Correction: Luminescence and photoelectrochemical properties of size-selected aqueous copper-doped Ag-In-S quantum dots.

[This corrects the article DOI: 10.1039/C8RA00257F.].

Fluorescent AgInS/ZnS quantum dots microplate and lateral flow immunoassays for folic acid determination in juice samples.

A noninstrumental rapid test for folic acid (FA) detection with visual results evaluation utilizing bright water-stable AgInS/ZnS (AIS/ZnS) quantum dots (QDs) is reported . AIS/ZnS QDs are hydrophilic photostable nanocrystals with size < 7 nm and emission in the visible range. They were synthesized directly in the water phase by a simple method compared to the synthesis of other QDs and conjugated with monoclonal antibodies specific for FA via ligand carboxyl groups. The conjugate was used for the development of instrumental qualitative and rapid quantitative FA detection methods. The competitive fluorescent microplate immunosorbent assay provided a limit of detection of 0.1 ng/mL FA and half maximal inhibitory concentration (IC50) of 24 ng/mL FA. The analytical signal was measured at ʎex = 410 nm and ʎem=590 nm. The proposed method showed no cross-reaction with other group B vitamins. For FA screening in juice samples, the lateral flow immunoassay was developed with a visual cutoff level of 3 µg/mL. In our perception, the developed methods are convenient for proving the perception of the AIS/ZnS QDs application as a luminescent label for immunoassay and are effective for FA detection. Graphical abstract.

Luminescence and photoelectrochemical properties of size-selected aqueous copper-doped Ag-In-S quantum dots.

Ternary luminescent copper and silver indium sulfide quantum dots (QDs) can be an attractive alternative to cadmium and lead chalcogenide QDs. The optical properties of Cu-In-S and Ag-In-S (AIS) QDs vary over a broad range depending on the QD composition and size. The implementation of ternary QDs as emitters in bio-sensing applications can be boosted by the development of mild and reproducible syntheses directly in aqueous solutions as well as the methods of shifting the photoluminescence (PL) bands of such QDs as far as possible into the near IR spectral range. In the present work, the copper-doping of aqueous non-stoichiometric AIS QDs was found to result in a red shift of the PL band maximum from around 630 nm to ∼780 nm and PL quenching. The deposition of a ZnS shell results in PL intensity recovery with the highest quantum yield of 15%, with almost not change in the PL band position, opposite to the undoped AIS QDs. Size-selective precipitation using 2-propanol as a non-solvent allows discrimination of up to 9 fractions of Cu-doped AIS/ZnS QDs with the average sizes in the fractions varying from around 3 to 2 nm and smaller and with reasonably the same composition irrespective of the QD size. The decrease of the average QD size results in a blue PL shift yielding a series of bright luminophors with the emission color varies from deep-red to bluish-green and the PL efficiency increases from 11% for the first fraction to up to 58% for the smallest Cu-doped AIS/ZnS QDs. The rate constant of the radiative recombination of the size-selected Cu-doped AIS/ZnS QDs revealed a steady growth with the QD size decrease as a result of the size-dependent enhancement of the spatial exciton confinement. The copper doping was found to result in an enhancement of the photoelectrochemical activity of CAIS/ZnS QDs introduced as spectral sensitizers of mesoporous titania photoanodes of liquid-junction solar cells.

Structural chemistry of A2MX4 compounds (X = O, F) with isolated tetrahedral anions: search for the densest structure types.

The packing density of various structures is important not only for understanding and the prediction of high-pressure phase transitions, but also because of its reported correlation with thermodynamic stability. Plotting the cube root of formula volume against the cation radii (R) for nine morphotropic series with isolated tetrahedral anions, A(2)MO(4) (M = Si, Ge, S, Se, Cr, Mn, Mo, W) and A(2)BeF(4), permits the comparison of packing densities for 13 structure types (about 80 individual compounds and several solid solutions) stable at (or near) ambient temperature. The spinel type is the densest. The next densest types are those of K(2)MoO(4), Tl(2)CrO(4), ß-Ca(2)SiO(4), ß-K(2)SO(4), Ag(2)CrO(4) and Sr(2)GeO(4). In three series (M = Ge, Mo, W) the densest type comes with somewhat intermediate values of R, and not the largest, in contrast to the classical homology rule. Another contradiction with traditional views is that some of the densest phases have abnormally low overall binding energies. The correlation between packing density and coordination number (CN) is better when CN of A counts entire MX(4) groups rather than individual X atoms; many, but not all, A(2)MX(4) structures have binary A(2)M analogues (of course, A and M are not necessarily the same in these structure types). The most frequent arrangement of A around M is of the Ni(2)In type: a (distorted) pentacapped trigonal prism.