钴
氮化碳
光催化
材料科学
原位
耐火材料(行星科学)
配体(生物化学)
催化作用
氮化物
齿合度
光化学
碳纤维
降级(电信)
化学工程
化学
无机化学
纳米技术
金属
有机化学
冶金
复合材料
受体
工程类
复合数
电信
生物化学
图层(电子)
计算机科学
作者
Yang Yang,Guangming Zeng,Danlian Huang,Chen Zhang,Donghui He,Chengyun Zhou,Wenjun Wang,Weiping Xiong,Biao Song,Huan Yi,Shujing Ye,Xiaoya Ren
出处
期刊:Small
[Wiley]
日期:2020-06-22
卷期号:16 (29)
被引量:301
标识
DOI:10.1002/smll.202001634
摘要
Abstract Semiconductor photocatalysis is a promising technology to tackle refractory antibiotics contamination in water. Herein, a facile in situ growth strategy is developed to implant single‐atom cobalt in polymeric carbon nitride (pCN) via the bidentate ligand for efficient photocatalytic degradation of oxytetracycline (OTC). The atomic characterizations indicate that single‐atom cobalt is successfully anchored on pCN by covalently forming the CoO bond and CoN bond, which will strengthen the interaction between single‐atom cobalt and pCN. This single‐atom cobalt can efficiently expand optical absorption, increase electron density, facilitate charge separation and transfer, and promote OTC degradation. As the optimal sample, Co(1.28%)pCN presents an outstanding apparent rate constant for OTC degradation (0.038 min −1 ) under visible light irradiation, which is about 3.7 times than that of the pristine pCN. The electron spin resonance (ESR) tests and reactive species trapping experiments demonstrate that the 1 O 2 , h + , •O 2 − , and •OH are responsible for OTC degradation. This work develops a new way to construct single‐atom‐modified pCN and provides a green and highly efficient strategy for refractory antibiotics removal.
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