TY - JOUR
T1 - A Facile One-Pot Synthetic Approach Towards CB@PCN-222(Fe) Composites for Simultaneous Electrochemical Detection of Dihydroxybenzene Isomers
AU - Chen, Wen Yi
AU - Li, Xu Shan
AU - Zou, Xin
AU - Sun, Qian
AU - Gao, En Qing
N1 - Publisher Copyright:
© 2023 The Electrochemical Society (“ECS”). Published on behalf of ECS by IOP Publishing Limited.
PY - 2023
Y1 - 2023
N2 - A novel porphyrin-metal organic frameworks (MOFs) based hybrid composite was created by combining conductive carbon black (CB) and PCN-222(Fe) (PCN = porous coordination network) via a one-pot strategy. The proposed material unquestionably takes advantage of the high specific area from MOFs and the strong conductivity of CB, which contributes to the contact with analytes and detection sensitivity. A series of analyses showed that the proposed modified electrode could be an alternative candidate for electrochemical detection of dihydroxybenzene isomers. A good linear correlation occurred between the differential pulse voltammetry current and the concentration of hydroquinone (HQ), catechol (CC) and resorcinol (RC) under the optimized conditions. With low detection limits (0.122, 0.094 and 0.243 μM) at the ranges (0.5-280, 0.5-280 and 0.5-320 μM) of these isomers mentioned above, the sensor exhibited good cost-effectiveness, repeatability and stability. Our methodology drives us to directly analyze the dihydroxybenzene isomers in actual samples with dependable recovery, further broadening the electrochemical detection field for environmental pollutants based on porphyrin MOFs.
AB - A novel porphyrin-metal organic frameworks (MOFs) based hybrid composite was created by combining conductive carbon black (CB) and PCN-222(Fe) (PCN = porous coordination network) via a one-pot strategy. The proposed material unquestionably takes advantage of the high specific area from MOFs and the strong conductivity of CB, which contributes to the contact with analytes and detection sensitivity. A series of analyses showed that the proposed modified electrode could be an alternative candidate for electrochemical detection of dihydroxybenzene isomers. A good linear correlation occurred between the differential pulse voltammetry current and the concentration of hydroquinone (HQ), catechol (CC) and resorcinol (RC) under the optimized conditions. With low detection limits (0.122, 0.094 and 0.243 μM) at the ranges (0.5-280, 0.5-280 and 0.5-320 μM) of these isomers mentioned above, the sensor exhibited good cost-effectiveness, repeatability and stability. Our methodology drives us to directly analyze the dihydroxybenzene isomers in actual samples with dependable recovery, further broadening the electrochemical detection field for environmental pollutants based on porphyrin MOFs.
UR - https://www.scopus.com/pages/publications/85180009278
U2 - 10.1149/1945-7111/ad0ea1
DO - 10.1149/1945-7111/ad0ea1
M3 - 文章
AN - SCOPUS:85180009278
SN - 0013-4651
VL - 170
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 12
M1 - 127501
ER -