Pyrrolic nitrogen-doped carbon sandwiched monolayer MoS<Subscript>2</Subscript> vertically anchored on graphene oxide for high-performance sodium-ion battery anodes

In this work, a novel pyrrolic nitrogen-doped carbon sandwiched monolayer MoS₂ hybrid was prepared. This sandwiched hybrid vertically anchors on graphene oxide as anode materials for sodium-ion batteries. Such electrode was fabricated by facile ionic liquid-assisted reflux and annealing methods. Owing to rational structure and enhancement from pyrrolic nitrogen dopant, this unique MoS₂/C-graphene hybrid exhibits reversible specific capacity of 486 mAh g^?1 after 1000 cycles with a low average fading capacity of 0.15 mAh g^?1 (fading cyclic rate of ca. 0.03% per cycle). A capacity of 330 mAh g^?1 is remained at the current densities of 10.0 A g^?1. The proposed strategy provides a convenient way to create new pyrrolic nitrogen-doped hybrids for energy field and other related applications.     

一种用于肿瘤治疗的高光热转换效率和高稳定性的光热剂

基于香豆素荧光团设计合成了一种光热剂(ECEI),其光热转换效率可达 85.78%。此外,冷热循环的实验结果表明,ECEI 具有良好的光稳定性。即使在线粒体膜电位受损的情况下,ECEI 也能有效靶向线粒体,在激光照射下诱导癌细胞死亡。这使 ECEI能够最大程度地破坏线粒体,从而抑制肿瘤细胞的繁殖。对小鼠肿瘤照射 1次后,小鼠肿瘤在 10 d内逐渐消失,这表明ECEI具有良好的肿瘤抑制效果。     

Aggregation-induced emission compounds as new assisted matrices for laser desorption/ionization time-of-flight mass spectrometry

Here, N,N′-bis(4-hydroxylsalicylidene)-p-phenylenediamine (BSPD-OH), N,N′-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe) and N,N′-bis(salicylidene)-p-phenylenediamine (BSPD), which belong to the same category of aggregation-induced emission (AIE) compounds based on Schiff base reactions, were synthesized and applied as new matrices in the analysis of small molecules by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). This type of AIE compounds can be good MALDI matrices. Conventional organic matrices often produce large amounts of matrix ions, hindering the analysis of low molecular weight (LMW) compounds. However, these AIE compounds generate few matrix ions and less background interference because their presence as aggregates decreases the generation of matrix interference. The sensitivity of the AIE matrix is high because the aggregates can improve the absorption of the applied laser emissions. We can regulate the ionization efficiency of the AIE matrix by changing its aggregation state. During this study, BSPD-OH exhibited better ionization efficiency than the other two AIE matrices because it has more phenolic hydroxyl groups. BSPD-OH was successfully applied to the analysis of various LMW compounds including amino acids, organic amine compounds, isoquinoline compounds and fluoroquinolones compounds. This material also can be employed during the qualitative and quantitative analysis of LMW metabolites in human urine without requiring complicated separation processes.     

Phase and morphology controllable synthesis of Sb2O3 microcrystals

A simple and facile solution route has been developed for phase and morphology controllable synthesis of antimony trioxide (Sb₂O₃) microcrystals. Orthorhombic phase and cubic phase Sb₂O₃ microcrystals have been selectively synthesized in high yield. The products were characterized by powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). The as-obtained microcrystals exhibited a variety of morphologies and structures, such as microspindles, nanoplates, and octahedra. Several experimental parameters have been investigated to gain morphology control of Sb₂O₃ microcrystals. Based on the time-dependent experimental results, an aggregation, and recrystallization mechanism was proposed to describe the formation process of these novel microstructures.     

