Lead halide perovskite quantum dots (QDs) are promising candidates for future lighting applications, due to their high quantum yield, narrow full width at half maximum (FWHM), and wide color gamut. However, the toxicity of lead represents a potential obstacle to their utilization. Although tin(II) has been used to replace lead in films and QDs, the high intrinsic defect density and oxidation vulnerability typically leads to unsatisfactory material properties. Bismuth, with much lower toxicity than lead, is promising to constitute lead-free perovskite materials because Bi is isoelectronic to Pb and more stable than Sn . Herein we report, for the first time, the synthesis and optical characterization of MA Bi Br perovskite QDs with photoluminescence quantum yield (PLQY) up to 12 %, which is much higher than Sn-based perovskite nanocrystals. Furthermore, the photoluminescence (PL) peaks of MA Bi X QDs could be easily tuned from 360 to 540 nm through anion exchange.
Photodetectors convert light signals into current or voltage outputs and are widely used for imaging, sensing, and spectroscopy. Perovskite-based photodetectors have shown high sensitivity and fast response due to the unprecedented low recombination loss in this solution processed semiconductor. Among various types of CHNHPbI morphology (film, single crystal, nanowire), single-crystalline CHNHPbI nanowires are particularly interesting for photodetection because of their reduced grain boundary, morphological anisotropy, and excellent mechanical flexibility. The concomitant disadvantage associated with the CHNHPbI nanowire photodetectors is their large surface area, which catalyzes carrier recombination and material decomposition, thus significantly degrading device performance and stability. Here we solved this key problem by introducing oleic acid soaking to passivate surface defects of CHNHPbI nanowires, which leads to a device with much improved stability and unprecedented sensitivity (measured detectivity of 2 × 10 Jones). By taking advantage of their one-dimensional geometry, we also showcased, for the first time, the linear dichroic photodetection of our CHNHPbI nanowire photodetector.
A combination
of visible light photocatalysis and gold catalysis
is applied to a ring expansion–oxidative arylation reaction.
The reaction provides an entry into functionalized cyclic ketones
from the coupling reaction of alkenyl and allenyl cycloalkanols with
aryl diazonium salts. A mechanism involving generation of an electrophilic
gold(III)–aryl intermediate is proposed on the basis of mechanistic
studies, including time-resolved FT-IR spectroscopy.
Molecular doping of inorganic semiconductors is a rising topic in the field of organic/inorganic hybrid electronics. However, it is difficult to find dopant molecules which simultaneously exhibit strong reducibility and stability in ambient atmosphere, which are needed for n‐type doping of oxide semiconductors. Herein, successful n‐type doping of SnO2 is demonstrated by a simple, air‐robust, and cost‐effective triphenylphosphine oxide molecule. Strikingly, it is discovered that electrons are transferred from the R3P+O−σ‐bond to the peripheral tin atoms other than the directly interacted ones at the surface. That means those electrons are delocalized. The course is verified by multi‐photophysical characterizations. This doping effect accounts for the enhancement of conductivity and the decline of work function of SnO2, which enlarges the built‐in field from 0.01 to 0.07 eV and decreases the energy barrier from 0.55 to 0.39 eV at the SnO2/perovskite interface enabling an increase in the conversion efficiency of perovskite solar cells from 19.01% to 20.69%.
As an NNN-tridentate ligand, the 2,2':6',2"-terpyridine plays an important role in coordination chemistry. With three coordination sites and low LUMO, terpyridine and its derivatives are one of the typical Pincer ligand and/or non-innocent ligands in transition metal catalysis. Interesting catalytic reactivities have been obtained with these tpy-metal complexes targeting some challenging transformations, such as CC bond formation and hydrofunctionalization. On the other hand, terpyridine ligands can form "closed-shell" octahedral complexes, which provide a linear and stable linkage in supramolecular chemistry. Numerous supramolecular architectures have been achieved using modified terpyridine ligands including Sierpiński triangles, hexagonal gasket and supramolecular rosettes. This review presents a summary of recent progress regarding transition metal-terpyridine complexes with the focus on their applications in catalysis and supramolecular structure construction. Facile synthesis of terpyridine derivatives is also described. We hope this article can serve to provide some general perspectives of the terpyridine ligand and their applications in coordination chemistry.
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