No abstract

The breakthrough in Ln(III)-based SMMs with Schiff base ligands have been occurred for the last decade on account of their magnetic behavior, anisotropy and relaxation pathways. Herein, we review the synthetic strategy, from a structural point of view and magnetic properties of mono, di, tri and polynuclear Ln(III)-based single-molecule magnets mainly with Schiff bases of Salicylaldehyde origin. Special attention has been given to some important breakthroughs that are changing the perspective of this field with a special emphasis on slow magnetic relaxation. An overview of 50 Ln(III)-Schiff base complexes with SMM behavior, covering the period 2008–2020, which have been critical in understanding the magnetic interactions between the Ln(III)-centers, are presented and discussed in detail.

Herein, for the first time, a direct Z-scheme g-C 3 N 4 /NiFe 2 O 4 nanocomposite photocatalyst was prepared using facile one-pot hydrothermal method and characterized using XRD, FT-IR, DRS, PL, SEM, EDS, TEM, HRTEM, XPS, BET and VSM characterized techniques. The result reveals that the NiFe 2 O 4 nanoparticles are loaded on the g-C 3 N 4 sheets successfully. The photocatalytic activities of the as-prepared photocatalysts were evaluated for the degradation of methyl orange (MO) under visible light irradiation. It was shown that the photocatalytic activity of the g-C 3 N 4 /NiFe 2 O 4 nanocomposite is about 4.4 and 3 times higher than those of the pristine NiFe 2 O 4 and g-C 3 N 4 respectively. The enhanced photocatalytic activity could be ascribed to the formation of g-C 3 N 4 /NiFe 2 O 4 direct Z-scheme photocatalyst, which results in efficient space separation of photogenerated charge carriers. More importantly, the as-prepared Z-scheme photocatalyst can be recoverable easily from the solution by an external magnetic field and it shows almost the same activity for three consecutive cycles. Considering the simplicity of preparation method, this work will provide new insights into the design of high-performance magnetic Z-scheme photocatalysts for organic contaminate removal.

Magnetically recyclable C-doped TiO2/Fe3O4 (C-TiO2/Fe3O4) nanocomposite was successfully synthesized via a sol–gel method. The synthesized samples were characterized using SEM, energy-dispersive X-ray spectroscopy (EDS), FTIR, and UV-VIS diffuse reflectance spectroscopy (DRS) techniques. The results clearly showed that a C-TiO2/Fe3O4 nanocomposite was produced. The photocatalytic activities of the prepared pristine (TiO2), C-doped TiO2 (C-TiO2) and C-TiO2/Fe3O4 were evaluated by the photodegradation of methyl orange (MO) under natural sunlight. The effect of catalyst loading and MO concentration were studied and optimized. The C-TiO2/Fe3O4 nanocomposite exhibited an excellent photocatalytic activity (99.68%) that was higher than the TiO2 (55.41%) and C-TiO2 (70%) photocatalysts within 150 min. The magnetic nanocomposite could be easily recovered from the treated solution by applying external magnetic field. The C-TiO2/Fe3O4 composite showed excellent photocatalytic performance for four consecutive photocatalytic reactions. Thus, this work could provide a simple method for the mass production of highly photoactive and stable C-TiO2/Fe3O4 photocatalyst for environmental remediation.

No abstract

Magnetically recyclable direct Z-scheme CoFe2O4-loaded g-C3N4 photocatalyst material was fabricated using a facile hydrothermal technique and subsequently characterized by XRD, VSM, PL, FT-IR, EDX, DRS, SEM, and BET techniques. The characterization results confirmed that nanoparticles of CoFe2O4 are loaded on the surface of g-C3N4 sheets. The optical band gap of g-C3N4 has been decreased from 2.65 eV to 1.30 eV by means of the loading of CoFe2O4 nanoparticles onto the nanosheets of g-C3N4. This has enhanced the separation process of electron-hole. Under visible light irradiation, the photocatalytic activity of the developed direct Z-scheme CoFe2O4-loaded g-C3N4 photocatalyst was evaluated for the photodegradation of methylene blue (MB); during this process the MB decomposed by up to 98.86% in 140 min. Meanwhile, under the same irradiation and time conditions, the g-C3N4 and CoFe2O4 themselves degraded MB up to 74.92% and 51.53%, respectively. The direct Z-scheme CoFe2O4-loaded g-C3N4 material was recovered from the solution after the photocatalytic activity using an external magnet and studied to determine its stability. It was shown that the photoactivity did not change significantly after five consecutive cycles.