Effect of g-C3N4 amount on green synthesized GdFeO3/g-C3N4 nanocomposites as promising compounds for solid-state hydrogen storage

Abstract

Hydrogen energy is a key role in novel renewable energy production/consumption technologies. Traditional hydrogen energy systems are suffered from low density, high production cost, low efficiency, and storage complications. With the start of solid-state hydrogen storage technology, many of above deficiencies are fulfilled, however, there are several unknown points, particularly in metal oxides, which need more attention. Hydrogen sorption on the layered materials or inside porous materials is a hopeful key to drawbacks for high-performance hydrogen sorption. Hereupon, layered solids with the merit of hydrogen sorption are introduced, for the first time, including “nanostructured bimetal oxide (BMO)” and “graphitic carbon nitride (CN)”. Perovskites are ceramic and they are hard materials so they could be a favorable candidate for solid-state hydrogen storage. g-C3N4 has attractive features including high surface area, chemical stability, small band gap, and low-cost synthesis methods but also has great potential as an electrode material for energy storage capacitors. The main motivation for this study comes from the potential applications for perovskite materials and graphitic carbon nitride for the solid-state hydrogen storage method. The Perovskite type GdFeO3 nanostructures (as BMO) synthesized through sol-gel approach in front of natural source of Grape juice as both complexing agent and fuel. The experimental scrutinization ascertains an original fabrication of GdFeO3 (GF) nanostructures in Grape juice at 800 C, with an approximately uniform nanosized structure of 70 nm on average. The obtained pure GF nanostructures are then utilized for nanocomposite formation based on g-C3N4 (CN) with different amounts. The resulting nanocomposites with the ratio of 1:2 from GF:CN perform a preferable hydrogen sorption capacity, in terms of “maximum discharge capacity of 577 mAhg1 ” in 2 M KOH electrolyte. It should be declared that however, the discharge capacity of the nanostructured GF is 188 mAhg1 . It can be emphasized that these GF/CN nanocomposites can be utilized as hopeful hosts in an electrochemical hydrogen storage setup due to the synergic effect of g-C3N4 with essential characteristics in cooperation with BMO nanostructures as acceptable electrocatalysts.