Amorphous and perovskite Li3xLa(2/3)−xTiO3 (thin) films via chemical solution deposition: solid electrolytes for all-solid-state Li-ion batteries
Thin films of amorphous and crystalline perovskite Li 3x La (2/3)−x TiO 3 (LLT) (x = 0.117) are prepared by means of aqueous chemical solution deposition onto rutile TiO 2 thin films as an anode, yielding an electrochemical half-cell. The Li-ion conductivity of the pin-hole free, amorphous LLT thin...
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| Vydáno v: | Journal of sol-gel science and technology Ročník 73; číslo 3; s. 536 - 543 |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Boston
Springer US
01.03.2015
Springer Nature B.V |
| Témata: | |
| ISSN: | 0928-0707, 1573-4846 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | Thin films of amorphous and crystalline perovskite Li
3x
La
(2/3)−x
TiO
3
(LLT) (x = 0.117) are prepared by means of aqueous chemical solution deposition onto rutile TiO
2
thin films as an anode, yielding an electrochemical half-cell. The Li-ion conductivity of the pin-hole free, amorphous LLT thin film (90 nm thick) is 3.8 × 10
−8
S cm
−1
on Pt and 1.3 × 10
−8
S cm
−1
on rutile TiO
2
, while measuring perpendicular to the thin film direction with impedance spectroscopy. Grazing angle attenuated total reflectance-Fourier transform infrared spectroscopy shows that all organic precursor molecules have been decomposed at 500 °C. In addition, in situ (heating) X-ray diffraction analysis shows that phase pure crystalline perovskite LLT (x = 0.117) is formed on top of the rutile TiO
2
anode at 700 °C. Furthermore, thickness control is possible by varying the precursor solution concentration and the number of deposition cycles. The current study presents a promising synthesis route to develop all-solid-state battery devices based on multi-metal oxide materials using aqueous precursor chemistry. |
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| Bibliografie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
| ISSN: | 0928-0707 1573-4846 |
| DOI: | 10.1007/s10971-014-3511-5 |