A new approach for the design of alloy systems with multiprincipal elements is presented in this research. The Al x CoCrCuFeNi alloys with different aluminum contents (i.e., x values in molar ratio, x ϭ 0 to 3.0) were synthesized using a well-developed arc-melting and casting method. These alloys possessed simple fcc/bcc structures, and their phase diagram was predicted by microstructure characterization and differential thermal analyses. With little aluminum addition, the alloys were composed of a simple fcc solid-solution structure. As the aluminum content reached x ϭ 0.8, a bcc structure appeared and constructed with mixed fcc and bcc eutectic phases. Spinodal decomposition occurred further on when the aluminum contents were higher than x ϭ 1.0, leading to the formation of modulated plate structures. A single ordered bcc structure was obtained for aluminum contents larger than x ϭ 2.8. The effects of high mixing entropy and sluggish cooperative diffusion enhance the formation of simple solid-solution phases and submicronic structures with nanoprecipitates in the alloys with multiprincipal elements rather than intermetallic compounds.
Vanadium dioxide (VO2) is a promising material for developing energy-saving “smart windows,” owing to its infrared thermochromism induced by metal-insulator transition (MIT). However, its practical application is greatly limited by its relatively high critical temperature (~68°C), low luminous transmittance (<60%), and poor solar energy regulation ability (<15%). Here, we developed a reversible and nonvolatile electric field control of the MIT of a monoclinic VO2 film. With a solid electrolyte layer assisting gating treatment, we modulated the insertion/extraction of hydrogen into/from the VO2 lattice at room temperature, causing tristate phase transitions that enable control of light transmittance. The dramatic increase in visible/infrared transmittance due to the phase transition from the metallic (lightly H-doped) to the insulating (heavily H-doped) phase results in an increased solar energy regulation ability up to 26.5%, while maintaining 70.8% visible luminous transmittance. These results break all previous records and exceed the theoretical limit for traditional VO2 smart windows, making them ready for energy-saving utilization.
Hydrogenation is an effective way to tune the property of metal oxides. It can conventionally be performed by doping hydrogen into solid materials with noble-metal catalysis, high-temperature/pressure annealing treatment, or high-energy proton implantation in vacuum condition. Acid solution naturally provides a rich proton source, but it should cause corrosion rather than hydrogenation to metal oxides. Here we report a facile approach to hydrogenate monoclinic vanadium dioxide (VO2) in acid solution at ambient condition by placing a small piece of low workfunction metal (Al, Cu, Ag, Zn, or Fe) on VO2 surface. It is found that the attachment of a tiny metal particle (~1.0 mm) can lead to the complete hydrogenation of an entire wafer-size VO2 (>2 inch). Moreover, with the right choice of the metal a two-step insulator–metal–insulator phase modulation can even be achieved. An electron–proton co-doping mechanism has been proposed and verified by the first-principles calculations.
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