TY - JOUR
T1 - Spherical hexagonal tellurium nanocrystals
T2 - Fabrication and size-dependent structural phase transition at high pressure
AU - Deng, Zhengtao
AU - Bao, Zhongxing
AU - Cao, Li
AU - Chen, Dong
AU - Tang, Fangqiong
AU - Wang, Feifei
AU - Liu, Cuixia
AU - Zou, Bingsuo
AU - Muscat, Anthony J.
N1 - Funding Information:
We are grateful to Dimitrios Psaltis for many helpful discussions of the amplitudes of burst oscillations, especially about the role of X-ray color oscillations. We also thank Tod Stroh-mayer and Jean Swank for discussing their burst observations in advance of publication. This work was supported in part by NSF grant AST 96-18524, NASA grant NAG 5-2925, and NASA RXTE grants at the University of Illinois, and NASA grant NAG 5-2868 at the University of Chicago.
PY - 2008/1/30
Y1 - 2008/1/30
N2 - Single-crystalline spherical nearly monodisperse tellurium (Te) nanocrystals (NCs) with average diameters of 20 and 90 nm, respectively, have been fabricated for the first time by a facile solution sonochemistry process. The structural characterizations show that the as-synthesized Te NCs have pure hexagonal structure, as revealed by x-ray diffraction (XRD), selected-area electron diffraction (SAED), energy-dispersive x-ray (EDX) spectroscopy, and high-resolution transmission electron microscopy (HRTEM) methods. The size-dependent structural phase transition of Te NCs up to the high pressure of 20 GPa has been investigated in a diamond anvil cell using resistance measurement at room temperature, and compared with the behavior of bulk Te under identical conditions. The experimental results indicate that 20 nm Te NCs, 90 nm NCs, and bulk Te all undergo two phase transitions up to 20 GPa, their respective transition pressures being about 7.2 and 10.3 GPa, 5.9 and 8.8 GPa, and 4.0 and 6.8 GPa. This indicates that the phase transition pressures are higher for the smaller NCs. In this paper we discuss the size-dependent structural phase transitions, the sluggishness of the phase transition process, and the fluctuating properties of the phase transition products at high pressure. The present work might open an avenue to real-time detection of the dynamics of the phase transition in bulk and nanoscale materials at high pressure, and also could serve as a guide to tailoring the microscopic properties of materials.
AB - Single-crystalline spherical nearly monodisperse tellurium (Te) nanocrystals (NCs) with average diameters of 20 and 90 nm, respectively, have been fabricated for the first time by a facile solution sonochemistry process. The structural characterizations show that the as-synthesized Te NCs have pure hexagonal structure, as revealed by x-ray diffraction (XRD), selected-area electron diffraction (SAED), energy-dispersive x-ray (EDX) spectroscopy, and high-resolution transmission electron microscopy (HRTEM) methods. The size-dependent structural phase transition of Te NCs up to the high pressure of 20 GPa has been investigated in a diamond anvil cell using resistance measurement at room temperature, and compared with the behavior of bulk Te under identical conditions. The experimental results indicate that 20 nm Te NCs, 90 nm NCs, and bulk Te all undergo two phase transitions up to 20 GPa, their respective transition pressures being about 7.2 and 10.3 GPa, 5.9 and 8.8 GPa, and 4.0 and 6.8 GPa. This indicates that the phase transition pressures are higher for the smaller NCs. In this paper we discuss the size-dependent structural phase transitions, the sluggishness of the phase transition process, and the fluctuating properties of the phase transition products at high pressure. The present work might open an avenue to real-time detection of the dynamics of the phase transition in bulk and nanoscale materials at high pressure, and also could serve as a guide to tailoring the microscopic properties of materials.
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U2 - 10.1088/0957-4484/19/04/045707
DO - 10.1088/0957-4484/19/04/045707
M3 - Article
C2 - 21817524
AN - SCOPUS:38049003532
SN - 0957-4484
VL - 19
JO - Nanotechnology
JF - Nanotechnology
IS - 4
M1 - 045707
ER -