In this paper, we report on an in-house developed electronic nose (E-nose) for use with breath analysis. The unit consists of an array of 10 micro-electro-mechanical systems (MEMS) metal oxide (MOX) gas sensors produced by seven manufacturers. Breath sampling of end-tidal breath is achieved using a heated sample tube, capable of monitoring sampling-related parameters, such as carbon dioxide (CO2), humidity, and temperature. A simple mobile app was developed to receive real-time data from the device, using Wi-Fi communication. The system has been tested using chemical standards and exhaled breath samples from healthy volunteers, before and after taking a peppermint capsule. Results from chemical testing indicate that we can separate chemical standards (acetone, isopropanol and 1-propanol) and different concentrations of isobutylene. The analysis of exhaled breath samples demonstrate that we can distinguish between pre- and post-consumption of peppermint capsules; area under the curve (AUC): 0.81, sensitivity: 0.83 (0.59–0.96), specificity: 0.72 (0.47–0.90), p-value: <0.001. The functionality of the developed device has been demonstrated with the testing of chemical standards and a simplified breath study using peppermint capsules. It is our intention to deploy this system in a UK hospital in an upcoming breath research study.
In this paper, we report on the development of a highly sensitive and humidity-tolerant metal-oxide-based volatile organic compound (VOC) sensor, capable of rapidly detecting low concentrations of VOCs. For this, we successfully fabricated two different thicknesses of nickel oxide (NiO) sensors using a spin-coating technique and tested them with seven different common VOCs at 40% r.h. The measured film thickness of the spin-coated NiO was ~5 μm (S-5) and ~10 μm (S-10). The fastest response and recovery times for all VOCs were less than 80 s and 120 s, respectively. The highest response (Rg/Ra = 1.5 for 5 ppm ethanol) was observed at 350 °C for both sensors. Sensors were also tested in two different humidity conditions (40% and 90% r.h.). The humidity did not significantly influence the observed sensitivity of the films. Furthermore, S-10 NiO showed only a 3% drift in the baseline resistance between the two humidity conditions, making our sensor humidity-tolerant compared to traditional n-type sensors. Thus, we propose thick-film NiO (10 μm) sensing material as an interesting alternative VOC sensor that is fast and humidity-tolerant.
The development of a fast, stable metal oxide-based VOC sensor for the detection of trace-level ppb concentrations, remains a challenge. Recently, many composite materials have been investigated to try and develop sensors with these characteristics. Here, we report on the development of ZnO/MoO3 heterojunction thick film devices, fabricated by a spin-coating technique, to detect a wide range of VOCs at application relevant ppb level concentrations. For comparison, pristine ZnO and pristine MoO3 devices were also fabricated. Sensors were tested at different temperatures and resulting in an optimum temperature of 380°C. The sensors were tested towards 11 different VOCs at ppb concentrations. Of all the sensors tested, the heterojunction device showed the highest response to VOCs, with the highest sensitivity towards 200 ppb of ethanol (Ra/Rg = 12.84). The results compared well with the pristine materials, with the response of the ZnO material being 6 times smaller and MoO3 10 times smaller compared to their heterojunction counterpart. The response times of the heterojunction device were also faster, at around 30 sec compared with 120 sec for pristine materials.
Enhancing the performance of a chemo-resistive gas sensor is often challenging due to environmental humidity influencing its sensitivity and baseline resistance. One of the most promising ways of overcoming this challenge is through ultraviolet (UV) illumination of the sensing material. Most research has focused on using UV with in-house developed sensors, which has limited their widespread use. In this work, we have evaluated if UV can enhance the performance of commercially available MOX-based gas sensors. The performance of five different MOX sensors has been evaluated, specifically SGX Microtech MiCS6814 (thin-film triple sensor), FIGARO TGS2620 (n-type thick film), and Alphasense VOC sensor (p-type thick film). These sensors were tested towards isobutylene gas under UV light at different wavelengths (UV-278 nm and UV-365 nm) to investigate its effect on humidity, sensitivity, baseline drift, and recovery time of each sensor. We found the response time of thin-film sensors for reducing gases was improved by 70 s under UV- 365 nm at normal operating temperatures. In addition, all the sensors were left in a dirty environment and the humid-gas testing was repeated. However, due to their robust design, the sensitivity and baseline drift of all the sensors remained the same. This indicates that UV has only limited uses with commercial gas sensors.