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• A Box-Behnken design for graphite anodes slurries optimization was presented to highlight the importance of the component's interactions to obtained higher performed anodes of lithium-ion batteries customization. • The carbon black content is the most significant effect in both materials which is reflected in higher capacities and coulombic efficiencies. • For the overall behavior, the binder/carbon black interactions are relevant in terms not only of electrochemical performance but also in the obtention of more homogeneous and better adhesion anodes. The technological application of lithium-ion batteries (LIB) grows constantly, making customization of the batteries a current necessity and sometimes a challenge. In this paper we described carbon-slurry optimization process for anodes of lithium-ion batteries customization by using a surface response statistical experiment with four response variables such specific discharge capacity, coulombic efficiency, anodes mass deviation, and capacity retention. We studied two commercial graphite active materials by characterizing the materials via Raman spectroscopy, SEM, and electrochemical techniques. We corroborate the graphite structure for both materials but with morphological differences such as shape and particle size. The binder composition seems to interfere with the active carbon materials capabilities while it generates better performance for one of them. Although the chemical structure of both materials was confirmed to be the same via Raman experiments, SEM images shows critical morphological differences that interferes with the final slurry thus, affecting the electrochemical performance of the anodes. Further studies are required to understand ECSA and its possible effect on the charge/discharge capacities of the anodes. [Display omitted] [ABSTRACT FROM AUTHOR]

This work presents a comprehensive analysis of the impact of carbon nanotubes (CNT) and carbon nanofibers (CNF) composition on the performance of nano-Si anodes in lithium-ion batteries. The nano-Si anode suffers from chemo-mechanical issues caused by its large volumetric change (e.g., 280%) during cycling. One of the promising solutions in electrode level is to establish a robust electronic conduction pathway in Si anodes by incorporating CNT and CNF with high aspect ratios. The objective of this work is to quantitatively measure the performance improvement achieved by CNT and CNF based on their compositions and analyze the improvement mechanism through electrochemical methods. The results indicate that substituting a portion of carbon black with CNT and CNF in a range of 1 – 10 wt% can enhance the capacity retention (from 44% to around 60%) and the fast-charging and fast-discharging capabilities. Electrochemical impedance spectroscopy (EIS) and distribution of relaxation times (DRT) analyses revealed that 5% – 10% CNT and CNF conductors effectively suppressed contact impedances growths in Si anodes. In summary, our findings highlight the importance of precise control over the composition of CNT and CNF to achieve good electrode morphology and electrochemical properties for nano-Si anodes. [ABSTRACT FROM AUTHOR]

This work aims at better understanding the interactions existing between the liquid electrolyte and the solid composite electrode in a Li-ion battery. We substituted the common active material (e.g. LiNi 1/3 Mn 1/3 Co 1/3 O 2 or LiFePO 4) by an insulating (inactive) γ-Al 2 O 3 compound in order to detect and evidence the interaction between the carbon black electronic additive and the liquid electrolyte. Our study presents the characterization of charge (electrons and ions) transport at different scales by combining a high-frequency analysis performed by broadband dielectric spectroscopy (BDS, up to 1010 Hz), along with a low-frequency analysis performed by electrochemical impedance spectroscopy (EIS, down to 10−3 Hz). Two carbon black materials with two different specific surface areas (80 m2.g−1 and 65 m2.g−1, respectively) were studied. The electronic percolation threshold and the kinetics of impregnation of the hierarchical composite electrode by the liquid electrolyte have been determined with respect to the carbon black content. The significant influence of the adsorbtion of ions at the carbon black surface on the electrons transport is particularly highlighted and explained. [ABSTRACT FROM AUTHOR]

