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Gas sensor properties of Ag- and Pd-decorated SnO micro-disks to NO_2, H_2 and CO: Catalyst enhanced sensor response and selectivity

机译:用Ag和Pd装饰的SnO微盘对NO_2,H_2和CO的气体传感器性能:催化剂增强了传感器的响应和选择性

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摘要

The gas sensor response of tin monoxide micro-disks, functionalized with noble metal nanoparticles (Pd and Ag), to NO_2, H_2 and CO were studied by monitoring changes in their resistance upon exposure to the various gases. The tin monoxide, with unusually low Sn oxidation state, was synthetized by carbothermal reduction. Surface modification by Pd and Ag catalysts was achieved by coating the micro-disks by metallic nanoparticle dispersions, prepared by the polyol reduction process, followed by thermal treatment. SEM and TEM analysis showed nanoparticles to be well-dispersed over the SnO surfaces. The decorated SnO micro-disks exhibited high sensor response to reducing gases such as H_2 and CO. On the other hand, the catalytic particles tended to reduce the sensor response to oxidizing gases such as NO_2. The catalytic activity of Pd nanoparticles was tied to chemical sensitization while that of Ag nanoparticles to electronic sensitization. Impedance spectroscopy enabled deconvolution of different contributions to the sensor response with only the Ag-decorated specimens exhibiting two RC time constants. Thus, in contrast to undecorated and Pd-decorated specimens, nearly 80% of Ag modified SnO's response to H_2 was controlled by changes in the interface between particles and disks. Sensor response to H_2 was optimal at higher temperatures (300 ℃), NO_2 at 200 ℃ while that for Pd-decorated materials; maximum sensor response to CO was observed at lower temperatures (under 150℃), where CO absorption by metal nanoparticles is favored.
机译:通过监测它们暴露于各种气体后的电阻变化,研究了用贵金属纳米粒子(Pd和Ag)功能化的一氧化锡微盘对NO_2,H_2和CO的气体传感器响应。通过碳热还原合成了具有极低Sn氧化态的一氧化锡。 Pd和Ag催化剂的表面改性是通过用多元醇还原工艺制备的金属纳米颗粒分散体涂覆微盘,然后进行热处理来实现的。 SEM和TEM分析表明纳米颗粒在SnO表面上分散良好。装饰的SnO微型磁盘对还原气体(例如H_2和CO)表现出较高的传感器响应。另一方面,催化颗粒倾向于降低传感器对氧化气体(例如NO_2)的响应。 Pd纳米颗粒的催化活性与化学增感有关,而Ag纳米颗粒的催化活性与电子增感有关。阻抗光谱法仅在显示两个RC时间常数的经过Ag修饰的样本上就能对传感器响应的不同贡献进行解卷积。因此,与未装饰和Pd装饰的样品相反,近80%的Ag修饰的SnO对H_2的响应是由颗粒和圆盘之间的界面变化控制的。在较高温度(300℃)下传感器对H_2的响应最佳,在200℃下传感器对H_2的响应最佳,而对Pd装饰材料的响应则最佳。在较低的温度(低于150℃)下观察到对CO的最大传感器响应,其中金属纳米颗粒对CO的吸收是有利的。

著录项

  • 来源
    《Sensors and Actuators》 |2017年第2期|253-261|共9页
  • 作者单位

    Department of Physical-Chemistry, Sao Paulo State University, Araraquara, SP, 14800-900, Brazil;

    Department of Physical-Chemistry, Sao Paulo State University, Araraquara, SP, 14800-900, Brazil,Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA;

    Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA;

    Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA;

    Department of Physical-Chemistry, Sao Paulo State University, Araraquara, SP, 14800-900, Brazil;

    Department of Physical-Chemistry, Sao Paulo State University - UNESP, Rua Francisco Degni 55, Quitandinha, P.O. Box 355, CEP: 14800-900, Araraquara, Sao Paulo, Brazil;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Gas sensors; SnO; Catalyst; Impedance spectroscopy; Sensitization;

    机译:气体传感器;SnO;催化剂;阻抗谱;敏化;

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