Affiliation:
1. School of Chemistry and Chemical Engineering Anhui University 111 Jiulong Road Hefei 230601 China
2. School of Materials Science and Engineering Anhui University 111 Jiulong Road Hefei 230601 China
Abstract
AbstractOxygen vacancy (Vo), as one of the most common surface defects, significantly influence the physiochemical properties of metal oxides. However, it remains a challenge for existing techniques to visualize the evolution of Vo during redox process due to its heterogeneous distribution, small size, and dynamic nature. Herein, the real‐time monitoring of such microscopic interfacial events is reported by advantage of the high‐contrast fluorescence response of carbon dots (H‐CDs) to Vo. The green emissive H‐CDs possess a unique disc‐shaped structure and exceptional hydrophilicity, allowing their tight adhesion to the surfaces of Vo‐rich MgO by simple mixing. Subsequently, a water involved interfacial reaction occurred between H‐CDs and Vo, resulting in gradual quenching of the original green emission and simultaneously emergence of bright red fluorescence. Moreover, the spatiotemporal diffusion dynamics and reaction kinetics are investigated by confocal laser scanning microscopy, revealing the time‐dependent reorganization and structural heterogeneity at the interface. The finding provides a new toolbox for in situ imaging of Vo‐triggered phenomena at a microscopic level, which will be helpful in promoting the rational design of oxide materials.
Funder
Key Technologies Research and Development Program
National Natural Science Foundation of China