Novel Heterostructure-Based CoFe and Cobalt Oxysulfide Nanocubes for Effective Bifunctional Electrocatalytic Water and Urea Oxidation.

The development of effective oxygen evolution reaction (OER) and urea oxidation reaction (UOR) on heterostructure electrocatalysts with specific interfaces and characteristics provides a distinctive character. In this study, heterostructure nanocubes (NCs) comprising inner cobalt oxysulfide (CoOS) NCs and outer CoFe (CF) layered double hydroxide (LDH) are developed using a hydrothermal methodology. During the sulfidation process, the divalent sulfur ions (S2-) are released from the breakdown of the sulfur source and react with the Co-precursors on the surface leading to the transformation of CoOH nanorods into CoOS nanocubes. Further, X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) analyses reveal that the interactions at the interface of the CF@CoOS NCs significantly altered the electronic structure, thus enhancing the electrocatalytic performance. The optimal catalysts exhibited effective OER and UOR activities, the attained potentials are 1.51 and 1.36 V. This remarkable performance is attributable to the induction of electron transfer from the CoFe LDH to CoOS, which reduces the energy barrier of the intermediates for the OER and UOR. Furthermore, an alkaline water and urea two-cell electrolyzer assembled using CF@CoOS-2 NCs and Pt/C as the anode and cathode requires a cell voltage of 1.63 and 1.56 V along with a durability performance.

Stable 1T-MoS2 by Facile Phase Transition Synthesis for Efficient Electrocatalytic Oxygen Evolution Reaction.

The 1T phase of MoS2 exhibits much higher electrocatalytic activity and better stability than the 2H phase. However, the harsh conditions of 1T phase synthesis remain a significant challenge for various extensions and applications of MoS2. In this work, a simple hydrothermal-based synthesis method for the phase transition of MoS2 is being developed. For this, the NH2-MIL-125(Ti) (Ti MOF) is successfully utilized to induce the phase transition of MoS2 from 2H to 1T, achieving a high conversion ratio of ≈78.3%. The optimum phase-induced MoS2/Ti MOF heterostructure demonstrates enhanced oxygen evolution reaction (OER) performance, showing an overpotential of 290 mV at a current density of 10 mA cm-2. The density functional theory (DFT) calculations are demonstrating the benefits of this phase transition, determining the electronic properties and OER performance of MoS2.

Fabrication of g-C3N4@N-doped Bi2MoO6 heterostructure for enhanced visible-light-driven photocatalytic degradation of tetracycline pollutant.

An effective catalyst for the removal of antibiotic pollutants which severely impact water bodies and the environment is most favorable. In this study, g-C3N4 (gCN) and nitrogen-doped Bi2MoO6 (gCN-NBM) heterostructures are developed using a solvothermal process with enhanced photocatalytic degradation of tetracycline (TC) pollutants under visible-light irradiation. The experimental results confirm that nitrogen-doped Bi2MoO6 (NBM) nanomaterials were dispersed on the gCN surface, and a close combination of NBM and gCN leads to the efficient photocatalytic performance of TC. The photocatalytic efficiency of the heterostructure catalysts is four-fold higher than those of the pristine Bi2MoO6 catalysts owing to the excellent photogenerated charge separation and reduced recombination rate. Photocurrent measurements and electrochemical impedance spectra results disclose that the prepared heterostructure catalysts exhibit efficient photo-induced charge transfer. The electron spin resonance spectra and quenching experiments results reveal that superoxide radicals (.O2-) play a major role in TC degradation. This study presents a promising approach for designing efficient visible-light photocatalysts for environmental remediation applications.

Sonocatalytic degradation of ciprofloxacin and organic pollutant by 1T/2H phase MoS2 in Polyvinylidene fluoride nanocomposite membrane.

The development of recyclable catalysts with effective properties and stable reusability is great importance for the removal of different types of pollutants in wastewater. Herein, we have synthesized Polyvinylidene fluoride (PVDF) polymer and mixed-phase 1T/2H MoS2 for immobilizing the sonocatalyst material. Techniques such as FESEM, XRD, FTIR, XPS, and UV-vis spectra have been used for analyzing the structural, and morphological properties. The formation of a 1T/2H mixed phase in MoS2 has been revealed by XRD and XPS analysis. Consequently, the sonocatalytic performance of the nanocomposite membrane was investigated through ciprofloxacin (CIP) and organic pollutants (Rhodamine B (RhB)). As a result, MoS2/PVDF (PM4) nanocomposite membrane exhibited a superior sonocatalytic activity with 94.37% and 84.37% of RhB and CIP degradation efficiency with pseudo-first-order kinetic constant (k) of 0.0187 min-1, and 0.0044 min-1. The sonocatalytic property of the nanocomposite membrane is related to 1T/2H mixed-phase and PVDF. Additionally, the metallic based 1T phase MoS2 helps to promote electrons and holes and reduce the recombination rate. Moreover, it promotes the generation of more hydroxy radicals (.OH), and superoxide radicals (∙O2-) play a significant role in sonocatalytic degradation of RhB pollutants. Thus, the improved sonocatalytic degradation of 1T/2H MoS2/PVDF composite membrane exhibited its application in real-time wastewater treatment.

Efficient sonocatalytic degradation of heavy metal and organic pollutants using CuS/MoS2 nanocomposites.

Eco-friendly and highly effective catalysts are receiving considerable attention for the removal of heavy-metal ions and organic pollutants. In this study, we developed CuS/MoS2 nanocomposite sonocatalysts to enhance the degradation rate of environmental contaminants by harnessing ultrasonic irradiation. The successful synthesis of nanocomposite sonocatalysts was confirmed by X-ray diffraction (XRD) analysis, and energy-dispersive X-ray spectroscopy. The incorporation of CuS into MoS2 resulted in a flower-like structure with an increased surface area. Importantly, the sonocatalytic efficiency was enhanced by increasing CuS concentration in the nanocomposites, achieving maximum removal efficiencies of 99% and 88.52% for rhodamine B (RhB) and Cr(VI), respectively. In addition, they showed excellent stability and recyclability over five consecutive cycles, without noticeable changes in the nanocomposite structure. Reactive oxygen species (ROS) used for the degradation were identified using ROS scavengers. We believe that this strategy of exploiting nanocomposite sonocatalysts has a great potential in the field of environmental catalysis.