Ordered deficient perovskite La2/3TiO3 films grown via molecular beam epitaxy

被引:0
|
作者
Weng, Joan [1 ,2 ]
Shin, Hyungki [1 ,2 ]
Godin, Simon [1 ,2 ]
Oudah, Mohamed [1 ,2 ]
Sutarto, Ronny [3 ]
Pons, Rebecca [1 ,2 ,4 ]
Davidson, Bruce A. [1 ,2 ]
Zou, Ke [1 ,2 ]
机构
[1] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 1Z1, Canada
[2] Univ British Columbia, Quantum Matter Inst, Vancouver, BC V6T 1Z4, Canada
[3] Canadian Light Source, Saskatoon, SK S7N 2V3, Canada
[4] Max Plack Inst Solid State Res, Heisenbergstr 1, D-70569 Stuttgart, Germany
来源
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
LITHIUM INSERTION; TRANSITION; INTERFACES; VACANCIES; CERAMICS; CRYSTAL; LA;
D O I
10.1116/6.0003091
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As the parent compound of a promising solid electrolyte material Li3xLa2/3-xTiO3, the perovskite La2/3TiO3 has potential for advancing research on Li-intercalated ionic conductors. Epitaxial La2/3TiO3 films have been grown by molecular beam epitaxy using a growth process consisting of deposition and annealing cycles, with in situ monitoring by electron diffraction. X-ray absorption spectroscopy confirms the tetravalent state of Ti in La2/3TiO3, and the as-grown films are insulating. X-ray diffraction reveals the presence of half-order peaks, indicating a doubling of the pseudocubic perovskite unit cell due to the ordering of La vacancies in alternating A-site layers. These results demonstrate that single-phase, vacancy-ordered epitaxial films of La2/3TiO3 can be stabilized with excellent crystalline and electronic properties over wafer-sized areas, making possible Li-ion intercalation studies in films with well-defined domain boundary properties. Such boundaries are known to profoundly influence Li-ion conduction within the material. Understanding the effects of domain boundaries on Li-ion conduction could lead to improvements in solid-state battery technology and pave the way for the development of more efficient and safer energy storage devices.
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页数:8
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