Y.H. Cai, Yong Zhang, Jilong Zheng, Rongyang Kou, Zhida Gao, Yanyan Song, Chenxi Zhao
Two-dimensional (2D) metal oxide semiconductor-based gas sensors usually suffer from limited sensitivity and sluggish recovery at ppb levels due to the intrinsic interlayer restacking and poor out-of-plane charge transport. Herein, TiO 2 nanotubular arrays (NTAs) acting as a scaffold were applied to grown 2D highly dispersed curved BiOBr nanosheets to form heterojunctions, thereby achieving full surface utilization in gaseous sensing reactions. Positron annihilation lifetime spectroscopy verified the presence of three types of defects (V O, V Br, and V BrBiBr ) in the as-formed BiOBr nanosheets; Monte Carlo simulations further revealed that these curved nanosheets exhibited a substantially increased target collision frequency and higher adsorption probability compared to planar structures. Using gaseous NO 2 molecules as the model target, the interface−defect−morphology synergistic effect enabled the resulting BiOBr/TiO 2 NTA composite to exhibit high activity in NO 2 sensing reactions even at room temperature, with a detection linear range from 1 ppb to 10 ppm (LOD = 0.12 ppb), sensitive response, excellent selectivity, satisfactory humidity tolerance, and superior operational stability (>60 days). In situ Raman analysis demonstrated that vacancy-mediated NO 2 adsorption contributed to the excellent sensing performance, which was further confirmed by strong NO 2 adsorption energy (−2.553 eV) and midgap defect state-triggered efficient charge transfer. This work not only provides an effective route for designing gas sensing materials but also paves a new way for preparing 2D materials with abundant active surfaces for catalytic applications.