ZnO Nano-Flowers Assembled on Carbon Fiber Textile for High-Performance Supercapacitor’s Electrode

Herein, a crystalline nano-flowers structured zinc oxide (ZnO) was directly grown on carbon fiber textile (CFT) substrate via a simple hydrothermal process and fabricated with a binder-free electrode (denoted as ZnO@CFT) for supercapacitor (SC) utilization. The ZnO@CFT electrode revealed a 201 F·g−1 specific capacitance at 1 A·g−1 with admirable stability of >90% maintained after 3000 cycles at 10 A·g−1. These impressive findings are responsible for the exceedingly open channels for well-organized and efficient diffusion of effective electrolytic conduction via ZnO and CFT. Consequently, accurate and consistent structural and morphological manufacturing engineering is well regarded when increasing electrode materials’ effective surface area and intrinsic electrical conduction capability. The crystalline structure of ZnO nano-flowers could pave the way for low-cost supercapacitors

Vanadium Carbide (V4C3) MXene as an Efficient Anode for Li-Ion and Na-Ion Batteries

Li-ion batteries (LIBs) and Na-ion batteries (SIBs) are deemed green and efficient electrochemical energy storage and generation devices; meanwhile, acquiring a competent anode remains a serious challenge. Herein, the density-functional theory (DFT) was employed to investigate the performance of V4C3 MXene as an anode for LIBs and SIBs. The results predict the outstanding electrical conductivity when Li/Na is loaded on V4C3. Both Li2xV4C3 and Na2xV4C3 (x = 0.125, 0.5, 1, 1.5, and 2) showed expected low-average open-circuit voltages of 0.38 V and 0.14 V, respectively, along with a good Li/Na storage capacity of (223 mAhg?1) and a good cycling performance. Furthermore, there was a low diffusion barrier of 0.048 eV for Li0.0625V4C3 and 0.023 eV for Na0.0625V4C3, implying the prompt intercalation/extraction of Li/Na. Based on the findings of the current study, V4C3-based materials may be utilized as an anode for Li/Na-ion batteries in future applications. 2022 by the authors.This work was financially funded by the authors express their gratitude for the support of the Researchers Supporting Project Number (RSP-2021/267) King Saud University, Riyadh, Saudi Arabia. This work is also supported by Scientific Research Fund of Hunan Provincial Education Department (No. 21B0637).Scopu

UV-Light Mediated Biosynthesis of Silver Nanowires; Characterization, Dye Degradation Potential and Kinetic Studies

Herrin, a simple and eco-friendly method for the synthesis of silver nanowires (Ag-NWs) has been reported. Silver nanowires were synthesized using Psidium guajava seed extract that acted as a reducing agent as well as a stabilizing agent for silver nitrate solution. Synthesis was carried out at 50 °C temperature under continuous UV-irradiation. Silver nanowires were initially characterized by a UV-visible and FTIR spectrophotometer. In addition, morphology and particle size of synthesized Ag-NWs were determined using Field Emission Scanning Electron Microscopy and X-ray diffraction (XRD) techniques. Nanowires were found to have 12.8 μm length and 200–500 nm diameter and cubic phase morphology. Furthermore, the catalytic potential of Ag-NWs for the degradation of methyl orange dye (MO) was determined. The selected dye was degraded successfully that confirmed the catalytic potential of Ag-NWs. The authors concluded that Ag-NWs can be synthesized using plant extract having excellent morphological features as well as impressive catalytic potential

Infrared spectroscopy of Ca(NH3)n complexes

Infrared spectra of Ca(NH3)n complexes in the gas phase have been recorded for the first time. The spectra are consistent with structures where the Ca atom resides inside one or more solvation shells of NH3 molecules. IR spectra were recorded using a photodissociation technique. A comparison of the spectra with those predicted from ab initio calculations suggests that Ca(NH3)8 has all NH3 molecules in a single solvent shell around the Ca atom, whereas the spectra of Ca(NH3)9 and Ca(NH3)10 are consistent with two-shell structures

Electrochemical detection and quantification of catechol based on a simple and sensitive poly(riboflavin) modified carbon nanotube paste electrode

In the present research work, selective and sensitive catechol (CT) detection and quantification were shown in the presence of resorcinol (RS) in 0.2 M phosphate buffer (PB) solution by preparing a low-cost, simple, and green carbon nanotube paste electrode (CNTPE) surface activated with electropolymerized riboflavin (PRF). The morphological, conductivity, and electrochemical features of the modified electrode (PRFMCNTPE) and bare carbon nanotube paste electrode (BCNTPE) materials were analyzed using electrochemical impedance spectroscopy (EIS), field emission scanning electron microscopy (FE-SEM), cyclic voltammetry (CV), and differential pulse voltammetry (DPV). The PRF-activated electrode displays outstanding sensitivity, stability, selectivity, reproducibility, and repeatability for the redox feature of CT with improved electrochemical current and declined electrochemical potential compared to BCNTPE. The peak currents of CT are correlated to the different CT concentrations (CV method: 6.0–60.0 μM & DPV method: 0.5–7.0 μM), and the obtained detection limit (DL) and quantification limit (QL) are found to be 0.025 μM and 0.085 μM (CV method) and 0.0039 μM and 0.0132 μM (DPV method), respectively. The prepared PRFMCNTPE material was advantageous for the examination of CT in environmentally important tap water sample as a real-time application

