In situ growth of CoFe-prussian blue analog nanospheres on ferrocene-functionalized ultrathin layered Ti3C2Tx MXene frameworks for efficient detection of xanthine

被引:38
作者
Chu, Mingyue [1 ]
Wang, Ying [1 ]
Xin, Jianjiao [1 ,2 ]
Zhang, Li [2 ]
Liu, Yikun [1 ]
Yang, Guixin [1 ]
Ma, Huiyuan [1 ]
Wang, Yingji [3 ]
Pang, Haijun [1 ]
Wang, Xinming [1 ]
机构
[1] Harbin Univ Sci & Technol, Sch Mat Sci & Chem Engn, Harbin 150040, Peoples R China
[2] Qiqihar Univ, Coll Mat Sci & Engn, Qiqihar 161006, Peoples R China
[3] Harbin Med Univ, Coll Pharm, Harbin 150081, Peoples R China
基金
中国国家自然科学基金;
关键词
Prussian blue analogues; Ferrocene; Xanthine; Electrochemical sensor; Ti3C2Tx MXene; ELECTROCHEMICAL SENSOR; URIC-ACID; ELECTRON-TRANSFER; ASCORBIC-ACID; CARBON NANOTUBES; DOPAMINE; POLYMER; ANODE; NANOCOMPOSITE; ACETAMINOPHEN;
D O I
10.1016/j.cej.2023.143866
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A funky electrochemical sensor for xanthine catching was proposed by growing CoFe-Prussian blue analogs (CoFe-PBA) in situ on ferrocene functionalized Ti3C2Tx MXene (Fc-Ti3C2Tx), denoted as CoFe-PBA/Fc-Ti3C2Tx. In this sensor, introduction of unique thin-layer structure Ti3C2Tx MXene as the interlayer spacers to accommodate ferrocene and CoFe-PBA prevented the restacking of MXene and CoFe-PBA, meanwhile gained higher conductivity. The CoFe-PBA/Fc-Ti3C2Tx was observed by SEM and TEM to possess abundant heteroatom-functionalized multiple-layers structure, and it was therefore endowed with a faster electron transfer rate and a greater electrochemically active surface area. Furthermore, the sensor was investigated using differential pulse voltammetr (DPV) and superiorelectrochemical sensing performance for xanthine detection was achieved with rather wide linear range (3 x 10-8 to 1.007 x 10-3 M), a remarkably low detection limit (0.002 & mu;M), and superior stability. The recovery rate of real sample analysis was acceptable, demonstrating the viability of using this electrochemical sensor in real applications.
引用
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页数:12
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