AI Article Synopsis

  • The study focuses on improving wastewater treatment by synthesizing zinc oxide (ZnO) and nickel-doped zinc oxide (Ni:ZnO) to enhance their photo catalytic capacity.
  • Annealing these materials boosts their photo catalytic activity by 65%, reduces average crystal size, and alters the optical band gap, making them more effective for pollutant breakdown.
  • The findings highlight the promising potential of using Ni:ZnO for practical wastewater treatment solutions, addressing urgent environmental challenges.

Article Abstract

Water scarcity and pollution has increased the need for innovative and effective waste water treatment methods. The presented study aims to tackle this difficulty by synthesizing zinc oxide (ZnO) and nickel (Ni) doped ZnO to improve their photo catalytic capacity. This study examines wastewater treatment and organic pollutant breakdown using nanotechnology. The annealing increases photo catalytic activity by 65%, thereby enhancing efficiency. XRD shows that annealing decreased the average crystal size of pure ZnO and nickel doped ZnO (Ni:ZnO) i.e., for pure ZnO average crystal size is decreased from 23.90 to 20.90 nm and for Ni:ZnO, 34.39-28.65 nm. SEM shows that un annealed samples have agglomerates, while annealed samples are quasi-spherical. Using diffuse reflectance spectroscopy (DRS), the study examines how annealing affects optical band gap. Annealed Ni:ZnO has a band gap of 3.09 eV, which is smaller as compared to un annealed Ni:ZnO (3.18 e V). Similarly, the decline in energy band gap is observed for pure ZnO too. This study highlights the significant capacity of Ni:ZnO, for un annealed and annealed synthesis, to effectively meet the urgent requirements for waste water treatment. The extensive research conducted in this work enhances our comprehension of photo catalytic materials and underscores its potential for practical implementation in addressing waste water-related environmental issues.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11411114PMC
http://dx.doi.org/10.1038/s41598-024-60258-5DOI Listing

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