The facile synthesis of 3D hierarchical flower-like TiO2 microspheres with enhanced photocatalytic activity

被引:8
|
作者
Rajput, Rekha B. [1 ]
Kale, Rohidas B. [1 ]
机构
[1] Inst Sci, Dept Phys, Madam Cama Rd, Mumbai, India
关键词
Solvothermal synthesis; 3D hierarchical flower-like TiO 2 microspheres; Nanorods; Photodegradation; Organic pollutants; METHYL-ORANGE DYE; SOLVOTHERMAL SYNTHESIS; HYDROTHERMAL SYNTHESIS; DEGRADATION; NANOPARTICLES; TEMPERATURE; WATER; PHOTODEGRADATION; PERFORMANCE; NANOSHEETS;
D O I
10.1016/j.jpcs.2023.111286
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A 3D hierarchical flower-like rutile TiO2 microspheres assembled by well-aligned 1D nanorods were efficiently synthesized using the solvothermal method at a temperature of 140 degrees C for 5 h. The synthesized TiO2 micro-spheres have an average crystallite size of about 6.9-8.4 nm. According to SEM, FESEM and TEM analysis, flower-like TiO2 microspheres are made up of nanorods that grow radially from the center and are several nm thick on average. The XRD, EDS and XPS analysis revealed that titanium and oxygen peaks were present with no other impurity peaks. The volume ratio of water and toluene plays a vital role that was significantly affecting the chemical properties of synthesized TiO2 materials. Compared to other samples, the hierarchical 3D TiO2 mi-crospheres Ti(1:1) had a small crystallite size, a lower bandgap, a comparatively large BET surface area of about 130 m2/g and a pore volume of 0.179 cm3/g, which revealed more favorable for photocatalytic activity. Ti(1:1) photocatalyst degraded MO by almost 96 and 94% within 50 and 40 min, respectively, when exposed to mercury light and sunlight. Also, it showed that within 60 min of mercury light irradiation, RhB degraded up to 65%. Additionally, an LC-MS study was performed for the degradation of MO dye solution and a possible degradation path was proposed.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] Synthesis of 3D hierarchical structure TiO2 and its photocatalytic activity
    Wang, Hongxia
    Li, Xinxing
    Tang, Liang
    PHYSICA B-CONDENSED MATTER, 2019, 556 : 31 - 35
  • [33] Hydrothermal Synthesis of Flower-like Hierarchical TiO2 Microspheres from Titanium Sulfate and Hexafluorosilicic Acid
    Shi Guo-Dong
    Song Jun
    Yang Liu-Liu
    Zhang Li-Xiong
    JOURNAL OF INORGANIC MATERIALS, 2014, 29 (08) : 891 - 896
  • [34] Liquid phase deposition of flower-like TiO2 microspheres decorated by ZIF-8 nanoparticles with enhanced photocatalytic activity
    Zhong, Wan-Ling
    Li, Chao
    Liu, Xiao-Ming
    Bai, Xiu-Kui
    Zhang, Gang-Sheng
    Lei, Cai-Xia
    MICROPOROUS AND MESOPOROUS MATERIALS, 2020, 306
  • [35] Dual co-catalysts Ag/Ti3C2/TiO2 hierarchical flower-like microspheres with enhanced photocatalytic H2-production activity
    Liu, Defa
    Sun, Bin
    Bai, Shuojie
    Gao, Tingting
    Zhou, Guowei
    CHINESE JOURNAL OF CATALYSIS, 2023, 50 : 273 - 283
  • [36] Progress in the synthesis and applications of hierarchical flower-like TiO2 nanostructures
    Zhijiao Wu
    Qian Wu
    Lixia Du
    Chao Jiang
    Lingyu Piao
    Particuology, 2014, 15 (04) : 61 - 70
  • [37] Progress in the synthesis and applications of hierarchical flower-like TiO2 nanostructures
    Wu, Zhijiao
    Wu, Qian
    Du, Lixia
    Jiang, Chao
    Piao, Lingyu
    PARTICUOLOGY, 2014, 15 : 61 - 70
  • [38] Flower-like TiO2 nanostructures with exposed {001} facets: Facile synthesis and enhanced photocatalysis
    Liu, Min
    Piao, Lingyu
    Lu, Weiming
    Ju, Siting
    Zhao, Lei
    Zhou, Chunlan
    Li, Hailing
    Wang, Wenjing
    NANOSCALE, 2010, 2 (07) : 1115 - 1117
  • [39] Large-Scale Fabrication of Rutile TiO2 with 3D Hierarchical Flower-Like Morphology
    Yao, Wenjun
    Zhuang, Wei
    Wang, Changsong
    Shi, Ronghua
    Lu, Xiaohua
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2016, 16 (12) : 12991 - 12995
  • [40] 3D hierarchical flower-like rutile TiO2 nanospheres-based versatile photocatalyst
    Du, Yibo
    Xu, Xiaoyu
    Lin, Lin
    Ge, Meiying
    He, Dannong
    JOURNAL OF MATERIALS SCIENCE, 2018, 53 (01) : 385 - 395