| 11. |
- Li, Fang-Yi, et al.
(författare)
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Inhibition of K-Ras4B-plasma membrane association with a membrane microdomain-targeting peptide
- 2020
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Ingår i: Chemical Science. - : Royal Society of Chemistry. - 2041-6520 .- 2041-6539. ; 11:3, s. 826-832
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Tidskriftsartikel (refereegranskat)abstract
- The association of K-Ras4B protein with plasma membrane (PM) is required for its signaling activity. Thus, direct inhibition of K-Ras4B-PM interaction could be a potential anti-Ras therapeutic strategy. However, it remains challenging to modulate such protein-PM interaction. Based on Ras isoform-specific PM microdomain localization patterns, we have developed a potent and isoform-selective peptide inhibitor, Memrasin, for detachment of K-Ras4B from the PM. Memrasin is one of the first direct inhibitors of K-Ras4B-PM interaction, and consists of a membrane l(d) region-binding sequence derived from the C-terminal region of K-Ras4B and an endosome-escape enhancing motif that can aggregate on membrane. It forms peptide-enriched domains in the l(d) region, abrogates the tethering of K-Ras4B to the PM and accordingly impairs Ras signaling activity, thereby efficiently decreasing the viability of several human lung cancer cells in a dose-responsive and K-Ras dependent manner. Memrasin provides a useful tool for exploring the biological function of K-Ras4B on or off the PM and a potential starting point for further development into anti-Ras therapeutics.
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| 12. |
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| 13. |
- Liang, Huali, et al.
(författare)
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Highly-ordered microstructure and well performance of LiNi0.6Mn0.2Co0.2O2 cathode material via the continuous microfluidic synthesis
- 2020
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Ingår i: Chemical Engineering Journal. - : Elsevier BV. - 1385-8947 .- 1873-3212. ; 394
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Tidskriftsartikel (refereegranskat)abstract
- Ni-rich layered oxides are potential cathode candidate's materials for Li-ion batteries due to their low cost and high energy density. However, it is difficult to reproducibly prepare uniformly distributed element and wellcontrolled morphology of Ni-rich layered oxide particles. This study develops a continuous microfluidic reaction process to synthesize spherical carbonate precursors (Ni0.6Mn0.2Co0.2CO3). The as-synthesized LiNi0.6Co0.2Mn0.2O2 materials exhibit well-defined microsphere morphology, uniform particles size distribution, better thermal stability and homogeneous transition metal distribution, due to the excellent mixing, well mass and heat transfer rate during the microfluidic reaction. Moreover, the as-prepared LiNi0.6Co0.2Mn0.2O2 materials achieve higher initial capacity, excellent electrochemical reversibility and capacity retention than that of the samples prepared by traditional co-precipitation. Therefore, our results demonstrate that microfluidic reaction is a simple and effective synthesis technology for preparing Ni-rich layered cathode.
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| 14. |
- Luo, Yang, et al.
(författare)
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Three-dimensional and temperature-dependent electronic structure of the heavy-fermion compound CePt2In7 studied by angle-resolved photoemission spectroscopy
- 2020
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Ingår i: Physical Review B. - : AMER PHYSICAL SOC. - 2469-9950 .- 2469-9969. ; 101:11
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Tidskriftsartikel (refereegranskat)abstract
- The three-dimensional and temperature-dependent electronic structures of the heavy-fermion superconductor CePt2In7 are investigated. Angle-resolved photoemission spectroscopy using variable photon energy establishes the existence of quasi-two- and three-dimensional Fermi surface topologies. Temperature-dependent 4d-4f on-resonance photoemission spectroscopies data reveal that heavy quasiparticle bands begin to form at a temperature well above the characteristic (coherence) temperature T+. The emergence of low-lying crystal electric field excitation may be responsible for the "relocalization" or the precursor to the establishment of heavy electrons coherence in heavy-fermion compounds. These findings provide critical insight into understanding the hybridization in heavy-fermion systems.
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| 15. |
- Xu, Hai-Sen, et al.
