Morphological peculiarities of the lithium electrode from the perspective of the Marcus-Hush-Chidsey model

This study employs the kinetics framework of Marcus-Hush-Chidsey(MHC)to investigate the charge transfer at the interface of lithium electrode and electrolyte in lithium(ion)-batteries.The chargetransfer rate constant is evaluated for different facets of lithium,namely(100),(110),(101),and(111)as a function of surface charge density with the aid of density functional theory(DFT)calculations.The results highlight and quantify the sensitivity of the rate of lithium plating and stripping to the surface orientation,surface charge density,and charge-transfer over-potential.An intrinsic kinetics competition among the different surface orientations is identified together with an asymmetry between the lithium plating and stripping and showcased to influence the deposit morphology and surface protrusions and indentations.

Effect of the anionic composition of sulfolane based electrolytes on the performances of lithium-sulfur batteries

In lithium-sulfur batteries,cell design,specifically electrolyte design,has a key impact on the battery performance.The effect of lithium salt anion donor number(DN)(DN[PF_(6)]^(-)=2.5,DN[N(SO_(2)CF_(3))_(2)]^(-)=5.4,DN[ClO_(4)]^(-)=8.4,DN[SO_(3)CF_(3)]^(-)=16.9,and DN[NO_(3)]^(-)=21.1)on the patterns of lithium-sulfur batteries and lithium metal electrode performances with sulfola ne-based electrolytes is investigated.An increase in DN of lithium salt anions leads to an increase in the depth and rate of electrochemical reduction of sulfur and long-chain lithium polysulfides and to a decrease in those for medium-and short-chain lithium polysulfides.DN of lithium salt anions has weak effect on the discharge capacity of lithium-sulfur batteries and the Coulomb efficiency during cycling,with the exception of LiSO_(3)CF_(3)and LiNO_(3).An increase in DN of lithium salt anions leads to an increase in the cycling duration of lithium metal anodes and to a decrease in the presence of lithium polysulfides.In sulfolane solutions of LiNO_(3)and LiSO_(3)CF_(3),lithium polysulfides do not affect the cycling duration of lithium metal anodes.

Simulation design of thin film lithium niobate electro-optic modulator with bimetallic layer electrodes

Thin-film lithium niobate electro-optical modulator will become the key device in the future optical communication,which has the advantages of high modulation rate,low half-wave voltage,large bandwidth,and easy integration compared with conventional bulk lithium niobate modulator.However,because the electrode gap of the lithium niobate film modulator is very narrow,when the microwave frequency gets higher,it leads to higher microwave loss,and the electro-optical performance of the modulator will be greatly reduced.Here,we propose a thin film lithium niobate electro-optic modulator with a bimetallic layer electrode structure to achieve microwave loss less than 8 dB/cm in the range of 200 GHz,exhibiting a voltage-length product of 1.1 V·cm and a 3 dB electro-optic bandwidth greater than 160 GHz.High-speed data transmission test has been performed,showing good performance.

A review on first principles based studies for improvement of cathode material of lithium ion batteries

Lithium ion batteries（LIBs） are currently best energy storage devices providing rechargeable electrical storage to wide variety of applications – from portable electronics to automobiles. Though, these batteries are fully adopted, widely used and commercialized, but researchers are still extensively working on their constituent materials and developing technology to improve their performance. A major part of related research activities is devoted to the electrode of the battery for improvement in its performance thereby addressing issues like safety, lifetime, specific capacity, energy density and most importantly abundance and cost. There are number of cathode materials that have been proposed and tested at laboratory scale and subsequently utilized in commercialized batteries ever since the appearance of LIBs. Owing to the availability of improved computational resources in the last decade, first principles calculation has become a reliable tool and played a vital role to predict the material properties of electrodes prior to their experimental analysis. This review gives a comprehensive insight and thorough analysis of the global research efforts related to the cathode materials based on first principles framework, sheds light on current status of knowledge and explores the ways forward.

A novel scrape-applied method for the manufacture of the membrane-electrode assembly of the fuel-cell system

This study investigates the transfer of the scrape-applied method from the electrodes of a lithium battery to the membrane-electrode assembly of fuel cells, including Proton Exchange Membrane Fuel Cells and Direct Methanol Fuel Cell. Three methods are commonly used to manufacture lithium battery electrodes： the roller-applied method, the spraying-applied method, and the scrape-applied method. This study develops novel scrape-applied equip- ment for lithium battery electrodes. This method is novel and suitable for producing fuel cell, better than other tradi- tional methods. In this study, the stability of coating process was tested by measuring the weight and thickness of a dry electrode. The stability and reproducibility of electrode fab- rication were examined by systematic data analysis. Finally, the study used a specially designed single cell composed of 16 conductive segments, which are insulated locally. The current passing through each segment was measured using Hall Effect sensors connected to the segment compartments. Based on the measured distribution of the local current in a segmented single cell, the influence of flooding and stoi- chiometry variation of feed gas was discussed in terms of electrochemical reaction rate. The experimental results serve as an important basis for future research in this field, which hold potential benefits to the academia and the industry.

