Photocatalytic Removal of Antibiotics on g-C3N4 Using Amorphous CuO as Cocatalysts

Amorphous CuO is considered as an excellent cocatalyst, owing to its large surface area and superior conductivity compared with its crystalline counterpart. The current work demonstrates a facile method to prepare amorphous CuO, which is grown on the surface of graphitic carbon nitride (g-C3N4) and is then applied for the photocatalytic degradation of tetracycline hydrochloride. The prepared CuO/g-C3N4 composite shows higher photocatalytic activities compared with bare g-C3N4. Efficient charge transfer between g-C3N4 and CuO is confirmed by the photocurrent response spectra and photoluminescence spectra. This work provides a facile approach to prepare low-cost composites for the photocatalytic degradation of antibiotics to safeguard the environment.

g-C3N4/Ca2Fe2O5 heterostructures for enhanced photocatalytic degradation of organic effluents under sunlight

Abstractg-C3N4/Ca2Fe2O5 heterostructures were successfully prepared by incorporating g-C3N4 into Ca2Fe2O5 (CFO). As prepared g-C3N4/CFO heterostructures were initially utilized to photodegrade organic effluent Methylene blue (MB) for optimization of photodegradation performance. 50% g-C3N4 content in CFO composition showed an enhanced photodegradation efficiency (~ 96%) over g-C3N4 (48.15%) and CFO (81.9%) due to mitigation of recombination of photogenerated charge carriers by Type-II heterojunction. The optimized composition of heterostructure was further tested for degradation of Bisphenol-A (BPA) under direct sunlight, exhibiting enhanced photodegradation efficiency of about 63.1% over g-C3N4 (17%) and CFO (45.1%). The photoelectrochemical studies at various potentials with and without light illumination showed significant improvement in photocurrent response for g-C3N4/Ca2Fe2O5 heterostructures (~ 1.9 mA) over CFO (~ 67.4 μA). These studies revealed efficient solar energy harvesting ability of g-C3N4/Ca2Fe2O5 heterostructures to be utilized for organic effluent treatment.

Synthesis, Characterization and Photoelectric Properties of Fe2O3 Incorporated TiO2 Photocatalyst Nanocomposites

In the present work we report the sol-gel synthesis of pure TiO2 and (TiO2)1−x(Fe2O3)x nanocomposites with different Fe2O3 contents (x = 0, 0.1, 0.5, and 1.0 for pure TiO2, Fe2O3 incorporated 0.1, 0.5, and pure Fe2O3 which are denoted as PT, 0.1F, 0.5F, and PF, respectively). The structural, morphological, optical, and surface texture of the prepared nanocomposites were characterized using various techniques. The structural studies confirm the strong influence of Fe2O3 contents on the crystallite sizes and dislocation values. The size of the crystallites was increased by the increase in Fe2O3 contents. The bandgap values elucidated from DRS analysis were decreased from 3.15 eV to 1.91 eV with increasing Fe2O3 contents. The N2-Physorption analysis has confirmed the mesoporous nature of the samples with a comparable specific surface area of 35 m2/g. The photoelectrochemical measurements (CV, CA and EIS) were performed to assess the photoelectric properties of the prepared materials. It was found that the PT samples have the highest catalytic activity and photocurrent response compared to other composites. The reduction in current density was as follows: 2.8, 1.65, 1.5 and 0.9 mA/cm2, while the photocurrent response was ca. 800, 450, 45, 35 µA/cm2 for PT, 0.1F, 0.5F and PF samples, respectively. The EIS results showed that the (TiO2)1−x(Fe2O3)x nanocomposites exhibit lower charge transfer resistance than pure titania and hematite samples.