Electroanalytical Detection of Indigo Carmine in Presence of Tartrazine Using a Poly(dl-phenylalanine) Modified Carbon Nanotube Paste Electrode

Certain dyes are deleterious to the biological system, including animals and plants living in the water sources, soil sources, and so on. Thus, the analysis of these dyes requires a potent, quick, and cost-effective approach to the environmental samples. The present research work shows a modest, low-cost, and eco-friendly electrochemical device based on poly(dl-phenylalanine)-layered carbon nanotube paste electrode (P(PAN)LCNTPE) material for indigo carmine (ICN) detection in the presence of tartrazine. The cyclic voltammetric, field emission scanning electron microscopy, and electrochemical impedance spectroscopic methods were operated for the detection of the redox nature of ICN and electrode material surface activities, respectively. In better operational circumstances, P(PAN)LCNTPE provided better catalytic activity for the redox action of ICN than the bare carbon nanotube paste electrode. The P(PAN)LCNTPE showed good electrochemical activity during the variation of ICN concentrations ranging from 0.2 µM to 10.0 µM with improved peak current, and the limit of detection was about 0.0216 µM. Moreover, the P(PAN)LCNTPE material was performed as a sensor of ICN in a tap water sample and shows adequate stability, repeatability, and reproducibility

Electroanalytical Detection of Indigo Carmine in Presence of Tartrazine Using a Poly(dl-phenylalanine) Modified Carbon Nanotube Paste Electrode

Certain dyes are deleterious to the biological system, including animals and plants living in the water sources, soil sources, and so on. Thus, the analysis of these dyes requires a potent, quick, and cost-effective approach to the environmental samples. The present research work shows a modest, low-cost, and eco-friendly electrochemical device based on poly(dl-phenylalanine)-layered carbon nanotube paste electrode (P(PAN)LCNTPE) material for indigo carmine (ICN) detection in the presence of tartrazine. The cyclic voltammetric, field emission scanning electron microscopy, and electrochemical impedance spectroscopic methods were operated for the detection of the redox nature of ICN and electrode material surface activities, respectively. In better operational circumstances, P(PAN)LCNTPE provided better catalytic activity for the redox action of ICN than the bare carbon nanotube paste electrode. The P(PAN)LCNTPE showed good electrochemical activity during the variation of ICN concentrations ranging from 0.2 µM to 10.0 µM with improved peak current, and the limit of detection was about 0.0216 µM. Moreover, the P(PAN)LCNTPE material was performed as a sensor of ICN in a tap water sample and shows adequate stability, repeatability, and reproducibility

Synthesis and Characterization of Sr-Doped ZnSe Nanoparticles for Catalytic and Biological Activities

The development of cost-effective and ecofriendly approaches toward water purification and antibacterial activity is a hot research topic in this era. Purposely, strontium-doped zinc selenide (Sr-doped ZnSe) nanoparticles, with different molar ratios of Sr2+ cations (0.01, 0.05, and 0.1), were prepared via the co-precipitation method, in which sodium borohydride (NaBH4) and 2-mercaptoethanol were employed as reducing and stabilizing agents, respectively. The ZnSe cubic structure expanded by Sr2+ cations was indicated by X-ray diffraction (XRD) analysis. The absorption of the chemical compounds on the surface was observed via Fourier transform infrared (FT-IR) spectroscopy. The optical orientation was measured by ultraviolet–visible diffused reflectance spectroscopy (UV-DRS) analysis. The surface area, morphology, and elemental purity were analyzed using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and energy-dispersive spectroscopy (EDS) analyses. The oxidation state and valency of the synthesized nanoparticles were analyzed using X-ray photoelectron spectroscopy (XPS). Sr-doped ZnSe nanoparticles were investigated for photocatalytic degradation of methyl orange (MO), and their antibacterial potential was investigated against different bacterial strains. The antibacterial activity examined against Staphylococcus aureus and Escherichia coli implied the excellent biological activity of the nanoparticles. Moreover, the Sr-doped ZnSe nanoparticles were evaluated by the successful degradation of methyl orange under visible light irradiation. Therefore, Sr-doped ZnSe nanoparticles have tremendous potential in biological and water remediation fields

Structural effects on the luminescence properties of CsPbI3 nanocrystals

Metal halide perovskite nanocrystals (NCs) are promising for photovoltaic and light-emitting applications. Due to the softness of their crystal lattice, structural modifications have a critical impact on their optoelectronic properties. Here we investigate the size-dependent optoelectronic properties of CsPbI3 NCs ranging from 7 to 17 nm, employing temperature and pressure as thermodynamic variables to modulate the energetics of the system and selectively tune the interatomic distances. By temperature-dependent photoluminescence spectroscopy, we have found that luminescence quenching channels exhibit increased non-radiative losses and weaker exciton-phonon coupling in bigger particles, in turn affecting the luminescence efficiency. Through pressure-dependent measurements up to 2.5 GPa, supported by XRD characterization, we revealed a NC-size dependent solid-solid phase transition from the γ-phase to the δ-phase. Importantly, the optical response to these structural changes strongly depends on the size of the NC. Our findings provide an interesting guideline to correlate the size and structural and optoelectronic properties of CsPbI3 NCs, important for engineering the functionalities of this class of soft semiconductors