Formation of NiFe_2O_4/Expanded Graphite Nanocomposites with Superior Lithium Storage Properties

A Ni Fe_2O_4/expanded graphite(Ni Fe_2O_4/EG)nanocomposite was prepared via a simple and inexpensive synthesis method. Its lithium storage properties were studied with the goal of applying it as an anode in a lithium-ion battery. The obtained nanocomposite exhibited a good cycle performance, with a capacity of 601 m Ah g^(-1)at a current of 1 A g^(-1)after 800 cycles. This good performance may beattributed to the enhanced electrical conductivity and layered structure of the EG. Its high mechanical strength could postpone the disintegration of the nanocomposite structure,efficiently accommodate volume changes in the Ni Fe_2O_4-based anodes, and alleviate aggregation of Ni Fe_2O_4 nanoparticles.

Preparation of Expanded Graphite-based Composites by One Step Impregnation

A new method for preparing expanded graphite-based composites （EGCs） was developed.The obtained samples were characterized by scanning electron microscopy （SEM）,transmission electron microscope （TEM） and nitrogen adsorption.The experimental results indicated that the EGCs was not simply mechanical mixture of EG and activated carbon,instead the activated carbon was coated on the surface of interior and external pores of the EG in the form of thin carbon layer.The thickness of the activated carbon layer was nearly one hundred nanometers by calculation.It was shown that the higher the impregnation ratio and the activation temperature were,the easier the porosity development would be.And the BET surface area and the total pore volume were as high as 1978 m2/g and 0.9917 cm3/g respectively at 350℃ with an impregnation ratio of 0.9.

Electrical Properties of Expanded Graphite Intercalation Compounds

The intercalation compounds of CuCl2 were synthesized with expanded graphite, whose magnitude of the electrical conductivity is about 10(3)S(.)cm(-1). Their electrical conductivity is 3 similar to6 times as high as that of the expanded graphite, and about 10 times as high as that of GIC made of the non-expanded graphite. The microanalysis results of chemical compounds by X-ray energy spectrum scanning of TEM testified that the atomic ratio of chloride and cupric is nonstoichoimetric. The multivalence and exchange of electrovalence of the cupric ion was confirmed by the XPS-ESCA. Vacancy of chlorine anion increases the concentration of charge carrier. The special stage structure, made of graphite and chloride, produces a weak chemical bond belt and provides a carrier space in the direction of GIC layer. These factors develop the electrical properties.

A graphitized expanded graphite cathode for aluminum-ion battery with excellent rate capability

Aluminum-ion battery(AIB)is very promising for its safety and large current charge–discharge.However,it is challenging to build a high-performance AIB system based on low-cost materials especially cathode&electrolyte.Despite the low-cost expanded graphite-triethylaminehydrochloride(EG-ET)system has been improved in cycle performance,its rate capability still remains a gap with the expensive graphene-alkylimidazoliumchloride AIB system.In this work,we treated the cheap EG appropriately through an industrial high-temperature process,employed the obtained EG3K(treated at 3000℃)cathode with AlCl_(3)-ET electrolyte,and built a novel,high-rate capability and double-cheap AIB system.The new EG3K-ET system achieved the cathode capacity of average 110 m Ah g^(-1)at 1 A g^(-1)with 18,000cycles,and retained the cathode capacity of 100 m Ah g^(-1)at 5 A g^(-1)with 27,500 cycles(fast charging of 72 s).Impressively,we demonstrated that a battery pack(EG3K-ET system,12 m Ah)had successfully driven the Model car running 100 m long.In addition,it was confirmed that the improvement of rate capability in the EG3K-ET system was mainly derived by deposition,and its capacity contribution ratio was about 53.7%.This work further promoted the application potential of the low-cost EG-ET AIB system.

Mechanism of Fume Suppression and Performance on Asphalt of Expanded Graphite for Pavement under High Temperature Condition

Fume suppression mechanisms and the effect of expanded graphite on the performance of asphalt were studied by applying infrared spectroscopy（FT-IR）, X-ray diffraction（XRD）, scanning electron microscopy（SEM） and comprehensive thermal analysis（TG, DSC）. The experimental results confirm that asphalt which is mixed with expandable graphite will expand in the process of hot mix, and the expanded graphite layer will swell by the light component in the asphalt. The light component in the asphalt and PAHs adsorption on expanded graphite surface or part of the plug in the expanded graphite layer between plates made nucleation crystallization growth. And the Van der Waals force and the bonding of the lattice can effectively restrain the asphalt fume release. Meanwhile, the expanding agent with oxidative can spread into the asphalt, leading to asphalt oxygenated and plastic abate, while the ductility decreases. Expanded graphite, SBS modifier and environment- friendly plasticizers are used to composite modified asphalt. According to asphalt fume release experiment, normal test of asphalt performance, Brookfield viscosity test, RTFOT test and asphalt mixture tests（high temperature stability, low temperature stability, water stability）, it has been proven that the modified asphalt’s performance is better than that of matrix asphalt and equivalent to that of SBS modified asphalt. Furthermore, it has good fume suppression effect.

