...
首页> 外文期刊>CERAMICS INTERNATIONAL >Synthesis and optical properties of Eu3+ ion-doped La2O2S2 via a solid state reaction method using La2O2SO4 as a raw material
【24h】

Synthesis and optical properties of Eu3+ ion-doped La2O2S2 via a solid state reaction method using La2O2SO4 as a raw material

机译:通过La2O2SO4作为原料的固态反应法通过固态反应方法合成和光学性质

获取原文
获取原文并翻译 | 示例

摘要

La2O2S2:Eu3+ was successfully synthesized by using La2O2SO4, Na2CO3 and sulphur as raw materials through a solid-state reaction (SSR) method. XRD results indicate that all of the diffraction peaks of the obtained sample are consistent with the standard pure phase of La2O2S2 with an optimal molar ratio (La2O2SO4:S:Na2CO3 = 1:30:5) and reaction temperature (500 degrees C). An infrared carbon and sulphur analysis instrument shows that the average value of the sulphur concentration in the target product is approximately 16.5039%, which is close to the theoretical data (17.1123%). The above-mentioned results illustrate the feasibility of the reaction process. SEM images show that the morphology of the product changed from a near-spherical (the precursor and La2O2SO4) to near-quadrilateral structure (La2O2S2) over the entire reaction process, with sizes varying from similar to 10 nm to similar to 200 nm. The optical band gap of La2O2S2 is approximately 2.55 eV, which is desired for photocatalytic applications. After being excited by a 325-nm laser at 77 K, La2O2S2:Eu3+ exhibited good photoluminescence properties, and a strong red emission at approximately 612 nm can be observed due to the D-5(0) - F-7(2) transition of Eu3+ ions.
机译:通过使用固态反应(SSR)方法,通过使用La2O 2 SO 4,Na 2 CO 3和硫作为原料成功合成La2O2S2:Eu3 +。 XRD结果表明所得样品的所有衍射峰与La2O2S2的标准纯相,具有最佳摩尔比(La2O2SO4:S:Na 2 CO 3 = 1:30:5)和反应温度(500℃)。红外碳和硫分析仪表表明,靶产物中硫浓度的平均值约为16.5039%,接近理论数据(17.1123%)。上述结果说明了反应过程的可行性。 SEM图像表明,在整个反应过程中,产品的形态从近球状(前体和La2O2SO4)变为近四边形结构(La2O2S2),尺寸不同于20nm至类似于200nm的尺寸。 La2O2S2的光带隙是约2.55eV,即光催化应用期望。在77k的325nm激光激发后,La2O2S2:Eu3 +表现出良好的光致发光性能,并且由于D-5(0) - &gt,可以观察到大约612nm的强烈的红色发射。 F-7(2)Eu3 +离子的转变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号