Engineering two-dimensional pores in freestanding TiO_2/graphene gel film for high performance lithium ion battery

As the key component of electrochemical energy storage devices, an electrode with superior ions transport pores is the important premise for high electrochemical performance. In this paper, we developed a unique solution process to prepare freestanding TiO_2/graphene hydrogel electrode with tunable density and porous structures. By incorporating room temperature ionic liquids（RTILs）, even upon drying, the non-volatile RTILs that remained in the gel film would preserve the efficient ion transport channels and prevent the electrode from closely stacking, to develop dense yet porous structures. As a result, the dense TiO_2/graphene gel film as an electrode for lithium ion battery displayed a good gravimetric electrochemical performance and more importantly a high volumetric performance.

Recent progress on electro-sorption technology for lithium recovery from aqueous sources

Lithium is known as the“white petroleum”of the electrification era,and the global demand for lithium grows rapidly with the quick development of new energy industry.The aqueous solutions,such as salt lake brine,underground brine,and seawater,have large lithium reserves,thus this kind of lithium resource has become a research hotspot recently.Compared with other lithium extraction technologies,electro-sorption method shows good prospects for practical applications with advantages in the aspects of efficiency,recovery ratio,cost,and environment.Herein,this review covers recent progress on electro-sorption technology for lithium recovery from aqueous solutions,including the concept illustration,research progress of the applied working electrodes and counter electrodes,and the evaluation indicators of electro-sorption system.Meanwhile,some prospects for the development of this technology are also proposed.We hope this review is beneficial for the construction of high-efficient electrochemical lithium recovery system to achieve an adequate lithium supply in the future.

A high-performance lithium anode based on N-doped composite graphene

Lithium(Li)metal is the most promising electrode for next-gene ration rechargeable batteries.In order to push the commercialization of the lithium metal batteries,a kind of nitrogen(N)-doped composite graphene(NCG)adopted as the Li plating host was prepared to regulate Li metal nucleation and suppress dendrite growth.Furthermore,a new kind of sandwich-type composite lithium metal(STCL)electrode was developed to improve its application.The STCL electrode can be used as convenient as a piece of Li foil but no dendrite growth.In a symmetric battery,the STCL electrode cycled for more than 4500 h with the overpotential of less than 40 mV.And due to the creative design,the STCL promises the Li-S battery with a prolonged cycling lifespan.

Microfibrillated Cellulose Based Ink for Eco-Sustainable Screen Printed Flexible Electrodes in Lithium Ion Batteries

Free organic solvent ink containing graphite, carboxymethyl cellulose and microfibrillated cellulose as active material, dispersing and binder, respectively, has been formulated to produce flexible and eco- sustainable electrodes for lithium ion batteries. Content ratio of components and dispersion protocol were tailored in order to have theological properties suitable for a large and cheap manufacturing process as well as screen printing. The bio-sourced printed electrodes exhibit a high porosity value of 70% that limits the electrochemical performances. However, the calendering process enhances electrode performances by increasing the reversible capacity from 85 until 315 mAh/g and reducing porosity to an optimal value of 34%. Moreover the introduction of 2% w/w of monofluoro-ethylene carbonate in the electrolyte reduced their reversible capacity loss of 11% in the printed electrode.

High capacity lithium-manganese-nickel-oxide composite cathodes with low irreversible capacity loss and good cycle life for lithium ion batteries

We report a method to eliminate the irreversible capacity of 0.4Li_2MnO_3·0.6LiNi_(0.5)Mn_(0.5)O_2(Li_(1.17)Ni_(0.25)Mn_(0.583)O_2) by decreasing lithium content to yield integrated layered-spinel structures.XRD patterns,High-resolution TEM image and electrochemical cycling of the materials in lithium cells revealed features consistent with the presence of spinel phase within the materials.When discharged to about 2.8 V,the spinel phase of LiM_2O_4(M=Ni,Mn) can transform to rock-salt phase of Li_2M_2O_4(M=Ni,Mn) during which the tetravalent manganese ions are reduced to an oxidation state of 3.0.So the spinel phase can act as a host to insert back the extracted lithium ions(from the layered matrix) that could not embed back into the layered lattice to eliminate the irreversible capacity loss and increase the discharge capacity.Their electrochemical properties at room temperature showed a high capacity(about 275 mAh g^(-1) at 0.1 C) and exhibited good cycling performance.