Porous LiMn2O4 Microspheres With Different Pore Size: Preparation and Application as Cathode Materials for Lithium Ion Batteries

Author(s):  
Shiyou Li ◽  
Konglei Zhu ◽  
Jinliang Liu ◽  
Dongni Zhao ◽  
Xiaoling Cui

Three types of LiMn2O4 (LMO) microspheres with different pore size are prepared by a facile method, using porous MnCO3–MnO2 and Mn2O3 microspheres as the self-supporting template, for lithium ion batteries (LIBs) cathode material. Briefly, Mn2O3 and MnO2 microspheres are heated in air at 600 °C for 10 h to synthesize porous Mn2O3 spheres. Then the mixture of as-prepared spherical Mn2O3 and LiNO3 is calcined to obtain the LMOs. The morphology and structure of LMOs are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and nitrogen adsorption/desorption analyses. The result shows that the maximum pore diameters of LMOs are 17 nm, 19 nm, and 11 nm, respectively. All LMOs microspheres are composed of similar sized nanoparticles; however, the surface of these microspheres is strewed with dense tinier pores or sparse larger pores. Generally, the nanoparticles will reduce the path of Li+ ion diffusion and increases the reaction sites for lithium insertion/extraction. Moreover, the pores can provide buffer spaces for the volume changes during charge–discharge process. The electrochemical performances of LMOs are investigated and LMO2 exhibits extremely good electrochemical behavior, especially the rate capability. The as-prepared LMO2 delivers a discharge capacity of 124.3 mAh g−1 at 0.5 C, retaining 79.6 mAh g−1 even at 5 C. The LMO2 sample also shows good capacity retention of 96.9% after 100 cycles at 0.5 C.

Nanoscale ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 4445-4451 ◽  
Author(s):  
Weiqin Li ◽  
Cuihua An ◽  
Huinan Guo ◽  
Yan Zhang ◽  
Kai Chen ◽  
...  

The mesoporous MnFe2O4@C nanorods has been prepared using self-template method. Benefiting from the synergistic effect of carbon coating and mesoporous feature, MnFe2O4@C displays outstanding electrochemical performances for LIBs.


2017 ◽  
Vol 8 ◽  
pp. 1297-1306 ◽  
Author(s):  
Jin Zhang ◽  
Yibing Cai ◽  
Xuebin Hou ◽  
Xiaofei Song ◽  
Pengfei Lv ◽  
...  

Titanium dioxide (TiO2) nanofibers have been widely applied in various fields including photocatalysis, energy storage and solar cells due to the advantages of low cost, high abundance and nontoxicity. However, the low conductivity of ions and bulk electrons hinder its rapid development in lithium-ion batteries (LIB). In order to improve the electrochemical performances of TiO2 nanomaterials as anode for LIB, hierarchically porous TiO2 nanofibers with different tetrabutyl titanate (TBT)/paraffin oil ratios were prepared as anode for LIB via a versatile single-nozzle microemulsion electrospinning (ME-ES) method followed by calcining. The experimental results indicated that TiO2 nanofibers with the higher TBT/paraffin oil ratio demonstrated more axially aligned channels and a larger specific surface area. Furthermore, they presented superior lithium-ion storage properties in terms of specific capacity, rate capability and cycling performance compared with solid TiO2 nanofibers for LIB. The initial discharge and charge capacity of porous TiO2 nanofibers with a TBT/paraffin oil ratio of 2.25 reached up to 634.72 and 390.42 mAh·g−1, thus resulting in a coulombic efficiency of 61.51%; and the discharge capacity maintained 264.56 mAh·g−1 after 100 cycles, which was much higher than that of solid TiO2 nanofibers. TiO2 nanofibers with TBT/paraffin oil ratio of 2.25 still obtained a high reversible capacity of 204.53 mAh·g−1 when current density returned back to 40 mA·g−1 after 60 cycles at increasing stepwise current density from 40 mA·g−1 to 800 mA·g−1. Herein, hierarchically porous TiO2 nanofibers have the potential to be applied as anode for lithium-ion batteries in practical applications.


2014 ◽  
Vol 07 (06) ◽  
pp. 1440013 ◽  
Author(s):  
Xiangjun Li ◽  
Hongxing Xin ◽  
Xiaoying Qin ◽  
Xueqin Yuan ◽  
Di Li ◽  
...  

