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Updated: Jan 7, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Atom-level tuning of Co single-atom catalysts to regulate the peroxymonosulfate activation pathway for wastewater
Lin Niu1, Qitao Lei1, Zhi Tang1
1State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, PR China.
Abstract:
The precise manipulation of reactive species generation in advanced oxidation processes remains a fundamental challenge in environmental catalysis, primarily due to the elusive structure-activity relationships at the atomic scale. In this study, we systematically synthesized a variety of cobalt-based SACs with precisely tuned nitrogen coordination numbers (Co-N4, Co-N3, and Co-N2), creating a gradient of nitrogen vacancies. This special structure directly modulated the electronic density of cobalt active sites and enhance catalytic performance in peroxymonosulfate (PMS) activation. The Co-N2 catalysts displayed the best catalytic performance with only 0.2 mM PMS, and 95.0 % of sulfathiazole (STZ) was degraded within 40 min followed by Co-N3 (91.0 %) and Co-N4 (75.5 %) catalysts. The kobs values in cobalt-based SACs/PMS systems correlated well (R2 = 0.9952) with N vacancy intensity as well as C chemical state (C-C/C-N/C-O, R2 = 0.9994-0.6829) as well as N chemical state (pyrrolic N/pyridinic N, R2 = 0.7991-0.9990) between the STZ and cobalt-based SACs/PMS systems. Particularly, while Co-N4 primarily facilitated non-radical pathways (1O2), the reduced coordination in Co-N3 and Co-N2 promoted a dual radical/non-radical mechanism, generating sulfate radicals (SO4•-), hydroxyl radicals (•OH), and 1O2 simultaneously. Density functional theory calculations confirm that reduced N-coordination (Co-N2) optimizes charge redistribution (increased the Bader charge transfer from 0.766 to 0.859 e), lengthening the O-O bond (from 1.468 Å to 1.522 Å) in PMS and boosting the contribution of radical active species 15.8-fold versus Co-N4. The Co-N2/PMS system exhibits high activity and strong anti-interference capability against various pollutants, coexisting ions, and natural water matrices. This work provides atomic-level insights into how coordination engineering governs reactive species evolution, offering a new insight for designing high-performance SACs in environmental remediation applications.
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