Photocatalytic hydrogen production and pollutant degradation using a heterogeneous photocatalyst remains an alternative route for mitigating the impending pollution and energy crisis. Hence, the development of cost-effective and environmentally friendly semiconducting materials with high solar light captivation nature is imperative. To overcome this challenge, α-MnO nanorod (NR)-modified MOF UiO-66-NH (UNH) was prepared via a facile solvothermal method, which is efficient toward H evolution and oxy-tetracycline hydrochloride (O-TCH) degradation.
View Article and Find Full Text PDFPhotocatalysis, as an amenable and effective process, can be adopted for pollution remediation and to alleviate the ongoing energy crisis. In this case, recently, metal organic frameworks (MOFs) have attracted increasing attention in the field of photocatalysis owning to their unique characteristics including large specific surface area, tuneable pore architecture, mouldable framework composition, tuneable band structure, and exceptional photon absorption tendency complimented with superior anti-recombination of excitons. Among the plethora of frameworks, inner transition metal based-MOFs (IT-MOFs) have started to garner significant traction as photocatalysts due to their distinct characteristics compared to conventional transition metal-based frameworks.
View Article and Find Full Text PDFIn the existing eco-crisis, designing and engineering an efficient as well as water stable photocatalyst for energy conversion and pollutant abatement remains crucial. In this regard, a mixed linker type zirconium metal organic framework (Zr-MOF) with terepthalic acid based ditopic linkers were utilized to design a single component photocatalyst through single step solvothermal method to utilize photons from visible light illumination towards hydrogen energy (H) production and Tetracycline Hydrochloride (TCH) degradation. The one pot synthesized mixed linker based Zr-MOF displays visible light absorption through band gap tuning, superior exciton segregation and oxygen vacancy that cumulatively supports the enhancement in the photocatalytic output with respect to their pristine counterparts.
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