Rubrene micro-crystals from solution routes: their crystallography, morphology and optical properties

被引:170
作者
Huang, Liwei [1 ,2 ]
Liao, Qing [1 ]
Shi, Qiang [1 ]
Fu, Hongbing [1 ]
Ma, Jinshi [1 ]
Yao, Jiannian [1 ]
机构
[1] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[2] Chinese Acad Sci, Inst Chem, State Key Lab Struct Chem Unstable & Stable Speci, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
SMALL ORGANIC-MOLECULES; THIN-FILM TRANSISTORS; SINGLE-CRYSTALS; STIMULATED-EMISSION; CRYSTALLIZATION; TRANSPORT; SUPERSATURATION; SEMICONDUCTORS; POLYMORPHS; GROWTH;
D O I
10.1039/b914334c
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
A series of rubrene micro-crystals (MCs) with controllable sizes and shapes, ranging from one-dimensional (1D) ribbons to 2D rhombic and hexagonal plates, have bee prepared by employing the reprecipitation method. Based on X-ray diffraction analysis, the crystal structures of 1D ribbons and 2D plates have been identified to be triclinic and monoclinic phases, respectively, rather than the commonly reported orthorhombic phase for vacuum-deposited rubrene crystals. In our system, adjustment of the monomer concentration of rubrene, which in turn determines the supersaturation (beta) for crystallization, paved the way for kinetic control over the nucleation and growth processes. Combining with theoretical calculations, we found that transformation from a triclinic phase at low supersaturation to a monoclinic phase at high supersaturation was responsible for the morphology change from 1D ribbons to 2D plates. Both ensemble and single-particle spectroscopy clarifies that 1D ribbons and 2D plates show distinct optical properties, probably related to their different solid-state structures in triclinic and monoclinic crystals. Moreover, scanning near-field optical microscopy reveals that the ribbons show waveguiding along a 1D direction, and the plates in a 2D plane.
引用
收藏
页码:159 / 166
页数:8
相关论文
共 51 条
[1]  
*ACC INC, 2005, MAT STUD VERS 3 2
[2]  
Akopyan Z.A., 1962, ZH STRUKT KHIM, V3, P602
[3]   Nucleation phenomena during the crystallisation and precipitation of Abecarnil [J].
Beckmann, W .
JOURNAL OF CRYSTAL GROWTH, 1999, 198 :1307-1314
[4]  
Bernstein J, 1999, ANGEW CHEM INT EDIT, V38, P3440, DOI 10.1002/(SICI)1521-3773(19991203)38:23<3440::AID-ANIE3440>3.0.CO
[5]  
2-#
[6]   Explanation for the supersaturation-dependent morphology of monoclinic paracetamol [J].
Boerrigter, SXM ;
Cuppen, HM ;
Ristic, RI ;
Sherwood, JN ;
Bennema, P ;
Meekes, H .
CRYSTAL GROWTH & DESIGN, 2002, 2 (05) :357-361
[7]   Effect of structural modifications in the spectral and laser properties of perylenediimide derivatives [J].
Calzado, Eva M. ;
Villalvilla, Jose M. ;
Boj, Pedro G. ;
Quintana, Jose A. ;
Gomez, Rafael ;
Segura, Jose L. ;
Diaz-Garcia, Maria A. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (36) :13595-13605
[8]   The influence of side chains on the structures and properties of functionalized pentacenes [J].
Chen, Jihua ;
Subramanian, Sankar ;
Parkin, Sean R. ;
Siegler, Maxime ;
Gallup, Kaitlin ;
Haughn, Chelsea ;
Martin, David C. ;
Anthony, John E. .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (17) :1961-1969
[9]   Effect of supersaturation on the crystallization of phenylbutazone polymorphs [J].
Datta, S ;
Grant, DJW .
CRYSTAL RESEARCH AND TECHNOLOGY, 2005, 40 (03) :233-242
[10]   Experimental and computational growth morphology of two polymorphs of a yellow isoxazolone dye [J].
Deij, MA ;
Aret, E ;
Boerrigter, SXM ;
van Meervelt, L ;
Deroover, G ;
Meekes, H ;
Vlieg, E .
LANGMUIR, 2005, 21 (09) :3831-3837