Electrochemical water splitting of 3D binder-free hydrothermally synthesized Co3O4/unidirectional carbon cloth.

The development of hydrogen energy sources based on electrochemical water splitting is of increasing interest due to its advantages in energy and environmental fields. In this study, Co3O4 was decorated on carbon cloth (CC) by a hydrothermal method and was used as an electrode for water splitting. The structural and morphological properties of the materials are assessed using a range of reliable techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) with EDX mapping, and diffuse reflectance spectroscopy (DRS). Results indicate that the Co3O4/CC material was synthesized at 140 °C for 9 h and calcined at 350 °C achieving a superior overall water-splitting activity in the direction of hydrogen evolution reaction (HER) reaction than that of the oxygen evolution reaction (OER). In detail, HER characteristics with an overpotential at -0.234 V and a current density at 10 mA cm-2. In addition, the Co3O4/CC material also gives overpotential at 0.54 V for OER process. Furthermore, the electrochemical surface area of Co3O4/CC material is 7.6 times higher than CC electrode. Moreover, the CC fabric is destroyed when the annealing temperature is higher than 350 °C, leading to a significant decrease in the activity of Co3O4/CC. The as-prepared Co3O4 shows good adhesion and stability based on CC substrate without binder substance or further treatment of CC.

Fe2O3/diatomite materials as efficient photo-Fenton catalysts for ciprofloxacin removal.

In this study, we used Fe2O3/diatomite material system toward ciprofloxacin (CIP) photo-Fenton removal in water under visible light (vis) excitation. The characterization of Fe2O3/diatomite catalysts was determined by X-ray diffraction patterns, Fourier-transform infrared analysis, inductively coupled plasma mass spectrometry, and scanning electron microscopy. The photo-Fenton catalytic activity of the Fe2O3/diatomite was appraised by the removal efficiency of the CIP throughout the effect of the H2O2 with various parameters such as initial pH, catalyst amount, and H2O2 amount. The results indicate that 0.2 gL-1 Fe2O3/diatomite catalysts achieved the highest performance at approximately 90.03% with a 50 µL H2O2 concentration. Furthermore, the Fe2O3/diatomite catalysts have high stability, with over 80% CIP removed after five cycles. This study is inspired to develop a potential material for photo-Fenton degradation of antibiotics in wastewater.