INORGANIC CHEMISTRY COMMUNICATION, cilt.177, sa.114388, ss.1-11, 2025 (SCI-Expanded)
In this study, photocatalytic and magnetic Ni (metal)/NiO (metal oxide)
nanoparticles (NPs) were synthesized and coated with small amounts of Pt
(1, 3, and 5 %) using a modified polyol process. The X-ray diffraction
results confirmed that the Ni/NiO NPs exhibited a mixed cubic phase of
Ni and NiO after calcination at 600 °C for 1 h. After loading 1 %, 3 %,
and 5 % Pt onto the Ni/NiO surface, broad Pt peaks became visible in the
XRD for the 5 % Pt sample, indicating the formation of a separate
crystalline Pt phase. Scanning electron microscopy and energy-dispersive
X-ray spectroscopy analyses revealed an average particle size of
approximately 30 nm, confirming impurity-free synthesis. All samples
demonstrated enhanced adsorption capabilities, with the 3 % Pt-loaded
Ni/NiO sample removing up to 60 % of methylene blue within 1 h under
sunlight. The 5 % Pt-loaded Ni/NiO exhibited the highest photocatalytic
performance, achieving a rate constant of 0.01779 min−1 and a
degradation efficiency of approximately 91 %. This improvement is
attributed to the role of Pt in facilitating charge separation and
acting as an electron sink, which suppresses charge carrier
recombination. Additionally, Pt increases the number of active sites,
further improving photocatalytic efficiency. Magnetization vs.
temperature measurements indicated that increasing the Pt content from
1 % to 5 % reduced the total magnetization owing to the paramagnetic
contribution of Pt in the Ni/NiO structure. The highest coercivity,
exchange bias, saturation magnetization, and remanent magnetization
values for Ni/NiO sample were determined from hysteresis loops at 5 K,
measuring 389.6 Oe, 28.1 Oe, 4.91 emu/g and 1.58 emu/g, respectively.
These results highlight the potential of Pt-deposited Ni/NiO NPs to
improve adsorption and photocatalytic activity, offering valuable
insights for pollutant degradation and magnetically recoverable
nanocatalysis of environmental remediation applications.