TY - JOUR
T1 - Nickel Oxide and Nickel Co-doped Graphitic Carbon Nitride Nanocomposites and its Octylphenol Sensing Application
AU - Gong, Wanyun
AU - Zou, Jing
AU - Zhang, Sheng
AU - Zhou, Xin
AU - Jiang, Jizhou
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We would like to thank the National Science Foundation of China (Grant. 21471122) and Wuhan Institute of Technology Graduate Student Education Innovation Fund (CX 2014011) for financial support. The measurements of NiO-Ni-GCN were performed in the Analytical Instrumentation Center of Wuhan Institute of Technology.
PY - 2015/11/16
Y1 - 2015/11/16
N2 - Nickel oxide and nickel co-doped graphitic carbon nitride (NiO-Ni-GCN) nanocomposites were successfully prepared by thermal treatment of melamine and NiCl2 6H2O. NiO-Ni-GCN nanocomposites showed superior electrochemical catalytic activity for the oxidation of octylphenol to pure GCN. A detection method of octylphenol in environmental water samples was developed based at NiO-Ni-GCN nanocomposites modified electrode under infrared light irradiation. Differential pulse voltammetry was used as the analytic technique of octylphenol, exhibiting stable and specific concentration-dependent oxidation signal in the presence of octylphenol in the range of 10nM to 1μM and 1μM to 50μM, with a detection limit of 3.3nM (3S/N). © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
AB - Nickel oxide and nickel co-doped graphitic carbon nitride (NiO-Ni-GCN) nanocomposites were successfully prepared by thermal treatment of melamine and NiCl2 6H2O. NiO-Ni-GCN nanocomposites showed superior electrochemical catalytic activity for the oxidation of octylphenol to pure GCN. A detection method of octylphenol in environmental water samples was developed based at NiO-Ni-GCN nanocomposites modified electrode under infrared light irradiation. Differential pulse voltammetry was used as the analytic technique of octylphenol, exhibiting stable and specific concentration-dependent oxidation signal in the presence of octylphenol in the range of 10nM to 1μM and 1μM to 50μM, with a detection limit of 3.3nM (3S/N). © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
UR - http://hdl.handle.net/10754/621565
UR - http://onlinelibrary.wiley.com/doi/10.1002/elan.201500491/full
UR - http://www.scopus.com/inward/record.url?scp=84954157686&partnerID=8YFLogxK
U2 - 10.1002/elan.201500491
DO - 10.1002/elan.201500491
M3 - Article
SN - 1040-0397
VL - 28
SP - 227
EP - 234
JO - Electroanalysis
JF - Electroanalysis
IS - 1
ER -