表征半导体金属氧化物传感器甲烷响应随时间的变化

IF 3.5 Q3 ENVIRONMENTAL SCIENCES
Adil Shah, Olivier Laurent, Grégoire Broquet, Clément Romand and Philippe Ciais
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引用次数: 0

摘要

基于半导体的费加罗田口气体传感器(TGS)对包括甲烷在内的还原性气体很敏感。TGS甲烷响应可以通过使用甲烷摩尔分数([CH4])增强时的电阻与参考电阻之间的比值来表征,参考电阻代表在相同环境条件下,具有相同背景气体成分,但在参考[CH4]水平下的采样。环境变量的影响,包括水摩尔分数([H2O]),预计将在该电阻比中抵消,从而允许独立的[CH4]表征。本研究旨在研究[CH4]电阻比特征随时间变化的原因,包括电阻比与[H2O]无关的假设。在合成空气(SCS)测试的传感器表征过程中,在受控条件下采样了精确的气体混合物,结果表明[H2O]会影响阻力比甲烷表征,尽管这种影响的重要性取决于参考气体。在类似的环境条件和气体混合物下,还进行了三次SCS测试,间隔为137天,然后是295天。[CH4]电阻比响应在第一个时间间隔期间发生显著变化,表明某些固有的东西改变了传感器的行为,但在第二个时间间隔期间可以忽略不计,表明自然老化不是传感器行为的关键驱动因素。额外的SCS试验显示,暴露于硫化氢后[CH4]电阻比反应持续变化;这可能导致相隔137天进行的受控SCS测试之间发生变化,尽管其他大气物种也可能对此负责。这是实验室测试和最终传感器应用的重要考虑因素。同时,功率损耗和采样干燥空气对不同TGS的影响可以忽略不计。此外,在大约25个月的时间里,总共进行了147次成功的环境空气(SCA)测试,其中少量高[CH4]气体与室外环境空气混合。当SCA测试被限制在类似SCS测试之间的第二个(295天)时间窗口时,SCA测试显示时间与[CH4]反应之间的相关性较弱。剩余观察到的SCA测试与时间的相关性可归因于[H2O]随时间的变化,支持SCS测试结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Characterising changes in the methane response of a semiconductor-based metal oxide sensor over time

Characterising changes in the methane response of a semiconductor-based metal oxide sensor over time

The semiconductor-based Figaro Taguchi Gas Sensor (TGS) is sensitive to reducing gases, including methane. TGS methane response can be characterised by using the ratio between resistance in the presence of methane mole fraction ([CH4]) enhancements and a reference resistance, representative of sampling under the same environmental conditions and with the same background gas composition, but at a reference [CH4] level. Effects of environmental variables, including water mole fraction ([H2O]), are expected to cancel in this resistance ratio, allowing for independent [CH4] characterisation. This work seeks to examine the cause of changes in [CH4] resistance ratio characterisation over time, including the hypothesis that resistance ratios are independent of [H2O]. Precise gas blends were sampled under controlled conditions during sensor characterisation in synthetic air (SCS) tests, which showed [H2O] to influence resistance ratio methane characterisation, although this effect's importance depends on the reference gas. Three SCS tests were also performed with gaps of 137 days followed by 295 days, all under similar environmental conditions and gas blends. [CH4] resistance ratio response changed significantly during the first time gap, suggesting that something inherently changed sensor behaviour, but negligibly during the second time gap, suggesting that natural ageing is not otherwise a key driver of sensor behaviour. Additional SCS tests showed persistent changes in [CH4] resistance ratio response following hydrogen sulphide exposure; this may have caused a change between controlled SCS tests conducted 137 days apart, although other atmospheric species may also have been responsible. This is an important consideration for laboratory testing and final sensor application. Meanwhile, power loss and sampling dry air negligibly affected a different TGS. In addition, a total of 147 successful sensor characterisation in ambient air (SCA) tests occurred irregularly over approximately 25 months, where small amounts of gas with a high [CH4] were blended with ambient outdoor air. SCA tests showed a weaker correlation between time and [CH4] response when restricted to the period covering the second (295-day) time window between the similar SCS tests. A residual observed SCA testing correlation with time could be attributed to changes in [H2O] over time, supporting SCS testing conclusions.

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