AI Article Synopsis

  • Medium-entropy alloy aerogels (MEAAs) combine the benefits of multimetallic alloys and aerogels, making them promising for catalytic applications despite challenges in achieving a single-phase structure.
  • A new strategy for creating ultralight 3D porous MEAAs with a density of just 39.3 mg/cm³ is introduced, utilizing auto-combustion and low-temperature reduction to ensure proper mixing of metal precursors.
  • These MEAAs demonstrate superior catalytic performance in methanol oxidation, showcasing high activity levels and enabling a more efficient methanol-oxidation-assisted water electrolyzer that operates at a significantly lower voltage than traditional systems.

Article Abstract

Medium-entropy alloy aerogels (MEAAs) with the advantages of both multimetallic alloys and aerogels are promising new materials in catalytic applications. However, limited by the immiscible behavior of different metals, achieving single-phase MEAAs is still a grand challenge. Herein, a general strategy for preparing ultralight 3D porous MEAAs with the lowest density of 39.3 mg cm among the metal materials is reported, through combining auto-combustion and subsequent low-temperature reduction procedures. The homogenous mixing of precursors at the ionic level makes the short-range diffusion of metal atoms possible to drive the formation of single-phase MEAAs. As a proof of concept in catalysis, as-synthesized Ni Co Fe Cu MEAAs exhibit a high mass activity of 1.62 A mg and specific activity of 132.24 mA cm toward methanol oxidation reactions, much higher than those of the low-entropy counterparts. In situ Fourier transform infrared and NMR spectroscopies reveal that MEAAs can enable highly selective conversion of methanol to formate. Most importantly, a methanol-oxidation-assisted MEAAs-based water electrolyzer can achieve a low cell voltage of 1.476 V at 10 mA cm for making value-added formate at the anode and H at the cathode, 173 mV lower than that of traditional alkaline water electrolyzers.

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Source
http://dx.doi.org/10.1002/adma.202202943DOI Listing

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