Insights on the mechanism of Na-ion storage in expanded graphite anode

Currently,Na-ion battery(NIB) has become one of the most potential alternatives for Li-ion batteries due to the safety and low cost.As a promising anode for Na-ion storage,expanded graphite has attracted considerable attention.However,the sodiation-desodiation process is still unclear.In our work,we obtain expanded graphite through slight modified Hummer's method and subsequent thermal treatment,which exhibits excellent cycling stability.Even at a high current density of 1 A g^(-1),our expanded graphite still remains a high reversible capacity of 100 mA h g^(-1) after 2600 cycles.Furthermore,we also investigate the electrochemical mechanism of our expanded graphite for Na-ion storage by operando Raman technique,which illuminate the electrochemical reaction during different sodiation-desodiation processes.

Preparation and Characterization of TiO_2/Expanded Graphite

In order to obtain anatase TiO2/expanded graphite with high expansion volume, titania gel was introduced to expandable graphite surface by sol-gel process, and then the composite was expanded and calcined at high tempera- ture. The samples were analysed by using scanning electron microscope （SEM）, X-ray diffraction（XRD）, energy disperse spectroscopy （EDS）, and differential scanning calorimetry （DSC）. The optimal conditions for preparation are as follows： the molar ratio of tetrabutyl orthotitanate to triethanolamine is 1 ： 0.4, and the calcination and expansion temperature is in the range of 650--750 ~C. Under such conditions, the expansion volume of composites could reach 98 mE/g, and the mass loss ratio is less than 5%. The analysis shows that lower temperature and smaller particle size of graphite are helpful to the formation of anatase-type of TiO2, but larger particle size will lead to lower mass loss ratio, and higher temperature and larger particle size will lead to higher expansion volume.

ZnO-Embedded Expanded Graphite Composite Anodes with Controlled Charge Storage Mechanism Enabling Operation of Lithium-Ion Batteries at Ultra-Low Temperatures

As lithium(Li)-ion batteries expand their applications,operating over a wide temperature range becomes increasingly important.However,the lowtemperature performance of conventional graphite anodes is severely hampered by the poor diffusion kinetics of Li ions(Li^(+)).Here,zinc oxide(ZnO) nanoparticles are incorporated into the expanded graphite to improve Li^(+)diffusion kinetics,resulting in a significant improvement in lowtemperature performance.The ZnO-embedded expanded graphite anodes are investigated with different amounts of ZnO to establish the structurecharge storage mechanism-performance relationship with a focus on lowtemperature applications.Electrochemical analysis reveals that the ZnOembedded expanded graphite anode with nano-sized ZnO maintains a large portion of the diffusion-controlled charge storage mechanism at an ultra-low temperature of-50℃ Due to this significantly enhanced Li^(+)diffusion rate,a full cell with the ZnO-embedded expanded graphite anode and a LiNi_(0.88)Co_(0.09)Al_(0.03)O_(2)cathode delivers high capacities of 176 mAh g^(-1)at20℃ and 86 mAh g^(-1)at-50℃ at a high rate of 1 C.The outstanding low-temperature performance of the composite anode by improving the Li^(+)diffusion kinetics provides important scientific insights into the fundamental design principles of anodes for low-temperature Li-ion battery operation.

Adsorption mechanism of expanded graphite for oil and dyes

Expanded graphite （r-;G） shows higher adsorption capacity for oils than for dyes. To illustrate the different adsorption mechanism of EG for these pollutants, adsorption capacities of dyes and oil on EG were firstly studied. And then stepwise adsorption for oils was carried out with EG which has been saturated firstly by dyes, the difference between adsorbance of oil on EG was checked with deviation analysis. Scanning electronic microscopy （SEM） analysis was used to show structure difference of EG adsorbed different adsorbates. These used adsorbates were SD300 oil, basic fuchsine, Auramine lake yellow O and acid brilliant red 3B. The adsorption isotherm of dyes on EG is type 11 or type 1, and their equilibrium adsorbances are less than 1.0 g/g. While, adsorbance for SD300 oil can reach 104.5 g/g. Deviation analysis for stepwise adsorbances of oil shows no statistical significance. EG saturated firstly by dyes, still has an average adsorption capacity of 35 g/g for SD300 oil, and it does not change with the initial dyes concentration. SEM photos illustrate the adsorption of oil on EG is mainly filling, In the adsorption of dyes, there is severe breakage of the V-type pore and shrinkage of the particle. Kinetic difference is analyzed also.

