Harnessing plasma-generated reactive species for the synthesis of different phases of molybdenum oxide to study adsorption and photocatalytic activity.

This study employs plasma-liquid interaction technique to synthesize different phases of molybdenum oxide using air and argon as plasma-forming gases. In situ plasma-generated nitrogen species primarily NO3-/NO2- and hydrogen species (H+) facilitate the reduction of the molybdenum precursor anion (Mo7O24-). The reduced Mo species subsequently reacts with reactive oxygen species, forming MoO6 octahedra, which is the building block of a molybdenum oxide crystal. Varied concentrations of NO3-/NO2- and H+ species in air and argon plasma treatment significantly influence the growth process. Air plasma synthesis yields hexagonal molybdenum oxide microrods, which upon calcination changes its phase to orthorhombic 2D layered structure. Moreover, the argon plasma synthesized sample exhibits a mixed phase of hexagonal and orthorhombic molybdenum oxide due to the heavy argon ion bombardment, inducing material porosity and surface oxygen vacancies. The mixed-phase material exhibits superior adsorption and photo-degradation towards cationic dye compared to the other two phases. The higher photocatalytic performance may be responsible for the extended lifetime of the photo-generated charge carriers possessed by the mixed-phase material. Radical scavenging tests have identified holes and hydroxyl radicals as the key reactive species that take part in the photo-degradation process.

Unveiling the Potential of Covalent Organic Framework Electrocatalyst for Enhanced Oxygen Evolution.

The potential for sustainable energy and carbon neutrality has expanded with the development of a highly active electrocatalyst for the oxygen evolution reaction (OER). Covalent Organic Frameworks (COF) have recently garnered attention because of their enormous potential in a number of cutting-edge application sectors, such as gas storage, sensors, fuel cells, and active catalytic supports. A simple and effective COF constructed and integrated by post-alteration plasma modification facilitates high electrocatalytic OER activity under alkaline conditions. Variations in parameters such as voltage and treatment duration have been employed to enhance the factor that demonstrates high OER performance. The overpotential and Tafel slope are the lowest of all when using an optimized parameter, such as plasma treatment for 30 min utilizing 6 kV of voltage, PT-30 COF, measuring 390 mV at a current density of 10 mA.cm-2 and 69 mV.dec-1, respectively, as compared to 652 mV and 235 mV.dec-1 for the Pristine-COF. Our findings provide a method for broadening the scope by post-functionalizing the parent framework for effective water splitting.

Post-Transition State Direct Dynamics Simulations on the Ozonolysis of Catechol in an N2 Bath and Comparison with Gas-Phase Results.

Chemical dynamics simulations on the post-transition state dynamics of ozonolysis of catechol are performed in this article using a newly developed QM + MM simulation model. The reaction is performed in a bath of N2 molecules equilibrated at 300 K. Two bath densities, namely, 20 and 324 kg/m3, are considered for the simulation. The excitation temperatures of a catechol-O3 moiety are taken as 800, 1000, and 1500 K for each density. At these new excitation temperatures, the gas-phase results are also computed to compare the results and quantify the effect of surrounding molecules on this reaction. Like the previous findings, five reaction channels are observed in the present investigation, producing CO2, CO, O2, small carboxylic acid (SCA), and H2O. The probabilities of these products are discussed with the role of bath densities. Results from the gas-phase simulation and density of 20 kg/m3 are very similar, whereas results differ significantly at a higher bath density of 324 kg/m3. The rate constants for the unimolecular channel at each temperature and density are also calculated and reported. The QM + MM setup used here can also be used for other chemical reactions, where the solvent effect is important.

Visiblelight-induced ternary electron donor-acceptor complex enabled synthesis of 2-(2-hydrazinyl) thiazole derivatives and the assessment of their antioxidant and antidiabetic therapeutic potential.

A mild and eco-friendly visible-light-induced synthesis of 2-(2-hydrazinyl) thiazole from readily accessible thiosemicarbazide, carbonyl, and phenacyl bromide in the absence of a metal catalyst and/or any extrinsic photosensitizer is reported. This approach only requires a source of visible light and a green solvent at room temperature to produce the medicinally privileged scaffolds of hydrazinyl-thiazole derivatives in good to outstanding yields. Experimental studies support the in situ formation of a visible-light-absorbing, photosensitized colored ternary EDA complex. The next step is to prepare a pair of radicals in an excited state, which makes it easier to prepare thiazole derivatives through a SET and PCET process. DFT calculations additionally supported the mechanistic analysis of the course of the reaction. The antioxidant and antidiabetic properties of some of the compounds in the synthesized library were tested in vitro. All the investigated compounds demonstrated appreciable antioxidant activity, as evidenced by the reducing power experiment and the IC50 values of the DPPH radical scavenging experiment. Furthermore, the IC50 values for 4c, 4d, and 4g also demonstrated a strong α-amylase inhibitory effect.

Post-Transition-State Direct Dynamics Simulations on the Ozonolysis of Catechol.

On-the-fly dynamics simulations are performed for the reaction of catechol + O3. The post transition state (TS) dynamics is studied at temperatures of 400 and 500 K. The PM7 semiempirical method is employed for calculating the potential energy gradient needed for integrating Hamilton's equations of motion. This semiempirical method provides excellent agreement in terms of energy and geometry of the TSs as well as minimum energy states of the system with respect to B3LYP/6-311+G (2df, 2p) calculated results. In the dynamics, first, a peroxyacid is formed, which further dissociates to different fragments. Four major channels forming CO, CO2, H2O, and small carboxylic acid (SCA) fragments are seen in this reaction. Rates of each of the channels and the overall unimolecular reaction are calculated at both temperatures. Branching ratios of all these product channels are calculated and compared with experiment. The minimum energy profile of CO2, CO, and H2O channels are calculated. A qualitative estimate of activation energies for all the channels are obtained and compared with the explicit TS energies of three product channels, which ultimately correlate with the reaction probabilities.

Novel single-step synthesis and shape transformation of Au/CuO micro/nanocomposites using plasma-liquid interaction.

We report a novel single-step synthesis method of metal/metal oxide composites and transformation of the shape of the oxide material by Plasma-Liquid Interaction. Considering the potential applications of noble metal nanoparticle decorated copper oxide composites, we synthesize Au/CuO micro/nanocomposites by generating plasma between two copper electrodes inside a gold precursor (HAuCl4) solution. Simultaneous synthesis of CuO and Au nanoparticles from the electrode material and from the precursor solution respectively is possible due to the interaction of energetic electrons and other active species formed in the plasma zone. Moreover, the process does not require any external stabilizing and reducing chemical agents. The method provides a remarkable tunability of the materials' physical and chemical properties by only controlling the precursor solution concentration. By controlling process parameters, the shape of CuO particles can be transformed from spindles to sheet-like and the size of Au nanoparticles can also be varied. It influences the particles' specific surface area and total pore volume. Plasmonic property of Au nanoparticles is also observed i.e. optical tunability can be achieved. The process is found to be effective for synthesis of desired nanomaterials having various energy storage and solar light-driven photocatalytic applications.