High-efficiency CO₂ conversion via mechano-driven dynamic strain engineering of ZnO nanostructures

Strain engineering involves intentionally inducing lattice distortion in materials to manipulate their electronic and geometric properties, along with the accompanying bond strength between reactants and catalysts. This approach presents an appealing pathway to optimize catalytic performance. However, it confronts challenges in achieving precise control, scalability and controllable modulation of intermediate species' adsorption and desorption. Herein, we report a dynamic strain engineering method achieved through ultrasonic cavitation-induced high and low-pressure cycles, enabling periodically adjustable adsorption/desorption properties while bypassing complex synthesis procedures. Illustrated using ZnO and CO2 piezo-reduction reaction as a demonstration, theoretical studies initially predict that adsorption of intermediates *COOH can be regulated within a specific range of strains. Under ultrasonic stimulation, ZnO catalyst with dynamic strain engineering exhibits a CO yield of similar to 98.8 mu mol center dot g(-1)center dot h(-1), approximately 16.5 times higher than that achieved under ultraviolet light irradiation without dynamic strain engineering, despite the latter having a considerably stronger input power. Furthermore, we delve into the factors linked to dynamic strain amplitude and frequency. This dynamic strain engineering approach streamlines catalyst preparation and presents innovative possibilities for controlled manipulation of intermediate specie's adsorption/desorption, with potential applications across a wide range of catalytic systems