Photomultiplication-Type Organic Photodetectors with High EQE-Bandwidth Product by Introducing a Perovskite Quantum Dot Interlayer

A photomultiplication (PM)-type organic photodetector (OPD) that exploits the ionic motion in CsPbI₃ perovskite quantum dots (QDs) is demonstrated. The device uses a QD monolayer as a PM-inducing interlayer and a donor–acceptor bulk heterojunction (BHJ) layer as a photoactive layer. When the device is illuminated, negative ions in the CsPbI₃ QD migrate and accumulate near the interface between the QDs and the electrode; these processes induce hole injection from the electrode and yield the PM phenomenon with an external quantum efficiency (EQE) >2000% at a 3 V applied bias. It is confirmed that the ionic motion of the CsPbI₃ QDs can induce a shift in the work function of the QD/electrode interface and that the dynamics of ionic motion determines the response speed of the device. The PM OPD showed a large EQE-bandwidth product >10⁶ Hz with a −3 dB frequency of 125 kHz at 3 V, which is one of the highest response speeds reported for a PM OPD. The PM-inducing strategy that exploits ionic motion of the interlayer is a potential approach to achieving high-efficiency PM OPDs.     

Clustering-based adaptive low-power subframe configuration with load-aware offsetting in dense heterogeneous networks

Heterogeneous Networks (HetNets) and cell densification represent promising solutions for the surging data traffic demand in wireless networks. In dense HetNets, user traffic is steered toward the Low-Power Node (LPN) when possible to enhance the user throughput and system capacity by increasing the area spectral efficiency. However, because of the transmit power differences in different tiers of HetNets and irregular service demand, a load imbalance typically exists among different serving nodes. To offload more traffic to LPNs and coordinate the Inter-Cell Interference (ICI), Third-Generation Partnership Project (3GPP) has facilitated the development of the Cell Range Expansion (CRE), enhanced Inter-Cell Interference Coordination (eICIC) and Further enhanced ICIC (FeICIC). In this paper, we develop a cell clustering-based load-aware offsetting and an adaptive Low-Power Subframe (LPS) approach. Our solution allows the separation of User Association (UA) functions at the User Equipment (UE) and network server such that users can make a simple cell-selection decision similar to that in the maximum Received Signal Strength (max-RSS) based UA scheme, where the network server computes the load-aware offsetting and required LPS periods based on the load conditions of the system. The proposed solution is evaluated using system-level simulations wherein the results correspond to performance changes in different service regions. Results show that our method effectively solves the offloading and interference coordination problems in dense HetNets.     

In Situ Management of Ions Migration to Control Hysteresis Effect for Planar Heterojunction Perovskite Solar Cells

As one of the most promising photovoltaic materials, the efficiency of inorganic–organic hybrid halide perovskite solar cells (PSCs) has reached 25.5% in 2020. However, the stability and hysteresis remain primary challenges before it can become a commercial photovoltaic technology. Therefore, those issues have drawn significant attention for photovoltaic applications. In this work, a study of the PSCs hysteresis improvement is presented based on a combination of first-principles simulations, scanning electron microscopy images, and time-dependent photocurrent measurements. It indicates the hysteresis led by the ion migration and accumulation is mainly localized at the two interfaces: one is between electron transport layer and active layer, and the other is between active layer and hole transport layer. Considering the massive defects at the grain boundaries (GBs), they lower the potential barriers significantly. The defect density at GBs is therefore reduced via the in situ passivation of PbI₂ crystals. The hysteresis index is decreased from 22.43% down to 1.04%, and results in an improvement in efficiency from 17.12% up to 20.10%. Following the understanding of defect-induced hysteresis, an approach to improve the hysteresis is provided, which can be integrated into the fabrication process and widely applied to enhance the performance of PSCs.     

Determination of low levels of polymer additives migrating from polypropylene to food simulated liquids by capillary SFC and solvent venting injection

Summary Methods for the determination of specific migration of polymer additives from polypropylene to aqueous acetic acid and isooctane have been studied. The migrants were extracted from aqueous acetic acid and characterized by supercritical fluid chromatography (SFC) with flame ionization detection (FID) and mass spectrometry (MS). The isooctane simulant was concentrated and injected directly into the SFC. Injection of extracts after incubation, using the solvent venting injection technique in the SFC, enabled additive concentrations as low as 10 ppb in 150 ml simulant to be determined, corresponding to a specific migration level of approximately 1 g additive/dm² polymer.     

