催化作用
过硫酸盐
活动站点
光化学
拉曼光谱
化学
密度泛函理论
吸收光谱法
光谱学
金属有机骨架
材料科学
化学工程
计算化学
有机化学
物理
量子力学
光学
工程类
吸附
作者
Dongpeng Zhang,Yanxiao Li,Pengfei Wang,Jinyong Qu,Yi Li,Sihui Zhan
标识
DOI:10.1038/s41467-023-39228-4
摘要
In heterogeneous catalysis, uncovering the dynamic evolution of active sites in the working conditions is crucial to realizing increased activity and enhanced stability of catalyst in Fenton-like activation. Herein, we capture the dynamic changes in the unit cell of Co/La-SrTiO3 catalyst during the exemplary peroxymonosulfate activation process using X-ray absorption spectroscopy and in situ Raman spectroscopy, revealing the substrate tuned its structural evolution, which is the reversible stretching vibration of O-Sr-O and Co/Ti-O bonds in different orientations. This process effectively promotes the generation of key SO5* intermediates, which is beneficial to the formation of 1O2 and SO4•- from persulfate on the Co active site. Density functional theory and X-ray absorption spectroscopy show that the optimized structural distortion enhanced the metal-oxygen bond strength by tuning the eg orbitals and increased the number of transferred electrons to peroxymonosulfate by about 3-fold, achieving excellent efficiency and stability in removing organic pollutants.
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