催化作用
罗丹明B
降级(电信)
纳米针
镍
氢氧化物
钴
化学
金属
氧化物
化学工程
氧化钴
材料科学
无机化学
纳米技术
纳米结构
有机化学
光催化
工程类
电信
计算机科学
作者
Hsing‐Hua Chen,Young‐Kwon Park,Eilhann E. Kwon,Yiu Fai Tsang,Xuan‐Thanh Bui,Ta Cong Khiem,Siming You,Chechia Hu,Kun‐Yi Andrew Lin
标识
DOI:10.1016/j.jcis.2021.11.186
摘要
While metal oxides are conventionally proposed for activating monopersulfate (MPS) to degrade refractory contaminants, metal sulfides have recently gained increased attention for MPS activation because these sulfides exhibit more reactive redox characteristics to enhance the catalytic activation of MPS. The present study attempts to develop a novel material comprised of metal sulfides with 3D hierarchical nanostructures to activate MPS. Specifically, a 3D hierarchically structured catalyst was fabricated by growing CuCo-layered double hydroxide (LDH) on nickel foam (NF), followed by direct sulfurization, affording Cu/CoS@NF (CCSNF). CCSNF could exhibit a unique morphology of floral bunches comprised of nano-needles, residing on the NF surfaces. Compared with its precursor, CuCo-LDH@NF, oxide analogue, and CuCo2O4@NF, CCSNF possessed superior physical and chemical properties, including larger surface area and pore volume, higher current density, and lower charge transfer resistance. These features render CCSNF a much more effective catalyst than CuCo-LDH@NF and CuCo2O4@NF for activating MPS to degrade Rhodamine B (RB). In particular, RB degradation by CCSNF-activated MPS required an activation energy only 26.8 kJ/mol, which is much lower than the reported values. The activation mechanism and degradation pathway of RB degradation by CCSNF-activated MPS were investigated and validated through experimental evidences and density function theory calculations.
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