光催化
降级(电信)
煅烧
纳米颗粒
光降解
化学
尖晶石
刚果红
化学工程
微晶
废水
甲基蓝
核化学
工业废水处理
傅里叶变换红外光谱
罗丹明B
甲基橙
材料科学
氧化物
吸附
钴
碎石
拉曼光谱
反铁磁性
锌
矿物学
无机化学
环境化学
作者
R. Krishna Priya,S. Sebastiammal,Santhamoorthy Madhappan,Perumal Asaithambi,Kokila Thirupathi,Seong-Cheol Kim,Phan Thi Tuong Vy
标识
DOI:10.1080/03601234.2025.2610898
摘要
In the present work, Co3O4 nanoparticles (Co3O4 NPs) were prepared by calcination of a hydrothermally synthesized Co-MOF precursor. The X-ray diffraction (XRD) analysis results confirmed the formation of Co3O4 NPs with well-defined cubic spinel oxide (Fd-3m phase) with an average crystallite size of ∼22 nm, while Fourier transform-infrared (FTIR) spectra supported the presence of Co-O bonding through prominent vibrational modes at 562 and 663 cm-1. The SEM images demonstrated that the Co3O4 NPs possess porous flower-like morphology, and EDAX confirmed the existence of cobalt and oxygen atoms. The PL analysis reveals prominent defect-related emissions in Co3O4 nanoparticles, confirming abundant defect states that can enhance their photocatalytic activity. The vibrating sample magnetometry (VSM) analysis demonstrated antiferromagnetic behavior, which was consistent with nanoscale Co3O4 NPs. The prepared Co3O4 NPs displayed superior photocatalytic activity toward the degradation of emerging wastewater pollutants. The experimental results demonstrated that about 96% degradation of herbal cigarette detritus in 160 min, and almost complete degradation of industrial dyes, namely Janus Green B, Methyl Violet 2B, and Congo Red in 30, 60, and 40 min, respectively, under UV-light irradiation.
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