scholarly journals Complete Three-Electron Vanadium Redox in NASICON-Type Na3VSc(PO4)3 Electrode Material for Na-Ion Batteries

2021 ◽  
Author(s):  
Tatiana I. Perfilyeva ◽  
Oleg A. Drozhzhin ◽  
Anastasia M. Alekseeva ◽  
Maxim V. Zakharkin ◽  
Andrey V. Mironov ◽  
...  
Keyword(s):  
Electrode Material ◽  
Ex Situ ◽  
Initial Structure ◽  
Voltage Range ◽  
Fourier Transformed Infrared Spectroscopy ◽  
Nasicon Type ◽  
Positive Electrode Material ◽  
Electrochemical Capacity ◽  
Solution Mechanism ◽  
Vanadium Redox

Abstract Here we introduce a new NASICON-type Na3VSc(PO4)3 positive electrode material for Na-ion batteries demonstrating reversible (de)intercalation of 3 Na cations per formula unit within a wide voltage range with complex voltage-composition dependence. The total electrochemical capacity of the material is 170 mAh/g, which corresponds to the complete three-electron V2+/V3+/V4+/V5+ process. All the (de)sodiation stages follow a predominantly solid-solution mechanism, as shown by operando X-ray powder diffraction. The oxidation of vanadium up to +5 upon the charge of Na3VSc(PO4)3 to 4.5 V vs. Na/Na+ causes the significant transformation of the unit cell. According to ex situ Fourier-transformed infrared spectroscopy it is accompanied by the increasing distortion of the vanadium coordination environment and shortening of the vanadium-oxygen bonds. This leads to the irreversible character of the charge-discharge curve, and the initial structure can be restored after the strong overdischarge to ≈1.5 V vs. Na/Na+.

NASICON-type Na3V2(PO4)3 as a new positive electrode material for rechargeable aluminium battery

2018 ◽  
Vol 260 ◽  
pp. 798-804 ◽  
Author(s):  
Francisco Nacimiento ◽  
Marta Cabello ◽  
Ricardo Alcántara ◽  
Pedro Lavela ◽  
José L. Tirado
Keyword(s):  
Electrode Material ◽  
Positive Electrode ◽  
Nasicon Type ◽  
Positive Electrode Material

scholarly journals Electrochemical study on nickel aluminum layered double hydroxides as high-performance electrode material for lithium-ion batteries based on sodium alginate binder

2021 ◽  
Author(s):  
Xinyue Li ◽  
Marco Fortunato ◽  
Anna Maria Cardinale ◽  
Angelina Sarapulova ◽  
Christian Njel ◽  
...  
Keyword(s):  
Lithium Ion Batteries ◽  
Electrode Material ◽  
Photoelectron Spectroscopy ◽  
Negative Electrode ◽  
Lithium Ion ◽  
Electrochemical Study ◽  
Ex Situ ◽  
Potential Range ◽  
X Ray ◽  
Storage Mechanism

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.

Sal wood sawdust derived highly mesoporous carbon as prospective electrode material for vanadium redox flow batteries

2019 ◽  
Vol 834 ◽  
pp. 94-100 ◽  
Author(s):  
Makhan Maharjan ◽  
Nyunt Wai ◽  
Andrei Veksha ◽  
Apostolos Giannis ◽  
Tuti Mariana Lim ◽  
...  
Keyword(s):  
Electrode Material ◽  
Mesoporous Carbon ◽  
Redox Flow Batteries ◽  
Wood Sawdust ◽  
Flow Batteries ◽  
Vanadium Redox

scholarly journals In-Situ Tools Used in Vanadium Redox Flow Battery Research—Review

Batteries ◽  
2021 ◽  
Vol 7 (3) ◽  
pp. 53
Author(s):  
Purna C. Ghimire ◽  
Arjun Bhattarai ◽  
Tuti M. Lim ◽  
Nyunt Wai ◽  
Maria Skyllas-Kazacos ◽  
...  
Keyword(s):  
Energy Storage ◽  
Cell Performance ◽  
Vanadium Redox Flow Battery ◽  
Ex Situ ◽  
Diagnostic Tools ◽  
Research Review ◽  
Redox Flow Battery ◽  
Flow Battery ◽  
Vanadium Redox

Progress in renewable energy production has directed interest in advanced developments of energy storage systems. The all-vanadium redox flow battery (VRFB) is one of the attractive technologies for large scale energy storage due to its design versatility and scalability, longevity, good round-trip efficiencies, stable capacity and safety. Despite these advantages, the deployment of the vanadium battery has been limited due to vanadium and cell material costs, as well as supply issues. Improving stack power density can lower the cost per kW power output and therefore, intensive research and development is currently ongoing to improve cell performance by increasing electrode activity, reducing cell resistance, improving membrane selectivity and ionic conductivity, etc. In order to evaluate the cell performance arising from this intensive R&D, numerous physical, electrochemical and chemical techniques are employed, which are mostly carried out ex situ, particularly on cell characterizations. However, this approach is unable to provide in-depth insights into the changes within the cell during operation. Therefore, in situ diagnostic tools have been developed to acquire information relating to the design, operating parameters and cell materials during VRFB operation. This paper reviews in situ diagnostic tools used to realize an in-depth insight into the VRFBs. A systematic review of the previous research in the field is presented with the advantages and limitations of each technique being discussed, along with the recommendations to guide researchers to identify the most appropriate technique for specific investigations.

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