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1.
Nanotechnology ; 35(33)2024 May 28.
Artículo en Inglés | MEDLINE | ID: mdl-38729124

RESUMEN

Li metal batteries with polymer electrolyte are of great interest for next-generation batteries for high safety and high energy density. However, uneven deposition on the lithium metal surface can greatly affect battery life. Therefore, surface modification on the Li metal become necessary to achieve good performance. Herein, an artificial solid electrolyte interface (SEI) modified lithium metal anode is prepared using cation-polymerization process, as triggered by PF5generated from CsPF6. As a result, the polarization voltage of Li||Li symmetric battery assembled with artificial SEI-modified Li metal anode was stable with a small over-potential of 25 mV after 3000 h at current density of 1.5 mA cm-2. Electrochemical performance of Li||NCM 622 (LiNi0.6Co0.2Mn0.2O2) full cell with soft-matter polymer electrolyte is significantly improved than bare Li-metal, the capacity retention is 75% after 120 cycles with N/P = 3:1 at a cut-off voltage of 4.3 V. Our work has shed lights on the commercialization of Li metal battery with polymer electrolyte.

2.
Comput Math Methods Med ; 2017: 5285810, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28894474

RESUMEN

The Middle East respiratory syndrome (MERS) coronavirus, a newly identified pathogen, causes severe pneumonia in humans. MERS is caused by a coronavirus known as MERS-CoV, which attacks the respiratory system. The recently defined receptor for MERS-CoV, dipeptidyl peptidase 4 (DPP4), is generally expressed in endothelial and epithelial cells and has been shown to be present on cultured human nonciliated bronchiolar epithelium cells. In this paper, a class of novel four-dimensional dynamic model describing the infection of MERS-CoV is given, and then global stability of the equilibria of the model is discussed. Our results show that the spread of MERS-CoV can also be controlled by decreasing the expression rate of DPP4.


Asunto(s)
Infecciones por Coronavirus/enzimología , Infecciones por Coronavirus/epidemiología , Dipeptidil Peptidasa 4/genética , Interacciones Huésped-Patógeno , Modelos Biológicos , Regulación Enzimológica de la Expresión Génica , Humanos , Coronavirus del Síndrome Respiratorio de Oriente Medio/metabolismo , Receptores Virales/metabolismo , Mucosa Respiratoria/enzimología , Mucosa Respiratoria/virología
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