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Engineered interfaces and nano-scale...
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Nandasiri, Manjula I.
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Engineered interfaces and nano-scale thin films for solid oxide fuel cell electrolytes.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Engineered interfaces and nano-scale thin films for solid oxide fuel cell electrolytes./
作者:
Nandasiri, Manjula I.
面頁冊數:
120 p.
附註:
Source: Dissertation Abstracts International, Volume: 74-10(E), Section: B.
Contained By:
Dissertation Abstracts International74-10B(E).
標題:
Physics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3570762
ISBN:
9781303165245
Engineered interfaces and nano-scale thin films for solid oxide fuel cell electrolytes.
Nandasiri, Manjula I.
Engineered interfaces and nano-scale thin films for solid oxide fuel cell electrolytes.
- 120 p.
Source: Dissertation Abstracts International, Volume: 74-10(E), Section: B.
Thesis (Ph.D.)--Western Michigan University, 2013.
This item must not be sold to any third party vendors.
Solid state electrolytes with high oxygen ionic conductivity at low temperatures are required to develop cost effective and efficient solid oxide fuel cells. This study investigates the influence of engineered interfaces on the oxygen ionic conductivity of nano-scale multilayer thin film electrolytes. The epitaxial Sm2O3 doped CeO2 (SDC) and Sc2O3 stabilized ZrO2 (ScSZ) are selected as the alternative layers for the proposed multilayer thin film electrolyte based on the optimum structural, chemical, and electrical properties reported in the previous studies. The epitaxial SDC(111)/ScSZ(111) multilayer thin films are grown on high purity Al2O3(0001) substrates by oxygen-plasma assisted molecular beam epitaxy. Prior to the deposition of multilayers, the growth parameters are optimized for epitaxial CeO 2, ZrO2, SDC, and ScSZ thin films.
ISBN: 9781303165245Subjects--Topical Terms:
516296
Physics.
Engineered interfaces and nano-scale thin films for solid oxide fuel cell electrolytes.
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Source: Dissertation Abstracts International, Volume: 74-10(E), Section: B.
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Adviser: Asghar N. Kayani.
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Solid state electrolytes with high oxygen ionic conductivity at low temperatures are required to develop cost effective and efficient solid oxide fuel cells. This study investigates the influence of engineered interfaces on the oxygen ionic conductivity of nano-scale multilayer thin film electrolytes. The epitaxial Sm2O3 doped CeO2 (SDC) and Sc2O3 stabilized ZrO2 (ScSZ) are selected as the alternative layers for the proposed multilayer thin film electrolyte based on the optimum structural, chemical, and electrical properties reported in the previous studies. The epitaxial SDC(111)/ScSZ(111) multilayer thin films are grown on high purity Al2O3(0001) substrates by oxygen-plasma assisted molecular beam epitaxy. Prior to the deposition of multilayers, the growth parameters are optimized for epitaxial CeO 2, ZrO2, SDC, and ScSZ thin films.
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The epitaxial orientation and surface morphology of CeO2 thin films shows dependency on the growth rate. Epitaxial CeO2(111) is obtained at relatively high growth rates (>9 A/min) at a substrate temperature of 650°C and an oxygen partial pressure of 2 x 10 -5 Torr. The same growth parameters are used for the deposition of ZrO2 thin films. ZrO2 exhibits both monoclinic and cubic phases, which is stabilized in the cubic structure by doping with Sc 2O3. The Sm and Sc evaporation rates are varied during the growth to obtain thin films of 15 mol % SmO1.5 doped CeO2 and 20 mol % ScO1.5 stabilized ZrO2, respectively. The SDC/ScSZ multilayer thin films are grown using the same growth parameters by varying the number of layers.
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The SDC/ScSZ multilayer thin films show significant enhancement in the oxygen ionic conductivity in comparison to single layer SDC and ScSZ thin films. The increase in the oxygen ionic conductivity with the increase in number of layers can be attributed to lattice mismatch induced ionic conductivity along the interfaces. The 8-layer film exhibits the maximum oxygen ionic conductivity with one order of magnitude enhancement in the temperature range of 500-800°C compared to single layer thin films.
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