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首页> 外文期刊>Journal of Materials Science >Effect of electrodes and zeolite cover layer on hydrocarbon sensing with p-type perovskite SrTi0.8Fe0.2O3-δ thick and thin films
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Effect of electrodes and zeolite cover layer on hydrocarbon sensing with p-type perovskite SrTi0.8Fe0.2O3-δ thick and thin films

机译:电极和沸石覆盖层对p型钙钛矿SrTi0.8 Fe0.2 O3-δ厚膜和薄膜的碳氢化合物感测的影响

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Screen-printed thick film as well as pulsed laser deposited thin film sensors of the perovskite SrTi0.8Fe0.2O3-δ (STF20) with gold electrodes present poor hydrocarbon selectivity when exposed to different gases (hydrocarbons, hydrogen, NO, and CO). By employing Pt-electrodes, response to H2 and CO is eliminated. In the case of thick film devices, only NO cross interference persists. The selectivity of the thick films is further increased by applying a Pt doped zeolite (ZSM-5) as a cover layer. By adjusting the thickness of the ZSM-5 cover layer, the film selectively senses mainly saturated hydrocarbons such as propane, suppressing the response towards all the other gases. This effect is attributed to the catalytic effect of the high Pt-content of the ZSM-5 zeolite. Application of a ZSM-5 cover layer to thin films enhances the sensor output response to propane, thus reducing selectivity for unsaturated hydrocarbons. A sensor configuration having Pt electrodes on top of an STF20 thick film with an additional 50 μm cover layer of ZSM-5 was found to be the most suitable to selectively sense saturated hydrocarbons. Thin film STF20 sensors equipped with Pt-IDC electrodes and without the zeolite cover layer, were found to perform best for unsaturated hydrocarbons at 400°C.
机译:带有金电极的钙钛矿SrTi0.8 Fe0.2 O3-δ(STF20)的丝网印刷厚膜以及脉冲激光沉积薄膜传感器在暴露时表现出较差的烃选择性转化为不同的气体(碳氢化合物,氢气,NO和CO)。通过使用Pt电极,消除了对H2 和CO的响应。在厚膜器件的情况下,仅NO交叉干扰持续存在。通过应用掺杂Pt的沸石(ZSM-5)作为覆盖层,可以进一步提高厚膜的选择性。通过调整ZSM-5覆盖层的厚度,该膜可以选择性地检测主要饱和的烃(例如丙烷),从而抑制了对所有其他气体的响应。该作用归因于ZSM-5沸石的高Pt含量的催化作用。将ZSM-5覆盖层应用于薄膜可增强传感器对丙烷的输出响应,从而降低对不饱和烃的选择性。发现在STF20厚膜的顶部具有Pt电极并带有额外的50μmZSM-5覆盖层的传感器配置最适合选择性地检测饱和烃。发现配备Pt-IDC电极且没有沸石覆盖层的STF20薄膜传感器在400°C下对不饱和烃的性能最佳。

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  • 来源
    《Journal of Materials Science 》 |2006年第18期| 5828-5835| 共8页
  • 作者单位

    Functional Materials University of Bayreuth;

    Functional Materials University of Bayreuth;

    Functional Materials University of Bayreuth;

    Institute for Chemical Process and Environmental Technology National Research Council of Canada;

    Institute for Chemical Process and Environmental Technology National Research Council of Canada;

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