Transformation of hydrothermally derived nanowire cluster intermediates into CdSiO3 nanobelts

被引:15
作者
Manjunatha, C. [1 ,2 ,3 ]
Nagabhushana, B. M. [1 ,2 ]
Nagabhushana, H. [4 ]
Chakradhar, R. P. S. [5 ]
机构
[1] MS Ramaiah Inst Technol, Dept Chem, Bangalore 560054, Karnataka, India
[2] Visvesvaraya Technol Univ, Belgaum 590018, India
[3] RV Coll Engn, Dept Chem, Bangalore 560059, Karnataka, India
[4] Tumkur Univ, CNR, Tumkur 572103, India
[5] CSIR Natl Aerosp Labs, Bangalore 560017, Karnataka, India
关键词
LONG-LASTING PHOSPHORESCENCE; LUMINESCENCE PROPERTIES; CRYSTAL-GROWTH; PHOTOLUMINESCENCE; DECOMPOSITION; AFTERGLOW; NANORODS; COPPER; CO;
D O I
10.1039/c2jm34356h
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
In this communication, we demonstrate that cadmium metasilicate nanobelts could be fabricated via a facile, eco-friendly, low cost hydrothermal treatment in the absence of surfactants and organic additives, followed by calcination. The monoclinic phase formation of the sample is described in detail by powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA) and fourier transform infrared (FT-IR) studies. The field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) measurements of as-formed samples and samples calcined at 600 degrees C for 3 h indicate that the as-formed CdSiO3 sample consists of entangled nano-wire bundles with diameters ranging from 20 to 80 nm and lengths in the order of several micrometers. The calcined sample consists of nanobelts of slightly increased diameter and increased length compared to the as-formed samples. The selected area electron diffraction (SAED) and high resolution transmission electron microscopy (HRTEM) images reflect the polycrystalline nature of nanobelts. The probable mechanism for the formation of nanobelts is also discussed.
引用
收藏
页码:22392 / 22397
页数:6
相关论文
共 32 条
[1]  
Alvani AAS, 2005, J LUMIN, V115, P147, DOI 10.1016/j.jlumin.2005.03.009
[2]   Aggregation-based crystal growth and microstructure development in natural iron oxyhydroxide biomineralization products [J].
Banfield, JF ;
Welch, SA ;
Zhang, HZ ;
Ebert, TT ;
Penn, RL .
SCIENCE, 2000, 289 (5480) :751-754
[3]   Higher-order organization by mesoscale self-assembly and transformation of hybrid nanostructures [J].
Cölfen, H ;
Mann, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (21) :2350-2365
[4]   Mesocrystals:: Inorganic superstructures made by highly parallel crystallization and controlled alignment [J].
Cölfen, H ;
Antonietti, M .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (35) :5576-5591
[5]  
Douglas B. E., 1994, CONCEPTS MODELS INOR, P242
[6]   Luminescent properties of Sr2MgSi2O7 and Ca2MgSi2O7 long lasting phosphors activated by Eu2+, Dy3+ [J].
Fei, Q ;
Chang, CK ;
Mao, DL .
JOURNAL OF ALLOYS AND COMPOUNDS, 2005, 390 (1-2) :133-137
[7]  
Hosokawa M, 2008, NANOPARTICLE TECHNOLOGY HANDBOOK, pV, DOI 10.1016/B978-044453122-3.50001-5
[8]   Y2SiO5:Ce phosphor particles 0.5-1.4 μm in size with spherical morphology [J].
Kang, YC ;
Lenggoro, IW ;
Park, SB ;
Okuyama, K .
JOURNAL OF SOLID STATE CHEMISTRY, 1999, 146 (01) :168-175
[9]   Observation of energy transfer from host to rare earth ions in Pr3+-doped USA long-lasting phosphor [J].
Kuang, Jinyong ;
Liu, Yingliang .
CHEMICAL PHYSICS LETTERS, 2006, 424 (1-3) :58-62
[10]   Luminescence properties of CdSiO3:Mn2+ phosphor [J].
Lei, BF ;
Liu, YL ;
Ye, Z ;
Shi, CS .
JOURNAL OF LUMINESCENCE, 2004, 109 (3-4) :215-219