Nitrogen-doped
graphitic biochar (NBC) has boosted the development
of nonradical peroxymonosulfate (PMS) activation in environmental
remediation. However, the specific role of nitrogen species played
in NBC-based nonradical carbocatalysis remains vaguely interpreted.
To pinpoint the critical nitrogen speciation, a sophisticated thermo-mechanochemical
manipulation was exploited to prepare a series of NBCs with similar
dimensional structures and oxygen levels but different nitrogen species
(i.e., dopants and vacancies). Different
from conventional perspectives, nonradical NBC-based carbocatalysis
was found to be preferably determined by the nitrogen vacancies more
than their parent nitrogen dopants. Raman depth analysis evidenced
that a complete transformation of nitrogen dopants into nitrogen vacancies
could be achieved at 800 °C, where an excellent nonradical abatement
of 4-chlorophenol (4-CH, 90.9% removal) was found for the NBC800 with
a low PMS consumption (1.24 mM). According to PMS adsorption experiments,
nitrogen vacancies exhibited the highest affinity toward the PMS molecules
compared to nitrogen dopants, which accounted for the superior carbocatalysis.
Electron paramagnetic resonance and Raman spectroscopic analyses indicated
that the original PMS molecules were bound to positively charged nitrogen
vacancies, and a robust metastable complex (*HSO5
–) evolved subsequently via hydrogen abstraction
by adjacent persistent free radicals. In situ Raman
techniques could be adopted to estimate the level of nitrogen vacancies
associated with the polarization of electron distribution. The flexible
feature and practical prospects of nitrogen vacancy-based carbocatalysis
were also observed in the remediation of simulated phenolic industrial
wastewater. Overall, this study unravels the dilemma in the current
NBC-based nonradical carbocatalysis and advances our understanding
of nitrogen doping technology for next-generation biochar design.
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