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以硝酸镧和硝酸铜为起始原料,柠檬酸为络合剂,分别以蒸馏水、乙醇、乙二醇和乙二醇甲醚为溶剂,采用溶胶-凝胶法制备了La2CuO4纳米晶。通过X射线衍射(XRD)、红外光谱(IR)、扫描电子显微镜(SEM)和紫外-可见-近红外光谱(UV-Vis-NIR)等方法对La2CuO4粉体进行了测试和表征;研究了不同溶剂对La2CuO4相组成、官能团、显微结构以及光学性能的影响。结果表明,以蒸馏水、乙醇和乙二醇为溶剂,600℃煅烧保温2h,均能获得单一La2CuO4物相,而以乙二醇甲醚为溶剂时,产物含有杂质相,所得粉体的形貌依次为网片状、蜂窝状、网状和块状。根据UV-Vis-NIR分析,所得La2CuO4的光学带隙分别为1.37、1.30、1.33和1.32eV。

La2CuO4 crystallites were prepared via a sol-gel process using lanthanum nitrate and cupric nitrate as raw materials, citric acid as complexing agent, while distilled water, ethanol, ethylene glycol and ethylene glycol monomethyl ether as solvent, respectively. The influences of different solvents on phase composition, functional group, microstructure and optical property of as-prepared La2 CuO4 crystallites were investigated by X-ray diffraction, infrared spectrum, scanning electron microscope and UV-Vis-Nir spectrophotometer. Results show that single La2CuO4 crystallites can be obtained after calcining at 600°C for 2h, except ethylene glycol monomethyl ether as solvent. The morphologies of the samples are nets flake, honeycomb, mesh and blocks when the solvent is distilled water, ethanol, ethylene glycol and ethylene glycol monomethyl ether, respectively. According to UV-Vis-Nir spectral analysis, the corresponding optical band gap of La2CuO4 crystallites was about 1.37, 1.30, 1.33 and 1.32eV.

参考文献

[1] Zhou X H;Cao Q X;Hu Y et al.[J].Sensors and Actuators B:Chemical,2001,77:443-446.
[2] 石晓波,傅海萍,李春根,汪德先.镧-镍复合氧化物纳米微粒的固相合成及其催化性能[J].化学研究与应用,2003(06):815-816.
[3] 张雪黎,罗来涛.A2BO4类钙钛矿型复合氧化物在催化领域的应用研究进展[J].工业催化,2006(03):6-10.
[4] 赵伟杰,赵辉,霍丽华,高山.厚膜型La2CuO4的氧敏性能[J].应用化学,2007(12):1409-1413.
[5] Sugai S;Takayanagi Y;Hayamizu N;Muroi T .Spin and phonon contribution to the superconductivity in La2-xSrxCuO4[J].The journal of physics and chemistry of solids,2008(12):3058-3063.
[6] Lan YC.;Cao YG.;Huang JK.;Che GC.;Liu GD.;Xu YP.;Xu T.;Li JY.;Chen XL. .Structure and superconducting properties of chemically oxidized La2CuO4+y under hydrothermal conditions[J].Physica, C. Superconductivity and its applications,2000(1/2):151-156.
[7] Gao, LZ;Chua, HT;Kawi, S .The direct decomposition of NO over the La2CUO4 nanofiber catalyst[J].Journal of Solid State Chemistry,2008(10):2804-2807.
[8] 刘钰,杨向光,刘玉敏,吴越.La2CuO4的制备及其对催化消除NO活性的影响[J].物理化学学报,1999(06):506-511.
[9] Spijker H;Simon D;Ooms F .[J].International Journal of Hydrogen Energy,2008,33:6414-6419.
[10] 杨东升,吴柏枚,郑卫华,杨宏顺,李波,曹烈兆.氧掺杂La2CuO4的热导[J].低温物理学报,2001(01):44-47.
[11] Hirayama T;Nakagawa M;Oda Y .[J].Solid State Communications,2000,113:121-124.
[12] 张悦,张磊,邓积光,魏丽,戴洪兴,何洪.水热法制备特定形貌单晶 La2-xSrxCuO4 及甲烷催化氧化性能[J].催化学报,2009(04):347-354.
[13] 王晓辉,周延春.La2 CuO4前驱物粉体的自蔓延燃烧合成及其晶化[J].材料研究学报,2001(04):387-393.
[14] Pankove J I .[J].Thin Solid Films,1982,90(02):172.
[15] Terauchi M;Tanaka M .[J].Micron,1999,30:371-377.
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