Lithium and Mn rich solid solution materials Li [ Li 0.26 Ni 0.07 Co 0.07 Mn 0.56] O 2 were synthesized by a carbonate co-precipitation method and modified with a layer of graphene. The graphene-modified cathodes exhibit improved rate capability and cycling performance as compared to the bare cathodes. Electrochemical impedance spectroscopy (EIS) analyses reveal that the improved electrochemical performances are due to acceleration kinetics of lithium-ion diffusion and the charge transfer reaction of the graphene-modified cathodes.


2017 ◽  
Vol 373 ◽  
pp. 299-302
Author(s):  
Bo Zhou ◽  
Chong Yang Li ◽  
Ning Qi ◽  
Zhi Quan Chen

Porous ZnO were synthesized with soft template method using zinc acetate Zn (CH3COO)2·2H2O as precursor and block copolymer F127 as the surfactant. Nitrogen adsorption-desorption measurements indicate that the ZnO sample contains large pores with mean diameter of about 30 nm. However, both small-angle X-ray diffraction and transmission electron microscope measurements indicate that the pore ordering is missing. Positron lifetime measurements reveal two long lifetime components in the porous ZnO. The longest lifetime τ4 (75 ns) corresponds to ortho-positronium (o-Ps) annihilation in large pores. The pore size estimated from τ4 is about 10.6 nm. This is much smaller than that estimated from Nitrogen adsorption-desorption measurements. In addition, the intensity I4 is only about 2.2%. This is probably due to the chemical quenching and/or inhibition of positronium formation induced by ZnO, which reduces o-Ps lifetime and intensity, and leads to under estimation of the pore size.


2015 ◽  
Vol 814 ◽  
pp. 358-364
Author(s):  
Peng Xiao Huang ◽  
Shui Hua Tang ◽  
Hui Peng ◽  
Xing Li

Graphitized-Carbon coated Li4Ti5O12/C (Li4Ti5O12/GC) composites were prepared from Li2CO3, TiO2 and aromatic resorcinol via a facile rheological phase method. The microstructure and morphology of the samples were determined by XRD and SEM. The electrochemical performances of the samples were characterized by galvanostatic charge-discharge test and electrochemical impedance spectroscopy (EIS). The results reveal that the coating of graphitized carbon could effectively enhance the charge/transfer kinetics of the Li4Ti5O12 electrode. The Li4Ti5O12/GC could deliver a discharge specific capacity of 166 mAh/g at 0.2 C, 148 mAh/g at 1.0 C, 142 mAh/g at 3.0 C, 138 mAh/g at 5.0 C and 127 mAh/g at 10.0 C, respectively, and it still could remain at 132 mAh/g after cycled at 5.0 C for 100 cycles. The excellent rate capability of the Li4Ti5O12/C makes it a promising anode material for high rate lithium ion batteries.


2018 ◽  
Vol 271 ◽  
pp. 9-17 ◽  
Author(s):  
Lkhagvajav Sarantuya ◽  
Galsan Sevjidsuren ◽  
Pagvajav Altantsog ◽  
Namsrai Tsogbadrakh

Nanosized spinel Li4Ti5O12 was successfully synthesized by a solid state reaction method at 800°C according to the Li4Ti5O12cubic spinel phase structure. In this synthesizing process, anatase TiO2and Li2CO3were used as reactants. The average grain size of the synthesized powders was around 200 nm. The synthesized Li4Ti5O12powder was characterized X-ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray spectrometry (EDS), and Specific Surface Area Analyzer (BET, Brunner-Emmett-Teller) respectively. X-ray diffraction results show that calcination temperature and time have the important effects on the crystal structure of Li4Ti5O12powder. In this study, we used a first principle method, based on the density functional theory to explore electronic and structural properties of Li4Ti5O12, as anode material for lithium ion batteries. Differences on these properties between delithiation state Li4Ti5O12and lithiation state Li7Ti5O12are compared. All the predicted structural and electrochemical properties agree closely with the experimental findings in literature. The average intercalation voltage of 1.4V during charging/discharging were obtained. We have shown that the Li4Ti5O12material exhibits insulating behavior with the band gap of 3.16 and 3.90 eV using the GGA and GGA+U+J0calculations respectively. Li7Ti5O12becomes metallic as Li atoms inserted in Li4Ti5O12material. Spinel Li4Ti5O12has been regarded as an attractive anode material for the development of high-power lithium-ion batteries because of its unique attributes of high safety and rate capability.


