A dual-mode sensing platform coupling two-signal ratiometric and colorimetric methods for detecting Au3+ based on surface state-regulated carbon nanodot.

The considerable risk posed by Au3+ residues to the environment and human health has sparked interest in researching Au3+ monitoring techniques. The detection results in the usual ratio mode are more reliable. In this work, we develop a dual-mode strategy based on reducing carbon dots coupling with two-signal ratiometric and colorimetric methods for high-sensitivity, good-selectivity, and wide-range detection of Au3+. Cyan carbon dots (C-CDs) were synthesized by a simple and efficient one-step hydrothermal method. The C-CDs with rich amino group used m-phenylenediamine as carbon source, which made it have the potential as a reducing agent. After the addition of Au3+, Au3+ was reduced to Au0, generating stable gold nanoparticles (AuNPs). The fluorescence signal (F490) of C-CDs decreased. At the same time, the large size of AuNPs enhances the second-order scattering signal (S770) and produces the UV-visible absorption peak of AuNPs. Therefore, the dual-mode sensing strategy combining S770/F490 ratiometric and colorimetric detection of Au3+ is realized with high accuracy and sensitivity. Au3+ was determined in real samples and a good recovery was obtained. The dual-mode method has good performance and practicality, so it shows great potential for environment testing in a simple and reliable way.

An intelligent "chemical tongue" for high-order monitoring ATP-related physiological phosphates and ATP hydrolysis through diverse transduction principles.

For discriminating diverse analytes and monitoring a specific chemical reaction, the emerging multi-channel "chemical nose/tongue" is challenging multi-material "chemical nose/tongue". The former contributes greatly to integrating different transduction principles from a single sensing material, avoiding the need for complex design, high cost, and tedious operation involved with the latter. Therefore, this high-order sensing puts a particular emphasis on the effects of encapsulation. Herein, the plasmonic gold nanoparticles (Au NPs) are encapsulated as a core into the fluorescent guanine monophosphate-Tb3+ infinite coordination polymer nanoparticles (GMP-Tb ICPs) to obtain a core-shell nanocomposite named Au NPs@GMP-Tb ICPs. Hence, a dual-channel "chemical tongue" based on Au NPs@GMP-Tb ICPs is present to realize high-order sensing of adenosine triphosphate (ATP)-related physiological phosphates and the monitoring of ATP hydrolysis. Considering the affinity of Tb3+ towards P-O bonds, four inorganic phosphates and three nucleotide phosphates with different phosphate group numbers and steric hindrance effect directly regulate two stimulus responses (fluorescence intensity and UV-vis absorbance) of Au NPs@GMP-Tb ICPs. Robust statistical methods, such as linear discriminant analysis and hierarchical cluster analysis, are used to recognize each phosphate by the developed sensor array either in the aqueous solution or in complex media such as serum, together with efficiently monitored ATP hydrolysis at different intervals. These findings and blind test clarify that the designed "chemical tongue" guarantees interference resistance and strengthens analytical capacity, together with offering valuable insight into "lab-on-a-nanoparticle" development for monitoring specific chemical reactions.

Construction of an effective ratiometric fluorescent sensing platform for specific and visual detection of mercury ions based on target-triggered the inhibition on inner filter effect.

Sensitive and selective determination of mercury ion (Hg2+) is critical for human health and environmental monitoring. Herein we construct an effective ratiometric fluorescent sensing platform by combining green fluorescent polymer carbon dots (PCDs) and red fluorescent tetraphenylporphyrin tetrasulfonic acid hydrate (TPPS) for specific and visual detection of Hg2+. The fluorescence of PCDs can be quenched by TPPS through inner filter effect (IEF). In the presence of both Mn2+ and Hg2+, however, Hg2+ can expedite the complexation of TPPS and Mn2+, which causes the decrease in both fluorescence and absorption of TPPS, accompanied by the fluorescence recovery of PCDs due to the subdued IFE between TPPS and PCDs. Based on the change of fluorescence signal, a ratiometric fluorescent sensing platform is constructed for specific and visual detection of Hg2+. The proposed approach presents a fine linear range for Hg2+ over the range of 10-200 nM with a detection limit of 0.038 nM. Moreover, an easily distinguishable fluorescence color change from pink to green with the increase of Hg2+ concentration can be observed by the naked eye under a UV lamp. Such a simple and effective method shows great potential for visual sensing of Hg2+ in on-site and resource-limited settings.