The Dai Group published their work “Room temperature synthesis of high-entropy Prussian blue analogues” in Nano Energy.
High-entropy Prussian blue analogues (HEPBAs) integrating the highly dispersed active sites of high-entropy materials with intrinsic 3D diffusion channels and the redox-active sites of Prussian blue analogues have great potential in electrochemical applications but have not been realized. In this work, a series of HEPBAs were successfully synthesized under room temperature combining mechanochemistry with wet chemistry for the first time.
High-entropy Prussian blue analogues (HEPBAs) were fabricated by combining mechanochemistry with wet chemistry. As an optimal element combination, high-entropy K(MgMnFeNiCu)Fe(CN)6 exhibited enhanced higher capacitances than all the single-component PBAs.
The group also published their work “Overcoming the phase separation within high-entropy metal carbide by poly(ionic liquid)s†” in Chemical Communications.
High-entropy crystalline materials are attracting more attention. In principle, high-entropy metal carbides (HMCs) that contain five or more metal ions, possess more negative free energy value during catalysis. But its preparation is challenging because of the immiscibility of multi metal cations in a single carbide solid solution.
Here, a rational strategy for preparing HMC is proposed via a coordination-assisted crystallization process in the presence of Br-based poly(ionic liquids). Through this method, Mo0.2W0.2V0.2Cr0.2Nb0.2C nanoparticles, with a single cubic phase structure, incorporated on porous carbon, are obtained (HMC@NC). By combination of well dispersed small particle size (∼4 nm), high surface area (∼270 m2 g−1), and high-entropy phase, HMC@NC can function as a promising catalyst for the dehydrogenation of ethylbenzene. Unexpected activity (EB conv.: 73%) and thermal stability (>100 h on steam) at 450 °C are observed. Such a facile synthetic strategy may inspire the fabrication of other types of HMCs for more specific tasks.