• Facile vacuum-assisted filtration method was used to assemble ERGO/MoS 2 -based films. • USER reaction quickly expanded the structure of graphene oxide-based films. • The most electrochemically active film was with the ratio 1:1 of ERGO to ex-MoS 2. • The displayed discharge capacity of ERGO/MoS 2 –1 (ratio 1:1) is 916 mAh/g. • Reduced graphene oxide-based films electrodes do not utilize non-active materials. In this paper, thin free standing films based on ultrafast self-expanded reduced graphene oxide (ERGO) and exfoliated molybdenum disulfide (ex-MoS 2) were prepared via vacuum-assisted filtration and tested as anodes in Li-ion half-cells. Three films with GO to ex-MoS 2 ratio of 1:1, 1:2 and 2:1 were assembled (ERGO/MoS 2 –1, ERGO/MoS 2 –2, ERGO/MoS 2 –3, respectively). Reduction of GO-based films was conducted via ultrafast self-expanded reaction (USER) in Ar atmosphere. This process not only immediately reduced GO but also significantly expanded films structure. The sample with the highest specific capacity and the highest stability consisted of GO and ex-MoS 2 with ratio of 1:1. The anode composed of this film showed approximately 6 times higher discharge capacity (916 mAh/g at 50 mA/g) than reference film (RGO/MoS 2 –1) where graphene oxide was thermally reduced in a furnace (145 mAh/g at 50 mA/g). Such high performance is associated with the expanded structure of ERGO allowing better lithiation yield and served as a protection of ex-MoS 2 against overexpanding upon charging/discharging process. What is more, the proposed Li-ion half-cells are free of any non-active materials e.g. carbon black or poly(vinyl difluoride) which are commonly used in batteries increasing the cost of the whole energy storage device. [Display omitted] [ABSTRACT FROM AUTHOR]

• Nanosized VC was synthesized by disproportionation of V(IV) ions in molten salt. • The VC powder have excellent dispersibility and uniform size distribution. • The VC exhibits desirable electrochemical performances as an anode in LIBs and SIBs. • It is a new insight into the synthesis of high-performance carbide as anode in metal-ion batteries. Nanosized VC with an average particle size of ∼40 nm was synthesized by disproportionation of V(IV) ions on acetylene black template in molten (Na,K)Cl at 950 °C holding for 5 h. The as-synthesized VC has exhibited desirable electrochemical performances as an anode in lithium-ion batteries (LIBs), delivered a reversible discharge capacity of 597.8 mAh g−1 at 0.1 A g−1 and ∼397.8 mAh g−1 at 0.5 A g−1 in 200 consecutive cycles. It is noteworthy that nanosized VC also displayed impressive charge-discharge capacities in sodium-ion batteries (SIBs), released ∼252.5 mAh g−1 at 0.1 A g−1. This work provides a new insight into the preparation of high-performance carbide ceramics as anodes in metal-ion batteries. [Display omitted] Well-distributed nanosized VC was synthesized by a convenient and efficient synthesis method, utilizing disproportionation reaction of V(IV) in molten salt, exhibits excellent electrochemical performances in lithium ion batteries. [ABSTRACT FROM AUTHOR]

Amorphous metal-organic gel (MOG) can be applied as anode for lithium ion batteries (LIBs) due to its advantages of the controllable structure and the adjustable pore size. In this work, M-MOGs (M=Ni, Zr, Fe, Al, Cr) membranes were fabricated by drop casting method and used as LIB anodes for the first time. They exhibited the excellent electrochemical performance, which were much better than metal-organic frameworks (MOFs) or MOGs without membrane formation of the same metal atom. There was no need to add carbon black, binder or organic solvent when fabricating the membrane electrode which can be attributed to the excellent electronic conductibility of membrane and the viscosity of MOGs. At the same time, the prepared MOGs have the self-healable property which can effectively restrain volume expansion during the lithium ion intercalation/extraction process. In five membrane electrodes, Ni-MOG membrane had a great specific capacity reaching to 1710.1 mA h g−1 at the current density of 100 mA g−1, and remained at 1245.5 mA h g−1 after 30 cycles with high rate performance. Furthermore, the coulombic efficiency was nearly 100% after 100 cycles at a high current density of 2 A g−1 or 5 A g−1. The conductivities of the five MOG membranes were between 10−8 and 10−7 S m−1, indicating that the membrane anodes had semiconductor property. It can be seen that amorphous MOG membrane is a promising anode material for LIBs. [Display omitted] [ABSTRACT FROM AUTHOR]