Alqahtani Zahrah, Grell Martin
Physics Department, Faculty of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Llyfrgell Bangor, Ffordd Gwynedd, Bangor LL57 1DT, UK.
Sensors (Basel). 2024 Jan 9;24(2):407. doi: 10.3390/s24020407.
Hydrogen sulphide (HS) is a toxic gas soluble in water, HS, as a weak acid. Since HS usually originates from the decomposition of faecal matter, its presence also indicates sewage dumping and possible parallel waterborne pathogens associated with sewage. We here present a low footprint ('frugal') HS sensor as an accessible resource for water quality monitoring. As a sensing mechanism, we find the chemical affinity of thiols to gold (Au) translates to HS. When an Au electrode is used as a control gate (CG) or floating gate (FG) electrode in the electric double layer (EDL) pool of an extended gate field effect transistor (EGFET) sensor, EGFET transfer characteristics shift along the CG voltage axis in response to HS. We rationalise this by the interface potential from the adsorption of polar HS molecules to the electrode. The sign of the shift changes between Au CG and Au FG, and cancels when both electrodes are Au. The sensor is selective for HS over the components of urine, nor does urine suppress the sensor's ability to detect HS. Electrodes can be recovered for repeated use by washing in 1M HCl. Quantitatively, CG voltage shift is fitted by a Langmuir-Freundlich (LF) model, supporting dipole adsorption over an ionic (Nernstian) response mechanism. We find a limit-of-detection of 14.9 nM, 100 times below potability.
硫化氢(HS)是一种可溶于水的有毒气体,HS为弱酸。由于HS通常源自粪便分解,其存在也表明有污水倾倒以及可能存在与污水相关的水传播病原体。我们在此展示一种低占用空间(“节俭型”)的HS传感器,作为一种可用于水质监测的资源。作为一种传感机制,我们发现硫醇与金(Au)的化学亲和力可转化为对HS的检测。当在扩展栅场效应晶体管(EGFET)传感器的双电层(EDL)池中使用金电极作为控制栅(CG)或浮栅(FG)电极时,EGFET的转移特性会随着HS的变化而沿CG电压轴移动。我们通过极性HS分子吸附到电极产生的界面电位来对此进行解释。在金CG和金FG之间,移动的方向会发生变化,而当两个电极均为金时,这种变化会相互抵消。该传感器对HS的选择性高于尿液成分,尿液也不会抑制传感器检测HS的能力。通过在1M盐酸中清洗,电极可回收并重复使用。从定量角度来看,CG电压偏移符合朗缪尔 - 弗伦德利希(LF)模型,这支持了偶极吸附而非离子(能斯特)响应机制。我们发现该传感器的检测限为14.9 nM,比饮用水标准低100倍。