Abstract

The use of visible light to propel chemical reactions is an exciting area of study that is crucial in the current socioeconomic environment. However, various photocatalysts have been developed to harness visible light, which consume high energy during synthesis. Thus, synthesizing photocatalysts at gel-liquid interfaces in ambient conditions is of scientific importance. Herein, we report an environmentally benign sodium alginate gel being used as a biopolymer template to synthesize copper sulfide (CuS) nanostructures at the gel-liquid interface. The driving force for the synthesis of CuS nanostructures is varied by changing the pH of the reaction medium (i.e., pH 7.4, 10, and 13) to tailor the morphology of CuS nanostructures. The CuS nanoflakes obtained at pH 7.4 transform into nanocubes when the pH is raised to 10, and the nanostructures deform at the pH of 13. Fourier transform infrared spectroscopy (FTIR) confirms all the characteristic stretching of sodium alginate, whereas the CuS nanostructures are crystallized in a hexagonal crystal system, as revealed by the powder X-ray diffraction analysis. The high-resolution X-ray photoelectron spectroscopy (XPS) spectra show the +2 and -2 oxidation states of copper (Cu) and sulfur (S) ions, respectively. The CuS nanoflakes physisorbed a higher concentration of greenhouse CO2 gas. Owing to a lower band gap of CuS nanoflakes synthesized at a pH of 7.4, compared to other CuS nanostructures prepared at pH 10 and 13, CuS photocatalytically degrades 95% of crystal violet and 98% of methylene blue aqueous dye solutions in 60 and 90 min, respectively, under blue light illumination. Additionally, sodium alginate-copper sulfide (SA-CuS) nanostructures synthesized at a pH of 7.4 demonstrate excellent performance in photoredox reactions to convert ferricyanide to ferrocyanide. The current research opens the door to developing new photocatalytic pathways for a wide range of photochemical reactions involving nanoparticle-impregnated alginate composites prepared on gel interfaces.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call