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Page 10 of 21                         Chen et al. J Mater Inf 2022;2:19  https://dx.doi.org/10.20517/jmi.2022.23










































                Figure 6. Schematic of (A) HT experimental setup for synthesizing alloys with a large composition space. (B) RF-ICP synthesis of HEAs
                using mixed pure metal powders. Fast RF-ICP synthesis of alloys using powder mixtures: (C) typical optical microscopy (OM) images
                showing the evolution of porosity in the Cu Ni  alloy under different heating times; (D) temperature profile of RF-ICP synthesis.
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                Reproduced  with  permission  . Copyright  2021,  Wiley-VCH.  RF-ICP:  radio  frequency  inductively  coupled  plasma;  MEA:
                medium-entropy alloy; HEA: high-entropy alloy.
               fashion. The achieved knowledge was the key to improving the subsequent screening and alloy design. This
               work indicates that HT theoretical calculations, synthesis and characterization are no longer bottlenecks for
               the development of HEAs. Note that these methodologies were used to develop HEAs with optimum
               mechanical properties. It is still challenging to achieve desired catalytic performances in these HT
               synthesized HEA catalysts, as it is difficult to control the surface properties, morphology and particle size of
               the synthesized HEAs, which are crucial in the field of catalysis.


               To extend the application of HEAs in the catalysis field, Yao et al. reported a HT synthesis technique for the
               compositional  design  and  rapid  thermal-shock  treatment  of  ultrafine  HEA  nanoclusters
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               (PtPdRhRuIrFeCoNi) with a homogeneous alloy structure, as shown in Figure 8A . In this process, carbon
               materials with surface defects were used as the supports to ensure the size uniformity for the different
               composition samples. The HT HEA catalyst systems were then rapidly tested by scanning droplet cell
               analysis [Figure 8B] for their electrochemical ORR. Their corresponding catalytic performance is displayed
               in Figure 8C and D, where the two best-performing HEA catalysts were quickly identified. This work
               indicates that the rapid synthesis and compositional exploration of HEAs by HT techniques are very
               efficient for exploring HEA catalysts.
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