Bimetallic conductive molecular 2D metal-organic framework @ 2D MXene nanosheet heterostructure for lithium storage.

Two-dimensional metal-organic frameworks (2D MOFs) have been considered to be one type of potential cathodes for lithium storage due to their regular channels and devisable redox-active sites. However, the relatively low electrical conductivity and weak long-term cyclability hindered their development. Herein, we report an optimized bimetallic conductive 2D MOF (CoNi(HHTP)) for enhanced lithium-ion storage.

Confinement of ZIF-67-derived N, Co-doped C@Si on a 2D MXene for enhanced lithium storage.

A heterostructure composed of ZIF-67-derived nitrogen and cobalt-doped carbon enfolded silicon (C@Si) nanoparticles anchored on 2D MXene layers was constructed for boosting the performance of lithium-ion batteries (LIBs). The heterostructure anode demonstrated a high initial discharge capacity of 3021 mA h g at 0.2 A g, retaining outstanding cycling stability with a reversible capacity of 520 mA h g at 2000 mA g, and the coulombic efficiency remained above 97% after 500 cycles.

One-Pot Hydrothermal-Derived rGO/MXene/Sulfur Composite Aerogels as Free-Standing Cathodes in Lithium-Sulfur Batteries.

The confinement and high utilization of sulfur in the cathodes is critical for improved cycling performance of lithium-sulfur batteries. In this case one-pot hydrothermal strategy is developed to produce rGO/MXene/sulfur composite aerogels where sulfur is in situ trapped in the 3D rGO/MXene conductive skeleton. The optimized composite aerogels as free-standing cathodes delivery a specific capacity of 951 mAhg after 100 cycles at 0.

Enhanced uranium separation by charge enabling γ-MnO with oxygen vacancies.

Numerous efforts have been devoted to understanding the electron transfer process of uranium (UO) on adsorbent materials, whereas the potential oxygen vacancies (OVs) in metal oxides have long been overlooked. Once these interactions are taken into account, the emerging molecular orbital effects undoubtedly affect the adsorption process. Here, we synthesized CC/γ-MnO by growing MnO on carbon cloth (CC), followed by the creation of oxygen vacancies (OVs) through electrochemical methods to form CC/γ-MnO-OVs.

Efficient adsorption of methyl orange and methyl blue dyes by a novel triptycene-based hyper-crosslinked porous polymer.

It is still a great challenge to develop new materials for the highly efficient entrapment of organic dyes from aqueous solution. Herein, a novel triptycene-based hyper-crosslinked porous polymer (TPP-PP) was designed and synthesized by a simple Friedel-Crafts reaction. The obtained polymer TPP-PP has a high surface area, abundant pore structure and stable thermal performance.

Discerning Tyrosine Phosphorylation from Multiple Phosphorylations Using a Nanofluidic Logic Platform.

Discerning tyrosine phosphorylation (pTyr) catalyzed by Tyr kinase is central to the revelation of oncogenic mechanisms and the development of targeted anticancer drugs. Despite some techniques, this goal remains challenging, especially when faced with the interference of multiple phosphorylation events, including serine (pSer) and threonine phosphorylation (pThr). We describe here a functional polymer-modified artificial ion nanochannel, which enables the sensitive and selective recognition of phosphotyrosine (pY) peptide by the distinct ionic current change.

Benzothiazolyl and Benzoxazolyl Hydrazones Function as Zinc Metallochaperones to Reactivate Mutant p53.

We identified a set of thiosemicarbazone (TSC) metal ion chelators that reactivate specific zinc-deficient p53 mutants using a mechanism called zinc metallochaperones (ZMCs) that restore zinc binding by shuttling zinc into cells. We defined biophysical and cellular assays necessary for structure-activity relationship studies using this mechanism. We investigated an alternative class of zinc scaffolds that differ from TSCs by substitution of the thiocarbamoyl moiety with benzothiazolyl, benzoxazolyl, and benzimidazolyl hydrazones.

Functional Nanochannels for Sensing Tyrosine Phosphorylation.

Tyrosine phosphorylation (pTyr), much of which occurred on localized multiple sites, initiates cellular signaling, governs cellular functions, and its dysregulation is implicated in many diseases, especially cancers. pTyr-specific sensing is of great significance for understanding disease states and developing targeted anticancer drugs, however, it is very challenging due to the slight difference from serine (pSer) or threonine phosphorylation (pThr). Here we present polyethylenimine--phenylguanidine (PEI-PG)-modified nanochannels that can address the challenge.

Biomimetic nanochannels for the discrimination of sialylated glycans a tug-of-war between glycan binding and polymer shrinkage.

Sialylated glycans that are attached to cell surface mediate diverse cellular processes such as immune responses, pathogen binding, and cancer progression. Precise determination of sialylated glycans, particularly their linkage isomers that can trigger distinct biological events and are indicative of different cancer types, remains a challenge, due to their complicated composition and limited structural differences. Here, we present a biomimetic nanochannels system integrated with the responsive polymer polyethyleneimine--glucopyranoside (Glc-PEI) to solve this problem.

Combinatorial Therapy of Zinc Metallochaperones with Mutant p53 Reactivation and Diminished Copper Binding.

Chemotherapy and radiation are more effective in wild-type (WT) p53 tumors due to p53 activation. This is one rationale for developing drugs that reactivate mutant p53 to synergize with chemotherapy and radiation. Zinc metallochaperones (ZMC) are a new class of mutant p53 reactivators that restore WT structure and function to zinc-deficient p53 mutants.

