Carbon dots (CDs) possess unique optical properties such as tunable photoluminescence (PL) and excitation dependent multicolor emission. The quenching and recovery of the fluorescence of CDs can be utilized for detecting analytes. The PL mechanisms of CDs have been discussed in previous articles, but the quenching mechanisms of CDs have not been summarized so far. Quenching mechanisms include static quenching, dynamic quenching, Förster resonance energy transfer (FRET), photoinduced electron transfer (PET), surface energy transfer (SET), Dexter energy transfer (DET) and inner filter effect (IFE). Following an introduction, the review (with 88 refs.) first summarizes the various kinds of quenching mechanisms of CDs (including static quenching, dynamic quenching, FRET, PET and IFE), the principles of these quenching mechanisms, and the methods of distinguishing these quenching mechanisms. This is followed by an overview on applications of the various quenching mechanisms in detection and imaging.

Surface functional groups strongly affect the properties of carbon dots (CDs). Amino, carboxy, and hydroxy groups are most commonly encountered in CDs, and they can be introduced via covalent and noncovalent modification. This article (with 116 refs.) reviews the progress made in the past few years. Following an introduction into the field, a large section covers methods for covalent modification (via amide coupling reactions, silylation, and other reactions including esterification, sulfonylation and copolymerization). Next section reviews methods for noncovalent modifications (π interactions, complexation/chelation, and electrostatic interactions). The resulting modified CDs are powerful nanomaterials for targeting and extracting analytes, and in drug release. The modification of the surface also affects fluorescence quantum yields, complexation capacity, the color of fluorescence, and their quenching capability. Current challenges are critically assessed in the concluding section. Graphical abstract The modification methods of carbon dots (CDs) includes covalent and noncovalent. Covalent modifications include amidation, silylation, esterification, sulfonylation and copolymerization reaction. Noncovalent modifications include electrostatic interactions, complexation and π interactions.

A series of Sn-doped TiO2 with Sn content ranging from 0.25 to 1 mol % were successfully synthesized by the hydrothermal method, and its performance as the photoanode of dye-sensitized solar cells (DSSCs) was investigated. TEM and XRD results indicate that the doping has no effect on the morphology and the crystal form of TiO2. The shift of XRD peaks observed at higher angle and the XPS results indicate Sn4+ ions incorporation into the TiO2 lattice. The flatband potential of Sn-TiO2 films shifts from −0.505 V (vs SCE) to −0.55 V with increasing Sn content from 0 to 1 mol at. %, which is beneficial to the increase of V oc. The higher transfer rate of electrons in the Sn-doped TiO2 films than in the undoped TiO2 films is confirmed by IMPS measurements, which is favorable to the higher J sc. IMVS and EIS measurements indicate that the charge recombination increases with increasing Sn doping content. Taking these factors, the optimum efficiency of 8.31% was found at 0.5 mol % Sn-doped TiO2 based DSSCs, which gave an efficiency improved by 12.1% compared with that of the cells based on pure TiO2 (7.45%). This work shows that Sn-doped TiO2 is a most interesting material and has good potential for application in photoenergy conversion devices.