Tunable structural and optical properties of CuInS colloidal quantum dots as photovoltaic absorbers.

Facile phase selective synthesis of CuInS (CIS) nanostructures has been an important pursuit because of the opportunity for tunable optical properties of the phases, and in this respect is investigated by hot-injection colloidal synthesis in this study. Relatively monodispersed colloidal quantum dots (3.8-5.

The passivating effect of cadmium in PbS/CdS colloidal quantum dots probed by nm-scale depth profiling.

Achieving control of the surface chemistry of colloidal quantum dots (CQDs) is essential to fully exploit their properties in solar cells, but direct measurement of the chemistry and electronic structure in the outermost atomic layers is challenging. Here we probe the surface oxidation and passivation of cation-exchanged PbS/CdS core/shell CQDs with sub nm-scale precision using synchrotron-radiation-excited depth-profiling photoemission. We investigate the surface composition of the topmost 1-2.

Erratum: Ultrafast Charge Dynamics in Trap-Free and Surface-Trapping Colloidal Quantum Dots.

[This corrects the article DOI: 10.1002/advs.201500088.

Ultrafast Charge Dynamics in Trap-Free and Surface-Trapping Colloidal Quantum Dots.

Ultrafast transient absorption spectroscopy is used to study subnanosecond charge dynamics in CdTe colloidal quantum dots. After treatment with chloride ions, these can become free of surface traps that produce nonradiative recombination. A comparison between these dots and the same dots before treatment enables new insights into the effect of surface trapping on ultrafast charge dynamics.

Effect of Chloride Passivation on Recombination Dynamics in CdTe Colloidal Quantum Dots.

Colloidal quantum dots (CQDs) can be used in conjunction with organic charge-transporting layers to produce light-emitting diodes, solar cells and other devices. The efficacy of CQDs in these applications is reduced by the non-radiative recombination associated with surface traps. Here we investigate the effect on the recombination dynamics in CdTe CQDs of the passivation of these surface traps by chloride ions.

Near-unity quantum yields from chloride treated CdTe colloidal quantum dots.

Colloidal quantum dots (CQDs) are promising materials for novel light sources and solar energy conversion. However, trap states associated with the CQD surface can produce non-radiative charge recombination that significantly reduces device performance. Here a facile post-synthetic treatment of CdTe CQDs is demonstrated that uses chloride ions to achieve near-complete suppression of surface trapping, resulting in an increase of photoluminescence (PL) quantum yield (QY) from ca.

Size dependence of ultrafast charge dynamics in monodisperse Au nanoparticles supported on TiO₂ colloidal spheres.

Sub-nanosecond charge dynamics in monodisperse Au nanoparticles (NPs) supported on TiO2 colloidal spheres are studied as a function of NP diameter using ultrafast transient absorption spectroscopy. The decay of the transmittance changes observed in the region of the plasmon resonance of the Au NPs following photoexcitation of the TiO2 spheres are well-described by a bi-exponential function consisting of a fast component of 2 ps duration associated with electron-phonon scattering, followed by a slow and relatively weak component associated with phonon-phonon scattering. The decay constant characterising the latter component was found to be dependent on the size of the Au NPs, rising from 49 ± 3 to 128 ± 6 ps as the diameter of the Au NPs increased from 12.