Structural, spectral, thermal, dielectric, mechanical and optical properties of urea L-alanine acetate single crystals

被引:32
|
作者
Jaikumar, D. [2 ]
Kalainathan, S. [1 ]
Bhagavannarayana, G. [3 ]
机构
[1] VIT Univ, Div Phys, SAS, Vellore 632014, Tamil Nadu, India
[2] Voorhees Coll, Dept Phys, Vellore 632001, Tamil Nadu, India
[3] Natl Phys Lab, CGC Sect, New Delhi 110012, India
关键词
Growth from solution; Organic compounds; Nonlinear optical materials; X-ray diffraction; Thermal analysis; Microhardness; SOLUTION GROWTH; NLO MATERIAL; MALIC ACID;
D O I
10.1016/j.physb.2010.02.053
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
A new organic nonlinear optical crystal, urea L-alanine acetate (ULAA) has been grown by solution growth using slow cooling technique with the vision to improve the properties of the L-alanine crystals. Urea and L-alanine material were mixed in the molar ratio 1:4. Solubility and metastable zone width were determined. Single crystal XRD analyses revealed that the crystal lattice of ULAA is orthorhombic ;system, primitive lattice with cell parameters a=5.7971 angstrom, b=6.0391 angstrom, c=12.3276 angstrom with space group P2(1)2(1)2(1) (D-2(4)). High-resolution X-ray diffraction (HR-XRD) analysis was carried out to study their crystalline perfection. FTIR spectrum was recorded to identify the presence of functional groups and molecular structure was confirmed by H-1 NMR spectrum. From the mass spectrum, the ratio of compound formation of ULAA was analyzed. Thermal strength of the grown crystal has been studied using thermo-gravimetric (TG) and differential thermal analysis (DTA). Dielectric measurements reveal that the grown crystals have very low dielectric loss. The mechanical behavior was studied by Vickers microhardness test. The grown crystals were found to be transparent in the entire visible region. Preliminary measurement using Kurtz powder technique with Nd-YAG laser light of wavelength 1064 nm indicates that their second harmonic generation (SHG) efficiency is roughly equal to that of pure KDP. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2394 / 2400
页数:7
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