Enhanced Electrochemical Performance of LiNi0.8Co0.1Mn0.1O2 Cathode Materials by Al2O3 Coating

Author(s):  
Yaohua Feng ◽  
Hui Xu ◽  
Bo Wang ◽  
Shimin Wang ◽  
Ling Ai ◽  
...  

Abstract The Ni-rich LiNi0.8Co0.1Mn0.1O2 (NCM811) is considered as a promising high capacity (more than 160 mAh/g) cathode for lithium-ion batteries. However, NCM811 suffers the rapid capacity fading and potential safety hazard during cycling, which hinders further commercial application. Herein, a homogeneous Al2O3 film is successfully coated on the NCM811 surface by the liquid phase deposition. The Al2O3 coating layer is evidenced by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. The results clearly demonstrate that the Al2O3 film is uniformly covered on the NCM811. In particular, the 2 wt% Al2O3-coated materials delivers a high discharge capacity of 162.2 mAh/g and with retention of 82.67% after 100 cycles at 0.5 C than that of the pristine NCM811 electrode with retention of 64.90% and discharge capacity of 111.50 mAh/g. The improved electrochemical performance can be ascribed to the thin and dense coating layer not only effectively inhibits the direct contact between the material and the electrolyte but also promotes the transfer of Li+ in the layered structure material.

Materials ◽  
2019 ◽  
Vol 12 (16) ◽  
pp. 2630 ◽  
Author(s):  
Yuyao Zhang ◽  
Jun Li ◽  
Wenyao Li ◽  
Danning Kang

TiO2 is regarded as a prospective electrode material owing to its excellent electrochemical properties such as the excellent cycling stability and the high safety. However, its low capacity and low electronic conductivity greatly restrict the further improvement in electrochemical performance. A new strategy was put forward to solve the above defects involved in TiO2 in which the low capacity was enhanced by nanomerization and porosity of TiO2, and the low electronic conductivity was improved by introducing Ag with a high conductivity. One-dimensional mesoporous Ag nanoparticles-embedded TiO2 nanofibers (Ag@TiO2 nanofibers) were successfully synthesized via a one-step electrospinning process combined with subsequent annealing treatment in this study. The microstructure and morphology of mesoporous TiO2@Ag nanofibers were confirmed by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and nitrogen adsorption–desorption. TiO2 nanofibers mainly consisted of a large amount of anatase TiO2, accompanied with traces of rutile TiO2. Ag nanoparticles were uniformly distributed throughout TiO2 nanofibers and promoted the transformation of TiO2 from the anatase to the rutile. The corresponding electrochemical performances are measured by galvanostatic charge-discharge, cycle stability, rate performance, cycle voltammetry, and electrochemical impedance spectroscopy measurements in this research, with pristine TiO2 nanofibers as the reference. The results indicated that the introduction of Ag nanoparticles into TiO2 nanofibers significantly improved the diffusion coefficient of Li ions (5.42 × 10−9 cm2⋅s−1 for pristine TiO2, 1.96 × 10−8 cm2⋅s−1 for Ag@TiO2), and the electronic conductivity of TiO2 (1.69 × 10−5 S⋅cm−1 for pristine TiO2, and 1.99 × 10−5 S⋅cm−1 for Ag@TiO2), based on which the comprehensive electrochemical performance were greatly enhanced. The coulombic efficiency of the Ag@TiO2 nanofibers electrode at the first three cycles was about 56%, 93%, and 96%, which was higher than that without Ag (48%, 66%, and 79%). The Ag@TiO2 nanofibers electrode exhibited a higher specific discharge capacity of about 128.23 mAh⋅g−1 when compared with that without Ag (72.76 mAh·g−1) after 100 cycles at 100 mA·g−1. With the current density sharply increased from 40 mA·g−1 to 1000 mA·g−1, the higher average discharge capacity of 56.35 mAh·g−1 was remained in the electrode with Ag, when compared with the electrode without Ag (average discharge capacity of about 12.14 mAh·g−1). When the current density was returned to 40 mA·g−1, 80.36% of the initial value was returned (about 162.25 mAh·g−1) in the electrode with Ag, which was evidently superior to that without Ag (about 86.50 mAh·g−1, only 55.42% of the initial value). One-dimensional mesoporous Ag@TiO2 nanofibers can be regarded as a potential and promising candidate as anode materials for lithium ion batteries.


2019 ◽  
Vol 9 (19) ◽  
pp. 4032 ◽  
Author(s):  
Luis Zuniga ◽  
Gabriel Gonzalez ◽  
Roberto Orrostieta Chavez ◽  
Jason C. Myers ◽  
Timothy P. Lodge ◽  
...  

