Rare earth (Gd, La) co-doped ZnO nanoflowers for direct sunlight driven photocatalytic activity

被引:50
|
作者
Palanivel, Baskaran [1 ]
Macadangdang Jr, Romulo R. [2 ]
Hossain, Md Shahadat [3 ]
Alharthi, Fahad A. [4 ]
Kumar, Mohanraj [5 ]
Chang, Jih-Hsing [5 ]
Gedi, Sreedevi [6 ]
机构
[1] Kings Engn Coll, Dept Phys, Kancheepuram 602117, Tamil Nadu, India
[2] Far Eastern Univ, Inst Arts & Sci, Dept Med Technol, Manila, Philippines
[3] Utsunomiya Univ, Grad Sch Engn, Dept Innovat Syst Engn, Yoto 7-1-2, Utsunomiya, Tochigi 3218585, Japan
[4] King Saud Univ, Coll Sci, Chem Dept, Riyadh 1145, Saudi Arabia
[5] Chaoyang Univ Technol, Dept Environm Engn & Management, 168 Jifeng E Rd, Taichung 41349, Taiwan
[6] Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, South Korea
关键词
Gd; La; ZnO; Nanoflower; Photocatalyst; Sunlight; DEGRADATION; NANOPARTICLES; DYE; NANORODS;
D O I
10.1016/j.jre.2022.01.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work Gd/La@ZnO nanoflower photocatalyst was successfully synthesized by a co-precipitation method and applied for rhodamine B (Rh B) and tetracycline (TCN) degradation under direct sunlight irradiation. The doping of rare earth elements extends the optical absorption wavelength of ZnO from UV region (390 nm) to visible-light region (401 nm). In addition, the co-doped ZnO nanoflower exhibits a lower charge recombination efficiency which was confirmed by photoluminescence emission analysis. Moreover, the co-doped ZnO nanoflower exhibits the maximum degradation efficiency of 91% for Rh B and 74% for TCN under sunlight irradiation. The calculated synergistic index of co-doped ZnO is higher than that of the pure ZnO. Reactive radicals' production was confirmed by terephthalic acid (TA) and nitro-blue tetrazolium (NBT) tests. The holes and hydroxyl (center dot OH) radicals play the major role in degradation reaction and it was confirmed by scavenger's test. Moreover, the recycling test confirms the stability of the photocatalyst. (c) 2022 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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