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Synthesis of ceramic cell materials from polymer precursors for electrolytic decomposition of no

机译:来自聚合物前体的陶瓷细胞材料的合成NO电解分解

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The synthesis of dense Ce{sub}(1-x)Gd{sub}xO{sub}(2-δ)(CGO) and porous La{sub}(1-x)Sr{sub}xCo{sub}(1-y)Fe{sub}yO{sub}3 (LSCF) electrode thin films was investigated by means of dip- or spin-coating from precursor solutions with mixing nitrates and organic solvent of polyhydroxyl alcohols. The microstructure of the CGO thin films can be changed from dense to porous by changing the species of solvents. The crystallization of the CCO thin film can be enhanced by using polymerized precursor solutions. Dense CGO thin films can be formed directly on porous LSCF substrate with certain surface porosity. The porous LSCF thin films were prepared by using solutions containing the organic solvent, polyethylene glycol. The spin-coated LSCF cathode cell showed higher efficiency for NO decomposition than the platinum-cathode cell.
机译:致密CE {sub}(1-x)gd {sub}(2-Δ)(cgO)和多孔la {sub}(1-x)sr {sub} xco {sub}合成合成 - 即通过用来自前体溶液的浸涂或旋涂,通过用混合硝酸盐和多羟基醇的有机溶剂来研究Fe {Sub} 3(LSCF)电极薄膜。通过改变溶剂种类来从致密到多孔改变CgO薄膜的微观结构。通过使用聚合的前体溶液,可以增强CCO薄膜的结晶。致密的CgO薄膜可以直接形成在多孔LSCF基板上,具有一定的表面孔隙率。通过使用含有有机溶剂,聚乙二醇的溶液制备多孔LSCF薄膜。旋涂的LSCF阴极细胞显示比铂 - 阴极电池的分解更高。

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