A molecular-like Au4Ru2 cluster supported on TiO2 with oxygen vacancies enables light harvesting to drive the fixation of N2.

Ionic movement inside organometal halide perovskites (OMHP) materials has been widely reported to be linked with stability issues in the perovskite-based optoelectronic devices. However, the dynamic processes of the ionic movement and how they influence the devices are still not well-understood. In this work, we applied an external electric field to the CH 3 NH 3 PbI 3 crystal and simultaneously monitored the PL behaviors. Two successive PL responses were observed in the same location of the crystal. First, an irreversible PL quenching was observed caused by the photo-annealing effect under an electric field accompanied by a permanent morphology change. The annealed area also showed reversible PL variation, which was attributed to the activation− deactivation of the radiative recombination centers induced by the migration of the iodine ions. Such results can help us gain a deep insight into how the ionic movements in OMHPs influence the performance of the perovskite-based optoelectronic devices under working conditions.

Carbon dots (CDs), as emerging luminescent nanomaterials, possess excellent but complex properties, and thus, they have attracted immense attention for their applications. Further practical application of CDs has been hindered by their limited photostability and photoluminescence intermittency. In this study, we demonstrated that an antioxidant (Trolox) can dramatically enhance the photostability and minimize the photoblinking of CDs without affecting their native spectral characteristics. Significant photoluminescence enhancement and stabilization were observed with the addition of Trolox in ensemble level. Meanwhile, strikingly stable emissions from individual CDs have been observed in the presence of Trolox in single-particle-level experiments. Our observations revealed that the charged state of CDs can be effectively recovered to a neutral state by Trolox via electron transfer. These results prove that the combination of antioxidants and CDs is a powerful means to improve their fluorescence robustness, which is crucial for applications that demand long-lived, nonblinking emission.

No abstract

Nonblinking colloidal quantum dots (QDs) are significant to their applications as single-photon sources or light-emitting materials. Herein, a simple heatup method was developed to synthesize high-qualityWZ-CdSe/CdS core−shell colloidal QDs, which achieved a near-unity photoluminescence quantum yield (PLQY). It was found that the blinking behavior of such QDs was completely suppressed at high excitation intensities, and ultra-stable PL emission was observed. For this reason, a systematic investigation was conducted, revealing that the complete blinking suppression was attributed mainly to the efficient multiexciton emission at high excitation intensities. Such high-quality QDs with nonblinking behaviors and nearly ideal PL properties at high excitation intensities have massive potential applications in various robust conditions, including QD display screens, single-particle tracks, and single-photon sources.