化学
检出限
荧光
氧化还原
纳米技术
降级(电信)
氧气
再现性
化学工程
相对标准差
自来水
化学稳定性
氧传感器
原位
催化作用
微球
选择性
组合化学
表面改性
作者
Qimin Zhao,Jiayi Huang,Yongkang Yan,Danhua Ge,Tao Liu,Xiaojun Chen
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-11-20
卷期号:41 (48): 32421-32431
被引量:3
标识
DOI:10.1021/acs.langmuir.5c04201
摘要
Developing light-responsive nanozymes with integrated activity and stability holds significant importance for highly sensitive and accurate sensing in food safety and environmental protection. Herein, we developed a dual-mode (colorimetric and fluorescent) sensor based on an Fe-doped TiO 2 nanosphere for d -penicillamine (D-PA) detection. The unique hollow structure of Fe-TiO 2 provides a large surface area and abundant oxygen vacancies while facilitating rapid Fe(II)/Fe(III) cycling, collectively resulting in enhanced light-responsive peroxidase (POD)-like activity. Under light irradiation, the Fe-TiO 2 promoted the generation of abundant reactive oxygen species, which oxidize TMB to blue oxTMB. Furthermore, the Fukui index and reaction kinetic trials indicated that the detection mechanism was primarily based on the antioxidant effect and redox activity of D-PA. The proposed sensor demonstrated detection limits (LODs) of 0.054 μM (colorimetric) and 0.40 μM (fluorescence), with 92.2–107.4% recovery and relative standard deviation < 4.4% in milk, tap water, and fetal bovine serum, along with outstanding reproducibility and stability. This work provides new insights to synthesize light-responsive nanozymes and integrated multimode sensing platforms.
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