电迁移微离子色谱及其应用

本文提出一种新型的离子色谱方法,采用恒电流电场代替机械泵输送离子,研制出体积小、重量轻、成本低、易操作的电迁移微离子色谱仪,并检测了几种常见的阴离子,Cl~-、Br~-、NO_2~-的检测极限为10~(-11)～10~(-12)mol,峰高和保留时间重现性相对标准偏差均<3％,进样量与峰高的线性关系良好。     

C→N Migrations of the ethoxycarbonyl group in reactions of ortho-substituted aryl isocyanates with the 1,3-zwitterion derived from triisopropylphosphine and ethyl 2-cyanoacrylate

The reactions of meta—para-substituted aryl isocyanates with phosphorus-containing 1,3-zwitterions, which proceed with the CN migration of the CO₂Et group to form the corresponding carbamates, were extended to ortho-substituted aryl isocyanates. The influence of the steric and electronic effects of the ortho substituents in the aromatic rings of aryl isocyanates on the ease of this rearrangement is qualitatively considered.     

1,3-Migration of a phenyl group in the conversion of (Me3Si)2(PhMe2Si)CSiMePhX into (Me3Si)2(Ph2MeSi)CSiMe2Y species

The finding that compounds of the type (Me₃Si)₂(PhMe₂Si)CSiMePhX react with electrophiles to give very predominantly rearranged products (Me₃Si)₂(Ph₂MeSi)CSiMe₂Y, which would be expected to be thermodynamically disfavoured, can be rationalized in terms of a mechanism in which the anchimerically-assisted departure of X⁻ gives the Ph-bridged cation [(Me₃Si)₂

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MePh]⁺ which is attacked by the nucleophile at the less hindered centre bearing two Me groups rather than that bearing one Me and one Ph group, with the outcome determined by kinetic rather than thermodynamic factors. Both (Me₃Si)₂(Ph₂MeSi)CSiMe₂Br and its isomer (Me₃Si)₂(PhMe₂Si)CSiMePhBr react with AgBF₄ in CH₂Cl₂ or Et₂O to give >95% of the fluoride (Me₃Si)₂(Ph₂MeSi)CSiMe₂F. Reaction of the bromide (Me₃Si)₂(PhMe₂Si)CSiMePhBr with AgO₂CCF₃ in Et₂O, and that of the hydride (Me₃Si)₂(PhMe₂Si)CSiMePhH with ICl in CCl₄, likewise give >95% of the rearranged (Me₃Si)₂(Ph₂MeSi)CSiMe₂O₂CCF₃ and (Me₃Si)₂(Ph₂MeSi)CSiMe₂Cl, respectively.     

Thermal cyclization of N-[2-(2-propenyl)-1-naphthyl] ketenimines: intramolecular Diels-Alder reaction versus [1,5] hydrogen migration. Synthesis of dibenz[b,h]acridines and benzo[h]quinolines

The thermal treatment of N-(2-propenyl)-1-naphthylamines provided the expected aza-Claisen rearranged products, 2-(2-propenyl)-1-naphthylamines and benz[g]indoles, these last derived from an intramolecular hydroamination reaction on those primary products. The 2-(2-propenyl)-1-naphthylamines were converted into their triphenylphosphazene derivatives, which by aza-Wittig reaction with disubstituted ketenes yielded N-[2-(2-propenyl)-1-naphthyl] ketenimines. The heating of these ketenimines in boiling toluene induced their cyclization either via an intramolecular Diels-Alder reaction, to afford dibenz[b,h]acridines, or via [1,5] hydrogen migration from the sp³ carbon atom of the propenyl substituent to the central carbon atom of the ketenimine fragment, followed by a 6π electrocyclic ring closure, to give benzo[h]quinolines.     

Reaction of a 5α-bromo-6β,19-epoxysteroid with BF3·Et2O/Ac2O: An evidence of a cyclic bromonium cation

Treatment of 3β-acetoxy-5-bromo-6β,19-epoxy-5α-androstan-17-one with Ac₂O and BF₃·OEt₂, produced the cleavage of the epoxy moiety and migration of the bromine atom to afford 3β,19-diacetoxy-6α-bromo-5-hydroxy-5β-androst-17-one in high yield.