Size-Dependent Phase Map and Phase Transformation Kinetics for Nanometric Iron(III) Oxides (γ → ε → α Pathway)

被引:75
作者
Lee, Seungyeol [1 ]
Xu, Huifang [1 ]
机构
[1] Univ Wisconsin, Dept Geosci, NASA, Astrobiol Inst, Madison, WI 53706 USA
关键词
RAY-POWDER DIFFRACTION; GIANT COERCIVE FIELD; MAGNETIC-PROPERTIES; IRON-OXIDES; IN-SITU; CRYSTAL-STRUCTURE; WAVE ABSORBER; GAMMA-FE2O3; TEMPERATURE; NANOPARTICLES;
D O I
10.1021/acs.jpcc.6b05287
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
Nanometric iron(III) oxide has been of great interest in a wide range of fields due to its magnetic properties, eminent biochemical characteristics, and potential for technological applications. Among iron oxides, epsilon-Fe2O3 is considered as a remarkable phase due to its giant coercive field at room temperature and ferromagnetic resonance capability. Here we present the first size dependent phase map for epsilon-Fe2O3 via a gamma -> epsilon -> alpha pathway together with the activation energies for the phase transformations, based on X-ray powder diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). HRTEM images of epsilon-Fe2O3 nanocrystals show both inversion and pseudohexagonal twins, which are fundamentally important for understanding the correlation between its nanostructure and magnetic properties. Two activation energies for gamma-Fe2O3 -> alpha-Fe2O3 phase transformations are 186.37 +/- 9.89 and 174.58 +/- 2.24 kJ mol(-1), respectively. The results provide useful information about the size, crystal structure, and transformation of the nanometric iron oxide polymorphs for applications in areas of developing engineered materials.
引用
收藏
页码:13316 / 13322
页数:7
相关论文
共 36 条
[1]   Kinetics of consecutive reactions: First reaction, first-order; second reaction, zeroth-order [J].
Ball, DW .
JOURNAL OF CHEMICAL EDUCATION, 1998, 75 (07) :917-919
[2]   In situ and time resolved study of the γ/α-Fe2O3 transition in nanometric particles [J].
Belin, T. ;
Millot, N. ;
Bovet, N. ;
Gailhanou, M. .
JOURNAL OF SOLID STATE CHEMISTRY, 2007, 180 (08) :2377-2385
[3]  
BLAKE RL, 1966, AM MINERAL, V51, P123
[4]   α-Fe2O3 versus β-Fe2O3: Controlling the Phase of the Transformation Product of ε-Fe2O3 in the Fe2O3/SiO2 System [J].
Brazda, Petr ;
Kohout, Jaroslav ;
Bezdicka, Petr ;
Kmjec, Tomas .
CRYSTAL GROWTH & DESIGN, 2014, 14 (03) :1039-1046
[5]   ADSORPTION OF WATER-VAPOR BY IRON-OXIDES .2. WATER ISOTHERMS AND X-RAY PHOTOELECTRON-SPECTROSCOPY [J].
CLARKE, NS ;
HALL, PG .
LANGMUIR, 1991, 7 (04) :678-682
[6]   Learning from the past: Rare ε-Fe2O3 in the ancient black-glazed Jian (Tenmoku) wares [J].
Dejoie, Catherine ;
Sciau, Philippe ;
Li, Weidong ;
Noe, Laure ;
Mehta, Apurva ;
Chen, Kai ;
Luo, Hongjie ;
Kunz, Martin ;
Tamura, Nobumichi ;
Liu, Zhi .
SCIENTIFIC REPORTS, 2014, 4
[7]   Enhancement of the phase transformation temperature of γ-Fe2O3 by Zn2+ doping [J].
Deka, Sasanka ;
Joy, Pattayil Alias .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (05) :453-456
[8]   Nanowire structural evolution from Fe3O4 to ε-Fe2O3 [J].
Ding, Yong ;
Morber, Jenny Ruth ;
Snyder, Robert L. ;
Wang, Zhong Lin .
ADVANCED FUNCTIONAL MATERIALS, 2007, 17 (07) :1172-1178
[9]   High- and low-temperature crystal and magnetic structures of ε-Fe2O3 and their correlation to its magnetic properties [J].
Gich, M. ;
Frontera, C. ;
Roig, A. ;
Taboada, E. ;
Molins, E. ;
Rechenberg, H. R. ;
Ardisson, J. D. ;
Macedo, W. A. A. ;
Ritter, C. ;
Hardy, V. ;
Sort, J. ;
Skumryev, V. ;
Nogues, J. .
CHEMISTRY OF MATERIALS, 2006, 18 (16) :3889-3897
[10]   Large coercivity and low-temperature magnetic reorientation in ε-Fe2O3 nanoparticles -: art. no. 044307 [J].
Gich, M ;
Roig, A ;
Frontera, C ;
Molins, E ;
Sort, J ;
Popovici, M ;
Chouteau, G ;
Marero, DMY ;
Nogués, J .
JOURNAL OF APPLIED PHYSICS, 2005, 98 (04)