Transforming Plastics to Single Atom Catalysts for Peroxymonosulfate Activation: Axial Chloride Coordination Intensified Electron Transfer Pathway

S Shiying Ren (School of Chemical Engineering) Y Yantao Wang L Lei Shi (School of Health Management Guangzhou Medical University Guangzhou China) X Xin Xu S Shuang Zhong (School of Chemical Engineering) K Kunsheng Hu H Hongyu Zhou (Department of Gynecology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University) Z Zhong‐Shuai Zhu (School of Chemical Engineering The University of Adelaide Adelaide SA 5005 Australia) P Peng Zhou W Wenjie Tian J Jian Zuo J Jiabao Yi (Department of Chemical Engineering and Interdisciplinary Research Center for Hydrogen Technologies and Carbon Management (IRC‐HTCM) King Fahd University of Petroleum and Minerals Dhahran Kingdom of Saudi Arabia) X Xiaohong Guan (Department of Environmental Science, Institute of Eco-Chongming, School of Ecological and Environmental Sciences) X Xiaoguang Duan S Shaobin Wang

Abstract

AbstractTransforming plastics into single‐atom catalysts is a promising strategy for upcycling waste plastics into value‐added functional materials. Herein, a graphene‐based single‐atom catalyst with atomically dispersed FeN4Cl sites (Fe─N/Cl─C) is produced from high‐density polyethylene wastes via one‐pot catalytic pyrolysis. The Fe─N/Cl─C catalyst exhibited much higher turnover frequency and surface area normalized activity (Kac) compared with the Fe─N─C catalyst without axial Cl modulation. Both experiments and density functional theory (DFT) computations demonstrated that the axial incorporation of chloride fine‐tuned the coordination environment of FeN4 sites and enhanced peroxymonosulfate (PMS) activation because of improved conductivity and modulated spin state. In situ, Raman, and infrared spectroscopic techniques revealed that PMS is activated by the Fe─N/Cl─C catalyst through an electron transfer process. The formation of a key PMS* intermediate at the Fe site effectively elevated the redox capacity of the catalyst surface to realize a fast degradation of diverse pollutants. The non‐radical oxidation manner secures high selectivity toward target pollutants and high chemical utilization efficiency. A continuous operation in a column reactor also demonstrated the high efficiency and stability of the (Fe─N/Cl─C + PMS) system for practical water treatment.

Article Details

Volume / Issue Vol. 37, Issue 8
Published February 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (15)

S

Shiying Ren

School of Chemical Engineering

Y

Yantao Wang

L

Lei Shi

School of Health Management Guangzhou Medical University Guangzhou China

X

Xin Xu

S

Shuang Zhong

School of Chemical Engineering

K

Kunsheng Hu

H

Hongyu Zhou

Department of Gynecology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

Z

Zhong‐Shuai Zhu

School of Chemical Engineering The University of Adelaide Adelaide SA 5005 Australia

P

Peng Zhou

W

Wenjie Tian

J

Jian Zuo

J

Jiabao Yi

Department of Chemical Engineering and Interdisciplinary Research Center for Hydrogen Technologies and Carbon Management (IRC‐HTCM) King Fahd University of Petroleum and Minerals Dhahran Kingdom of Saudi Arabia

X

Xiaohong Guan

Department of Environmental Science, Institute of Eco-Chongming, School of Ecological and Environmental Sciences

X

Xiaoguang Duan

S

Shaobin Wang