TY - JOUR
T1 - Photocatalytic and electrochemical exploration of a novel Pd modified FeVO4/ZrO2 nanocomposite materials for organic pollutant decontaminants in water
AU - Kumari, Monika
AU - Kumar, Naveen
AU - Sharma, Raj Kishore
AU - Tahir, Muhammad
AU - Kumar, Vinod
AU - Singh, Pardeep
AU - Raizada, Pankaj
AU - Kumar, Suresh
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/4/1
Y1 - 2025/4/1
N2 - The present investigation is focused on the synthesis of FeVO4/ZrO2 photocatalysts with varying percentages of FeVO4 on ZrO2 (10 % 20 % and 30 % wt%) and subsequent deposition of Pd on these binary composites at different Pd weight percentages (2 %, 3 %, and 5 % wt%). ZrO2 and FeVO4 were synthesized using the hydrothermal method. FeVO4 is integrated in situ onto ZrO2 in the binary composite followed by Pd deposition by chemical reduction. The fabricated materials comprehensively analyzed their crystalline structures, morphological characteristics, charge carrier recombination dynamics, band gap energies, chemical compositions, and surface charge. This analysis employed sophisticated methods, including XRD, XPS, UV–Vis DRS, HRTEM, EDX, PL, FESEM, and Zeta potential analysis. The efficacy of photocatalysts was determined on two organic pollutants: the antibiotic ciprofloxacin (CP) and the cationic dye Rhodamine B (RhB). The incorporation of FeVO4 significantly enhanced degradation efficiency compared to using the pure ZrO2 photocatalyst alone. The heterojunctions in binary composites facilitated efficient charge separation and enhanced light harvesting, thereby augmenting the photocatalytic efficiency of the synthesized composites. Furthermore, subsequent Pd deposition further augmented the photocatalytic efficiency to a greater extent due to the surface plasmon effect. Among the ternary composites, ZFPd-2 (3 % wt% Pd on 20 % FeVO4/ZrO2) exhibited the highest degradation efficiencies, achieving 95.43 % degradation for RhB and 91.44 % for CP within 180 min. Trapping agents were utilized to examine the role of active species during the degradation process. Photogenerated holes and electrons were identified as active species in RhB degradation, whereas in CP degradation, oxygen radicals and holes predominated. The effect of pH on the photocatalytic performance of the photocatalyst was also investigated, along with the reusability and stability of the photocatalyst over five cycles. Electrochemical analysis via Mott-Schottky curves and EIS supported higher donor density and lower charge resistance after composite formation.
AB - The present investigation is focused on the synthesis of FeVO4/ZrO2 photocatalysts with varying percentages of FeVO4 on ZrO2 (10 % 20 % and 30 % wt%) and subsequent deposition of Pd on these binary composites at different Pd weight percentages (2 %, 3 %, and 5 % wt%). ZrO2 and FeVO4 were synthesized using the hydrothermal method. FeVO4 is integrated in situ onto ZrO2 in the binary composite followed by Pd deposition by chemical reduction. The fabricated materials comprehensively analyzed their crystalline structures, morphological characteristics, charge carrier recombination dynamics, band gap energies, chemical compositions, and surface charge. This analysis employed sophisticated methods, including XRD, XPS, UV–Vis DRS, HRTEM, EDX, PL, FESEM, and Zeta potential analysis. The efficacy of photocatalysts was determined on two organic pollutants: the antibiotic ciprofloxacin (CP) and the cationic dye Rhodamine B (RhB). The incorporation of FeVO4 significantly enhanced degradation efficiency compared to using the pure ZrO2 photocatalyst alone. The heterojunctions in binary composites facilitated efficient charge separation and enhanced light harvesting, thereby augmenting the photocatalytic efficiency of the synthesized composites. Furthermore, subsequent Pd deposition further augmented the photocatalytic efficiency to a greater extent due to the surface plasmon effect. Among the ternary composites, ZFPd-2 (3 % wt% Pd on 20 % FeVO4/ZrO2) exhibited the highest degradation efficiencies, achieving 95.43 % degradation for RhB and 91.44 % for CP within 180 min. Trapping agents were utilized to examine the role of active species during the degradation process. Photogenerated holes and electrons were identified as active species in RhB degradation, whereas in CP degradation, oxygen radicals and holes predominated. The effect of pH on the photocatalytic performance of the photocatalyst was also investigated, along with the reusability and stability of the photocatalyst over five cycles. Electrochemical analysis via Mott-Schottky curves and EIS supported higher donor density and lower charge resistance after composite formation.
KW - Composite
KW - Degradation
KW - FeVO
KW - Pd
KW - Photocatalysis
KW - ZrO
UR - http://www.scopus.com/inward/record.url?scp=85216448188&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85216448188&partnerID=8YFLogxK
U2 - 10.1016/j.molliq.2025.127013
DO - 10.1016/j.molliq.2025.127013
M3 - Article
AN - SCOPUS:85216448188
SN - 0167-7322
VL - 423
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
M1 - 127013
ER -