Studies on photoluminescence, electrochemical sensors, and photocatalysis using Ho3+-doped MgAl2O4 nanophosphors

被引:3
作者
Manjula, S. N. [1 ,2 ]
Chandrasekhar, M. [2 ]
Kumar, M. R. Anil [3 ]
Bhoomika, V. [4 ]
Raghavendra, N. [2 ]
Somashekar, M. N. [5 ]
Ravikumar, C. R. [2 ]
Nagabhushana, H. [5 ,6 ]
机构
[1] SJR Coll Women, Dept Phys, Bengaluru, India
[2] East West Inst Technol, Res Ctr, Dept Sci, VTU, Bangalore 560091, India
[3] Concordia Univ, Gina Cody Sch Engn & Comp Sci, Dept Chem & Mat Engn, Montreal, PQ H3G 2W1, Canada
[4] East West Inst Technol, Dept Civil Engn, VTU, Bangalore 560091, India
[5] SS Margol Degree Coll Arts Sci & Commerce, Dept Chem, Shahabad 585228, Karnataka, India
[6] Tumkur Univ, Prof CNR Rao Ctr Adv Mat, Tumkur, India
关键词
Nanophosphors; MgAl2O4:HO3+; Solution combustion; Photocatalysis; Electrochemical sensor; HEAT-TREATMENT; PHOSPHORS; SPINEL; LUMINESCENCE; LASER; MN;
D O I
10.1007/s13738-024-02992-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ho3+-doped MgAl2O4 nanophosphors (1-11 mol%) were synthesized via solution combustion method and oxalyldihydrazide used as fuel. The findings revealed a range of band gap energies between 4.86 and 5.42 eV. Ho3+ ions in the host undergo f-f transitions that are triggered at 406 nm, and as a result, exhibit discrete photoluminescence emission peaks between 406 and 605 nm. Enhanced MgAl2O4 has chromaticity diagram (CIE) coordinates from orange-red to yellow region and 97% color purity. Photocatalytic properties of NPs under UV light led to the discovery that a rapid orange-red dye is activated at 493 nm. Fast orange-red dye removal using the new photocatalysts and MgAl2O4:Ho3+ nanophosphors has been demonstrated. The investigation showed that 89.02% of the dye lost its color after being exposed to radiation for 120 min. The cyclic voltametric method can detect lead pollution using the modified MgAl2O4:Ho3+ carbon paste electrode. Based on their electrochemical performance, we conclude that MgAl2O4:Ho3+ nanophosphors are effective lead detecting electrode materials.
引用
收藏
页码:1245 / 1257
页数:13
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