Abstract

Increasing attention has been focused in the area of multi-mode sensing method for on-site application to avoid the false positive results and enhance the accuracy label measurements. This article reports the synthesis of bright red fluorescent amphiphilic carbon dots (C-dots) as dualphase fluorescent nanosensor for selective detection of As3+ in water. One-pot solvothermal approach was chosen for the C-dots synthesis with a maximum fluorescence quantum yield of 47%. Bright red fluorescence of the C-dots was selectively weakened upon the treatment with As3+, although the other competing ions showed infectivity. Static quenching was proved behind this fluorescence attenuation by absorbance and time-resolved fluorescence spectroscopy. The amphiphilicity of synthesized C-dots has been utilized to detect As3+ in both liquid and solid phase. Aqueous dispersion of C-dots showed a dramatic fluorescence quenching efficiency of maximum 80%. To fabricate solid phase sensor, C-dots were successfully coated and absorbed on silica beads and cotton buds. These fluorescent solid matrices also displayed a relative good quenching efficiency (70–80%) towards As3+ without any leaching out of the C-dots from the solid surface. In addition, these C-dots showed an adequate potentiality to detect this ion in real water sample analysis. These findings would enable a great potentiality in the environmental water contaminants sensing technology.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.