A M?ssbauer investigation of nano-NiFe alloy/expanded graphite for electromagnetic shielding

A new material is prepared by impregnating the expanded graphite(EG) into ethanol solutions of metal acetate and then drying and reducing it in H2.It contains the EG and the nanoparticles of the magnetic Ni–Fe alloy for the electromagnetic shielding.Its morphology,phase structure,magnetic properties,and electromagnetic shielding effectiveness(SE) are investigated in our experiment.It shows that the morphology,the phase structure,and the magnetic property of the composite can be modified by altering the Ni content in the alloy nanoparticles.Interestingly,the SE can be enhanced to 54–70 d B at low frequencies(300 kHz–10 MHz) by dispersing the magnetic nanoparticles onto EG.

A novel approach for synthesis of expanded graphite and its enhanced lithium storage properties

Relying on the great success in portable and smart devices,lithium ion batteries(LIBs)have been considered as one of the leading technologies in electric vehicles(EVs)and stationary energy storage systems(ESSs).With the rapid development of EVs and ESSs,the technology upgrading of LIBs is highly demanded.As expected,it requires LIBs with improved power and energy densities[1].

Research on Complex Refraction Indices of Expanded Graphite

The expanded graphite (EG) with a low density and better extinction performance can be used in military as passive jamming material in IR and MMW bands. Its complex refractive index is a significant parameter for the extinction property. This paper presents a method to calculate the complex refractive index of EG. The reflection spectra of EG pellets were measured in the 0.24-2.6μm and 2.5-25μm bands, respectively. Based on the measurement results, the complex refractive index of EG in 5-10μm band was calculated by using Kramers-Kronig(K-K) relation and Bruggeman effective medium theory, and then the errors were analyzed. The results indicate that it is feasible to calculate the complex refractive index of EG based on its IR reflection spectra data.

Preparation and Properties of 1-octadecanol/1,3:2,4-di-(3,4-dimethyl) Benzylidene Sorbitol/Expanded Graphite Form-stable Composite Phase Change Material

A 1-octadecanol（OD）/1,3:2,4-di-（3,4-dimethyl） benzylidene sorbitol（DMDBS）/expander graphite（EG） composite was prepared as a form-stable phase change material（PCM） by vacuum melting method. The results of field emission-scanning electron microscopy（FE-SEM） showed that 1-octadecanol was restricted in the three-dimensional network formed by DMDBS and the honeycomb network formed by EG. X-ray diffraction（XRD） and Fourier transform infrared spectroscopy（FT-IR） results showed that no chemical reaction occurred among the components of composite PCM in the preparation process. The gel-to-sol transition temperature of the composite PCMs containing DMDBS was much higher than the melting point of pure 1-octadecanol. The improvements in preventing leakage and thermal stability limits were mainly attributed to the synergistic effect of the three-dimensional network formed by DMDBS and the honeycomb network formed by EG. Differential scanning calorimeter（DSC） was used to determine the latent heat and phase change temperature of the composite PCMs. During melting and freezing process the latent heat values of the PCM with the composition of 91% OD/3% DMDBS/6% EG were 214.9 and 185.9 kJ·kg-1, respectively. Its degree of supercooling was only 0.1 ℃. Thermal constant analyzer results showed that its thermal conductivity（κ） changed up to roughly 10 times over that of OD/DMDBS matrix.

Palmitic Acid-Lauric Acid/Expanded Graphite as Form-Stable Composite Phase Change Material for Low-Temperature Energy Storage Applications

Low thermal conductivity of binary fatty acid mixture of palmitic and lauric acids(PA-LA)within the value range of 0.15-0.17 W/(m·K)restricts its wide utilization as thermal energy storage material in the active regime of solar heating applications at low operating temperatures.Nevertheless,this mixture as phase change material(PCM)has a suitable phase-change temperature and heat of 36℃and 176.3 J/g,respectively.Hence,the objective of this study is to formulate a novel form-stable composite PCM with the PA-LA mixture and expanded graphite(EG)as a thermal enhancer.PA-LA eutectic mixture with varied concentrations of EG was prepared and characterized.The thermal conductivity of PA-LA/EG increased gradually with the mass of EG.Optimum thermal properties were observed in PA-LA/(5%EG)composite,where its melting(T_(m)),freezing temperature(T_(t)),latent melting heat and thermal conductivity was 35.53℃,34.84℃,174 J/g,and 1.19 W/(m·K),respectively.Also,the composite PCM is characterized by good chemical-thermal stability and thermal reliability for long-term usage.In conclusion,it can be utilized as a prospective form-stable PCM for thermal energy storage in solar heating systems,overheat treatment systems,and other thermal storage applications at low operating temperatures.

