Vanadium Pentoxide Gels from Liquid Crystals to Lithium Batteries

1994 ◽  
Vol 369 ◽  
Author(s):  
J. Livage ◽  
N. Baffier ◽  
J.P. Pereira-Ramos ◽  
P. Davidson
Keyword(s):  
Vanadium Pentoxide ◽  
Lithium Batteries ◽  
Mixed Oxides ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Solid State Reactions ◽  
Polymerization Process ◽  
Display Devices ◽  
Oriented Films ◽  
Vanadic Acid

AbstractVanadium pentoxide gels V205.nH20 are formed via the condensation of vanadic acid in aqueous solutions. They exhibit both ionic and electronic conductivity and could therefore be used as cathode materials in lithium batteries or electrochromic display devices. The polymerization process leads to ribbon-like vanadium pentoxide particles. In a given range of concentration, sols and gels exhibit a homogeneous lyotropic nematic phase in which the ribbons align in the same direction. Ordered fluid phases are thus obtained leading to oriented films when deposited onto flat substrates. Moreover, mixed oxides MxV205 (M = Na+, K+,Ba2+, Al3+, Fe3+,Fe3+,...) exhibiting some preferred orientation are obtained via ion exchange.These compounds exhibit improved lectrochemical properties (specific capacity, cycling properties) compared to usual mixed oxides prepared via solid state reactions.

Combustion Synthesis of Sr-Substituted LaCo0.4Fe0.6O3 Powders

1992 ◽  
Vol 271 ◽  
Author(s):  
J. J. Kingsley ◽  
L. A. Chick ◽  
G. W. Coffey ◽  
D. E. McCready ◽  
L. R. Pederson
Keyword(s):  
Solid State ◽  
Metal Oxides ◽  
Mixed Oxides ◽  
Electronic Conductivity ◽  
Solid State Reactions ◽  
Bet Surface Area ◽  
Metal Nitrates ◽  
Subsequent Calcination ◽  
Multi Phase ◽  
Sorption Characteristics

ABSTRACTSr-substituted perovskite LaCo0.4Fe0.6O3 is known to have excellent mixed ionic and electronic conductivity and increased O2 sorption characteristics. These perovskites are usually prepared by lengthy solid-state reactions of the component oxides at temperatures near 1150°C, and often produce inhomogeneous, multi-phase powders. Presently, it has been prepared by the calcination of combustion-derived fine mixed oxides at 850°C in 6 hrs. Combustion reactions are carried out using precursor solutions containing the corresponding metal nitrates (oxidizers) and glycine (fuel) at 250°C. The metal oxides produced by this process and subsequent calcination were characterized by XRD, TEM and BET surface area analysis.

scholarly journals PEDOT-Coated Red Phosphorus Nanosphere Anodes for Pseudocapacitive Potassium-Ion Storage

Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1732
Author(s):  
Dan Zhao ◽  
Qian Zhao ◽  
Zhenyu Wang ◽  
Lan Feng ◽  
Jinying Zhang ◽  
...  
Keyword(s):  
Surface Engineering ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Lithium Ion ◽  
Average Diameter ◽  
Potassium Ion ◽  
Red Phosphorus ◽  
Fast Charging ◽  
Potential Alternative ◽  
High Theoretical Capacity

Potassium-ion batteries (KIBs) have come up as a potential alternative to lithium-ion batteries due to abundant potassium storage in the crust. Red phosphorus is a promising anode material for KIBs with abundant resources and high theoretical capacity. Nevertheless, large volume expansion, low electronic conductivity, and limited K+ charging speed in red phosphorus upon cycling have severely hindered the development of red phosphorus-based anodes. To obtain improved conductivity and structural stability, surface engineering of red phosphorus is required. Poly(3,4-ethylenedioxythiophene) (PEDOT)-coated red phosphorus nanospheres (RPNP@PEDOT) with an average diameter of 60 nm were synthesized via a facile solution-phase approach. PEDOT can relieve the volume change of red phosphorus and promote electron/ion transportation during charge−discharge cycles, which is partially corroborated by our DFT calculations. A specific capacity of 402 mAh g−1 at 0.1 A g−1 after 40 cycles, and a specific capacity of 302 mAh g−1 at 0.5 A g−1 after 275 cycles, were achieved by RPNP@PEDOT anode with a high pseudocapacitive contribution of 62%. The surface–interface engineering for the organic–inorganic composite of RPNP@PEDOT provides a novel perspective for broad applications of red phosphorus-based KIBs in fast charging occasions.

