In the current study, a simple hydrothermal method was used to successfully synthesize NaTaO3 and Ag, N doped NaTaO3 catalysts. The band edge potential was accessible through UV–visible spectroscopic analysis, and the diffraction peak was easily indexed as an orthorhombic structure. The values of the predicted crystallite sizes for the undoped NaTaO3, Ag-doped, and N-doped NaTaO3 nanoparticles are 61.03 nm, 48.9 nm, and 53.50 nm, respectively. Pure, Ag, and N doped NaTaO3 nanocubes were discovered to exhibit band gap energies of 3.62, 3.60, and 3.57 eV, respectively, based on the UV-Vis examination. Moreover, a Field Emission Scanning Electron Microscopy study confirmed the presence of cubic (3-D) shape. An HRTEM examination verified that the material is polycrystalline. The Ta, Na, N, and O are present at binding energies of 26.09, 1073, 405.7, and 526.6 eV, respectively, according to the XPS spectra. The pure, silver (Ag), and nitrogen (N) doped NaTaO3 photocatalysts have photocatalytic H2 evolution rates of 556 µmolh−1, 2834 µmolh−1 and 3266 µmolh−1, respectively. Without a co-catalyst, the maximal rate of H2 generation under UV light has not yet been attained for the N-doped NaTaO3 perovskite with its cubic (3-D) structure. Furthermore, even after three days, the improved photocatalyst demonstrates 87 % of photocatalytic activity in the reliability test.
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