Abstract
Excess consumption of fluoride through drinking water and its detrimental effects on human health have been a serious global concern. Therefore, frequent monitoring as well as quantitative determination of fluoride ion (F-) concentration in aqueous media is of vital importance. Herein, we have developed a facile and highly sensitive spectroscopic technique for selective detection of F- in aqueous media using aluminium phthalocyanine chloride (AlPc-Cl) as a sensor. The absorbance as well as steady-state fluorescence intensity of AlPc-Cl has been found to decrease in presence of F- which has been used as a marker for the determination of fluoride ion concentration in water. The structural change in AlPc-Cl after addition of F- has been thoroughly studied by using 19F NMR (Nuclear Magnetic Resonance) spectroscopy. Our detailed steady-state as well as time-resolved fluorescence studies reveal that the quenching mechanism is static in nature due to ground state complexation in between F- and AlPc-Cl molecules. The response of the sensor is found to be linear over the F- concentration regime from 0 to 6 parts per million (ppm) with a detection limit of 0.05 ppm. Additionally, it shows an excellent selectivity as well as an insignificant change in sensitivity even in the presence of interfering iron and aluminium ions. Based on the detailed photophysical study, we have further developed a low cost and portable prototype device which shows an excellent sensitivity with the detection limit of 0.10 ppm. This prototype device has a high prospect for real-time monitoring of fluoride ion concentration especially in remote areas.