(författare)
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Single crystal of a one-dimensional metallo-covalent organic framework
- 2020
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Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 11:1
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Tidskriftsartikel (refereegranskat)abstract
- Although polymers have been studied for well over a century, there are few examples of covalently linked polymer crystals synthesised directly from solution. One-dimensional (1D) covalent polymers that are packed into a framework structure can be viewed as a 1D covalent organic framework (COF), but making a single crystal of this has been elusive. Herein, by combining labile metal coordination and dynamic covalent chemistry, we discover a strategy to synthesise single-crystal metallo-COFs under solvothermal conditions. The single-crystal structure is rigorously solved using single-crystal electron diffraction technique. The non-centrosymmetric metallo-COF allows second harmonic generation. Due to the presence of syntactic pendant amine groups along the polymer chains, the metallopolymer crystal can be further cross-linked into a crystalline woven network. Although polymers have been studied for well over a century, there are few examples of covalently linked polymer crystals synthesized directly from solution. Here, the authors demonstrate a strategy to synthesize single crystalline 1D metallo-covalent organic frameworks by combining dynamic covalent chemistry and metal-ligand coordination.
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| 16. |
- Xue, Xiaoyin, et al.
(författare)
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PEDOT:PSS @Molecular Sieve as Dual-Functional Additive to Enhance Electrochemical Performance and Stability of Ni-Rich NMC Lithium-Ion Batteries
- 2020
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Ingår i: Energy Technology. - : Wiley. - 2194-4288 .- 2194-4296. ; 8:10
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Tidskriftsartikel (refereegranskat)abstract
- Molecular sieves (MSs) coated with conductive polymer (PEDOT:PSS) are used as water scavengers to modify the nickel‐rich LiNi1–x–yCoxMnyO2 (NMC)‐layered cathode. This strategy proactively captures residual water in the battery system without affecting the transport performance of electrons and Li+ ions. The moisture content and nuclear magnetic resonance (NMR) tests show that MSs after coating still maintain good water absorption characteristics and inhibit the decomposition of the electrolyte. The conductivity of the PEDOT:PSS@MS‐NMC electrode is 1.08 × 10−4 S cm−1, which is improved by 63.9%, compared with the MS‐NMC electrode. Through X‐ray photoelectron spectroscopy, transmission electron microscopy, and scanning electron microscopy measurements, it is also shown that the surface structure stability and particle integrity for PEDOT:PSS@MS‐NMC electrode is well retained. After 500 cycles, the capacity retention of the composite cathode is 71.3%, which is higher than that of the NMC (38.3%) and MS‐NMC cathode (62.4%). This is a novel and effective strategy to suppress side reactions at the electrode interface and improve electrode stability, capacity retention, and cycle performance of the Ni‐rich NMC cathode.
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| 17. |
- Yang, Fu-Sheng, et al.
(författare)
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Chromosome-level genome assembly of a parent species of widely cultivated azaleas
- 2020
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Ingår i: Nature Communications. - : Nature Publishing Group. - 2041-1723. ; 11:1
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Tidskriftsartikel (refereegranskat)abstract
- Azaleas (Ericaceae) comprise one of the most diverse ornamental plants, renowned for their cultural and economic importance. We present a chromosome-scale genome assembly for Rhododendron simsii, the primary ancestor of azalea cultivars. Genome analyses unveil the remnants of an ancient whole-genome duplication preceding the radiation of most Ericaceae, likely contributing to the genomic architecture of flowering time. Small-scale gene duplications contribute to the expansion of gene families involved in azalea pigment biosynthesis. We reconstruct entire metabolic pathways for anthocyanins and carotenoids and their potential regulatory networks by detailed analysis of time-ordered gene co-expression networks. MYB, bHLH, and WD40 transcription factors may collectively regulate anthocyanin accumulation in R. simsii, particularly at the initial stages of flower coloration, and with WRKY transcription factors controlling progressive flower coloring at later stages. This work provides a cornerstone for understanding the underlying genetics governing flower timing and coloration and could accelerate selective breeding in azalea. Azaleas are one of the most diverse ornamental plants and have cultural and economic importance. Here, the authors report a chromosome-scale genome assembly for the primary ancestor of the azalea cultivar Rhododendro simsi and identify transcription factors that may function in flower coloration at different stages.
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| 18. |
- Zhai, Pan, et al.
