Mercaptopropionic acid (MPA) capped CdTe quantum dots (QDs) with particle size 3 nm have been successfully synthesized in aqueous medium by hydrothermal synthesis method. And the effects of different metal ions on MPA capped CdTe QDs fluorescence were studied using fluorescence spectrometry. The results demonstrated that at the same concentration level, Ag + could strongly quench CdTe QDs fluorescence, and the other metal ions had little effect on CdTe QDs fluorescence except Cu 2+ . On the basis of this fact, a rapid, simple, highly sensitive and selective method based on fluorescence quenching principle for Ag + detection in aqueous solution was proposed. Under optimal conditions, the quenched fluorescence intensity ( F 0 – F ) increased linearly with the concentration of Ag + ranging from 4 × 10 −7 to 32 × 10 −7 mol L −1 . The limit of detection for Ag + was 4.106 × 10 −8 mol L −1 . The obtained plot of F 0 / F versus [Ag + ] was an upward curvature, concave towards the y -axis, rather than a straight line. The modified form of the Stern–Volmer equation was third order in Ag + concentration. According to the modified Stern–Volmer equation, it can be inferred that dynamic quenching and static quenching simultaneously occurred when Ag + interacted with MPA capped CdTe QDs. At the same time other factors might also influence the quenching process. Based on this study, hydrothermal synthesized MPA capped CdTe QDs with particle size 3 nm may be used as a novel fluorescence probe to quantificationally and selectively detect Ag + .
Yang Huang,Zanyong Zhuang,Xiaogang Xue,Jinsheng Zheng,Zhang Lin
So far, the photoluminescence (PL) properties optimization of mercaptopropionic acid (MPA) capped CdTe has yet to be understood from a perspective of growth kinetics. In this work, the growth kinetics, size distribution and PL properties of CdTe quantum dots (QDs) grown in MPA aqueous solutions of two extreme concentrations, i.e. 0 mM and 50 mM, were systematically investigated. The studies revealed that CdTe QDs coarsen in low and high concentrations of MPA followed different growth kinetics, i.e. a mixed OA (Oriented Attachment)–OR (Ostwald Ripening) growth and an OA dominated growth, respectively. Moreover, the OR growth in a low MPA concentration solution was found to be disadvantageous for narrowing the size distribution but favourable for enhancing fluorescence, while the OA growth in a high MPA concentration solution is beneficial for focusing and controlling the particle size. Further activation energy calculations indicate that the extra MPA that forbids the OR growth and retards the OA growth is favourable for slowing the particle growth, thus achieving CdTe QDs with a controlled size and narrow distribution. Furthermore, the kinetics study reveals how the introduction of concentrated surface ligands affects the PL properties (FWHM and intensity) of the material.
The topic of intermolecular interactions enhancing electron tunneling between protein residues on biofilm surface has been investigated by some theoretical studies. However, few of experimental studies could confirm this viewpoint. In this work, the Mercaptopropionic acid self-assembled monolayer (MPA SAM) with terminal carboxyl groups was constructed, as a simplified model for functionalized biomimic membrane. The electron tunneling rate constant of ferrocenylmethanol redox process on SAM was obtained from experimental results of scanning electrochemical microscopy . It is found that the electron tunneling across MPA SAM is faster than that of contrastive Methyl mercaptopropionate SAM. This result is attributed to the intermolecular interactions between the redox and MPA molecules. The conditions of lower pH and weaker ion pair effect all benefit the formation of the intermolecular interactions, resulting the enhancement of electron tunneling more obvious. Based on this, this kind of intermolecular interaction is inferred to be intermolecular hydrogen bond . Our work may have contributions to exploring electron tunneling between protein residues on biofilm surface.