We report results on the electrochemical performance of flexible and binder-free α-Fe2O3/TiO2/carbon composite fiber anodes for lithium-ion batteries (LIBs). The composite fibers were produced via centrifugal spinning and subsequent thermal processing. The fibers were prepared from a precursor solution containing PVP/iron (III) acetylacetonate/titanium (IV) butoxide/ethanol/acetic acid followed by oxidation at 200 °C in air and then carbonization at 550 °C under flowing argon. The morphology and structure of the composite fibers were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). These ternary composite fiber anodes showed an improved electrochemical performance compared to the pristine TiO2/C and α-Fe2O3/C composite fiber electrodes. The α-Fe2O3/TiO2/C composite fibers also showed a superior cycling performance with a specific capacity of 340 mAh g−1 after 100 cycles at a current density of 100 mA g−1, compared to 61 mAh g−1 and 121 mAh g−1 for TiO2/C and α-Fe2O3/C composite electrodes, respectively. The improved electrochemical performance and the simple processing of these metal oxide/carbon composite fibers make them promising candidates for the next generation and cost-effective flexible binder-free anodes for LIBs.


RSC Advances ◽  
2016 ◽  
Vol 6 (27) ◽  
pp. 22625-22632 ◽  
Author(s):  
Honglong Zhang ◽  
Bing Li ◽  
Jing Wang ◽  
Bihe Wu ◽  
Tao Fu ◽  
...  

The Li2MnO3-coated LiNi0.8Co0.1Mn0.1O2 shows a higher discharge capacity and a better capacity retention. The coating layer can protect the NCM active materials from CO2, suppressing the formation of Li2CO3 on the surface of NCM materials.


2013 ◽  
Vol 01 (04) ◽  
pp. 1340017
Author(s):  
ZAILEI ZHANG ◽  
YANHONG WANG ◽  
MEIJU ZHANG ◽  
QIANGQIANG TAN ◽  
FABING SU

We report a facile chemical vapor deposition (CVD) method to grow silicon/carbon ( Si / C ) microspheres on commercial graphite microsphere (GMs) surface to prepare Si / C / GMs composite anode materials for Li -ion batteries. The CVD synthesis is conducted at 900°C using methyltrichlorosilane ( CH 3 SiCl 3) as both the Si and C precursor, which is a cheap byproduct in organosilane industry. The samples are characterized by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, thermogravimetric analysis, Raman spectroscopy and X-ray photoelectron spectroscopy. It is found that the obtained Si / C / GMs composites are composed of Si nanocrystals, amorphous carbon and GMs. The CVD time significantly influences the morphology and electrochemical performance of the Si / C / GMs composite materials. The Si / C / GMs composite materials prepared at CVD condition of 900°C for 4 h possess improved electrochemical properties, showing a discharge capacity of 821.4 mAh g−1 at a rate of 50 mA g−1, and a good cycling performance (i.e., a reversible capacity of 565.2 mAh g−1 is retained after 50 cycles). The enhanced electrochemical performance is attributed to the formation of Si / C microsphere network among GMs, which increases the electronic conductivity and is able to buffer the large volume changes of Si during lithium ion insertion/extraction.


Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1730 ◽  
Author(s):  
Ha Tran Huu ◽  
Xuan Dieu Nguyen Thi ◽  
Kim Nguyen Van ◽  
Sung Jin Kim ◽  
Vien Vo

The demand for well-designed nanostructured composites with enhanced electrochemical performance for lithium-ion batteries electrode materials has been emerging. In order to improve the electrochemical performance of MoS2-based anode materials, MoS2 nanosheets integrated with g-C3N4 (MoS2/g-C3N4 composite) was synthesized by a facile heating treatment from the precursors of thiourea and sodium molybdate at 550 °C under N2 gas flow. The structure and composition of MoS2/g-C3N4 were confirmed by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, infrared spectroscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis and elemental analysis. The lithium storage capability of the MoS2/g-C3N4 composite was evaluated, indicating high capacity and stable cycling performance at 1 C (A·g−1) with a reversible capacity of 1204 mA·h·g−1 for 200 cycles. This result is believed the role of g-C3N4 as a supporting material to accommodate the volume change and improve charge transport for nanostructured MoS2. Additionally, the contribution of the pseudocapacitive effect was also calculated to further clarify the enhancement in Li-ion storage performance of the composite.


2020 ◽  
Vol 8 ◽  
Author(s):  
Jiequn Liu ◽  
Shengkui Zhong ◽  
Qingrong Chen ◽  
Luchao Meng ◽  
Qianyi Wang ◽  
...  

Compositing with metal oxides is proved to be an efficient strategy to improve electrochemical performance of anode material Li4Ti5O12 for lithium-ion batteries. Herein, spherical Li4Ti5O12/NiO composite powders have been successfully prepared via a spray drying method. X-ray diffraction and high-resolution transmission electron microscopy results demonstrate that crystal structure of the powders is spinel. Scanning electron microscopy results show that NiO uniformly distributes throughout Li4Ti5O12 matrix. It is found that compositing with NiO increases both discharge platform capacity and rate stability of Li4Ti5O12. The as-prepared Li4Ti5O12/NiO (5%) exhibits a high initial discharge capacity of 381.3 mAh g−1 at 0.1 C, and a discharge capacity of 194.7 mAh g−1 at an ultrahigh rate of 20 C.


