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Detecting alcohol vapors using two-dimensional copper-based Ruddlesden–Popper perovskites
The detection of alcohol vapors has many important applications, such as measuring the breath ethanol content to prevent drug-impaired driving. A medical application is the detection of 1-propanol because this compound was found to be a potential marker for lung cancer screening. This work reports a...
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Published in: | Applied physics letters 2020-11, Vol.117 (22) |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The detection of alcohol vapors has many important applications, such as measuring the breath ethanol content to prevent drug-impaired driving. A medical application is the detection of 1-propanol because this compound was found to be a potential marker for lung cancer screening. This work reports an alcohol sensor using the two-dimensional Ruddlesden–Popper perovskite bis(phenethylammonium) tetrachlorocuprate—(PEA)2CuCl4, also known as phenethylammonium copper chloride—as the sensing material. The device is based on a change in conductance upon exposure to alcohol vapors. A comparison between pristine (PEA)2CuCl4 and (PEA)2CuCl4 after a treatment with ultraviolet light shows that the latter has a higher conductance. Devices made with this UV-converted material show a strong response to 1-propanol vapors, starting from a concentration around 2000 parts per million (ppm). Additionally, these devices demonstrate stable behavior in a nitrogen atmosphere. During the stabilization of the 1-propanol flow rate, the concentration fluctuates. These fluctuations were detected by monitoring the current of the device over time, down to steps in 100 ppm around a concentration of 8000 ppm. The conductance of the devices decreases in contact with air. However, this process can be reversed by additional ultraviolet illumination, thereby making the devices reusable. |
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ISSN: | 0003-6951 1077-3118 |
DOI: | 10.1063/5.0033370 |