Ball-milled FeP/graphite as a low-cost anode material for the sodium-ion battery

Phosphorus is a promising anode material for sodium batteries with a theoretical capacity of 2596 mA h g-1. However, phosphorus has a low electrical conductivity of 1 x 10-14 S cm-1, which results in poor cycling and rate performances. Even if it is alloyed with conductive Fe, it still delivers a poor electrochemical performance. In this article, a FeP/graphite composite has been synthesized using a simple, cheap, and productive method of low energy ball-milling, which is an efficient way to improve the electrical conductivity of the FeP compound. The cycling performance was improved significantly, and when the current density increased to 500 mA g-1, the FeP/graphite composite could still deliver 134 mA h g-1, which was more than twice the capacity of the FeP compound alone. Our results suggest that by using a low-energy ball-milling method, a promising FeP/graphite anode material can be synthesized for the sodium battery

Binder-free and carbon-free 3D porous air electrode for Li-O2 batteries with high efficiency, high capacity, and long life

Pt-Gd alloy polycrystalline thin film is deposited on 3D nickel foam by pulsed laser deposition method serving as a whole binder/carbon-free air electrode, showing great catalytic activity enhancement as an efficient bifunctional catalyst for the oxygen reduction and evolution reactions in lithium oxygen batteries. The porous structure can facilitate rapid O2 and electrolyte diffusion, as well as forming a continuous conductive network throughout the whole energy conversion process. It shows a favorable cycle performance in the full discharge/charge model, owing to the high catalytic activity of the Pt-Gd alloy composite and 3D porous nickel foam structure. Specially, excellent cycling performance under capacity limited mode is also demonstrated, in which the terminal discharge voltage is higher than 2.5 V and the terminal charge voltage is lower than 3.7 V after 100 cycles at a current density of 0.1 mA cm−2. Therefore, this electrocatalyst is a promising bifunctional electrocatalyst for lithium oxygen batteries and this depositing high-efficient electrocatalyst on porous substrate with polycrystalline thin film by pulsed laser deposition is also a promising technique in the future lithium oxygen batteries research

A germanium/single-walled carbon nanotube composite paper as a free-standing anode for lithium-ion batteries

Paper-like free-standing germanium (Ge) and single-walled carbon nanotube (SWCNT) composite anodes were synthesized by the vacuum filtration of Ge/SWCNT composites, which were prepared by a facile aqueous-based method. The samples were characterized by X-ray diffraction, field emission scanning electron microscopy, and transmission electron microscopy. Electrochemical measurements demonstrate that the Ge/SWCNT composite paper anode with the weight percentage of 32% Ge delivered a specific discharge capacity of 417 mA h g−1 after 40 cycles at a current density of 25 mA g−1, 117% higher than the pure SWCNT paper anode. The SWCNTs not only function as a flexible mechanical support for strain release, but also provide excellent electrically conducting channels, while the nanosized Ge particles contribute to improving the discharge capacity of the paper anode

Room-Temperature Sodium-Sulfur Batteries: A Comprehensive Review on Research Progress and Cell Chemistry

Room temperature sodium-sulfur (RT-Na/S) batteries have recently regained a great deal of attention due to their high theoretical energy density and low cost, which make them promising candidates for application in large-scale energy storage, especially in stationary energy storage, such as with electrical grids. Research on this system is currently in its infancy, and it is encountering severe challenges in terms of low electroactivity, limited cycle life, and serious self-charging. Moreover, the reaction mechanism of S with Na ions varies with the electrolyte that is applied, and is very complicated and hard to detect due to the multi-step reactions and the formation of various polysulfides. Therefore, understanding the chemistry and optimizing the nanostructure of electrodes for RT-Na/S batteries are critical for their advancement and practical application in the future. In the present review, the electrochemical reactions between Na and S are reviewed, as well as recent progress on the crucial cathode materials. Furthermore, attention also is paid to electrolytes, separators, and cell configuration. Additionally, current challenges and future perspectives for the RT-Na/S batteries are discussed, and potential research directions toward improving RT-Na/S cells are proposed at the end

Capillary-Induced Ge Uniformly Distributed in N-Doped Carbon Nanotubes with Enhanced Li-Storage Performance

Germanium (Ge) is a prospective anode material for lithium-ion batteries, as it possesses large theoretical capacity, outstanding lithium-ion diffusivity, and excellent electrical conductivity. Ge suffers from drastic capacity decay and poor rate performance, however, owing to its low electrical conductivity and huge volume expansion during cycling processes. Herein, a novel strategy has been developed to synthesize a Ge at N-doped carbon nanotubes (Ge at N-CNTs) composite with Ge nanoparticles uniformly distributed in the N-CNTs by using capillary action. This unique structure could effectively buffer large volume expansion. When evaluated as an anode material, the Ge at N-CNTs demonstrate enhanced cycling stability and excellent rate capabilities

High-surface-area -Fe2O3/carbon nanocomposite: one-step synthesis and its highly reversible and enhanced high-rate lithium storage properties

