| نویسندگان | Mohammad Reza Doosti,,shaghayegh laleh,Jose Miguel Sansano |
| نشریه | Frontiers in Chemistry |
| شماره صفحات | 1013349-1013366 |
| شماره سریال | 10 |
| شماره مجلد | 1 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2022 |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | سوئیس |
| نمایه نشریه | JCR،Scopus |
چکیده مقاله
In this study, a new solar light-driven magnetic heterogeneous photocatalyst,
denoted as ZnO/NiFe2O4/Co3O4, is successfully prepared. FT-IR, XPS, XRD,
VSM, DRS, FESEM, TEM, EDS, elemental mapping, and ICP analysis are
accomplished for full characterization of this catalyst. FESEM and TEM
analyses of the photocatalyt clearly affirm the formation of a hexagonal
structure of ZnO (25–40 nm) and the cubic structure of NiFe2O4 and Co3O4
(10–25 nm). Furthermore, the HRTEM images of the photocatalyst verify some
key lattice fringes related to the photocatalyt structure. These data are in very
good agreement with XRD analysis results. According to the ICP analysis, the
molar ratio of ZnO/NiFe2O4/Co3O4 composite is obtained to be 1:0.75:0.5.
Moreover, magnetization measurements reveals that the ZnO/NiFe2O4/Co3O4
has a superparamagnetic behavior with saturation magnetization of 32.38 emu/
g. UV-vis DRS analysis indicates that the photocatalyst has a boosted and strong
light response. ZnO/NiFe2O4/Co3O4, with band gap energy of about 2.65 eV
[estimated according to the Tauc plot of (αhν)2 vs. hν], exhibits strong potential
towards the efficacious degradation of tetracycline (TC) by natural solar light. It
is supposed that the synergistic optical effects between ZnO, NiFe2O4, and
Co3O4 species is responsible for the increased photocatalytic performance of
this photocatalyst under the optimal conditions (photocatalyst dosage =
0.02 g L−1, TC concentration = 30 mg L−1, pH = 9, irradiation time = 20 min,
and TC degradation efficiency = 98%). The kinetic study of this degradation
process is evaluated and it is well-matched with the pseudo-first-order kinetics.
Based on the radical quenching tests, it can be perceived that •O2− species and
holes are the major contributors in such a process, whereas the •OH radicals
identify to have no major participation. The application of this methodology is
implemented in a facile and low-cost photocatalytic approach to easily degrade
TC by using a very low amount of the photocatalyst under natural sunlight
source in an air atmosphere. The convenient magnetic isolation and reuse of
the photocatalyst, and almost complete mineralization of TC (based on TOCanalysis), are surveyed too, which further highlights the operational application
of the current method. Notably, this method has the preferred performance
among the very few methods reported for the photocatalytic degradation of TC
under natural sunlight. It is assumed that the achievements of this
photocatalytic method have opened an avenue for sustainable
environmental remediation of a broad range of contaminants.
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