東華大學圖書館 |

Language: English

Help

回圖書館首頁

手機版館藏查詢

Back

Switch To: Labeled | MARC Mode | ISBD

Atomistic simulations of barium tita...

Zhang, Qingsong.

Linked to FindBook

Google Book

Amazon

博客來

Atomistic simulations of barium titanate.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Atomistic simulations of barium titanate./
Author:	Zhang, Qingsong.
Description:	100 p.
Notes:	Source: Dissertation Abstracts International, Volume: 66-05, Section: B, page: 2776.
Contained By:	Dissertation Abstracts International66-05B.
Subject:	Physics, Condensed Matter. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3176101
ISBN:	9780542158148

Atomistic simulations of barium titanate.
Zhang, Qingsong.

Atomistic simulations of barium titanate. - 100 p.

Source: Dissertation Abstracts International, Volume: 66-05, Section: B, page: 2776.

Thesis (Ph.D.)--California Institute of Technology, 2004.

We present the Polarizable Charge Equilibration (P-QEq) force field to include self-consistent atomic polarization and charge transfer in molecular dynamics of materials. The short-range Pauli repulsion effects are described by two body potentials without exclusions. A linear self-consistent field solution to the charge transfer is proposed for charge transfer in large systems. The P-QEq is parameterized for BaTiO3 based on quantum mechanics calculations (DFT with GGA) and applied to the study of the phase transitions, domain walls and oxygen vacancies.

ISBN: 9780542158148Subjects--Topical Terms:

1018743
Physics, Condensed Matter.

Atomistic simulations of barium titanate.
LDR:03106nmm 2200313 4500 001 1833227
005 20070926083715.5
008 130610s2004 eng d
020 $a 9780542158148
035 $a (UMI)AAI3176101
035 $a AAI3176101
040 $a UMI $c UMI
100 1 $a Zhang, Qingsong. $3 1921936
245 1 0 $a Atomistic simulations of barium titanate.
300 $a 100 p.
500 $a Source: Dissertation Abstracts International, Volume: 66-05, Section: B, page: 2776.
500 $a Adviser: William A. Goddard, III.
502 $a Thesis (Ph.D.)--California Institute of Technology, 2004.
520 $a We present the Polarizable Charge Equilibration (P-QEq) force field to include self-consistent atomic polarization and charge transfer in molecular dynamics of materials. The short-range Pauli repulsion effects are described by two body potentials without exclusions. A linear self-consistent field solution to the charge transfer is proposed for charge transfer in large systems. The P-QEq is parameterized for BaTiO3 based on quantum mechanics calculations (DFT with GGA) and applied to the study of the phase transitions, domain walls and oxygen vacancies.
520 $a Frozen phonon analysis reveals that the three high-temperature BaTiO 3 phases in the displacive model are unstable. Within their corresponding macroscopic phase symmetries, the smallest stable phase structures are achieved by antiferroelectric distortions from unstable phonons at the Brillouin zone boundaries. The antiferroelectric distortions soften phonons, reduce zero point energies and increase vibrational entropies. A correct BaTiO 3 phase transition sequence and comparable transition temperatures are obtained by free energy calculations. The inelastic coherent scattering functions of these phases agree with X-ray diffraction experiments.
520 $a BaTiO3 180° domain wall is Ba-centered with abrupt polarization switching across the wall. The center of BaTiO3 90° domain wall is close to its orthogonal phase. There are transition layers from the wall centers to the internal domains in the types of domain walls. Polarization variation in these transition layers induces polarization charge and free charge transfer. This effect causes a strong bipolar electric field in BaTiO 3 90° domain wall.
520 $a Oxygen vacancies are frozen at room temperature, and mobile near the Curie temperature. In the tetragonal phase, the broken Ti-O chains are frozen, reducing switchable polarization. Due to charge redistribution and local relaxation, oxygen vacancy interaction is short-range and anisotropic. Two oxygen vacancies can form a stable pair state, where two broken Ti-O chains are aligned parallel. Oxygen vacancy clusters can form dendritic structures as a result of local relaxation and charge interaction.
590 $a School code: 0037.
650 4 $a Physics, Condensed Matter. $3 1018743
650 4 $a Engineering, Materials Science. $3 1017759
690 $a 0611
690 $a 0794
710 2 0 $a California Institute of Technology. $3 726902
773 0 $t Dissertation Abstracts International $g 66-05B.
790 1 0 $a Goddard, William A., III, $e advisor
790 $a 0037
791 $a Ph.D.
792 $a 2004
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3176101