层状双氢氧化物
光催化
苯酚
氢氧化物
材料科学
带隙
扫描电子显微镜
傅里叶变换红外光谱
密度泛函理论
核化学
化学
热液循环
红外线的
分析化学(期刊)
催化作用
无机化学
化学工程
有机化学
光学
复合材料
计算化学
工程类
物理
光电子学
作者
Yuxiu Fu,Yaming Pang,Zheng Yu-shu,Xiaoli Song,Liguo Gao
标识
DOI:10.1002/slct.202203035
摘要
Abstract Mg 2+ ‐Mo 6+ ‐Al 3+ ‐MoO 4 2− ‐Layered double hydroxides (LDHs) materials were successfully prepared via a hydrothermal method by doping Mo 6+ in hydroxide laminates and inserting MoO 4 2− to replace the interlayer anions of LDHs materials. The samples were characterized by X‐ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscope (TEM), Fourier transform infrared spectrometer (FTIRS) and ultraviolet‐visible spectrophotometer (UV). The electronic density of states was calculated using the density functional theory (DFT) of Vienna Ab‐initio Simulation Package (VASP). The effects of Mo 6+ and MoO 4 2− on the structure, morphology, electronic structure and photocatalytic performance of Mg 2+ ‐Al 3+ ‐LDHs were systematically studied. The conditions for phenol degradation by Mg 2+ ‐Mo 6+ ‐Al 3+ ‐MoO 4 2− ‐LDHs were optimized by single factor analysis and response surface methodology. The results show that the MoO 4 2− anion reduces the band gap width and thus enhances the absorption of low‐energy photons. The interaction between cations and anions enhances the photocatalytic performance. When the dosage of Mg 2+ ‐Mo 6+ ‐Al 3+ ‐MoO 4 2− ‐LDHs was 0.03 g, the temperature was 40 °C and the visible light irradiation was 15 min, the removal rate of phenol reached 94.76 %.
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