Hollow-structured α-Fe2O3/carbon (HIOC) nanocomposite with a high surface area of around 260 m2 g−1 was synthesized by a one-step, in situ, and industrially-oriented spray pyrolysis method using iron lactate and sucrose solution as the precursors. The small α-Fe2O3 nanocrystals were highly dispersed inside amorphous carbon to form a carbon nanocomposite. Electrochemical measurements showed that the carbon played an important role in affecting both the cycle life and the rate capability of the electrode. The HIOC composites showed the best electrochemical performance in terms of high capacity (1210 mAh g−1 at a current density of 0.1 C), enhanced rate capability and excellent cycle stability (720 mAh g−1 at a current density of 2 C up to 220 cycles). HIOC nanocomposite can also be used in other potential applications, such as in gas sensors, catalysts, and biomedical applications because it is easily dispersed in water and has a high surface area

Host structural stabilization of Li1.232Mn0.615Ni0.154O2 through K-doping attempt: toward superior electrochemical performances

Lithium-rich layered cathodes are known famously for its superior capacity over traditional layered oxides but trapped for lower initial coulombic efficiency, poorer rate capability and worse cyclic stability in spite of diverse attempts. Herein, a new K-stabilized Li-rich layered cathode synthesized through a simple oxalate co-precipitation is reported for its super electrochemical performances. Compared with pristine Li-rich layered cathode, K-stabilized one reaches a higher initial coulombic efficiency of 87% from 76% and outruns for 94% of capacity retention and 244 mAh g-1 of discharge capacity at 0.5C after 100 cycles. Moreover, 133 mAh g-1 of discharge capacity can be delivered even charged at 10C showing a highly-improved rate capability. X-ray diffraction and electrochemical impedance spectroscopy tests show that enlarged Li slab layer caused by K+ accommodation can provide facile Li+ diffusion paths and facilitate Li+ migration from the crystal lattice. As a consequence, the introduction of K+ in the host layered structure can inhibit the detrimental spinel structure growth during cycling. Therefore, the K-stabilized Li-rich layered materials can be considered to be an attractive alternative to meet with the higher power and energy density demands of advanced lithium-ion battery

Lini0.5mn1.5o4 spinel cathode using room temperature ionic liquid as electrolyte

In this study, LiNi0.5Mn1.5O4 (LNMO) nanoparticles were prepared as a 5 V cathode material via a rheological phase method and annealed at different temperatures: 680 ◦C, 750 ◦C, and 820 ◦C. The sample annealed at 750 ◦C shows the best performance. A room temperature ionic liquid (RTIL) containing 1 M lithium bis(trifluoromethanesulfonyl) imide (LiNTf2) in N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl) imide (C4mpyrNTf2) was used as novel electrolyte in conjunction with the LNMO cathodes and their electrochemical properties have been investigated. The results show that the LNMO using RTIL as electrolyte has better coulombic efficiency and comparable discharge capacities to those of the cells assembled with standard liquid electrolyte (1 M LiPF6 in ethylene carbonate/diethyl carbonate). Electrochemical impedance spectroscopy shows that the RTIL is much more stable as the electrolyte for LiNi0.5Mn1.5O4 than the conventional electrolyte

Heteroaromatic organic compound with conjugated multi-carbonyl as cathode material for rechargeable lithium batteries

The heteroaromatic organic compound, N,N\u27-diphenyl-1,4,5,8-naphthalenetetra-carboxylic diimide (DP-NTCDI-250) as the cathode material of lithium batteries is prepared through a simple one-pot N-acylation reaction of 1,4,5,8-naphthalenetetra-carboxylic dianhydride (NTCDA) with phenylamine (PA) in DMF solution followed by heat treatment in 250 °C. The as prepared sample is characterized by the combination of elemental analysis, NMR, FT-IR, TGA, XRD, SEM and TEM. The electrochemical measurements show that DP-NTCDI-250 can deliver an initial discharge capacity of 170 mAh g-1 at the current density of 25 mA g-1. The capacity of 119 mAh g-1 can be retained after 100 cycles. Even at the high current density of 500 mA g-1, its capacity still reaches 105 mAh g-1, indicating its high rate capability. Therefore, the as-prepared DP-NTCDI-250 could be a promising candidate as low cost cathode materials for lithium batteries

Nickel sulfide nanocrystals on nitrogen-doped porous carbon nanotubes with high-efficiency electrocatalysis for room-temperature sodium-sulfur batteries

Polysulfide dissolution and slow electrochemical kinetics of conversion reactions lead to low utilization of sulfur cathodes that inhibits further development of room-temperature sodium-sulfur batteries. Here we report a multifunctional sulfur host, NiS2 nanocrystals implanted in nitrogen-doped porous carbon nanotubes, which is rationally designed to achieve high polysulfide immobilization and conversion. Attributable to the synergetic effect of physical confinement and chemical bonding, the high electronic conductivity of the matrix, closed porous structure, and polarized additives of the multifunctional sulfur host effectively immobilize polysulfides. Significantly, the electrocatalytic behaviors of the Lewis base matrix and the NiS2 component are clearly evidenced by operando synchrotron X-ray diffraction and density functional theory with strong adsorption of polysulfides and high conversion of soluble polysulfides into insoluble Na2S2/Na2S. Thus, the as-obtained sulfur cathodes exhibit excellent performance in room-temperature Na/S batteries