Hydrogen adsorption by a porous bimetallic solid solution carbide MAX phases synthesized in an open atmosphere

Abstract

Multilayer and porosity are significant traits for energy storage materials, especially for hydrogen storage and utilization. However, the material must first undergo subsequent sequential investigation for accurate quantification to be a candidate for hydrogen storage. The mixed metallic MAX phase and their derivatives MXene have the potential to be used for hydrogen storage. In this paper, we describe the formation of low temperature (1100 °C), porous, and high purity (84.92 %) bimetallic solid solution Titanium Vanadium Aluminum Carbide (TiVAlxC) MAX phases in an open atmosphere, where the variation of x, e.g., Al mole content, is critical for obtaining high purity metallic solid solution MAX phases. The BET comparative analysis shows the textural features of the TiVAlxC with change in Al and end phases, i.e., Ti2AlC (Titanium Aluminum Carbide) and (Vanadium Aluminum Carbide) V2AlC. The outcomes are evident that impurity, crystallinity, and crystallite size impact the textural properties of the synthesized MAX phases. Corelative findings on accurate quantification of hydrogen uptake based upon textural properties. The gravimetric hydrogen storage capacity of Ti2AlC, TiVAl1.3C, and V2AlC phases are 0.33, 0.62, and 1.29%wt, respectively. The gravimetric analysis provided valuable insights into the isothermal hydrogen adsorption of TiVAlxC and its end phases, demonstrating these materials' ability to be used for future hydrogen storage.