A copper-based metal-organic framework decorated with electrodeposited Fe2O3 nanoparticles for electrochemical nitrite sensing

被引:23
作者
Amali, R. K. A. [1 ,2 ,3 ]
Lim, H. N. [1 ,2 ,3 ]
Ibrahim, I. [1 ,2 ,3 ]
Zainal, Z. [3 ]
Ahmad, S. A. A. [3 ]
机构
[1] Univ Putra Malaysia, Inst Nanosci & Nanotechnol, Foundry Reticular Mat Sustainably Lab, Upm Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Inst Nanosci & Nanotechnol, Funct Nanotechnol Devices Lab, Upm Serdang 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Fac Sci, Dept Chem, Upm Serdang 43400, Selangor, Malaysia
关键词
Copper-based metal-organic framework; Fe2O3; nanoparticle; Electrochemical sensor; Amperometry; Nitrite; REDUCED GRAPHENE OXIDE; TRACE NITRITE; COMPOSITE; PLATFORM; SENSOR;
D O I
10.1007/s00604-022-05450-y
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An amperometric nitrite sensor is reported based on a screen-printed carbon electrode (SPCE) modified with copper(II)-benzene-1,4-dicarboxylate (Cu-BDC) frameworks and iron(III) oxide nanoparticles (Fe2O3 NPs). First, copper(I) oxide (Cu2O) nanocubes were synthesized, followed by a solvothermal reaction between Cu2O and H2BDC to form square plate-like Cu-BDC frameworks. Then, Fe2O3 NPs were electrodeposited on Cu-BDC frameworks using a potentiostatic method. The Fe2O3@Cu-BDC nanocomposite benefits from high conductivity and large active surface area, offering excellent electrocatalytic activity for nitrite oxidation. Under optimal amperometric conditions (0.55 V vs. Ag/AgCl), the sensor has a linear range of 1 to 2000 mu M with a detection limit of 0.074 mu M (S/N = 3) and sensitivity of 220.59 mu A mM(-1) cm(-2). The sensor also provides good selectivity and reproducibility (RSD = 1.91%, n = 5). Furthermore, the sensor exhibits long-term stability, retaining 91.4% of its original current after 4 weeks of storage at room temperature. Finally, assessing nitrite in tap and mineral water samples revealed that the Fe2O3@Cu-BDC/SPCE has a promising prospect in amperometric nitrite detection.
引用
收藏
页数:10
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