Weiqing Zhu1, Juanjuan Gao1, Haiou Song2, Xuezhen Lin1, Shupeng Zhang1. 1. School of Chemical Engineering , Nanjing University of Science and Technology , Nanjing 210094 , P. R. China. 2. School of Environment , Nanjing Normal University , Nanjing 210097 , P. R. China.
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-Ox 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-Ox 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.
N-doped an class="Chemical">graphene (NG), n class="Chemical">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-Ox 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-Ox 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.
Entities:
Keywords:
N, S-co-doped graphene; aniline; nitrobenzene; p-phenylenediamine; sensor; synergistic effect