RESUMEN
Quantum cutting (QC) allows the conversion of high-energy photons into lower-energy photons, exhibiting great potential for infrared communications. Yb-doped perovskite nanocrystals can achieve an efficient QC process with extremely high photoluminescence quantum yield (PLQY) thanks to the favorable Yb3+ incorporation in the perovskite structure. However, conventionally used oleic acid-oleylamine-based ligand pairs cause instability issues due to highly dynamic binding to surface states that have curbed their potential applications. Herein, zwitterionic type C3-sulfobetaine 3-(N,N-Dimethylpalmitylammonio)propanesulfonate molecule is utilized to build a strong binding state on the nanocrystals' surface through a new phosphine oxide synthesis route. Leveraging machine learning and Bayesian Optimization workflow to determine optimal synthesis conditions, near-infrared PLQY above 190% is achieved. The high PLQY is well maintained after over three months of aging, under high-flux continuous UV irradiation, and long continuous annealing. This is the first report of highly efficient and stable perovskite quantum cutters, which will drive the study of fundamental physics phenomena and near-infrared quantum communications.
RESUMEN
Water stability is a crucial issue always addressed for commercial practical application of perovskite quantum dots (QDs). Recent advances in ligand engineering for in situ synthesis of water-stable perovskite QDs have attracted growing interest. However, the exact mechanism remains unclear. Here, the function of 4-bromobutyric acid (BBA) and oleylamine (OLA) is systematically studied in water-stable CsPbX3 (X = Br and I) QDs and confirms that the zwitterionic ligands generated in situ by BBA and OLA are anchored on the QDs surface, thus preventing water from penetrating into the QDs. Cs4PbBr6 intermediate crystal found in the crystal structure evolution process of CsPbX3 QD further reveals a complete crystallization process: PbX2 + CsX + Br- â Cs4PbBr6 crystals + X-â CsPbX3 QDs + Br-. Furthermore, it is found that the solvent coordination of the precursor solution has a significant effect on the crystallinity of Cs4PbBr6 intermediate crystal, while the Rb+ doping can effectively passivate the surface defects of CsPbX3 QDs, thereby jointly achieving photoluminescence quantum yields (PLQY) of 94.6% for CsPbBr3 QDs (88.2% for CsPbI3 QDs). This work provides new insights and guiding ideas for the green synthesis of high-quality and water-stable perovskite QDs.
RESUMEN
To best catch human eyes in next-generation displays, the updated recommendation 2020 (Rec. 2020) standard has called for ultrapure green emitters to be qualified with a narrow emission of 525-535 nm with a full width at half-maximum (fwhm) below 25 nm. However, it is still challenging to find an emitter which can simultaneously cover these two criteria. Instead of traditional II-VI group semiconductor quantum dots, perovskite nanocrystals (NCs) can render versatile emitting tunability to allow them access to the Rec. 2020 standard. Herein, to realize the critical window of Rec. 2020, we have proposed a scalable, room temperature synthesis route of formamidinium lead bromide (FAPbBr3) NCs using a sole ligand of sulfobetaine-18 (SBE-18). The as-synthesized FAPbBr3 NCs exhibit an ideal emission at 534 nm with an ultranarrow fwhm of 20.5 nm and a high photoluminescence quantum yield of 90.6%, overwhelming the FAPbBr3 nanoplates capped with oleic acid/oleylamine (OA/OAM). Introducing these high quality NCs into backlight displays, an ultrapure green backlight which covers ≈85.7% of the Rec. 2020 standard in the CIE 1931 color space is achieved, signifying the "greenest" backlight till now. Thus, we can foresee perovskite NCs as the most potential candidates for next-generation displays.
RESUMEN
A nanoparticle design featuring pH-responsive alkoxyphenyl acylsulfonamide ligands is reported herein. As a result of ligand structure, this nanoparticle is neutral at pHâ 7.4, becoming positively charged at tumorâ pH (<6.5). The particle uptake and cytotoxicity increase over this pHâ range. This pH-controlled uptake and toxicity makes this particle a promising tool for tumor selective therapy.