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Nature of the Synergistic Effect of N and S Co-Doped Graphene for the Enhanced Simultaneous Determination of Toxic Pollutants.

Authors :
Zhu W
Gao J
Song H
Lin X
Zhang S
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2019 Nov 27; Vol. 11 (47), pp. 44545-44555. Date of Electronic Publication: 2019 Nov 13.
Publication Year :
2019

Abstract

N-doped graphene (NG), S-doped graphene (SG), and N and S co-doped graphene nanocatalysts with different doping sequences (N-SG and S-NG) are successfully synthesized by a facile low-temperature hydrothermal method. By changing the synthetic sequence, S-NG significantly increases the electron transport rate of the sensor and the electrocatalytic ability compared to NG, SG, and N-SG due to the optimal proportion of doping element content and suitable N- and S-bonding configurations. The origin of the synergistic effect of N and S co-doped graphene is confirmed. Traces of S doping greatly enhance the electrochemical performance. The large volume of S-O <subscript>x</subscript> groups may prevent the analytes from approaching the catalytic sites of the sensing materials due to a steric hindrance effect. S-NG, which possesses less S-O <subscript>x</subscript> groups, exhibits better performance than N-SG. Pyridinic N plays an important role in enhancing the electrochemical activity and conductivity. The simultaneous determination of aniline (AN), p -phenylenediamine (PPD), and nitrobenzene (NB) as typical toxic pollutants is performed by employing the S-NG nanoarchitecture. The detection limits (S/N = 3) for AN, PPD, and NB are 0.023, 0.051, and 0.216 μM, respectively. In addition, the S-NG sensors also have excellent anti-interference, stability, and reproducibility. The precise control and synthesis of multiheteroatoms into graphene represent a promising strategy to enhance the electrocatalytic performance in energy and environmental fields.

Details

Language :
English
ISSN :
1944-8252
Volume :
11
Issue :
47
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
31675208
Full Text :
https://doi.org/10.1021/acsami.9b13211