The present study developed a new system of electrochemical water splitting using a boron doped diamond (BDD) electrode in the electrochemical reactor. The new method assessed the electrical current, acidity (pH), electrical conductivity, absorbance, dissipation, and splitting energies in addition to the water splitting efficiency of the overall process. Employing CuO NPs and ZnO NPs as catalysts induced a significant impact in reducing the dissipated energy and in increasing the efficiency of splitting water. Specifically, CuO NPs showed a significant enhancement in reducing the dissipated energy and in keeping the electrical current of the reaction stable. Meanwhile, the system catalyzed with ZnO NPs induced a similar impact as that for CuO NPs at a lower rate only. The energy dissipation rates in the system were found to be 48% and 65% by using CuO and ZnO NPs, respectively. However, the dissipation rate for the normalized system without catalysis (water buffer at pH = 6.5) is known to be 100%. The energy efficiency of the system was found to be 25% without catalysis, while it was found to be 82% for the system catalyzed with ZnO NPs compared to that for CuO NPs (normalized to 100%). The energy dissipated in the case of the non-catalyzed system was found to be the highest. Overall, water splitting catalyzed with CuO NPs exhibits the best performance under the applied experimental conditions by using the BDD/Niobium (Nb) electrodes.

The efficiency of boron doped diamond (BDD) in the electrochemical treatment of synthetically contaminated water with veratric acid (VA), one kind of polyphenolic type compounds, is investigated in this work. A BDD electrode was practically fabricated using hot filament chemical vapor deposition (HFCVD). Later on, the BDD electrode was implemented as an anode in a batch electrolytic reactor. The effect of operating factors such as the initial concentration of VA, NaCl addition, and supporting electrolyte type (H₂SO₄, H₃PO₄ and Na₂SO₄) was studied. The chemical oxygen demand (COD) measurements were conducted to study the VA electrolysis kinetics. The experimental data suggested that sodium sulfate was the best supporting electrolyte as the COD removal reached a percentage of 100% using 1 mmol/dm³ as VA concentration. The kinetics of the COD decay of the VA electrolysis were found to obey the pseudo-first order model. Remarkably, the electrolysis process is significantly speeded up once chloride is added to the reaction. The complete COD removal was achieved in 60 minutes of treatment.

Surface atomic arrangement and physical properties of aluminum ultrathin layers on c-Si(111)-7 × 7 and hydrogen-terminated c-Si(111)-1 × 1 surfaces deposited using molecular beam epitaxy were investigated. X-ray photoelectron spectroscopy spectra were collected in two configurations (take-off angle of 0° and 45°) to precisely determine the surface species. Moreover, 3D atomic force microscopy (AFM) images of the air-exposed samples were acquired to investigate the clustering formations in film structure. The deposition of the Al layers was monitored in situ using a reflection high-energy electron diffraction (RHEED) experiments to confirm the surface crystalline structure of the c-Si(111). The analysis of the RHEED patterns during the growth process suggests the settlement of aluminum atoms in Al(111)-1 × 1 clustered formations on both types of surfaces. The surface electrical conductivity in both configurations was tested against atmospheric oxidation. The results indicate differences in conductivity based on the formation of various alloys on the surface.