期刊
ACS APPLIED NANO MATERIALS
卷 6, 期 21, 页码 19981-19996出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsanm.3c03777
关键词
platinum; nickel; porous carbon nanosheets; dihydroxybenzene isomers; linear sweep voltammetry; real-time analysis
Ultrathin three-dimensional porous carbon nanosheets derived from Moringa oleifera barks were used as the carbon precursor in this study. Through a simple one-step pyrolysis technique, hierarchical PCN was generated using high temperature pyrolysis and KOH activation. Pt-Ni bimetallic nanoparticles were decorated on the ultrathin 3D PCN using the microwave-solvothermal approach. The Pt-Ni@PCN nanocomposite exhibited excellent electrochemical sensor performance for detecting dihydroxybenzene isomers.
Ultrathin three-dimensional (3D) interconnected porous carbon nanosheets (PCNs) derived from Moringa oleifera barks (commonly known as the drumstick tree) with electrochemical (EC) sensor performance was employed as the carbon precursor. In this study, we described a simple one-step pyrolysis technique to generate hierarchical PCN using a high-temperature pyrolysis and KOH activation procedure. Using the microwave-solvothermal approach, platinum-nickel bimetallic octahedral nanoparticles were decorated on ultrathin 3D PCN (referred to as Pt-Ni@PCN). The morphological, structural, and EC properties of the Pt-Ni@PCN nanocomposite were well characterized. Using cyclic voltammetry and linear sweep voltammetry, the dihydroxybenzene (DHB) isomers hydroquinone, catechol, and resorcinol were identified individually as well as simultaneously. The screen-printed carbon electrode-modified nanocomposite [Pt-Ni@PCN/screen-printed carbon electrode (SPCE)] served as an outstanding electron (e(-))-transfer mediator for DHB isomer oxidation, yielding limits of detection of 0.0093, 0.0263, and 0.0529 mu M, respectively. Also, the Pt-Ni@PCN/SPCE sensor has exceptional selectivity, long-term durability, reproducibility, repeatability, and anti-interference. Furthermore, the proposed sensor can be exploited to detect simultaneously environmental pollutants in river, lake, and tap water samples with good recovery rates.
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