Room-Temperature Ammonia Detection Using Layered Bi2Se3/Bi2O3: A Next-Generation Sensor Room-Temperature Ammonia Detection Using Layered Bi2Se3/Bi2O3: A Next-Generation Sensor AITranslate
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We demonstrate room-temperature NH3 sensors for the first time using liquid-phase-exfoliated layered n-Bi2Se3/p-Bi2O3 of four different compositions (Bi2Se3 in %:Bi2O3 in % = 27.1:72.9, 52:48, 64:36, and 77:23) by hydrothermal synthesis for 7, 14, 21, and 28 h which are named as B7, B14, B21, and B28, respectively. Sensor B14 exhibits superior sensing performance within a wide concentration range (5–180 ppm) of NH3 with high selectivity (among NH3, acetone, toluene, isopropyl alcohol, methyl amine, ethanol, methanol, and benzene) and a response (R = Ig/Ia) of 8.5 toward 180 ppm due to the maximum interaction between n-Bi2Se3 and p-Bi2O3. The sensor delivered a response time of 134.5 s and a faster recovery of 23.5 s with a limit of detection of 5 ppm. The sensing mechanism is explained on the basis of experimentally confirmed physisorption (decrement of response from 8.18 to 4.63 with the increase of operating temperature from 30 to 50 °C)-based charge transfer at the adsorption sites on the Bi2Se3 surface and modulation of barrier potential formed between n-Bi2Se3 and p-Bi2O3. Further, the long-term stability of the sensor over 90 days indicates potential candidature of the material to be used as a next-generation NH3 sensor at room temperature.
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DOI:https://doi.org/10.1021/acsaelm.2c01496
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We demonstrate room-temperature NH3 sensors for the first time using liquid-phase-exfoliated layered n-Bi2Se3/p-Bi2O3 of four different compositions (Bi2Se3 in %:Bi2O3 in % = 27.1:72.9, 52:48, 64:36, and 77:23) by hydrothermal synthesis for 7, 14, 21, and 28 h which are named as B7, B14, B21, and B28, respectively. Sensor B14 exhibits superior sensing performance within a wide concentration range (5–180 ppm) of NH3 with high selectivity (among NH3, acetone, toluene, isopropyl alcohol, methyl amine, ethanol, methanol, and benzene) and a response (R = Ig/Ia) of 8.5 toward 180 ppm due to the maximum interaction between n-Bi2Se3 and p-Bi2O3. The sensor delivered a response time of 134.5 s and a faster recovery of 23.5 s with a limit of detection of 5 ppm. The sensing mechanism is explained on the basis of experimentally confirmed physisorption (decrement of response from 8.18 to 4.63 with the increase of operating temperature from 30 to 50 °C)-based charge transfer at the adsorption sites on the Bi2Se3 surface and modulation of barrier potential formed between n-Bi2Se3 and p-Bi2O3. Further, the long-term stability of the sensor over 90 days indicates potential candidature of the material to be used as a next-generation NH3 sensor at room temperature.
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| GB/T 7714-2015 | [1] Biswajit Das, Sk Riyajuddin, Kaushik Ghosh, et al. ACS Applied Electronic Materials, 2023(5). DOI:10.1021/acsaelm.2c01496. |
| MLA | [1] Biswajit Das, et al., ACS Applied Electronic Materials, no. 5, 2023, https://doi.org/10.1021/acsaelm.2c01496. |
| APA | [1] Biswajit Das, Sk Riyajuddin, Kaushik Ghosh, & Ranajit Ghosh. (2023). ACS Applied Electronic Materials(5). https://doi.org/10.1021/acsaelm.2c01496 |
| IEEE | [1] Biswajit Das, Sk Riyajuddin, Kaushik Ghosh, and Ranajit Ghosh, ACS Applied Electronic Materials, no. 5, 2023, doi: 10.1021/acsaelm.2c01496. keywords: {layered Bi2Se3 NH3 sensing room temperature physisorption p−n heterojunction} |