scholarly journals Binary PMMA/PVDF blend film modified substrate enables superior lithium metal anode for lithium batteries

2021 ◽  
Author(s):  
Yuping Wu ◽  
Xiaosong Xiong ◽  
Ruoyu Zhi ◽  
Qi Zhou ◽  
Wenqi Yan ◽  
...  
Keyword(s):  
Electrode Material ◽  
Lithium Batteries ◽  
Specific Capacity ◽  
Lithium Metal ◽  
Next Generation ◽  
Safety Hazards ◽  
Blend Film ◽  
Metal Anode ◽  
Lithium Metal Anode ◽  
Metallic Lithium

Metallic lithium is an promising next generation electrode material due to its ultrahigh specific capacity and the lowest potential. However, short cycling lifespan and safety hazards have hindered the practical...

scholarly journals Wire-in-Wire TiO2/C Nanofibers Free-Standing Anodes for Li-Ion and K-Ion Batteries with Long Cycling Stability and High Capacity

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Die Su ◽  
Yi Pei ◽  
Li Liu ◽  
Zhixiao Liu ◽  
Junfang Liu ◽  
...  
Keyword(s):  
Critical Role ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
High Capacity ◽  
Cycling Stability ◽  
Free Standing ◽  
High Specific Capacity ◽  
Tetracarboxylic Dianhydride ◽  
Carbon Network

AbstractWearable and portable mobile phones play a critical role in the market, and one of the key technologies is the flexible electrode with high specific capacity and excellent mechanical flexibility. Herein, a wire-in-wire TiO2/C nanofibers (TiO2 ww/CN) film is synthesized via electrospinning with selenium as a structural inducer. The interconnected carbon network and unique wire-in-wire nanostructure cannot only improve electronic conductivity and induce effective charge transports, but also bring a superior mechanic flexibility. Ultimately, TiO2 ww/CN film shows outstanding electrochemical performance as free-standing electrodes in Li/K ion batteries. It shows a discharge capacity as high as 303 mAh g−1 at 5 A g−1 after 6000 cycles in Li half-cells, and the unique structure is well-reserved after long-term cycling. Moreover, even TiO2 has a large diffusion barrier of K+, TiO2 ww/CN film demonstrates excellent performance (259 mAh g−1 at 0.05 A g−1 after 1000 cycles) in K half-cells owing to extraordinary pseudocapacitive contribution. The Li/K full cells consisted of TiO2 ww/CN film anode and LiFePO4/Perylene-3,4,9,10-tetracarboxylic dianhydride cathode possess outstanding cycling stability and demonstrate practical application from lighting at least 19 LEDs. It is, therefore, expected that this material will find broad applications in portable and wearable Li/K-ion batteries.

Processing and Performance of V205 Xerogel, Aerogel, and Aerogellike Materials as Lithium Intercalation Hosts

1998 ◽  
Vol 548 ◽  
Author(s):  
Leland H. Manhart ◽  
Jun John Xu ◽  
Fabrice Coustier ◽  
Stefano Passerini ◽  
Boone B. Owens ◽  
...  
Keyword(s):  
Lithium Batteries ◽  
Methyl Formate ◽  
Sol Gel ◽  
Specific Capacity ◽  
Lithium Intercalation ◽  
Composite Electrodes ◽  
Rechargeable Lithium Batteries ◽  
Exchange Processes ◽  
And Performance ◽  
Sol Gel Synthesis

ABSTRACTVarious forms of vanadium pentoxide, including xerogel, aerogel, and aerogel-like forms, were prepared by sol-gel synthesis and processed by novel procedures following synthesis. It was demonstrated that the intrinsic thermodynamics of lithium intercalation of the ARG and ARG-like materials prepared by solvent exchange processes involving methyl formate (MF/ARG and MF/ARG-xslike) are identical, while they are drastically different from those of the parent XRG, which gives rise to significantly increased specific energies for the MF/ARG or MF/ARG-like as lithium intercalation hosts. All three forms are capable of reversibly intercalating up to four moles of Li+ ions per mole of V205 electrochemically and can be cathode candidates for rechargeable lithium batteries. Various processing methods for fabricating composite electrodes with the XRG led to specific capacity in the range of 300 to 350 mAh/g at C4Li/ 20 rate, and good cyclability.

