scholarly journals Advancing towards a Practical Magnesium Ion Battery

Materials ◽  
2021 ◽  
Vol 14 (23) ◽  
pp. 7488
Author(s):  
Alejandro Medina ◽  
Carlos Pérez-Vicente ◽  
Ricardo Alcántara
Keyword(s):  
Electrode Materials ◽  
Theoretical Calculations ◽  
Negative Electrode ◽  
Diffusion Path ◽  
Critical Issue ◽  
Magnesium Ion ◽  
Future Directions ◽  
Sustainable Systems ◽  
Magnesium Batteries ◽  
And Diffusion

A post-lithium battery era is envisaged, and it is urgent to find new and sustainable systems for energy storage. Multivalent metals, such as magnesium, are very promising to replace lithium, but the low mobility of magnesium ion and the lack of suitable electrolytes are serious concerns. This review mainly discusses the advantages and shortcomings of the new rechargeable magnesium batteries, the future directions and the possibility of using solid electrolytes. Special emphasis is put on the diversity of structures, and on the theoretical calculations about voltage and structures. A critical issue is to select the combination of the positive and negative electrode materials to achieve an optimum battery voltage. The theoretical calculations of the structure, intercalation voltage and diffusion path can be very useful for evaluating the materials and for comparison with the experimental results of the magnesium batteries which are not hassle-free.

scholarly journals The Principle of Introducing Halogen Ions Into β-FeOOH: Controlling Electronic Structure and Electrochemical Performance

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Dongbin Zhang ◽  
Xuzhao Han ◽  
Xianggui Kong ◽  
Fazhi Zhang ◽  
Xiaodong Lei
Keyword(s):  
Electronic Structure ◽  
Design Principle ◽  
Electrode Materials ◽  
Theoretical Calculations ◽  
Specific Capacity ◽  
Negative Electrode ◽  
Electrochemical Performances ◽  
Host Materials ◽  
Rate Capacity ◽  
High Valence State

AbstractCoordination tuning electronic structure of host materials is a quite effective strategy for activating and improving the intrinsic properties. Herein, halogen anion (X−)-incorporated β-FeOOH (β-FeOOH(X), X = F−, Cl−, and Br−) was investigated with a spontaneous adsorption process, which realized a great improvement of supercapacitor performances by adjusting the coordination geometry. Experiments coupled with theoretical calculations demonstrated that the change of Fe–O bond length and structural distortion of β-FeOOH, which is rooted in halogen ions embedment, led to the relatively narrow band gap. Because of the strong electronegativity of X−, the Fe element in β-FeOOH(X)s presented the unexpected high valence state (3 + δ), which is facilitating to adsorb SO32− species. Consequently, the designed β-FeOOH(X)s exhibited the good electric conductivity and enhanced the contact between electrode and electrolyte. When used as a negative electrode, the β-FeOOH(F) showed the excellent specific capacity of 391.9 F g−1 at 1 A g−1 current density, almost tenfold improvement compared with initial β-FeOOH, with the superior rate capacity and cyclic stability. This combinational design principle of electronic structure and electrochemical performances provides a promising way to develop advanced electrode materials for supercapacitor.

scholarly journals A Review of Electrospun Carbon Nanofiber-Based Negative Electrode Materials for Supercapacitors

Electrochem ◽  
2021 ◽  
Vol 2 (2) ◽  
pp. 236-250
Author(s):  
Arjun Prasad Tiwari ◽  
Tanka Mukhiya ◽  
Alagan Muthurasu ◽  
Kisan Chhetri ◽  
Minju Lee ◽  
...  
Keyword(s):  
Energy Storage ◽  
Electrode Materials ◽  
Carbon Nanofiber ◽  
Negative Electrode ◽  
Smart Devices ◽  
Potential Candidate ◽  
Free Standing ◽  
High Capacitance ◽  
Negative Electrode Materials ◽  
Carbon Based