Preparation and Photocatalytic Ability of Magnetic Nanosized Titania/Expanded Graphite Light Catalyst

By using hydrothermal synthesis method, successively adding tetrabutyl titanate and expandable flake graphite in 40 mL 0.95% NH4Cl solution prepared the nano TiO2/expandable flake graphite, which was then settled in muffle furnace in the expansion of 10 s under 800 ℃ and got nanosized TiO2/expanded graphite. Synthesized that with CoFe2O4 by chemical coprecipitation method finally prepared magnetic nanosized photocatalyst TiO2/expanded graphite. Magnetic nanosized TiO2/expanded graphite was studied on the photodegradation performance of methyl orange solution and the magnetic recovery after the degradation of methyl orange solution. The experiment result showed that in 50 mL 25 mg/L methyl orange solution joined 120 mg loading 50% TiO2 of the expanded graphite, exposed to ultraviolet irradiation for 1 h, the methyl orange decolorization ratio was 90%. When the load of CoFe2O4 in nanosized TiO2/expanded graphite reached 40%, its magnetic recovery efficiency reached 94.3%.

Regulated adsorption-diffusion and enhanced charge transfer in expanded graphite cohered with N,B bridge-doping carbon patches to boost K-ion storage

The great challenges are remained in constructing graphite-based anode with well built-in structures to accelerate kinetics and enhance stability in the advanced K-ion batteries(KIBs).Here,we firstly report the design of expanded graphite cohered by N,B bridge-doping carbon patches(NBEG)for efficient K-ion adsorption/diffusion and long-term durability.It is the B co-doping that plays a crucial role in maximizing doping-site utilization of N atoms,balancing the adsorption-diffusion kinetics,and promoting the charge transfer between NBEG and K ions.Especially,the robust lamellar structure,suitable interlayer distance,and rich active sites of the designed NBEG favor the rapid ion/electron transfer pathways and high K-ion storage capacity.Consequently,even at a low N,B doping concentration(4.36 at%,2.07 at%),NBEG anode shows prominent electrochemical performance for KIBs,surpassing most of the advanced carbon-based anodes.Kinetic studies,density functional theory simulations,and in-situ Raman spectroscopy are further performed to reveal the K-ion storage mechanism and confirm the critical actions of co-doping B.This work offers the new methods for graphite-electrode design and the deeper insights into their energy storage mechanisms in KIBs.

Fatty Acid/Expanded Graphite Encapsulating Form-Stable Phase Change Materials for Energy Storage

The lauric-myristic-palmitic acid( LA-MA-PA) ternary eutectic mixtures/expanded graphite( EG) composite phase change materials( PCMs) were prepared by absorbing LA-MA-PA into the porous network of EG. The optimum ratio of ternary eutectic mixtures to EG was determined to be 93∶7 without liquid LA-MA-PA leakage from the composite PCMs. In order to make the structure more stable, the composite PCMs were encapsulated by surface treatment agent to prepare LA-MA-PA/EG encapsulating form-stable PCMs which were characterized by scanning electron microscope( SEM),Fourier transformation infrared spectroscope( FT-IR),differential scanning calorimetry( DSC) and thermal treatment. The results showed there was no chemical reaction between surface treatment agent and LA-MA-PA,and the samples were compactly encapsulated which left almost no imprint on the filter paper after thermal treatment. The phase change temperature and latent heat of LA-MA-PA/EG encapsulating form-stable PCMs were tested to be29. 32 ℃ and 96. 20 J/g,respectively. Additionally,the heat transfer efficiency of heat storage was improved by the addition of EG.

Organically-Expanded Graphite/Octadecylamine: Structural, Thermal and Relaxation Evaluation

Natural graphite was chemically modified by an acid mixture (H2SO4/HNO3, 4:1) using sonication. The resulting material was then expanded with octadecylamine by the dispersion method. The sample was characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetry (TG), wide-angle X-ray diffraction (WAXD) and relaxometry—low-field nuclear magnetic resonance (LFNMR). The SEM images revealed the expansion of the graphite layers. The presence of CH absorption was detected in the infrared spectrum of the expanded sample. The WAXD showed an additional diffraction peak at lower 2θ angle, indicating that intercalation of octadecylamine was successful. The thermogravimetry curve revealed three degradation steps. Two of them could be attributed to different structures (delaminated and exfoliated). The relaxometry showed that the relaxation time was dependon the frequency and the curve of the graphite/octadecylamine presented two peaks—approximately before 106 Hz and after 107 Hz. The results permitted inferring that organically modified graphite was achieved.