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As a hot topic in materials science and chemistry, molecular stereoisomerism in organic molecules is a key factor in precisely tuning their molecular arrangements, dominating their self-assembly behavior and optimizing their hierarchical condensed structures. We demonstrate a supramolecular chiral oligofluorenol (2O8-DPFOH-SFX) with a hierarchical uniform crystalline structure by precisely controlling molecular stereoisomerism. The resulting ordered supramolecular framework presented exceptional crystalline-enhanced emission and excellent spectral stability.

Nontrivial topology and unconventional pairing are two central guiding principles in the contemporary search for and analysis of superconducting materials and heterostructure compounds. Previously, a topological superconductor has been predominantly conceived to result from a topologically nontrivial band subject to an intrinsic or external superconducting proximity effect. Here, we propose a new class of topological superconductors that are uniquely induced by unconventional pairing. They exhibit a boundary-obstructed higher-order topological character and, depending on their dimensionality, feature unprecedently robust Majorana bound states or hinge modes protected by chiral symmetry. We predict the 112 family of iron pnictides, such as Ca 1−x La x FeAs 2 , to be highly suited material candidates for our proposal, which can be tested by edge spectroscopy. Because of the boundary obstruction, the topologically nontrivial feature of the 112 pnictides does not reveal itself for a bulk-only torus band analysis without boundaries, and as such, it had evaded previous investigations. Our proposal not only opens a new arena for highly stable Majorana modes in high-temperature superconductors but also provides the smoking gun for extended s-wave order in the iron pnictides.

Three diazafluorene derivatives triphenylamine (TPA)(PDAF)n (n = 1, 2, 3) serving as small molecular elements are designed and synthesized via concentrated sulfuric acid mediated Friedel–Crafts reaction. With highly nonplanar topological configuration, TPA(PDAF)3 shows weaker intermolecular interaction in the solid states and thus exhibits single nanomolecular behavior, which is crucial for charge stored and retained in an organic field‐effect transistor (OFET) memory device. Furthermore, diazafluorene derivatives possess a completely separate highest occupied molecular orbital/lowest unoccupied molecular orbital, which offers ideal hole and electron trapping sites. As charge storage elements, triphenylamine groups provide the hole trapping sites, while diazafluorene units provide the electron trapping sites and act as a hole blocking group to restrain the leakage of stored holes trapped in triphenylamine. The pentacene‐based OFET memory device with solution‐processing TPA(PDAF)3 shows a good hole‐trapping ability, high hole trapping density (4.55 × 1012 cm−2), fast trapping speed (<20 ms), a large memory window (89 V), and a tunable ambipolar memory behavior. The optimized device shows a large ON/OFF current ratio (2.85 × 107), good charge retention (>104 s), and reliable endurance properties. This study suggests that diazafluorene based donor–acceptor small molecular elements have great promise for high‐performance OFET memory.

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We investigate the electronic physics of layered Ni-based trichalcogenide NiPX3 (X=S, Se), a member of transition-metal trichalcogenides (TMTs) with the chemical formula, ABX3. These Ni-based TMTs distinguish themselves from other TMTs as their low energy electronic physics can be effectively described by the two eg d-orbitals. The major band kinematics is characterized by the unusal long-range effective hopping between two third nearest-neighbor (TNN) Ni sites in the two-dimensional Ni honeycomb lattice so that the Ni lattice can be equivalently viewed as four weakly coupled honeycomb sublattices. Within each sublattice, the electronic physics is described by a strongly correlated two-orbital graphene-type model that results in an antiferromagnetic (AFM) ground state near half filling. We show that the low energy physics in a paramagnetic state is determined by the eight Dirac cones which locate at K, K , K 2 and K 2 points in the first Brillouin zone with a strong AFM fluctuation between two K(K ) and K 2 ( K 2 ) Dirac cones and carrier doping can sufficiently suppress the long-range AFM order and allow other competing orders, such as superconductivity, to emerge. The material can be an ideal system to study many exotic phenomena emerged from strong electron-electron correlation, including a potential d ± id superconducting state at high temperature.arXiv:1811.02333v1 [cond-mat.str-el]

When the self-gripping mesh compared with the conventional suture fixed Lichtenstein technique, while there was a difference in operative time, there were no differences in pain (chronic or acute) or other complications.