材料科学
氢传感器
抗坏血酸
贵金属
纳米颗粒
催化作用
氢
离解(化学)
化学工程
化学吸附
物理吸附
选择性
结晶度
热液循环
纳米技术
检出限
金属
化学
钯
物理化学
复合材料
色谱法
有机化学
冶金
工程类
食品科学
作者
Gaojie Li,Kai Du,Xinxin Wang,Xiaochen Wang,Boao Chen,Chun Qiu,Jiaqiang Xu
标识
DOI:10.1016/j.ijhydene.2023.06.263
摘要
This study is attempted to improve the hydrogen sensing performance of SnO2 based sensors by simultaneously employing two strategies of morphology control and noble metal loading. Therefore, SnO2 ultrathin nanosheets with thickness not exceeding 3.5 nm were successfully synthesized by a hydrothermal method and then different content of Pd nanoparticles were uniformly loaded onto SnO2 surface by in situ reduction with ascorbic acid. The gas sensing properties demonstrated that the introduction of Pd not only altered the selectivity of the SnO2 sensor from ethanol to hydrogen, but also significantly improved the gas sensitivity and reduced the working temperature. And the optimal 1.0%Pd/SnO2 sensor owned the highest sensitivity (75), fastest response-recovery property (21 s/13 s) to 20 ppm of hydrogen at 220 °C, and the actual detection limit is as low as 0.1 ppm. Furthermore, 1.0%Pd/SnO2 sensor exhibited excellent repeatability, reproducibility and acceptable anti-interference of humidity. The DFT studies suggest that the physisorption of the hydrogen molecules on the surface of SnO2, but chemisorption on the surface of Pd/SnO2. The improved H2 sensing performance of Pd/SnO2 sensor attributes its ultrathin thickness of SnO2 and catalytic dissociation of Pd to O2 and H2.
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