首页> 美国卫生研究院文献>Beilstein Journal of Nanotechnology >Low-temperature CO oxidation over Cu/Pt co-doped ZrO2 nanoparticles synthesized by solution combustion
【2h】

Low-temperature CO oxidation over Cu/Pt co-doped ZrO2 nanoparticles synthesized by solution combustion

机译:固溶燃烧合成Cu / Pt共掺杂ZrO2纳米粒子的低温CO氧化

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Zirconia (ZrO2) nanoparticles co-doped with Cu and Pt were applied as catalysts for carbon monoxide (CO) oxidation. These materials were prepared through solution combustion in order to obtain highly active and stable catalytic nanomaterials. This method allows Pt2+ and Cu2+ ions to dissolve into the ZrO2 lattice and thus creates oxygen vacancies due to lattice distortion and charge imbalance. High-resolution transmission electron microscopy (HRTEM) results showed Cu/Pt co-doped ZrO2 nanoparticles with a size of ca. 10 nm. X-ray diffraction (XRD) and Raman spectra confirmed cubic structure and larger oxygen vacancies. The nanoparticles showed excellent activity for CO oxidation. The temperature T 50 (the temperature at which 50% of CO are converted) was lowered by 175 °C in comparison to bare ZrO2. Further, they exhibited very high stability for CO reaction (time-on-stream ≈ 70 h). This is due to combined effect of smaller particle size, large oxygen vacancies, high specific surface area and better thermal stability of the Cu/Pt co-doped ZrO2 nanoparticles. The apparent activation energy for CO oxidation is found to be 45.6 kJ·mol−1. The CO conversion decreases with increase in gas hourly space velocity (GHSV) and initial CO concentration.
机译:共掺杂了Cu和Pt的氧化锆(ZrO2)纳米颗粒被用作一氧化碳(CO)氧​​化的催化剂。这些材料是通过溶液燃烧制备的,以获得高活性和稳定的催化纳米材料。该方法允许Pt 2 + 和Cu 2 + 离子溶解到ZrO2晶格中,从而由于晶格畸变和电荷不平衡而产生氧空位。高分辨率透射电子显微镜(HRTEM)结果表明,Cu / Pt共掺杂ZrO2纳米粒子的尺寸约为。 10纳米X射线衍射(XRD)和拉曼光谱证实立方结构和较大的氧空位。纳米颗粒显示出优异的CO氧化活性。与裸露的ZrO2相比,温度T 50(转化为50%的CO的温度)降低了175°C。此外,它们对CO反应表现出非常高的稳定性(运行时间≈70小时)。这是由于Cu / Pt共掺杂ZrO2纳米粒子的粒径较小,氧空位较大,比表面积高和热稳定性更好的综合作用所致。发现CO氧化的表观活化能为45.6 kJ·mol -1 。 CO转化率随气体时空速度(GHSV)和初始CO浓度的增加而降低。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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