Multifunctional Ni(OH)2/Ag composites for ultrasensitive SERS detection and efficient photocatalytic degradation of ciprofloxacin and methylene blue

被引:25
|
作者
Wen, Xiaojun [1 ]
Cheng, Huan [1 ]
Zhang, Weilong [1 ]
You, Lijun [2 ]
Li, Jumei [1 ]
机构
[1] Wuhan Inst Technol, Sch Chem & Environm Engn, Key Lab Novel Biomass based Environm & Energy Mat, Wuhan 430205, Peoples R China
[2] Fuzhou Univ, Coll Biol Sci & Engn, Fuzhou 350116, Peoples R China
基金
中国国家自然科学基金;
关键词
SERS; Recyclable sensing; Photocatalytic degradation; In-situ monitoring; Organic pollutants; GRAPHENE OXIDE;
D O I
10.1016/j.talanta.2023.125140
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
To enable the widespread application of surface-enhanced Raman scattering (SERS) technique in practical sensing of organic pollutants, it is essential to develop a reliable SERS substrate that offers both high sensitivity and reusability. In this study, we employed a simple and rapid in-situ deposition method to coat Ag nanoparticles onto flower-like Ni(OH)2 spheres, resulting in the formation of Ni(OH)2/Ag composites with excellent photocatalytic performance and SERS activity. These composites were used as a promising SERS analysis tool for effective detection of organic pollutants, including ciprofloxacin hydrochloride (CIP) and methylene blue (MB). Notably, the composites exhibited outstanding detection limits of 10-8 M for MB and 10-7 M for CIP, respectively, and showed a strong linear relationship between SERS intensities and the logarithmic concentration (R2 & GE; 0.97). Moreover, under simulated sunlight irradiation, the Ni(OH)2/Ag composites efficiently degraded MB and CIP molecules within a short period of 120 min for MB and 130 min for CIP. This demonstrated their practical reusability, as evidenced by their consistent performance over five cycles of SERS sensing. These findings underscore the significant potential of these composites for SERS-based detection of trace pollutants and ecological restoration through photocatalytic reactions in the future.
引用
收藏
页数:11
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