Supercritically exfoliated ultrathin vanadium pentoxide nanosheets with high rate capability for lithium batteries

2013 ◽  
Vol 15 (39) ◽  
pp. 16828 ◽  
Author(s):  
Qinyou An ◽  
Qiulong Wei ◽  
Liqiang Mai ◽  
Jiayang Fei ◽  
Xu Xu ◽  
...  
Keyword(s):  
Vanadium Pentoxide ◽  
Lithium Batteries ◽  
Rate Capability ◽  
High Rate ◽  
High Rate Capability

High-Capacity Derivatives Produced from Hydrolytic Lignin as Electrode Materials for Energy Storage and Conversion

2018 ◽  
Vol 386 ◽  
pp. 359-364
Author(s):  
Yury M. Nikolenko ◽  
Denis P. Opra ◽  
Alexander K. Tsvetnikov ◽  
Alexander Yu. Ustinov ◽  
Valery G. Kuryavyi ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Energy Storage ◽  
Electrode Materials ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Energy Storage And Conversion ◽  
Operating Voltage ◽  
X Ray ◽  
Thermally Activated ◽  
Hydrolytic Lignin

The hydrolytic lignin derivatives have been prepared via its physical activation (high-temperature heating in vacuum) followed by chemical modification (fluorination). The obtained products were characterized using scanning electron microscopy, X-ray diffraction, transmission electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy. It was found that the graphitized product of thermal activation up to 1000 °C at a low rate of < 2 °C/min under high vacuum shows an enhanced specific surface area (215 m2/g), that makes its potentially useful as sorbent, catalytic substrate or electrode material. To clarify the potentialities of hydrolytic lignin derivatives for energy storage and conversion, the electrochemical system with metallic lithium anode was applied. The galvanostatic discharge of battery at a current density of 100 μA/cm2between 3.0 and 0.5 V shows that the specific capacity of thermally activated derivative is equal to 845 mA·h/g, while the untreated lignin yields only 190 mA·h/g. The improve of the electrochemical performance of product originates from its graphitization, increasing electronic conductivity, and, possibly, enhanced ability to adsorb of oxygen. The fluorination of both the lignin and its thermally activated form results in higher operating voltage of battery, as seems, due to the involvement of fluorine bound to carbon in electrochemical process.

Constructing zigzag-like hollow mesoporous nanospheres MoO2/C with superior lithium storage performance

2021 ◽  
Author(s):  
Wencai Zhao ◽  
Y.F. Yuan ◽  
S.M. Yin ◽  
Gaoshen Cai ◽  
S.Y. Guo
Keyword(s):  
Reaction Kinetics ◽  
Discharge Capacity ◽  
Amorphous Carbon ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Rate Capability ◽  
Lithium Ion ◽  
Structure Design ◽  
Structure Stability ◽  
Lithium Storage

Abstract Hollow mesoporous nanospheres MoO2/C are successfully constructed through metal chelating reaction between molybdenum acetylacetone and glycerol as well as the Kirkendall effect induced by diammonium hydrogen phosphate. MoO2 nanoparticles coupled by amorphous carbon are assembled to unique zigzag-like hollow mesoporous nanosphere with large specific surface area of 147.7 m2 g-1 and main pore size of 8.7 nm. The content of carbon is 9.1%. As anode material for lithium-ion batteries, the composite shows high specific capacity and excellent cycling performance. At 0.2 A g-1, average discharge capacity stabilizes at 1092 mAh g-1. At 1 A g-1 after 700 cycles, the discharge capacity still reaches 512 mAh g-1. Impressively, the composite preserves intact after 700 cycles. Even at 5 A g-1, the discharge capacity can reach 321 mAh g-1, exhibiting superior rate capability. Various kinetics analyses demonstrate that in electrochemical reaction, the proportion of the surface capacitive effect is higher, and the composite has relatively high diffusion coefficient of Li ions and fast faradic reaction kinetics. Excellent lithium storge performance is attributed to the synergistic effect of zigzag-like hollow mesoporous nanosphere and amorphous carbon, which improves reaction kinetics, structure stability and electronic conductivity of MoO2. The present work provides a new useful structure design strategy for advanced energy storage application of MoO2.

