In recent years, much interest has been raised by materials with multi-purpose characteristics as the performance of electrochemical energy devices such as supercapacitors and photocatalytic activities depend strongly on the properties of materials. This study delineates various parameters like morphology, energy band gap, charge transfer resistance, different defect states, diffusion coefficient and functional groups adsorbed on the surface of material to assess the performance of supercapacitor electrodes and photocatalytic degradation efficiency of synthesised multi-dimensional ZnS nanostructures. Ethylenediamine (EN)-mediated multi-dimensional ZnS nanostructures were grown by the solvothermal route. One-dimensional (1D), 2D and 3D morphologies were obtained by varying the ratio of de-ionised water and EN, taken as 1:3, 1:2 and 1:1, respectively. The EN molecules effectively capped most of the surfaces of the ZnS nanoparticles formed, preventing agglomeration of nanoparticles due to the decrement in surface energy. The oriented attachment of these clusters resulted in the formation of 1D, 2D and 3D morphologies. The plausible chemistry in the formation of 1D, 2D and 3D nanostructures has been elaborated. Charge transfer properties of prepared electrodes have been examined using the electrochemical impedance spectroscopy (EIS) technique because better charge transfer causes diminishing electron/hole recombination and hence better photodegradation efficiency. Among the synthesised materials, the 2D nanostructure degraded the eosin Y dye to maximum 90.71% efficiency with rate constant 34 × 10 min. 2D nanostructures possess better charge transfer and hence better photodegradation efficiency. Various studies using methods of UV-vis, Fourier-transform infrared, Brunauer-Emmett-Teller, x-ray photoelectron spectroscopy and photoluminescence spectra are in good agreement with the obtained photodegradation results. After analysing cyclic voltammetry curves and EIS, a higher diffusion coefficient is obtained for 1D nanostructure material, hence a higher specific capacitance and higher energy density of 159.12 F g and 22.75 KWh kg are found in this case. Only 9% loss of specific capacitance is found after 1000 cycles, showing a relatively high cycling stability in 3D nanostructures. The excellent supercapacitive property can be attributed to the porous structure and high specific surface area. Thus, the synthesised multi-dimensional ZnS nanostructures are proved to be a potential candidate for both photocatalytic and supercapacitor electrode performance.
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http://dx.doi.org/10.1088/1361-6528/ab7604 | DOI Listing |
J Am Chem Soc
December 2024
Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States.
Designing catalysts with well-defined active sites with chemical functionality responsive to visible light has significant potential for overcoming scaling relations limiting chemical reactions over heterogeneous catalyst surfaces. Visible light can be leveraged to facilitate the removal of strongly bound species from well-defined single cationic sites (Rh) under mild conditions (323 K) when they are incorporated within a photoactive perovskite oxide (Rh-doped SrTiO). CO, a key intermediate in many chemistries, forms stable geminal dicarbonyl Rh complexes (Rh(CO)), that could act as site blockers or poisons during a catalytic cycle.
View Article and Find Full Text PDFMikrochim Acta
December 2024
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650500, People's Republic of China.
A novel copper and iron doped containing chitosan and heparin sodium carbon dots (CS-Cu,Fe/HS) nanozyme was formulated through a single-step microwave digestion method. CS-Cu,Fe/HS exhibits excellent peroxidase (POD)-like activity and positive charge characteristics, and it can oxidize the negatively charged 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) in the presence of HO to produce a green compound (ox-ABTS). Furthermore, CS-Cu,Fe/HS enhances electron transfer and provides additional active sites through the valence state transformations of Fe/Fe and Cu/Cu.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
Laboratory of Photoactive Nanocomposite Materials, Saint Petersburg State University, 199034 Saint-Petersburg, Russia.
In this study, we explore the charge transfer mechanism between WO and CuO in heterostructured WO/CuO electrodes and in a WO||CuO tandem photoelectrochemical cell. The physical-chemical characterizations of the individual WO and CuO electrodes and the heterostructured WO/CuO electrode by XRD, XPS, and SEM methods confirm the successful formation of the target systems. The results of photoelectrochemical studies infer that in both the heterostructured WO/CuO electrode and WO||CuO tandem photoelectrochemical cell, the major mechanism of charge transfer between WO and CuO is a realization of the Z-scheme.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
State Key Laboratory of Heavy Oil Processing, Institute of New Energy, College of New Energy, China University of Petroleum (East China), Qingdao 266580, China.
The integration of intermittent renewable energy sources into the energy supply has driven the need for large-scale energy storage technologies. Vanadium redox flow batteries (VRFBs) are considered promising due to their long lifespan, high safety, and flexible design. However, the graphite felt (GF) electrode, a critical component of VRFBs, faces challenges due to the scarcity of active sites, leading to low electrochemical activity.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
Department of Chemistry and Chemical Engineering, Taiyuan Institute of Technology, Taiyuan 030008, China.
Cisplatin-based platinum compounds are important clinical chemotherapeutic agents that participate in most tumor chemotherapy regimens. Through density-functional theory calculations, the formation and stability of the inorganic oxide carrier, the mechanisms of the hydrolysis reaction of the activated platinum compound, and its binding mechanism with DNA bases can be studied. The higher the oxidation state of Pt (II to IV), the more electrons transfer from the magnesia-gold composite material to the platinum compound.
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