Controllable size, shape and morphology of molybdic acid self-aggregated with rhodamine B to construct functional material

被引:15
作者
Guan, Zi Sheng [1 ]
Zhang, Yu [1 ]
Zhang, Qiang [1 ]
Li, Dong Xu [1 ]
机构
[1] Nanjing Univ Technol, Coll Mat Sci & Engn, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
rhodamine B-molybdic acid aggregates; self-aggregation; bulk solution; evaporation-enhanced conditions;
D O I
10.1016/j.jcis.2006.05.063
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Controllable size, shape and morphology of rhodamine B/molybdic acid (RBMA) aggregates were prepared from a self-aggregation reaction in a molybdic acid and rhodamine B (RhB) coexisting solution. Nanodisks, as well as microcrystal rods and polyhexagonal microcrystal rods, have been obtained in conventional bulk solutions at different temperatures. Large-sized network microcrystal rods and branched fractal aggregates constructed with nanosubunits after the nucleation duration of an ice-water-cooled process have also been achieved under the evaporation-enhanced conditions on glass substrates. The factors affecting the size, shape and morphology of RBMA aggregates including temperature, nucleation and growth, and processing conditions are discussed. The results show that photofunctional molecules (RhB) modified the surface of the molybdic acid particles and influenced their self-aggregation. The temperature and nucleation play key roles in the formation of RBMA aggregates. The structures of RBMA aggregates were characterized by X-ray diffraction, infrared spectra and elemental dispersive spectroscopy. The results indicate that the aggregates show the characteristics of RhB-mediated hydrated ammonium molybdenum bronze with the metastable hexagonal phase. Visible-light-induced electrons transfer reactions in the RBMA aggregates from rhodamine B molecules to MoO3 matrixes were measured by UV-vis spectra and X-ray photoelectron spectra, and the fluorescent image was observed by laser scanning confocal microscopy. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:113 / 122
页数:10
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