of configurational entropy. While there has been significant work exploring HE alloys and oxides, new families of HE materials are still being revealed. In this work we present the synthesis of a novel family of HE materials based on lanthanide oxysulfides. Here, we implement lanthanide dithiocarbamates as versatile precursors that can be mixed at the molecular scale prior to thermolysis in order to produce the high entropy oxysulfide. The target of our synthesis is the HE Ln 2 SO 2 phase, where Ln = Pr, Nd, Gd, Dy, Er and where Ln = Pr, Nd, Gd, Dy for 5 and 4 lanthanide samples, respectively. We confirmed the structure of samples produced by powder X-ray diffraction, electron microscopy, and high-resolution energy dispersive X-ray spectroscopy. Optical spectroscopy shows a broad emission feature centered around 450 nm as well as a peak in absorption at around 280 nm. From this data we calculate the band gap and Urbach energies of the materials produced.

The high-entropy alloy Al 0.5 CrFeCoNiCu has been shown to consist of two stable, face-centred cubic solid solutions at temperatures approaching its solidus; one rich in Cr, Fe, Co & Ni (dendritic) and the other rich in Cu (interdendritic).Whilst some studies have suggested that the high-temperature microstructure may be metastably retained to room temperature through rapid cooling, evidence of phase decomposition has also been reported. In this study, fine-scale precipitation has been observed in samples of Al 0.5 CrFeCoNiCu that have been rapidly cooled after casting, and water quenched following ageing for 1000 h at 1000 • C. Contrary to previous reports, in the as-cast state, the two facecentred cubic phases, as well as an L1 2 phase, were found in both dendritic and interdendritic areas, with the dendritic areas having undergone a spinodal decomposition. After ageing and quenching, L1 2 precipitates were found in both dendritic and interdendritic areas, and precipitates of the Cr-, Fe-, Co-and Ni-enriched face-centred cubic phase were found in the Cu-rich interdendritic regions. Given the nature of the heat treatments applied, the results suggest that precipitation in the alloy is rapid and cannot be avoided, even when the material is cooled quickly to room temperature.