二氧化锡
材料科学
氢传感器
纳米结构
结晶度
基质(水族馆)
介孔材料
氢
电阻率和电导率
锡
化学电阻器
溅射
沉积(地质)
电极
薄膜
分析化学(期刊)
纳米技术
化学工程
复合材料
化学
冶金
催化作用
钯
物理化学
海洋学
工程类
生物
古生物学
生物化学
色谱法
沉积物
地质学
有机化学
电气工程
作者
Nagih M. Shaalan,D. Hamad
标识
DOI:10.1016/j.apsusc.2022.153857
摘要
In this paper, tin dioxide (SnO2) mesoporous nanostructures (pores of 2 and 50 nm) were directly sputtered on a Pt-interdigitated electrode (gap length of 35 μm) with a slow deposition rate of 5 nm/min under a controlled substrate temperature of 100, 350, and 500 °C. It is found that the surface area was 0.22 × 104, 0.18 × 104, and 0.17 × 104 observed for the nanostructure prepared at 350 °C, 500 °C, and 100 °C, respectively. The film crystallinity increased with increasing the substrate temperature. The film prepared at 500 °C showed a lower resistivity in air. Most importantly, the sensor fabricated by using the nanostructure prepared at 500 °C exhibits excellent low-temperature (100 °C) H2 sensing properties. When this sensor is exposed to 1000 ppm (0.1%) H2, the sensor response is 30 × 103 %. The sensing performances are superior to those of most reported at higher temperature H2 sensors based on SnO2 materials. Interesting is the sensor selectivity, where the sensor prepared at 500 °C is selective toward H2 gas, while the sensor prepared at 350 °C is selective toward NO2 gas. The sensing performance of the sensor prepared at 500 °C for H2 (reducing gas) was attributed to a proposed mechanism of a coulomb interaction (electric dipole). The sensors exhibit two different behaviors of their electrical resistivities upon exposure to H2 gas at low and high temperatures. The gas sensing mechanisms for such behaviors were proposed to understand the sensor behavior. The current results may assist in realizing high selective sensors toward H2 for the commercial market.
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