催化作用
化学
钴
电子转移
X射线吸收光谱法
Atom(片上系统)
光化学
木质素
降级(电信)
吸收光谱法
无机化学
有机化学
物理
电信
嵌入式系统
量子力学
计算机科学
作者
Yuanfeng Qi,Jing Li,Yanqing Zhang,Qi Cao,Yanmei Si,Zhiren Wu,Muhammad Akram,Xing Xu
标识
DOI:10.1016/j.apcatb.2021.119910
摘要
In this work, a facile one-pot pyrolytic strategy was employed to fabricate a nitrogen coordinated Co single-atom catalyst (SA Co-N/C catalyst) by using lignin as carbon sources. The HAADF-STEM images and X-ray absorption spectra (XAS) analysis showed the isolated Co atoms less than 2 Å throughout the entire SA Co-N/C architecture. Results showed that the single-atom Co sites served as the main active sites for naproxen (NPX) degradation via peroxymonosulfate (PMS) activation. This was confirmed by the high positive correlation (R2 = 0.9675) between the rate constants and Co amounts in all SA Co-N/C catalysts. In particular, the as-prepared SA Co-N/C catalyst with a very small Co loading (2.45 wt.%) exhibited exceptional high turnover frequency (TOF) value for NPX (4.82 min−1), which is promising for the potential application prospect. Electron transfer was induced by the single-atom Co sites, which was the dominated mechanism for the NPX degradation.
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