A Fluorescent Probe for Investigating the Role of Biothiols in Signaling Pathways Associated with Cerebral Ischemia-Reperfusion Injury

Cerebral ischemia-reperfusion injury (CIRI) is intimately associated with the redox regulation of biothiol, a crucial antioxidant marker that precludes the onset of ROS. We designed a novel fluorescent probe, DCI-Ac-Py , showing various physicochemical properties, such as high selectivity, exceptional signal-to-noise ratio, near-infrared (NIR) optical window, and blood–brain barrier (BBB) penetrability, for detecting biothiols in the brain. The picolinate serves as a specific recognition group that is rapidly activated by biothiol and undergoes nucleophilic substitution with the adjacent acrylic ester to yield the desired NIR probe. Additionally, the probe's lipid solubility is improved through the inclusion of halogen atoms, which aids in penetrating the BBB. Using DCI-Ac-Py , we investigated changes of biothiols in vivo in the brains of mice during CIRI. We found that biothiol-mediated NF-kB classical (P65-related) and nonclassical (RelB-related) pathways contribute to abundant ROS production induced by CIRI and that biothiols are involved in redox regulation. These findings provide new insights into the study of CIRI and shed light on the physiological and pathological mechanisms of biothiols in the brain.     

基于纳米材料的细胞释放生物信号分子电化学传感器的研究进展

电化学传感器已被证实是一种检测细胞释放信号分子的有效方法.纳米材料如碳纳米材料、金属纳米颗粒,以及纳米复合材料等因其独特性质在电化学分析技术方面应用广泛.本文综述了近年来基于纳米材料的电化学传感器用于检测细胞中释放的信号分子的研究进展,并展望了其发展方向.     

Self-assembly of nanotubes and ordered mesostructures using weak interactions

Two simple organic compounds, 5-nitroisophthalic acid (npa) and 4,4′-bipyridine (bpy), were used as building blocks for supramolecular self-assembly by hydrothermal synthesis. SEM, TEM, and XRD were used to analyse the multi-step assembly process in which npa and bpy assembled into nanotubes (or nanobelts) of about 30–100 nm in diameter and several millimetres in length and microtubes (or microbelts). The tubes then further assembled to form complex ordered structures, such as pom-pom-shaped and flower-like mesostructures.     

Enhanced third‐order nonlinear optical properties determined in thin films using the Z‐scan technique: bis(μ‐4,4′‐oxydibenzoato)bis[(4′‐phenyl‐2,2′:6′,2′′‐terpyridine)cobalt(II)]

π‐Conjugated organic materials exhibit high and tunable nonlinear optical (NLO) properties, and fast response times. 4′‐Phenyl‐2,2′:6′,2′′‐terpyridine (PTP) is an important N‐heterocyclic ligand involving π‐conjugated systems, however, studies concerning the third‐order NLO properties of terpyridine transition metal complexes are limited. The title binuclear terpyridine Co^II complex, bis(μ‐4,4′‐oxydibenzoato)‐κ³O,O′:O′′;κ³O′′:O,O′‐bis[(4′‐phenyl‐2,2′:6′,2′′‐terpyridine‐κ³N,N′,N′′)cobalt(II)], [Co₂(C₁₄H₈O₅)₂(C₂₁H₁₅N₃)₂], (1), has been synthesized under hydrothermal conditions. In the crystal structure, each Co^II cation is surrounded by three N atoms of a PTP ligand and three O atoms, two from a bidentate and one from a symmetry‐related monodentate 4,4′‐oxydibenzoate (ODA²⁻) ligand, completing a distorted octahedral coordination geometry. Neighbouring [Co(PTP)]²⁺ units are bridged by ODA²⁻ ligands to form a ring‐like structure. The third‐order nonlinear optical (NLO) properties of (1) and PTP were determined in thin films using the Z‐scan technique. The title compound shows a strong third‐order NLO saturable absorption (SA), while PTP exhibits a third‐order NLO reverse saturable absorption (RSA). The absorptive coefficient β of (1) is −37.3 × 10⁻⁷ m W⁻¹, which is larger than that (8.96 × 10⁻⁷ m W⁻¹) of PTP. The third‐order NLO susceptibility χ⁽³⁾ values are calculated as 6.01 × 10⁻⁸ e.s.u. for (1) and 1.44 × 10⁻⁸ e.s.u. for PTP.     

Tunable white-light emission of lanthanide(III) hybrid material based on hectorite

Lanthanide(III) luminescent hybrid materials based on the layered hectorite have been successfully prepared, showing tunable emission colors as well as white light by varying the molar ratio between Eu³⁺ and Tb³⁺.