2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Raul-Augustin Mitran ◽  
Daniela Berger ◽  
Jeanina Pandele-Cusu ◽  
Cristian Matei

Mesoporous silica materials are promising nanocarriers for the development of drug delivery systems. In this study, the influence of pore size, volume, surface area, and doping the silica framework on the release kinetics of a model drug, metoprolol, has been studied. 20% or 50% wt. therapeutic agent was loaded into the carrier mesopores through incipient wetness impregnation. The carriers and drug-loaded samples have been characterized by small- and wide-angle X-ray diffraction, FT-IR spectroscopy, scanning electron microscopy, and nitrogen adsorption-desorption isotherms. The in vitro release profiles have been fitted using a three-parameter kinetic model and they have been explained in terms of the release rate during the burst and sustained release stages and the fraction of drug molecules released during the burst stage. The silica framework doping with aluminum was found to decrease the amount of drug released in the burst stage, without affecting the other kinetic parameters. The therapeutic agent release rates depend mainly on the pore size and volume of the mesoporous carriers and drug-loaded samples.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Seung-Hwan Lee ◽  
Bong-Soo Jin ◽  
Hyun-Soo Kim

AbstractBoron-doped Ni-rich LiNi0.84Co0.10Mn0.06O2 (B-NCM) cathode material is prepared and its electrochemical performances are investigated. The structural properties indicate that the incorporation of boron leads to highly-ordered layered structure and low cation disordering. All samples have high areal loadings of active materials (approximately 14.6 mg/cm2) that meets the requirement for commercialization. Among them, the 1.0 wt% boron-doped NCM (1.0B-NCM) shows the best electrochemical performances. The 1.0B-NCM delivers a discharge capacity of 205. 3 mAh g−1, cyclability of 93.1% after 50 cycles at 0.5 C and rate capability of 87.5% at 2 C. As a result, we can conclude that the 1.0B-NCM cathode can be regarded as a promising candidate for the next-generation lithium ion batteries.


Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3125 ◽  
Author(s):  
Yuan Wang ◽  
Chuanqiang Yin ◽  
Zhenglin Song ◽  
Qiulin Wang ◽  
Yu Lan ◽  
...  

Surface coating modification on a polyethylene separator serves as a promising way to meet the high requirements of thermal dimensional stability and excellent electrolyte wettability for lithium ion batteries (LIBs). In this paper, we report a new type of surface modified separator by coating polyvinylidene fluoride (PVDF) organic particles on traditional microporous polyethylene (PE) separators. The PE separator coated by PVDF particles (PE-PVDF separator) has higher porosity (61.4%), better electrolyte wettability (the contact angle to water was 3.28° ± 0.21°) and superior ionic conductivity (1.53 mS/cm) compared with the bare PE separator (51.2%, 111.3° ± 0.12°, 0.55 mS/cm). On one hand, the PVDF organic polymer has excellent organic electrolyte compatibility. On the other hand, the PVDF particles contain sub-micro spheres, of which the separator can possess a large specific surface area to absorb additional electrolyte. As a result, LIBs assembled using the PE-PVDF separator showed better electrochemical performances. For example, the button cell using a PE-PVDF as the separator had a higher capacity retention rate (70.01% capacity retention after 200 cycles at 0.5 C) than the bare PE separator (62.5% capacity retention after 200 cycles at 0.5 C). Moreover, the rate capability of LIBs was greatly improved as well—especially at larger current densities such as 2 C and 5 C.


Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1071
Author(s):  
Xuli Ding ◽  
Daowei Liang ◽  
Hongda Zhao

Although the silicon oxide (SiO2) as an anode material shows potential and promise for lithium-ion batteries (LIBs), owing to its high capacity, low cost, abundance, and safety, severe capacity decay and sluggish charge transfer during the discharge–charge process has caused a serious challenge for available applications. Herein, a novel 3D porous silicon oxide@Pourous Carbon@Tin (SiO2@Pc@Sn) composite anode material was firstly designed and synthesized by freeze-drying and thermal-melting self-assembly, in which SiO2 microparticles were encapsulated in the porous carbon as well as Sn nanoballs being uniformly dispersed in the SiO2@Pc-like sesame seeds, effectively constructing a robust and conductive 3D porous Jujube cake-like architecture that is beneficial for fast ion transfer and high structural stability. Such a SiO2@Pc@Sn micro-nano hierarchical structure as a LIBs anode exhibits a large reversible specific capacity ~520 mAh·g−1, initial coulombic efficiency (ICE) ~52%, outstanding rate capability, and excellent cycling stability over 100 cycles. Furthermore, the phase evolution and underlying electrochemical mechanism during the charge–discharge process were further uncovered by cyclic voltammetry (CV) investigation.


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