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The Potential Relationship Among HIF-1α and Protein Metabolism Soon after Hypoxic Ischemia along with Dual Results about Nerves.
2. Therefore, this green exfoliation of cationic SilkNFs may provide a biological platform of nanomaterials for applications as diverse as ion electronics, renewable energy, and sustainable nanotechnology.We report the excellent charge storage performance of high-energy Li-ion capacitors (LIC) fabricated from the mesoporous Co3O4 nanosheets as the conversion-type battery component and Jack fruit (Artocarpus heterophyllus) derived activated carbon as a supercapacitor electrode, especially at high temperatures (50 and 40 °C). Prior to the fabrication, the electrochemical prelithiation strategy was applied to Co3O4 to alleviate the irreversibility and enrich the Li-ions for electrochemical reactions (Co0 + Li2O). The LIC delivered a maximum energy density of ∼118 Wh kg-1 at a high temperature of 50 °C. The significant difference is observed at a high rate of 2.6 kW kg-1 at 50 °C with excellent cycle stability up to 3000 cycles, with a retention of ∼87% compared with the LIC cycled at room temperature (∼74%). The magnificent electrochemical performance clearly demonstrates that the mesoporous structure and residual carbon synergistically facilitated the Li+/electron transport and hinder undesirable side reactions with electrolytes to realize high-energy density at high temperatures.Next-generation electrocatalysts with smart integrated designs, maximizing the chemical cascade synergy for sustainable hydrogen production, are needed to address the urgent environmental threats, but scalable synthesis of precisely architectured nanohybrids rendering a few-nanometer interfacial controllability to augment the catalytic reactivity and operational stability is a major bottleneck. Herein, by inventing a surface-confined lateral growth of nanometer-thin and nanoporous two-dimensional (2D)-Pt on NiFe-LDH nanosheets, a highly reactive 2D-2D interfacially integrated nanoplatform is synthesized for an alkaline hydrogen evolution reaction (HER) which not only extracts high Pt-atomic utilization efficiency but also synergistically accelerates the water dissociation and hydrogen generation cascade on the colocalized Pt/M(OH) x active sites, endowing a 6.1-fold higher Pt mass activity than 20% Pt/C and also empowers a record-high HER operational stability for 50 h, due to the chemically enforced lamellar architecture. This work offers a gateway to produce active metal nanosheets tailored with a suitable active-template surface in order to invent and enforce futuristic catalysis technologies.Phototherapy, such as photodynamic therapy and photothermal therapy, holds great potential for modulation of Alzheimer's β-amyloid (Aβ) self-assembly. Unfortunately, current works for phototherapy of Alzheimer's disease (AD) are just employing either visible or first near-infrared (NIR-I) light with limited tissue penetration, which can not avoid damaging nearby normal tissues of AD patients through the dense skull and scalp. To overcome the shortcomings of AD phototherapy, herein we report an amyloid targeting, N-doped three-dimensional mesoporous carbon nanosphere (KD8@N-MCNs) as a second near-infrared (NIR-II) PTT agent. This makes it possible for photothermal dissociation of Aβ aggregates through the scalp and skull in a NIR-II window without hurting nearby normal tissues. Besides, KD8@N-MCNs have both superoxide dismutase and catalase activities, which can scavenge intracellular superfluous reactive oxygen species and alleviate neuroinflammation in vivo. Furthermore, KD8@N-MCNs efficiently cross the blood-brain barrier owing to the covalently grafted target peptides of KLVFFAED on the nanosphere surface. In vivo studies demonstrate that KD8@N-MCNs decrease Aβ deposits, ameliorate memory deficits, and alleviate neuroinflammation in the 3xTg-AD mouse model. Our work provides a biocompatible and non-invasive way to attenuate AD-associated pathology.Autophagy triggered by reactive oxygen species (ROS) in photodynamic therapy (PDT) generally exhibits an anti-apoptotic effect to promote cell survival. Herein, an innovative supramolecular nanoplatform was fabricated for enhanced PDT by converting the role of autophagy from pro-survival to pro-death. The respiration inhibitor 3-bromopyruvate (3BP), which can act as an autophagy promoter and hypoxia ameliorator, was integrated into photosensitizer chlorin e6 (Ce6)-encapsulated nanoparticles to combat hypoxic tumor. 3BP could inhibit respiration by down-regulating HK-II and GAPDH expression to significantly reduce intracellular oxygen consumption rate, which could relieve tumor hypoxia for enhanced photodynamic cancer therapy. More importantly, the autophagy level was significantly elevated by the combination of 3BP and PDT determined by Western blot, immunofluorescent imaging, and transmission electron microscopy. It was very surprising that excessively activated autophagy promoted cell apoptosis, leading to the changeover of autophagy from pro-survival to pro-death. Therefore, PDT combined with 3BP could achieve efficient cell proliferation inhibition and tumor regression. Furthermore, hypoxia-inducible factor-1α (HIF-1α) could be down-regulated after tumor hypoxia was relieved by 3BP. Tumor metastasis could then be effectively inhibited by eliminating primary tumors and down-regulating HIF-1α expression. These results provide an inspiration for future innovative approaches of cancer therapy by triggering pro-death autophagy.Contact electrification (CE) at interfaces is sensitive to the functional groups on the solid surface, but its mechanism is poorly understood, especially for the liquid-solid cases. A core controversy is the identity of the charge carriers (electrons or/and ions) in the CE between liquids and solids. Here, the CE between SiO2 surfaces with different functional groups and different liquids, including DI water and organic solutions, is systematically studied, and the contribution of electron transfer is distinguished