Improving the Structure and Cycling Stability of Ni-Rich Layered Cathodes by Dual Modification of Yttrium Doping and Surface Coating

2020 ◽  
Vol 12 (17) ◽  
pp. 19483-19494 ◽  
Author(s):  
Yan Huang ◽  
Shuang Cao ◽  
Xin Xie ◽  
Chao Wu ◽  
Sidra Jamil ◽  
...  
Nano Energy ◽  
2019 ◽  
Vol 62 ◽  
pp. 30-37 ◽  
Author(s):  
Xiaopeng Cheng ◽  
Jianming Zheng ◽  
Junxia Lu ◽  
Yonghe Li ◽  
Pengfei Yan ◽  
...  

Nano Energy ◽  
2021 ◽  
pp. 106665
Author(s):  
Xingyu Qu ◽  
He Huang ◽  
Tao Wan ◽  
Long Hu ◽  
Zhenlu Yu ◽  
...  

2020 ◽  
Vol 8 (8) ◽  
pp. 4252-4256 ◽  
Author(s):  
Zhijie Bi ◽  
Ning Zhao ◽  
Lina Ma ◽  
Chuan Shi ◽  
Zhengqian Fu ◽  
...  

LiMn2O4 cathodes coated with garnet electrolytes are constructed for improving cycling stability of solid lithium batteries.


1987 ◽  
Vol 58 (04) ◽  
pp. 1064-1067 ◽  
Author(s):  
K Kodama ◽  
B Pasche ◽  
P Olsson ◽  
J Swedenborg ◽  
L Adolfsson ◽  
...  

SummaryThe mode of F Xa inhibition was investigated on a thromboresistant surface with end-point attached partially depoly-merized heparin of an approximate molecular weight of 8000. Affinity chromatography revealed that one fourth of the heparin used in surface coating had high affinity for antithrombin III (AT). The heparin surface adsorbed AT from both human plasma and solutions of purified AT. By increasing the ionic strength in the AT solution the existence of high and low affinity sites could be shown. The uptake of AT was measured and the density of available high and low affinity sites was found to be in the range of 5 HTid 11 pic.omoles/cmf, respectively Thus the estimated density of biologically active high and low ailmity heparm respectively would be 40 and 90 ng/cm2 The heparin coating did not take up or exert F Xa inhibition by itself. With AT adsorbed on both high and low affinity heparin the surface had the capacity to inhibit several consecutive aliquots of F Xa exposed to the surface. When mainly high affinity sites were saturated with AT the inhibition capacity was considerably lower. Tt was demonstrated that the density of AT on both high and low affinity heparin determines the F Xa inhibition capacity whereas the amount of AT on high affinity sites limits the rate of the reaction. This implies that during the inhibition of F Xa there is a continuous surface-diffusion of AT from sites of a lower class to the high affinity sites where the F Xa/AT complex is formed and leaves the surface. The ability of the immobilized heparin to catalyze inhibition of F Xa is likely to be an important component for the thromboresistant properties of a heparin coating with non-compromized AT binding sequences.


2004 ◽  
Vol 11 (2) ◽  
pp. 133-150 ◽  
Author(s):  
M. B. Dizon ◽  
J. Yang ◽  
F. B. Cheung ◽  
J. L. Rempe ◽  
K. Y. Suh ◽  
...  

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