TY - JOUR
T1 - Phase-Controlled Multi-Element Oxide-Sulfide Heterostructure Toward High-Efficiency Electro-Fenton Oxidation
AU - Purba, Yemima
AU - Sari, Fitri Nur Indah
AU - Wei, Xuan Yu
AU - Su, Yen-Hsun
AU - Ting, Jyh-Ming
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Electron Fenton (EF) degradation often suffers from low in situ H2O2 electrosynthesis and Fe2+ regeneration. Herein, a novel multi-element oxide-sulfide heterostructure is reported, (FeVCoCuMn)2O3/(CuFeVCoMn)S, for efficient and stable EF degradation. The oxide-sulfide phase ratio is optimized through temperature control during the synthesis. Experimental data and theoretical calculations highlight the advantages of multi-metal doping in enhancing the H2O2 selectivity and Fe2⁺ regeneration. The multi-element oxide-sulfide heterostructure outperforms its subsystems by providing enhanced H2O2 electrosynthesis. Among the elements, the Cu, Co, Mn, V, and S donate electrons to the trivalent Fe3⁺ cations, thus enhancing the Fe2⁺ regeneration. Density functional theory calculations show that the characteristics of the heterostructure can be optimized based on the phase ratio, resulting in enhanced charge transfer and optimized intermediate binding strength. The (FeVCoCuMn)2O3/(CuFeVCoMn)S catalyst achieves 98% tetracycline degradation in 120 min and maintains 87% efficiency over ten cycles. This work provides an insight into the coexistence of multi-metal doping and heterostructure in obtaining an efficient and selective heterogeneous EF catalyst for wastewater treatment.
AB - Electron Fenton (EF) degradation often suffers from low in situ H2O2 electrosynthesis and Fe2+ regeneration. Herein, a novel multi-element oxide-sulfide heterostructure is reported, (FeVCoCuMn)2O3/(CuFeVCoMn)S, for efficient and stable EF degradation. The oxide-sulfide phase ratio is optimized through temperature control during the synthesis. Experimental data and theoretical calculations highlight the advantages of multi-metal doping in enhancing the H2O2 selectivity and Fe2⁺ regeneration. The multi-element oxide-sulfide heterostructure outperforms its subsystems by providing enhanced H2O2 electrosynthesis. Among the elements, the Cu, Co, Mn, V, and S donate electrons to the trivalent Fe3⁺ cations, thus enhancing the Fe2⁺ regeneration. Density functional theory calculations show that the characteristics of the heterostructure can be optimized based on the phase ratio, resulting in enhanced charge transfer and optimized intermediate binding strength. The (FeVCoCuMn)2O3/(CuFeVCoMn)S catalyst achieves 98% tetracycline degradation in 120 min and maintains 87% efficiency over ten cycles. This work provides an insight into the coexistence of multi-metal doping and heterostructure in obtaining an efficient and selective heterogeneous EF catalyst for wastewater treatment.
UR - https://www.scopus.com/pages/publications/105015396984
UR - https://www.scopus.com/pages/publications/105015396984#tab=citedBy
U2 - 10.1002/smtd.202501652
DO - 10.1002/smtd.202501652
M3 - Article
C2 - 40931589
AN - SCOPUS:105015396984
SN - 2366-9608
JO - Small Methods
JF - Small Methods
ER -