(författare)
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Ionic Conductive Thermoplastic Polymer Welding Layer for Low Electrode/Solid Electrolyte Interface Resistance
- 2020
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Ingår i: ACS Applied Energy Materials. - : AMER CHEMICAL SOC. - 2574-0962. ; 3:7, s. 7011-7019
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Tidskriftsartikel (refereegranskat)abstract
- The application of LAGP ceramic solid electrolytes is circumscribed by the large electrode/electrolyte interfacial resistance because of their rigidity and brittleness. Here, a highly cohesive composite polymer layer consisting of poly(vinylene carbonate)-thermoplastic polyurethanes (PVC-TPU) is coated onto both sides of the Li1.5Al0.5Ge1.5(PO4)(3) pellet to address the interfacial problems with the electrodes. The coated PVC-TPU acts as an ionic conductive welding layer to facilitate the interfacial contact of the LAGP pellet with both electrodes and decreases the interfacial resistance of the LAGP pellet against the cathode (from 1.4 x 10(6) to 3.8 x 10(3) Omega cm(2)) and the Li-metal anode (from 3.3 x 10(4) to 890 Omega cm(2)). The resulting composite solid-state electrolyte (CSSE) presents the synergistic effect of the LAGP ceramic pellet and the PVC-TPU layer in terms of electrochemical stability, ionic transport properties, and stable lithium plating/stripping cycling with a low overpotential for 1000 h. Consequently, the LiFePO4/Li solid-state batteries utilizing this CSSE deliver a high capacity retention of 95.3% after 100 cycles at room temperature with a high Coulombic efficiency exceeding 99.99% per cycle and lithium dendrite inhibition.
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| 19. |
- Zhao, Beibei, et al.
(författare)
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NaSn2(PO4)(3) submicro-particles for high performance Na/Li mixed-ion battery anodes
- 2020
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Ingår i: Journal of Alloys and Compounds. - : ELSEVIER SCIENCE SA. - 0925-8388 .- 1873-4669. ; 844
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Tidskriftsartikel (refereegranskat)abstract
- NaSn2(PO4)(3) has open framework, high ionic conductivity, low working potential, high theoretical capacity more than twice of graphite. However, its commercial application is limited by its low electrical conductivity and rapid capacity fading. To overcome this challenge, we synthesize NaSn2(PO4)(3) submicro-particles (around 100-300 nm in size) by hydrothermally assisted pyrolysis reactions. The synthesized NaSn2(PO4)(3) anode for Na/Li mixed-ion batteries delivers an ultrahigh initial discharge capacities, excellent rate performance and superior cycling stability. This design provides a promising pathway for developing high performance mixed-ion batteries. (C) 2020 Elsevier B.V. All rights reserved.
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| 20. |
- Zhao, Yi, et al.
(författare)
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Redox Dual-Cocatalyst-Modified CdS Double-Heterojunction Photocatalysts for Efficient Hydrogen Production
- 2020
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 12:41, s. 46073-46083
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Tidskriftsartikel (refereegranskat)abstract
- Cadmium sulfide (CdS) as one of the most common visible-light-responsive photocatalysts has been widely investigated for hydrogen generation. However, its low solar-hydrogen conversion efficiency caused by fast carrier recombination and poor catalytic activity hinders its practical applications. To address this issue, we develop a novel and highly efficient nickel-cobalt phosphide and phosphate cocatalyst-modified CdS (NiCoP/CdS/NiCoPi) photocatalyst for hydrogen evolution. The dual-cocatalysts were simultaneously deposited on CdS during one phosphating step by using sodium hypophosphate as the phosphorus source. After the loading of the dual-cocatalysts, the photocurrent of CdS significantly increased, while its electrical impedance and photoluminescence emission dramatically decreased, which indicates the enhancement of charge carrier separation. It was proposed that the NiCoP cocatalyst accepts electrons and promotes hydrogen evolution, while the NiCoPi cocatalyst donates electrons and accelerates the oxidation of sacrificial agents (e.g., lactic acid). Consequently, the visible-light-driven hydrogen evolution of this composite photocatalyst greatly improved. The dual-cocatalyst-modified CdS with a loading content of 5 mol % showed a high hydrogen evolution rate of 80.8 mmol.g(-1).h(-1), which was 202 times higher than that of bare CdS (0.4 mmol.g(-1).h(-1)). This is the highest enhancement factor for metal phosphide-modified CdS photocatalysts. It also exhibited remarkable stability in a continuous photocatalytic test with a total reaction time of 24 h.
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