摘要
Cells have greatly inspired advancements in chemical processes, including leveraging the idea of cascade catalysis to drive thermodynamically unfavorable reactions and mimicking the compartmentalized architecture to design novel nanostructures. Here, a single-particle cascade catalysis promoted gas sensing platform is inspired to be designed (denoted as CoSnO 3 @mCeO 2 ) by positionally assembling n-type mesoporous CeO 2 catalytic shell on p-type CoSnO 3 gas sensitive core. Uniform CoSn(OH) 6 @mCe(OH) x core–shell particles with tailored mesostructures, tunable large mesopores, and adjustable shell thicknesses are first constructed. After thermal treatment, CoSnO 3 @mCeO 2 particles are obtained, which serve as cascade catalysis enhanced sensitive layer for fabricating gas sensors with independent catalytic and sensing control. As a proof-of-concept, the CoSnO 3 @mCeO 2 gas sensors exhibit nearly three times higher acetone sensitivity ( R g /R a = 26.81–50 ppm) than individual CoSnO 3 sensors with an ultralow limit of detection of 5.22 ppb. The enhanced sensitivity is achieved through a tandem catalytic reforming-oxidation sensing procedure, which begins with the primary catalytic reforming of acetone to acetic acid in the mCeO 2 shell, followed by the secondary sensing reaction of acetic acid in the CoSnO 3 core. The design concept of cascade catalysis promotes gas sensor can serve as a paradigm for developing single-particle functional nanodevices for various applications.
危险品化学品经营许可证(带存储)