Novel plasma assisted preparation of ZnCuFeCr layered double hydroxides with improved photocatalytic performance of methyl orange degradation

被引:33
|
作者
Tao, Xumei [1 ]
Yang, Chen [1 ]
Huang, Liang [2 ]
Shang, Shuyong [3 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem Engn, State Key Lab Base Ecochem Engn, Qingdao 266042, Shandong, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Electromech Engn, Qingdao 266042, Shandong, Peoples R China
[3] Chengdu Normal Univ, Dept Sci Technol & Discipline Construct, Chengdu 611130, Sichuan, Peoples R China
关键词
Photocatalytic; Visible light; Layered double hydroxides; Methyl orange; ZnCuFeCr-LDHs; VISIBLE-LIGHT PHOTOCATALYSIS; HYDROGEN-PRODUCTION; CATALYTIC-ACTIVITY; BLUE DYE; SURFACE; CR(VI); TIO2; RECOMMENDATIONS; NANOCOMPOSITES; HYDROTALCITE;
D O I
10.1016/j.apsusc.2019.145053
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Plasma assisted preparation of ZnCuFeCr layered double hydroxides used as photocatalyst showed excellent photocatalytic performance on methyl orange degradation under visible light. The catalysts were characterized by XRD, SEM, XPS, BET, UV-Vis DRS, EPR and PL. Compared with the traditional co-precipitation method, the plasma-assisted preparation of layered double hydroxides had obvious advantages of visible light photocatalysis. Plasma assisted preparation resulted in a tighter arrangement of the laminate atoms and more stable crystal structure, increased the specific surface area, generated more oxygen vacancies and reduced photoelectron-hole recombination during photocatalysis. The reaction mechanism of the preparation process and photocatalytic reaction process was inferred. Meanwhile, the effects of preparation time on the degradation were investigated, and the optimal preparation conditions were obtained. The degradation rate of 1000 mL (20 mg/L) methyl orange could reach up to 96.8% within 42 min in visible light photocatalysis under the preparation conditions that discharge voltage of 30.9 kV, photocatalyst addition amount of 1 g/L.
引用
收藏
页数:10
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