Fabrication of SnO2/NGO hybrid nanocomposite as an effective photocatalyst for binary dye degradation under sunlight illumination

被引:14
|
作者
Kumar, Jothi Vinoth [1 ]
Karthika, Duraisamy [2 ]
Rosaiah, Pitcheri [3 ]
Devanesan, Sandhanasamy [4 ]
Mythili, R. [5 ]
Dhananjaya, Merum [6 ]
Joo, Sang Woo [6 ]
机构
[1] Kyung Hee Univ, Bio Nanocomposite Res Ctr, Dept Food & Nutr, Seoul 02447, South Korea
[2] OMR, Agni Coll Technol, Dept Chem Engn, Thazhambur 603103, Tamil Nadu, India
[3] Saveetha Inst Med & Tech Sci SIMATS, Saveetha Sch Engn, Dept Phys, Chennai 602105, India
[4] King Saud Univ, Coll Sci, Dept Phys & Astron, POB 2455, Riyadh 11451, Saudi Arabia
[5] Saveetha Univ, Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci, Dept Pharm, Chennai 600077, India
[6] Yeungnam Univ, Dept Mech Engn, 280 Daehak Ro, Gyongsan 38541, Gyeongbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Graphene oxide; Methylene blue; Methyl orange; SnO (2) /NGO nanocomposite; AZO DYES; TIO2; DECOLORIZATION; NANOPARTICLES; RAMAN;
D O I
10.1016/j.psep.2024.05.088
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We successfully synthesized nitrogen-doped graphene oxide grafting tin oxide nanoparticles (SnO2/NGO nanocomposite). To evaluate the surface, optical and morphology characterization of synthesized SnO2/NGO nanocomposites was done using various analytical techniques. The XRD data indicate the crystallinity of a high-purity SnO2/NGO nanocomposite in nature. The Raman spectra of the resultant SnO2/NGO nanocomposite exhibit moderate graphitization with a ID/IG intensity of 0.98. Under sunlight irradiation, the photocatalytic activity of a produced SnO2/NGO nanocomposite on the breakdown of toxic binary organic dyes (methylene blue/methyl orange) was examined. On MB and MO, the resultant SnO2/NGO nanocomposite had a maximum degradation efficiency of 150 mins and 89.4%, 93.7%, respectively. Furthermore, the simple and inexpensive hydrothermalderived SnO2/NGO nanocomposite exhibits rapid photocatalytic degradation on MB and MO when exposed to sunlight illumination.
引用
收藏
页码:398 / 405
页数:8
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