Ultrafast activation of peroxymonosulfate by single atom cobalt anchored on N-doped two-dimensional Ti3C2Tx MXene for organic pollutant degradation

Supported single-atom catalysts (SACs) have attracted great attention for organic pollutant degradation due to their exceptional catalytic activity and atomic utilization. In this work, we synthesized single Co atoms anchored on nitrogen-doped Ti 3 C 2 T x MXene (Co-N-Ti 3 C 2 T x ), leveraging its unique layered structure to create a nanoscale confinement environment that enhances catalytic performance. This spatial confinement, synergistically combined with nitrogen-induced electronic modulation, significantly promotes peroxymonosulfate (PMS) activation and accelerates electron transfer, resulting in ultrafast degradation of enrofloxacin (ENR). The Co-N-Ti 3 C 2 T x /PMS system exhibits catalytic activity 2.4 times higher than pristine Co-Ti 3 C 2 T x and outperforms previously reported catalysts for PMS-driven ENR removal. The quenching experiments, electron spin resonance (EPR) detection and electrochemical studies demonstrated that SO 4 •− and 1 O 2 are two main reactive species with electron transfer as the dominant reaction. First-principle calculations indicate that the introduction of N can enhance the PMS adsorption and promote the enrichment and supply of electrons to produce reactive species. Further, this catalyst also demonstrates outstanding durability after multiple cycles toward various organic pollutants. This study highlights the critical role of nanoscale confinement coupled with electronic tuning in single-atom catalysis, providing valuable insights for designing high-performance advanced oxidation systems to water purification. • Synergistic confinement and N modulation accelerate interfacial electron transfer. • Nitrogen doping enhances PMS adsorption and 1 O 2 reactive species generation. • Co-N-Ti 3 C 2 T x /PMS exhibits catalytic activity 2.4 times higher than Co-Ti 3 C 2 T x . • Outstanding durability after multiple cycles toward various organic pollutants

Authors

Institutions

Publication Details

Journal
Applied Catalysis B: Environmental
Published
2026-04-23
DOI
https://doi.org/10.1016/j.apcatb.2026.126854
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ultrafast activation of peroxymonosulfate by single atom cobalt anchored on N-doped two-dimensional Ti3C2Tx MXene for organic pollutant degradation

Shuangyou Bao, WeiWei Yang, Zongsu Wei, Kai Li et al.
Applied Catalysis B: Environmental
Advanced oxidation water treatment
article

Ultrafast activation of peroxymonosulfate by single atom cobalt anchored on N-doped two-dimensional Ti3C2Tx MXene for organic pollutant degradation

Shuangyou Bao, WeiWei Yang, Zongsu Wei, Kai Li, Yingjun Wang, Yongsheng Yu
article en

Abstract

Supported single-atom catalysts (SACs) have attracted great attention for organic pollutant degradation due to their exceptional catalytic activity and atomic utilization. In this work, we synthesized single Co atoms anchored on nitrogen-doped Ti 3 C 2 T x MXene (Co-N-Ti 3 C 2 T x ), leveraging its unique layered structure to create a nanoscale confinement environment that enhances catalytic performance. This spatial confinement, synergistically combined with nitrogen-induced electronic modulation, significantly promotes peroxymonosulfate (PMS) activation and accelerates electron transfer, resulting in ultrafast degradation of enrofloxacin (ENR). The Co-N-Ti 3 C 2 T x /PMS system exhibits catalytic activity 2.4 times higher than pristine Co-Ti 3 C 2 T x and outperforms previously reported catalysts for PMS-driven ENR removal. The quenching experiments, electron spin resonance (EPR) detection and electrochemical studies demonstrated that SO 4 •− and 1 O 2 are two main reactive species with electron transfer as the dominant reaction. First-principle calculations indicate that the introduction of N can enhance the PMS adsorption and promote the enrichment and supply of electrons to produce reactive species. Further, this catalyst also demonstrates outstanding durability after multiple cycles toward various organic pollutants. This study highlights the critical role of nanoscale confinement coupled with electronic tuning in single-atom catalysis, providing valuable insights for designing high-performance advanced oxidation systems to water purification. • Synergistic confinement and N modulation accelerate interfacial electron transfer. • Nitrogen doping enhances PMS adsorption and 1 O 2 reactive species generation. • Co-N-Ti 3 C 2 T x /PMS exhibits catalytic activity 2.4 times higher than Co-Ti 3 C 2 T x . • Outstanding durability after multiple cycles toward various organic pollutants

Applied Catalysis B: EnvironmentalVol. 394
Kunming University of Science and Technology (CN), Aarhus University (DK), Harbin Institute of Technology (CN)
National Natural Science Foundation of China, Aarhus Universitets Forskningsfond, China Scholarship Council, Danmarks Frie Forskningsfond, Natural Science Foundation of Heilongjiang Province, Novo Nordisk Fonden, Poul Due Jensens Fond
Openalex Percentile: Top 17%
Advanced oxidation water treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.