from that of ion transfer according to the charge decay behavior at surfaces at specific temperature, because electron release follows the thermionic emission theory. It is revealed that electron transfer plays an important role in the CE between liquids and functional group modified SiO2. Moreover, the electron transfer between the DI water and the SiO2 is found highly related to the electron affinity of the functional groups on the SiO2 surfaces, while the electron transfer between organic solutions and the SiO2 is independent of the functional groups, due to the limited ability of organic solutions to donate or gain electrons. An energy band model for the electron transfer between liquids and solids is further proposed, in which the effects of functional groups are considered. The discoveries in this work support the "two-step" model about the formation of an electric double-layer (Wang model), in which the electron transfer occurs first when the liquids contact the solids for the very first time.Multiple experiments provide evidence for photovoltaic, catalytic, optoelectronic, and plasmonic processes involving hot, i.e., high energy, electrons in nanoscale materials. ABBV-2222 However, the mechanisms of such processes remain elusive, because electrons rapidly lose energy by relaxation through dense manifolds of states. We demonstrate a long-lived hot electron state in a Pt nanocluster adsorbed on the MoS2 substrate. For this purpose, we develop a simulation technique, combining classical molecular dynamics based on machine learning potentials with ab initio nonadiabatic molecular dynamics and real-time time-dependent density functional theory. Choosing Pt20/MoS2 as a prototypical system, we find frequent shifting of a top atom in the Pt particle occurring on a 50 ps time scale. The distortion breaks particle symmetry and creates unsaturated chemical bonds. The lifetime of the localized state associated with the broken bonds is enhanced by a factor of 3. Hot electrons aggregate near the shifted atom and form a catalytic reaction center. Our findings prove that distortion of even a single atom can have important implications for nanoscale catalysis and plasmonics and provide insights for utilizing machine learning potentials to accelerate ab initio investigations of excited state dynamics in condensed matter systems.Single metal atom photocatalysts have received widespread attention due to the rational use of metal resources and maximum atom utilization efficiency. In particular, N-rich amorphous g-C3N4 is always used as a support to anchor single metal atoms. However, the enhancement of photocatalytic activity of g-C3N4 by introducing a single atom is limited due to the bulk morphology and the excess defects of amorphous g-C3N4. Here, we report crystalline g-C3N4 nanorod supported copper single atoms by molten salts and the reflux method. The prepared single Cu atoms/crystalline g-C3N4 photocatalyst (Cu-CCN) shows highly selective and efficient photocatalytic reduction of CO2 under the absence of any cocatalyst or sacrificial agent. The introduction of single Cu atoms can be used as the CO2 adsorption site, thus increasing the adsorption capacity of Cu-CCN samples to CO2. Theoretical calculation results show that reducing CO2 to CH4 on Cu-CCN samples is an entropy-increasing process, whereas reducing CO2 to CO is an entropy-decreasing process. As a result, the Cu-CCN samples exhibited enhanced photocatalytic CO2 reduction with nearly 100% selective photocatalytic CO2 to CO conversion. The mechanism of photocatalytic CO2 reduction over Cu-CCN samples was proposed based on in situ Fourier transform infrared spectra, X-ray absorption spectroscopy, and density functional theory calculation. link2 This work provides an in-depth understanding of the design of photocatalysts for enhancing active sites of the reactants.Branched heterostructured semiconductor nanoparticles such as core seeded tetrapods and octapods offer properties not seen in their spherical core-shell counterparts, but are challenging to synthesize with a large diversity of branch numbers via heterogeneous nucleation and growth processes alone. This work describes a process to facet-link matchstick-like Ag2S-tipped ZnS nanorods via their Ag2S tips, producing branched Ag2S-centered ZnS nanoparticles such as bipods, tripods, and in general multipods with 4 to 16 ZnS arms as a function of reaction time. The angle between nanorods in the bipods and tripods is found to be close to 120°, resulting in unexpected bent and trigonal planar geometry, respectively. link3 This is attributed to the exposed facets of the monoclinic Ag2S tips, their relative chemical reactivities, and their atomic composition. The formation of particles with an increasing number of branches takes place in a stepwise manner, thus making the facet-linking approach a facile synthesis route to systematically obtaining a diverse set of branched heterostructured semiconductor nanoparticles with a well-defined number of branches.The rising global human population and increased environmental stresses require a higher plant productivity while balancing the ecosystem using advanced nanoelectronic technologies. Although multifunctional wearable devices have played distinct roles in human healthcare monitoring and disease diagnosis, probing potential physiological health issues in plants poses a formidable challenge due to their biological complexity. Herein an integrated multimodal flexible sensor system is proposed for plant growth management using stacked ZnIn2S4(ZIS) nanosheets as the kernel sensing media. The proposed ZIS-based flexible sensor can not only perceive light illumination at a fast response (∼4 ms) but also monitor the humidity with a perdurable steady performance that has yet to be reported elsewhere. First-principles calculations reveal that the tunneling effect dominates the current model associated with humidity response. This finding guides the investigation on the plant stomatal functions by measuring plant transpiration.
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