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Lamellar phase separation and dynamic competition in La0.23Ca0.77MnO3
J Tao1, D Niebieskikwiat, M B Salamon
1Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Physical Review Letters
|May 21, 2005
Summary
Charge-ordered and charge-disordered domains coexist in La0.23Ca0.77MnO3. Below 170 K, a new phase emerges and dynamically competes with the existing one, linked to magnetic transitions.
Area of Science:
- Condensed Matter Physics
- Materials Science
- Solid-State Chemistry
Background:
- La0.23Ca0.77MnO3 exhibits complex phase behavior relevant to colossal magnetoresistance materials.
- Understanding domain coexistence and dynamics is crucial for electronic and magnetic applications.
Purpose of the Study:
- To investigate the coexistence and dynamical interplay of charge-ordered (CO) and charge-disordered (CD) domains in La0.23Ca0.77MnO3.
- To elucidate the structural and dynamical characteristics of these coexisting phases and their relationship with magnetic transitions.
Main Methods:
- High-resolution transmission electron microscopy (HR-TEM) for structural analysis.
- Resistivity measurements to probe phase transitions and dynamics.
- Analysis of domain morphology and orientation relative to superlattice vectors.
Main Results:
- Coexistence of lamellar charge-ordered (CO) and charge-disordered (CD) domains observed below approximately 170 K.
- A CD-monoclinic phase forms within the CO-orthorhombic matrix, with sheetlike morphology perpendicular to the CO superlattice q vector.
- Dynamic competition between CO and CD phases observed between 64 and 130 K, with the CD phase slowly advancing.
Conclusions:
- The study reveals a dynamic coexistence and competition between distinct charge ordering states in La0.23Ca0.77MnO3.
- The observed slow dynamics are linked to magnetic transitions, indicating significant magnetoelastic coupling effects.
- These findings provide insights into the complex phase behavior of manganites and their potential for tunable electronic properties.