MIL-125(Ti)-derived COOH functionalized TiO2 grafted molecularly imprinted polymers for photoelectrochemical sensing of ofloxacin

光电流 分子印迹聚合物 材料科学 检出限 表面改性 煅烧 化学工程 聚合物 氧氟沙星 选择性 纳米技术 化学 光电子学 有机化学 色谱法 催化作用 复合材料 抗生素 工程类 生物化学 环丙沙星
作者
Zheng Zhang,Lili Huang,Shuangchao Sheng,Caiyun Jiang,Yuping Wang
出处
期刊:Sensors and Actuators B-chemical [Elsevier BV]
卷期号:343: 130119-130119 被引量:61
标识
DOI:10.1016/j.snb.2021.130119
摘要

In this study, a molecularly imprinted polymers-assisted photoelectrochemical (MIPs-PEC) sensor was fabricated for the ultrasensitive detection of ofloxacin based on MIL-125(Ti)-derived COOH functionalized TiO2 grafted MIPs as the PEC signal probe. The COOH functionalized TiO2 (TiO2-C) with excellent conductivity, light absorption capacity and photoelectric conversion rate was obtained through one-step calcination of metal-organic framework (MIL-125(Ti)). It was worth mentioning that the photocurrent response signal of TiO2-C was much larger than that of MIL-125(Ti). Meanwhile, benefiting from the large specific surface area and abundant functional groups of cake-like TiO2-C, the grafting of MIPs as a recognition element becomes more convenient and robust. The [email protected]2-C with a large number of binding sites also had precise electron transfer channels due to the template molecules in the MIPs grafted TiO2-C were removed by photodesorption. Furthermore, this strategy of MIPs modification greatly promoted the selectivity and sensitivity of the established PEC sensor. Under optimal conditions, the [email protected]2-C/ITO PEC sensor had a good linear relationship with the OFL concentration in the range of 0.01–3000 ng mL−1, and the detection limit was calculated as 2.91 ng mL−1 (S/N = 3). Moreover, the prepared MIPs-PEC sensor exhibited excellent stability, interference resistance and practicability in real water samples. This work provided a new vision for the design of photoactive materials in PEC sensors and the monitoring of other pollutants in the environment.
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