RESUMO
One of the most practical and environmentally friendly ways to deal with the energy crises and global warming is to produce hydrogen as clean fuel by splitting water. The central obstacle for electrochemical water splitting is the use of expensive metal-based catalysts. For electrocatalytic hydrogen production, it is essential to fabricate an efficient catalyst for the counterpart oxygen evolution reaction (OER), which is a four-electron-transfer sluggish process. Here in this study, we have successfully fabricated cobalt-based ferrite nanoparticles over the surface of carbon nanotube fiber (CNTF) that was utilized as flexible anode materials for the OER and overall electrochemical water splitting reactions. Scanning electron microscopy images with elemental mapping showed the growth of nanoparticles over CNTF, while electrochemical characterization exhibited excellent electrocatalytic performance. Linear sweep voltammetry revealed the reduced overpotential value (260 mV@η10mAcm-2) with a small Tafel slope of 149 mV dec-1. Boosted electrochemical double layer capacitance (0.87 mF cm-2) for the modified electrode also reflects the higher surface area as compared to pristine CNTF (Cdl = 0.022 mF cm-2). Charge transfer resistance for the surface-modified CNTF showed the lower diameter in the Nyquist plot and was consequently associated with the better Faradaic process at the electrode/electrolyte interface. Overall, the as-fabricated electrode could be a promising alternative for the efficient electrochemical water splitting reaction as compared to expensive metal-based electrocatalysts.
RESUMO
The spread of organic pollutants in water spoils the environment, and among the best-known sorbents for removing organic compounds are carbonaceous materials. Sunflower seed waste (SFSW) was employed as a green and low-cost precursor to prepare carbon nanoparticles (CNPs) via pyrolysis, followed by a ball-milling process. The CNPs were treated with a nitric-sulfuric acid mixture (1:1) at 100 °C. The scanning electron microscopy (SEM) showed a particle size range of 38 to 45 nm, and the Brunauer-Emmett-Teller (BET) surface area was 162.9 m2 g-1. The elemental analysis was performed using energy-dispersive X-ray spectroscopy, and the functional groups on the CNPs were examined with Fourier transform infrared spectroscopy. Additionally, an X-ray diffractometer was employed to test the phase crystallinity of the prepared CNPs. The fabricated CNPs were used to adsorb ciprofloxacin (CFXN) and malachite green (MLG) from water. The experimentally obtained adsorption capacities for CFXN and MLG were 103.6 and 182.4 mg g-1, respectively. The kinetic investigation implied that the adsorption of both pollutants fitted the pseudo-first-order model, and the intraparticle diffusion step controlled the process. The equilibrium findings for CFXN and MLG sorption on the CNPs followed the Langmuir and the Fredulich isotherm models, respectively. It was concluded that both pollutants spontaneously adsorbed on the CNPs, with physisorption being the likely mechanism. Additionally, the FTIR analysis of the adsorbed CFXN showed the disappearance of some functional groups, suggesting a chemisorption contribution. The CNPs showed an excellent performance in removing CFXN and MLG from groundwater and seawater samples and possessed consistent efficiency during the recycle-reuse study. The application of CNPs to treat synthetically contaminated natural water samples indicated the complete remediation of polluted water using the ball-mill-fabricated CNPs.