scholarly journals MnO2/rGO/CNTs Framework as a Sulfur Host for High-Performance Li-S Batteries

Molecules ◽  
2020 ◽  
Vol 25 (8) ◽  
pp. 1989 ◽  
Author(s):  
Wei Dong ◽  
Lingqiang Meng ◽  
Xiaodong Hong ◽  
Sizhe Liu ◽  
Ding Shen ◽  
...  
Keyword(s):  
High Performance ◽  
Physical Adsorption ◽  
Rapid Development ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Framework Structure ◽  
Shuttle Effect ◽  
Lithium Sulfur Batteries ◽  
Lithium Sulfur ◽  
Initial Capacity

Lithium-sulfur batteries are very promising next-generation energy storage batteries due to their high theoretical specific capacity. However, the shuttle effect of lithium-sulfur batteries is one of the important bottlenecks that limits its rapid development. Herein, physical and chemical dual adsorption of lithium polysulfides are achieved by designing a novel framework structure consisting of MnO2, reduced graphene oxide (rGO), and carbon nanotubes (CNTs). The framework-structure composite of MnO2/rGO/CNTs is prepared by a simple hydrothermal method. The framework exhibits a uniform and abundant mesoporous structure (concentrating in ~12 nm). MnO2 is an α phase structure and the α-MnO2 also has a significant effect on the adsorption of lithium polysulfides. The rGO and CNTs provide a good physical adsorption interaction and good electronic conductivity for the dissolved polysulfides. As a result, the MnO2/rGO/CNTs/S cathode delivered a high initial capacity of 1201 mAh g−1 at 0.2 C. The average capacities were 916 mAh g−1, 736 mAh g−1, and 547 mAh g−1 at the current densities of 0.5 C, 1 C, and 2 C, respectively. In addition, when tested at 0.5 C, the MnO2/rGO/CNTs/S exhibited a high initial capacity of 1010 mAh g−1 and achieved 780 mAh g−1 after 200 cycles, with a low capacity decay rate of 0.11% per cycle. This framework-structure composite provides a simple way to improve the electrochemical performance of Li-S batteries.

scholarly journals Atomistic Modeling of Various Doped Mg2NiH4 as Conversion Electrode Materials for Lithium Storage

Crystals ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 254 ◽  
Author(s):  
Zhao Qian ◽  
Guanzhong Jiang ◽  
Yingying Ren ◽  
Xi Nie ◽  
Rajeev Ahuja
Keyword(s):  
Density Functional ◽  
Electrode Materials ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Density Functional Theory Calculations ◽  
Lithium Storage ◽  
Pure Material ◽  
Computational Screening ◽  
Electrochemical Capacity ◽  
Ti Doping

In this work, we have compared the potential applications of nine different elements doped Mg2NiH4 as conversion-type electrode materials in Li-ion batteries by means of state-of-the-art Density functional theory calculations. The electrochemical properties, such as specific capacity, volume change and average voltage, as well as the atomic and electronic structures of different doped systems have been investigated. The Na doping can improve the electrochemical capacity of the pristine material. Si and Ti doping can reduce the band gap and benefit the electronic conductivity of electrode materials. All of the nine doping elements can help to reduce the average voltage of negative electrodes and lead to reasonable volume changes. According to the computational screening, the Na, Si and Ti doping elements are thought to be promising to enhance the comprehensive properties of pure material. This theoretical study is proposed to encourage and expedite the development of metal-hydrides based lithium-storage materials.

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