2015 ◽  
Vol 2015 ◽  
pp. 1-8
Author(s):  
Liwei Su ◽  
Yali Sha ◽  
Jingkang Jiang ◽  
Lianbang Wang ◽  
Yuanhao Wang

Ultrathin carbon-coated LiMnPO4(ULMP/C) nanoplates were prepared through an ethylene glycol- (EG-) assisted pyrolysis method. Different from most of LiMnPO4/C works, the obtained ULMP/C possessed relatively small particle size (less than 50 nm in thickness) and preferable carbon coating (~1 nm in thickness, 2 wt.%). As a reference, LiMnPO4/C (LMP/C) composites were also fabricated via the traditional hydrothermal method. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), thermogravimetric analysis (TG), galvanostatic charge-discharge, and cyclic voltammetry (CV) were performed to characterize the crystalline phase, morphology, structure, carbon content, and electrochemical behaviors of samples. The electrochemical performance of bare and carbon-coated LiMnPO4was evaluated as cathodes in lithium ion batteries. As a result, the obtained ULMP/C nanoplates demonstrated much higher reversible capacities (110.9 mAh g−1after 50 cycles at 0.1 C) and rate performances than pure LMP and LMP/C composites. This facile and efficient EG-assisted pyrolysis method can enlighten us on exploiting advanced routes to modify active materials with ultrathin and homogeneous carbon layers.


Energies ◽  
2020 ◽  
Vol 13 (19) ◽  
pp. 5124
Author(s):  
Eun Hyuk Chung ◽  
Jong Pil Kim ◽  
Hyun Gyu Kim ◽  
Jae-Min Chung ◽  
Sei-Jin Lee ◽  
...  

It has been reported that improving electrical conductivity and maintaining stable structure during discharge/charge process are challenge for Si to be used as an anode for lithium ion batteries (LIB). To address this problem, milkweed (MW) was carbonized to prepare hollow carbon microtubes (HCMT) derived from biomass as an anode template for LIB. In order to improve electrical conductivity, various materials such as chitosan (CTS), agarose, and polyvinylidene fluoride (PVDF) are used as carbon source (C1, C2, and C3) by carbonization. Carbon coated HCMT@Si composits, HCMT@Si@C1, HCMT@Si@C1@C2, and HCMT@Si@C1@C3, have been successfully synthesized. Changes in structure and crystallinity of HCMT@Si composites were characterized by using X-ray diffraction (XRD). Specific surface area for samples was calculated by using BET (Brunauer–Emmett–Teller). Also, pore size and particle size were obtained by particle and pore size analysis system. The surface morphology was evaluated using high resolution scanning electron microscopy (HR-SEM), Field Emission transmission electron microscopy (TEM). The thermal properties of HCMT@Si composites were analyzed by thermogravimetric analysis (TGA). Our research was performed to study the synthesis and electrochemical performance of Si composite with HCMT by the carbonization of natural micro hollow milkweed to form an inner space. After carbonization at 900 °C for 2 h in N2 flow, inner diameter of HCMT obtained was about 10 μm. The electrochemical tests indicate that HCMT@Si@C1@C3 exhibits discharge capacity of 932.18 mAh/g at 0.5 A/g after 100 cycles.


Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 2025
Author(s):  
Ki Yoon Bae ◽  
Sung Ho Cho ◽  
Byung Hyuk Kim ◽  
Byung Dae Son ◽  
Woo Young Yoon

We developed a novel battery system consisting of a hybrid (LiCoO2 + LiV3O8) cathode in a cell with a hybrid (graphite + Li-metal) anode and compared it with currently used systems. The hybrid cathode was synthesized using various ratios of LiCoO2:LiV3O8, where the 80:20 wt% ratio yielded the best electrochemical performance. The graphite and Li-metal hybrid anode, the composition of which was calculated based on the amount of non-lithiated cathode material (LiV3O8), was used to synthesize a full cell. With the addition of LiV3O8, the discharge capacity of the LiCoO2 + LiV3O8 hybrid cathode increased from 142.03 to 182.88 mA h g−1 (a 28.76% improvement). The energy density of this cathode also increased significantly, from 545.96 to 629.24 W h kg−1 (a 15.21% improvement). The LiCoO2 + LiV3O8 hybrid cathode was characterized through X-ray diffraction analysis, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. Its electrochemical performance was analyzed using a battery-testing system and electrochemical impedance spectroscopy. We expect that optimized synthesis conditions will enable the development of a novel battery system with an increase in energy density and discharge capacity.


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