Sodium Alginate-CuS Nanostructures Synthesized at the Gel-Liquid Interface: An Efficient Photocatalyst for Redox Reaction and Water Remediation.

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.

A platinum nanoparticle doped self-assembled peptide bolaamphiphile hydrogel as an efficient electrocatalyst for the hydrogen evolution reaction.

Noble metal-based nanomaterials have shown great potential for catalytic application with higher selectivity and activity. Owing to their self-assembly properties with various molecular interactions, peptides play an essential role in the controlled synthesis of noble metal-based catalysts with high surface area. In this work, a phenylalanine (F) and tyrosine (Y) based peptide bolaamphiphile is prepared by solution-phase peptide synthesis. The peptide bolaamphiphile readily self-assembles into a hydrogel with a cross-linked nanofibrillar network. The platinum nanoparticles (Pt NPs) are in situ generated within the cross-linked nanofibrillar network of the hydrogel matrix of the peptide bolaamphiphile. Benefiting from the synergistic properties of the Pt nanoparticles doped on three-dimensional fibrous networks, Pt6@hydrogel shows efficient catalytic activity for the electrochemical hydrogen evolution reaction (HER) in 0.5 M H2SO4 solution. The Pt6@hydrogel requires an overpotential of 45 mV at -10 mA cm-2 with a Tafel slope of 52 mV dec-1. The Pt6@hydrogel also shows electrocatalytic activity in basic and neutral pH solutions. The excellent activity and stability of Pt6@hydrogel for the HER shows great potential for energy conversion applications.