Probing the Active Nitrogen Species in Nitrogen‐Doped Carbon Nanozymes for Enhanced Oxidase‐Like Activity

Nitrogen doping emerges as a potent approach to enhance the oxidase-like activity of carbon nanozymes. However, the unclear knowledge of the active nitrogen species within nitrogen-doped carbon nanozymes hinders the advancement of high-performance carbon nanozymes. Herein, a group of nitrogen-doped carbon (N/C) nanozymes with controllable nitrogen dopants are successfully synthesized via a dicyandiamide-assisted pyrolysis method. The intrinsic connection between different nitrogen configurations (pyridinic N, pyrrolic N, and graphitic N) in N/C nanozymes and the oxidase-like performance are experimentally investigated. The results confirm pyridinic N is the active nitrogen species in N/C nanozymes for enhanced oxidase-like activity. Theoretical calculations further reveal the potential regulatory mechanism is pyridinic N can increase the local charge density of neighboring carbon atoms and accelerate the adsorption and activation of molecular oxygen. Notably, the optimized N/C nanozyme with the highest pyridinic N ratio presents impressive oxidase-like performance, surpassing most of the previously reported oxidase-like materials. Moreover, the optimized N/C nanozyme exhibits excellent antibacterial properties and can be easily incorporated into common medical and hygiene products to give them spontaneous antibacterial properties. The work will facilitate the rational design of carbon nanozymes with high-performance oxidase-like activity for applications in the antibacterial field.

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Publication Details

Journal
Small
Published
2025-01-16
DOI
https://doi.org/10.1002/smll.202411273
Citations
19
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
9.84

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article

Probing the Active Nitrogen Species in Nitrogen‐Doped Carbon Nanozymes for Enhanced Oxidase‐Like Activity

Shou‐Qing Ni, Yue Pan, Yu Zhang, Lingshuai Kong et al.
19 citations
Small
Advanced Nanomaterials in Catalysis
9.84
article

Probing the Active Nitrogen Species in Nitrogen‐Doped Carbon Nanozymes for Enhanced Oxidase‐Like Activity

Shou‐Qing Ni, Yue Pan, Yu Zhang, Lingshuai Kong, Grzegorz Boczkaj, Yifeng Wang, Yang Liu, Shuang Han, Jinhua Zhan
article en
19 citations

Abstract

Nitrogen doping emerges as a potent approach to enhance the oxidase-like activity of carbon nanozymes. However, the unclear knowledge of the active nitrogen species within nitrogen-doped carbon nanozymes hinders the advancement of high-performance carbon nanozymes. Herein, a group of nitrogen-doped carbon (N/C) nanozymes with controllable nitrogen dopants are successfully synthesized via a dicyandiamide-assisted pyrolysis method. The intrinsic connection between different nitrogen configurations (pyridinic N, pyrrolic N, and graphitic N) in N/C nanozymes and the oxidase-like performance are experimentally investigated. The results confirm pyridinic N is the active nitrogen species in N/C nanozymes for enhanced oxidase-like activity. Theoretical calculations further reveal the potential regulatory mechanism is pyridinic N can increase the local charge density of neighboring carbon atoms and accelerate the adsorption and activation of molecular oxygen. Notably, the optimized N/C nanozyme with the highest pyridinic N ratio presents impressive oxidase-like performance, surpassing most of the previously reported oxidase-like materials. Moreover, the optimized N/C nanozyme exhibits excellent antibacterial properties and can be easily incorporated into common medical and hygiene products to give them spontaneous antibacterial properties. The work will facilitate the rational design of carbon nanozymes with high-performance oxidase-like activity for applications in the antibacterial field.

SmallVol. 21(9)
Shandong University (CN), Gdańsk University of Technology (PL), Korea University (KR), University of Gdańsk (PL)
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province
Openalex Percentile: Top 1%
Advanced Nanomaterials in Catalysis
9.84
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