The development of smart negative electrode materials with high capacitance for the uses in supercapacitors remains challenging. Although several types of electrode materials with high capacitance in energy storage have been reported, carbon-based materials are the most reliable electrodes due to their high conductivity, high power density, and excellent stability. The most common complaint about general carbon materials is that these electrode materials can hardly ever be used as free-standing electrodes. Free-standing carbon-based electrodes are in high demand and are a passionate topic of energy storage research. Electrospun nanofibers are a potential candidate to fill this gap. However, the as-spun carbon nanofibers (ECNFs) have low capacitance and low energy density on their own. To overcome the limitations of pure CNFs, increasing surface area, heteroatom doping and metal doping have been chosen. In this review, we introduce the negative electrode materials that have been developed so far. Moreover, this review focuses on the advances of electrospun nanofiber-based negative electrode materials and their limitations. We put forth a future perspective on how these limitations can be overcome to meet the demands of next-generation smart devices.

Electrodeposited MoO x films as negative electrode materials for redox supercapacitors

2017 ◽  
Vol 225 ◽  
pp. 19-28 ◽  
Author(s):  
Kush K. Upadhyay ◽  
Tuyen Nguyen ◽  
Teresa M. Silva ◽  
Maria J. Carmezim ◽  
M. Fatima Montemor
Keyword(s):  
Electrode Materials ◽  
Negative Electrode ◽  
Negative Electrode Materials

Recent progress in rechargeable lithium batteries with organic materials as promising electrodes

2016 ◽  
Vol 4 (19) ◽  
pp. 7091-7106 ◽  
Author(s):  
Jian Xie ◽  
Qichun Zhang
Keyword(s):  
Lithium Ion Batteries ◽  
Lithium Batteries ◽  
Recent Progress ◽  
Electrode Materials ◽  
Negative Electrode ◽  
Lithium Ion ◽  
Positive Electrode ◽  
Rechargeable Lithium Batteries ◽  
Organic Electrode ◽  
Negative Electrode Materials

Different organic electrode materials in lithium-ion batteries are divided into three types: positive electrode materials, negative electrode materials, and bi-functional electrode materials, and are further discussed.

scholarly journals Microstructure and Magnetic Properties of NdFeB Sintered Magnets Diffusion-Treated with Cu/Al Mixed Dyco Alloy-Powder

2017 ◽  
Vol 62 (2) ◽  
pp. 1263-1266 ◽  
Author(s):  
M.-W. Lee ◽  
K.-H. Bae ◽  
S.-R. Lee ◽  
H.-J. Kim ◽  
T.-S. Jang
Keyword(s):  
Grain Boundary ◽  
Diffusion Path ◽  
Boundary Phase ◽  
Core Shell ◽  
Phase Layer ◽  
Sintered Magnets ◽  
The Core ◽  
Shell Type ◽  
Property Changes ◽  
And Diffusion

AbstractWe investigated the microstructural and magnetic property changes of DyCo, Cu + DyCo, and Al + DyCo diffusion-treated NdFeB sintered magnets. The coercivity of all diffusion treated magnet was increased at 880ºC of 1stpost annealing(PA), by 6.1 kOe in Cu and 7.0 kOe in Al mixed DyCo coated magnets, whereas this increment was found to be relatively low (3.9 kOe) in the magnet coated with DyCo only. The diffusivity and diffusion depth of Dy were increased in those magnets which were treated with Cu or Al mixed DyCo, mainly due to comparatively easy diffusion path provided by Cu and Al because of their solubility with Ndrich grain boundary phase. The formation of Cu/Al-rich grain boundary phase might have enhanced the diffusivity of Dy-atoms. Moreover, relatively a large number of Dy atoms reached into the magnet and mostly segregated at the interface of Nd2Fe14B and grain boundary phases covering Nd2Fe14B grains so that the core-shell type structures were developed. The formation of highly anisotropic (Nd, Dy)2Fe14B phase layer, which acted as the shell in the core-shell type structure so as to prevent the reverse domain movement, was the cause of enhancing the coercivity of diffusion treated NdFeB magnets. Segregation of cobalt in Nd-rich TJP followed by the formation of Co-rich phase was beneficial for the coercivity enhancement, resulting in the stabilization of the metastable c-Nd2O3phase.

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