Excellent visible-light driven photocatalyst of (Al, Ni) co-doped ZnO structures for organic dye degradation

被引:86
|
作者
Reddy, I. Neelakanta [1 ]
Reddy, Ch Venkata [1 ]
Shim, Jaesool [1 ]
Akkinepally, Bhargav [1 ]
Cho, Migyung [2 ]
Yoo, Kisoo [1 ]
Kim, Dongseob [3 ]
机构
[1] Yeungnam Univ, Sch Mech Engn, Gyongsan 712749, South Korea
[2] Tongmyong Univ, Sch Informat Engn, Busan 608711, South Korea
[3] Inst Ind Technol KITECH, Aircraft Syst Technol Grp, Gyeongbuk Do 38822, South Korea
基金
新加坡国家研究基金会;
关键词
(Al; Ni) co-doped ZnO; Visible light; Free radical capture; Photocatalytic activity; Degradation kinetics; RESONANT RAMAN-SCATTERING; ZINC-OXIDE; METHYLENE-BLUE; THIN-FILMS; PHYSICAL-PROPERTIES; WATER-PURIFICATION; CATALYTIC-ACTIVITY; HIGHLY EFFICIENT; GREEN EMISSION; AU-ZNO;
D O I
10.1016/j.cattod.2018.07.030
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
(Al, Ni) co-doped ZnO nanostructures were synthesized by a simple ball-milling method. The samples prepared were extensively characterized using standard techniques. X-ray diffraction analysis confirmed the coexistence of Al and Ni in the ZnO sites. The pollutant photodegradation performances of the materials were assessed by studying the removal of methyl orange and Congo red under visible-light illumination. Of the photocatalysts prepared, 2%Al-2%Ni-ZnO was found to be the most active for pollutant degradation, effecting 100% removal of MO within 30 min under visible-light illumination. This excellent catalytic activity was attributed to the strong absorption of visible light and effective separation of photoinduced charge carriers. In addition, radical-scavenging experiments were conducted to identify the key reactive species formed in the reaction, allowing a mechanistic rationale for the superior photocatalytic activity of 2%Al-2%Ni-ZnO to be proposed.
引用
收藏
页码:277 / 285
页数:9
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