A highly efficient room-temperature NO2 gas sensor based on three-dimensional core–shell structured CoS2 bridged Co3O4@MoS2.

In recent years, two-dimensional transition metal dihalides have emerged as a subject of growing research interest in the field of gas sensing. This heightened attention can be attributed to their notable characteristics of high surface area ratios, customizable electronic properties of the layers, and a wide range of catalytic capabilities. These unique features make them promising candidates for gas sensing applications and warrant further investigation and exploration in this area. Practical applications of the original TMD (MoS2) gas sensors are limited by their poor gas sensing performance at room temperature (RT), including less-than-full recovery, long response times, and low response speeds. Addressing these challenges is crucial for improving their real-world usability. In this study, we synthesized three-component heterojunctions (Co3O4–CoS2@MoS2) with a controlled morphology and composition using different mass ratios of raw materials. The Co3O4–CoS2@MoS2-2 gas sensor demonstrated exceptional sensitivity to NO2 gas (Ra/Rg = 39.6 in 100 ppm) at room temperature, achieving an ultra-fast response time of merely 3.4 seconds in ambient air. This sensing behavior first benefits from Co3O4's high specific surface area and abundant oxygen vacancy concentration. The second is the synergistic effect of the heterogeneous structure between MoS2 and Co3O4. And finally, the electron holding capacity of the S atom in CoS2. The synergistic effect of the three factors promotes the gas-sensing performance of the sensor. The results we obtained show that this approach is viable to improve the sensing performance of metal oxides under RT conditions and can also be scaled up to include other 2D transition metal dihalide-based materials. [ABSTRACT FROM AUTHOR]