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A phosphine detection matrix using nanostructure modified porous silicon gas sensors

机译:使用纳米结构改性的多孔硅气体传感器的磷化氢检测矩阵

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We discuss the selective modification of porous silicon (PS) conductometric gas sensors for phosphine detection. Tin, nickel, copper and gold are electrolessly deposited onto nanopore covered microporous porous silicon surfaces forming SnO_x, NiO, Cu_xO and Au_xO nanostructured centers. Further studies have also been carried out with nanostructured alumina coated porous silicon. The porous silicon surface is analyzed for the metal oxides considered using XPS measurements. These experiments demonstrate that the indicated metals are deposited to the nanopore covered micropores of the PS interface and are oxidized to form metal oxide sites. The sensitivity change of these modified porous silicon gas sensor surfaces has been measured under l-5ppm PH_3 exposure. An improved sensitivity, of the order of 5 times that of untreated porous silicon, for 1 ppm exposure is observed. The selection of the nanostructure deposition is based on the hard to soft acid character of the nanostructured deposit and its subsequent effect on the physisorption of PH_3, an intermediate base. The observed behavior follows an inverse pattern IHSAB to the hard soft acid-base concept.
机译:我们讨论了用于磷化氢检测的多孔硅(PS)电导率气体传感器的选择性改进。锡,镍,铜和金化学沉积在纳米孔覆盖的微孔多孔硅表面上,形成SnO_x,NiO,Cu_xO和Au_xO纳米结构中心。还已经对纳米结构的氧化铝涂覆的多孔硅进行了进一步的研究。使用XPS测量分析多孔硅表面的金属氧化物。这些实验表明,所示金属沉积到PS界面的纳米孔覆盖的微孔上,并被氧化形成金属氧化物位点。这些改性的多孔硅气体传感器表面的灵敏度变化已在1-5 ppm PH_3暴露条件下进行了测量。观察到对于1 ppm的曝光,其灵敏度提高了未经处理的多孔硅的5倍左右。纳米结构沉积物的选择基于纳米结构沉积物的难于软酸的特性及其对PH_3(一种中间碱)的物理吸附的后续影响。观察到的行为遵循与硬软酸碱概念相反的模式IHSAB。

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