Therapeutic targeting of and mutant breast cancer through mutant p53 reactivation.

Triple negative breast cancer (TNBC) is an aggressive subset for which effective therapeutic approaches are needed. A significant proportion of TNBC patients harbor either germline or somatic mutations in , or epigenetic silencing of , which renders them deficient in DNA repair. Virtually all deficient breast cancers harbor mutations in suggesting that inactivation of p53 is a requirement for tumor progression in the setting of deficiency.

Effect of thermal treatment of Pd decorated Fe/C nanocatalysts on their catalytic performance for formic acid oxidation.

The thermal treatment of bimetallic nanocatalysts plays an important role in determining their catalytic performance. Here tuning the surface oxidized metal species of bimetallic Pd-Fe electrocatalysts for the formic acid (FA) oxidation reaction is reported and a correlation between the surface oxidized metal species of the Pd-Fe nanoparticles and their catalytic activities is proposed. The structural details of the Pd-Fe/C catalysts are characterized by X-ray diffraction, X-ray photoelectron spectroscopy and high-sensitivity low-energy ion scattering (HS-LEIS).

Strong Confinement Effects on Homocrystallization by Stereocomplex Crystals in Electrospun Polylactide Fibers.

In asymmetric poly(l-lactide)/poly(d-lactide) (PLLA/PDLA) blends, the pre-existing stereocomplex crystals can impose confinement effects on homocrystallization of uncomplexed PLLA among them. However, confinement effects are very weak in the blend films because of relatively large PLLA domains distributed in the skeleton of stereocomplex crystals. As a comparison, in the electrospun blend fibers, fine distribution of uncomplexed PLLA results in strong confinement effects.

Critical Composition of the β Form of Poly(vinylidene fluoride) in Miscible Crystalline/Crystalline Blends.

Crystallization and the polymorphic transition of poly(vinylidene fluoride) (PVDF) in its miscible blends with poly(butylene succinate) (PBS) from the melt has been investigated. The presence of a miscible PBS component lowers the crystallization temperature and the melting point of the PVDF component in the blends. It becomes more significant above a critical PBS content between 40 and 50 wt % where PVDF chains are dispersed in the matrix composed by PBS chains.

Characterization of the minimal length of functional SecA in Escherichia coli.

Previous studies showed that certain regions of E. coli SecA can be deleted from its N- and/or C-termini to complement a SecA amber ts mutant. In this study, we determined and characterized the dispensability of both ends of SecA molecules.

Transgenic expression of entire hepatitis B virus in mice induces hepatocarcinogenesis independent of chronic liver injury.

Hepatocellular carcinoma (HCC), the third leading cause of cancer deaths worldwide, is most commonly caused by chronic hepatitis B virus (HBV) infection. However, whether HBV plays any direct role in carcinogenesis, other than indirectly causing chronic liver injury by inciting the host immune response, remains unclear. We have established two independent transgenic mouse lines expressing the complete genome of a mutant HBV ("preS2 mutant") that is found at much higher frequencies in people with HCC than those without.

Unusual cold crystallization behavior in physically aged poly(L-lactide).

A comparative study of cold crystallization behavior in poly(L-lactide) (PLLA) annealed below and just above the glass transition temperature (T(g)) has been conducted. Annealing benefits the generation of local order and the subsequent cold crystallization process, which becomes significant in PLLA annealed just above T(g). Surprisingly, morphological observation reveals high density nuclei in PLLA annealed below T(g), contrary to its relatively slow crystallization kinetics.

Molecular origin of enhanced strength in the monofilament of syndiotactic polypropylene because of annealing: a micro-FTIR study.

The conformational and polymorphic transformations in the melt-spun monofilament of syndiotactic polypropylene upon annealing and subsequent stretching have been first explored by micro-FTIR studies. The results indicate that annealing of as-spun monofilament gives rise to an unusual increase in the molecular orientation of helical conformations in both amorphous phase and ordered crystals as a result of structural transitions of transplanar conformations to helical ones as well as mesophase to ordered crystals. The increased molecular orientation in the annealed monofilament is mainly responsible for the enhanced strength during stretching.

Micro-FTIR study of molecular orientation at crack tip in nylon 6/clay nanocomposite: insight into fracture mechanism.

A study on the mechanism for the degraded toughness in nylon 6/clay nanocomposite is explored in this article. Such a nanocomposite exhibits lower specific essential work of fracture we and specific nonessential work of fracture betawp than its pure nylon 6 counterpart, as revealed by essential work of fracture (EWF) measurements. Furthermore, the molecular orientation in a small region (20x20 microm2) ahead of crack tip, obtained from micro-FTIR measurements for the first time, is found to be lower in the nanocomposite during crack initiation and propagation.

Orientation and epitaxy in the injection-molded bars of linear low-density polyethylene/isotactic polypropylene blends: an infrared dichroism measurement.

In this article, molecular orientation of crystalline and amorphous phases of both linear low-density polyethylene (LLDPE) and isotactic polypropylene (iPP) and epitaxy in the LLDPE/iPP blends prepared via dynamic packing injection molding have been investigated with the aid of polarized Fourier transform infrared (FTIR) spectroscopy and two-dimensional X-ray scattering (2D-WAXS). In LLDPE-rich blends, LLDPE was oriented along the shear flow direction, and iPP kept very low orientation. No epitaxial growth between LLDPE and iPP was observed.