ZIF-8 derived Fe‒N coordination moieties anchored carbon nanocubes for efficient peroxymonosulfate activation via non-radical pathways: Role of FeNx sites

Developing high-efficient hybrids carbon catalysts for PMS-based advanced oxidation process (AOPs) are crucial in the field of environmental remediation. In this work, novel carbon nanocubes (xFe‒N‒C) with three-dimensional porous structure and abundant well-dispersed FeN x sites were obtained via a skillful cage-encapsulated-precursor pyrolysis strategy. The as-synthesized xFe‒N‒C exhibited superb activity for phenol degradation by activating peroxymonosulfate (PMS). Besides, the catalytic system not only possessed good recycling performance, wide pH adaptation and relatively low activation energy, but also had high resistance to environmental interference. Singlet oxygen ( 1 O 2 ) dominated non-radical process was responsible for phenol degradation rather than traditional radical pathways. Impressively, the doping level of Fe could regulate FeN x contents in catalysts, and the catalytic activity of xFe‒N‒C was greatly enhanced with increasing FeN x contents. Based on density functional theory calculations (DFT), the introduction of FeN x sites regulated the electronic structure of catalysts. Such electron-deficient Fe center acted as electron acceptor to receive electrons transmitted by the adsorbed PMS , thus generating highly reactive 1 O 2 for rapid phenol oxidation. This work provides a new insight into the innovation in transition metal-nitrogen hybrid carbon catalysts and highlights the pivotal roles of FeN x sites in 1 O 2 generation during PMS activation process.