Search

High performance device is the key issue for organic light‐emitting diodes (OLEDs) industrialization. In this instance, efficient hosts, emitters, as well as other functional layer materials are essential for the realization of high‐performance OLEDs. Herein, we develop a series of D−A type host materials, TPATRZ, CzTRZ, and POXTRZ with ortho‐linking strategy. The ortho‐linkage makes TPATRZ, CzTRZ, and POXTRZ highly twisted conformations, which reducing the degree of intramolecular conjugation and maintain high triplet energies of these materials. The red phosphorescence organic light emitting diodes by using Ir(piq)2(acac) as dopant, TPATRZ, CzTRZ, and POXTRZ as host materials achieved relative high device performance with over 20 % external quantum efficiency and flat efficiency roll‐off. The EQEs of the champion devices remain above 22 % at the practical luminance (500 and 1000 cd m−2). The device hosted by POXTRZ achieved the highest external quantum efficiency of 24.0 %, as well as smallest efficiency roll‐off of 6.3 % at 1000 cd m−2. These results further extend the possibilities of ortho‐linkage D−A type host materials and make them have a promising application in OLEDs. [ABSTRACT FROM AUTHOR]

Abstract: Compound {(EMIM)2[Zn7(μ4-O)2(1,4-ndc)6]}n (1) (EMIM=1-ethyl-3-methylimidazolium and 1,4-ndc=1,4-naphthalenedicarboxylate) has been synthesized by using the mixed ionic liquids of 1-ethyl-3-methylimidazolium tetrafluoroborate and 1-ethyl-3-methylimidazolium l-lactate as solvent. Compound 1 has a 3D anionic framework with bcu-(424·64) topology based on a unique heptanuclear [Zn7(μ4-O)(μ2-COO)10] cluster as secondary building unit. The imidazolium cation [EMIM]+ of the ionic liquid acting as extra framework charge-balancing species occupies the channels of the 3D anionic framework. The roles of the ionic liquid in ionothermal synthesis and crystallization of compound 1 are briefly discussed. The thermal and photoluminescent properties of compound 1 have also been investigated. [Copyright &y& Elsevier]

Mobile ad hoc networks (MANETs) have become a hot issue in the area of wireless networks for their non-infrastructure and mobile features. In this paper, a MANET is modeled so that the length of each link in the network is considered as a birth-death process and the space is reused for n times in the flooding process, which is named as an n-spatial reuse birth-death model ( n-SRBDM). We analyze the performance of the network under the dynamic source routing protocol (DSR) which is a famous reactive routing protocol. Some performance parameters of the route discovery are studied such as the probability distribution and the expectation of the flooding distance, the probability that a route is discovered by a query packet with a hop limit, the probability that a request packet finds a τ-time-valid route or a symmetric-valid route, and the average time needed to discover a valid route. For the route maintenance, some parameters are introduced and studied such as the average frequency of route recovery and the average time of a route to be valid. We compare the two models with spatial reuse and without spatial reuse by evaluating these parameters. It is shown that the spatial reuse model is much more effective in routing. [ABSTRACT FROM AUTHOR]

Fluorene is a classic three-membered polycyclic aromatic hydrocarbon, and it has been widely used in optoelectronic devices. Here we explore a simple and efficient strategy for the derivatization at the 2- and 3- positions in fluorene unit. By introducing different types of substituents, we design two pairs of 2,3-disubstituted fluorene isomers and use them as host materials for phosphorescent organic light-emitting diodes (PHOLEDs). The green PHOLEDs hosted by these fluorene derivatives realize high external quantum efficiencies (EQE) over 20 % with low efficiency roll-off. Particularly, the devices hosted by 2TRz3TPA and 2TPA3TRz achieve nearly 24 % EQE and 104 lm W -1 power efficiency. These results clearly demonstrate that the 2,3-disubstituted fluorene platforms are potentially useful for constructing host materials., (© 2022 Wiley-VCH GmbH.)

Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic nanozymes require more consideration regarding complicated tumor microenvironments to mimic biological enzymes, thus achieving superior nanozyme activity in vivo. Here we report a biomimetic hybrid nanozyme (named rMGB) which integrates natural enzyme glucose oxidase (GOx) with nanozyme manganese dioxide (MnO 2 ) by mutual promotion for maximizing the enzymatic activity of MnO 2 and GOx. Under hypoxia environment, we observed that MnO 2 could react with endogenous H 2 O 2 to produce O 2 for enhancing the catalytic efficiency of GOx for starvation therapy. Meanwhile, we confirmed that glucose oxidation generated gluconic acid and further improved the catalytic efficiency of MnO 2 subsequently. The biochemical reaction cycle, consisting of MnO 2 , O 2 , GOx, and H + , was triggered by the tumor microenvironment and accelerated each other so as to achieve self-supplied H + and accelerate O 2 generation, enhancing the starvation therapy, alleviating tumor hypoxia and accelerating the reactive oxygen species generation in photodynamic therapy. This biomimetic hybrid nanozyme would further facilitate the development of biological nanozymes for cancer treatment.