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
线性范围
氧氟沙星
电子转移
选择性
纳米技术
吸收(声学)
分子
嫁接
比表面积
卟啉
信号(编程语言)
光电传感器
组合化学
反应速率常数
生物传感器
分子印迹
核化学
光催化
化学
作者
Zheng Zhang,Lili Huang,Shuangchao Sheng,Caiyun Jiang,Yuping Wang
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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