Synthesis, X-Ray Analysis, and Electrochemical Study of Some Manganese Carbonyl Derivatives with 1,1′-Bis(diphenylphosphino)ferrocene, dppfe

1994 ◽  
Vol 67 (9) ◽  
pp. 2440-2446 ◽  
Author(s):  
Satoru Onaka ◽  
Masa-aki Haga ◽  
Shigeru Takagi ◽  
Mayumi Otsuka ◽  
Katuya Mizuno
Author(s):  
Xinyue Li ◽  
Marco Fortunato ◽  
Anna Maria Cardinale ◽  
Angelina Sarapulova ◽  
Christian Njel ◽  
...  

AbstractNickel aluminum layered double hydroxide (NiAl LDH) with nitrate in its interlayer is investigated as a negative electrode material for lithium-ion batteries (LIBs). The effect of the potential range (i.e., 0.01–3.0 V and 0.4–3.0 V vs. Li+/Li) and of the binder on the performance of the material is investigated in 1 M LiPF6 in EC/DMC vs. Li. The NiAl LDH electrode based on sodium alginate (SA) binder shows a high initial discharge specific capacity of 2586 mAh g−1 at 0.05 A g−1 and good stability in the potential range of 0.01–3.0 V vs. Li+/Li, which is better than what obtained with a polyvinylidene difluoride (PVDF)-based electrode. The NiAl LDH electrode with SA binder shows, after 400 cycles at 0.5 A g−1, a cycling retention of 42.2% with a capacity of 697 mAh g−1 and at a high current density of 1.0 A g−1 shows a retention of 27.6% with a capacity of 388 mAh g−1 over 1400 cycles. In the same conditions, the PVDF-based electrode retains only 15.6% with a capacity of 182 mAh g−1 and 8.5% with a capacity of 121 mAh g−1, respectively. Ex situ X-ray photoelectron spectroscopy (XPS) and ex situ X-ray absorption spectroscopy (XAS) reveal a conversion reaction mechanism during Li+ insertion into the NiAl LDH material. X-ray diffraction (XRD) and XPS have been combined with the electrochemical study to understand the effect of different cutoff potentials on the Li-ion storage mechanism. Graphical abstract The as-prepared NiAl-NO3−-LDH with the rhombohedral R-3 m space group is investigated as a negative electrode material for lithium-ion batteries (LIBs). The effect of the potential range (i.e., 0.01–3.0 V and 0.4–3.0 V vs. Li+/Li) and of the binder on the material’s performance is investigated in 1 M LiPF6 in EC/DMC vs. Li. Ex situ X-ray photoelectron spectroscopy (XPS) and ex situ X-ray absorption spectroscopy (XAS) reveal a conversion reaction mechanism during Li+ insertion into the NiAl LDH material. X-ray diffraction (XRD) and XPS have been combined with the electrochemical study to understand the effect of different cutoff potentials on the Li-ion storage mechanism. This work highlights the possibility of the direct application of NiAl LDH materials as negative electrodes for LIBs.


1998 ◽  
Vol 558 (1-2) ◽  
pp. 1-9 ◽  
Author(s):  
Arne Hörsken ◽  
Guodong Zheng ◽  
Mark Stradiotto ◽  
Christopher T.C. McCrory ◽  
Lijuan Li

2014 ◽  
Vol 752 ◽  
pp. 171-182 ◽  
Author(s):  
Marilé Landman ◽  
Renyuan Liu ◽  
Roan Fraser ◽  
Petrus H. van Rooyen ◽  
Jeanet Conradie

1969 ◽  
Vol 8 (8) ◽  
pp. 1801-1803 ◽  
Author(s):  
A. Denise George ◽  
M. Frederick Hawthorne

1985 ◽  
Vol 63 (8) ◽  
pp. 2261-2272 ◽  
Author(s):  
Brenda M. Louie ◽  
Steven J. Rettig ◽  
Alan Storr ◽  
James Trotter

The coordinating properties of a variety of unsymmetrical uninegative tridentate chelating "pyrazolylgallate" ligands have been studied using the tricarbonyl moieties "M(CO)3", where M = Mn or Re, as acceptor species. A series of monomeric, pseudo octahedral complexes has been characterized and a fac mode of coordination established for the tridentate gallate ligands from 1H nmr, ir measurements, and X-ray structure determinations. Nitrosylation of a selection of the rhenium tricarbonyl compounds has yielded a number of cationic rhenium mononitrosyl dicarbonyl species. The reactivity of these cations towards reducing agents has been investigated.


2012 ◽  
Vol 41 (19) ◽  
pp. 5832 ◽  
Author(s):  
Juan Zhao ◽  
Junsheng Wang ◽  
Junwei Zhao ◽  
Pengtao Ma ◽  
Jingping Wang ◽  
...  

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