Hydrothermal synthesis MoO3@CoMoO4 hybrid as an anode material for high performance lithium rechargeable batteries

2019 ◽  
Vol 12 (01) ◽  
pp. 1850104 ◽  
Author(s):  
Jinggao Wu ◽  
Qi Lai ◽  
Canyu Zhong
Keyword(s):  
Current Density ◽  
High Performance ◽  
High Current Density ◽  
Rate Capability ◽  
Lithium Ion ◽  
Charge Transfer Resistance ◽  
Rechargeable Batteries ◽  
Transfer Resistance ◽  
Lithium Rechargeable Batteries ◽  
One Step

MoO3@CoMoO4 hybrid is fabricated by a facile one-step hydrothermal method and is used as anode for lithium-ion battery (LIB). Compared to pristine MoO3, galvanostatic charge–discharge tests show that the hybrid electrode delivered a remarkable rate capability of 586.69[Formula: see text]mAh[Formula: see text]g[Formula: see text] at the high current density of 1000[Formula: see text]mA[Formula: see text]g[Formula: see text] and a greatly enhanced cyclic capacity of 887.36[Formula: see text]mA[Formula: see text]h[Formula: see text]g[Formula: see text] after 140 cycles at the current density of 200[Formula: see text]mA[Formula: see text]g[Formula: see text] (with capacity retention, 85.3%). The superior electrochemical properties could be ascribed to the synergistic effect of MoO3 and CoO nanostructure that results in the lower charge transfer resistance and the higher Li[Formula: see text] diffusion coefficient, thus leading to high performance Li[Formula: see text] reversibility storage.

Graphene-Wrapped FeOOH Nanorods with Enhanced Performance as Lithium-Ion Battery Anode

NANO ◽  
2020 ◽  
pp. 2150005
Author(s):  
Meng Sun ◽  
Zhipeng Cui ◽  
Huanqing Liu ◽  
Sijie Li ◽  
Qingye Zhang ◽  
...  
Keyword(s):  
High Performance ◽  
Electrode Materials ◽  
Electronic Conductivity ◽  
Rate Capability ◽  
Lithium Ion ◽  
Extraction Process ◽  
Hybrid Structure ◽  
Charge Transfer Resistance ◽  
Transfer Resistance ◽  
Distinctive Structure

FeOOH nanorods (NRs) wrapped by reduced graphene oxide (rGO) were fabricated using a facile solvothermal method. When used as anode materials for lithium-ion batteries (LIBs), the FeOOH NRs/rGO composites show a higher capacity (490[Formula: see text]mAh g[Formula: see text] after 100 cycles at a current density of 100[Formula: see text]mA g[Formula: see text] and better rate capability than pure FeOOH NRs. The enhanced electrochemical performance can be ascribed to the hybrid structure of FeOOH and rGO. On one hand, the introduction of rGO can improve electronic conductivity and reduce charge-transfer resistance for electrode materials. On the other hand, the distinctive structure (FeOOH NRs surrounded by flexible rGO) can effectively buffer large volume change during the Li[Formula: see text] insertion/extraction process. Our work provides a feasible strategy to obtain high-performance LIBs.

scholarly journals Conductive 2D metal-organic framework for high-performance cathodes in aqueous rechargeable zinc batteries

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Kwan Woo Nam ◽  
Sarah S. Park ◽  
Roberto dos Reis ◽  
Vinayak P. Dravid ◽  
Heejin Kim ◽  
...  
Keyword(s):  
High Performance ◽  
Large Scale ◽  
High Current Density ◽  
Metal Organic Framework ◽  
Lithium Ion ◽  
Rechargeable Batteries ◽  
Economic Feasibility ◽  
Interfacial Resistance ◽  
Metal Organic ◽  
Organic Framework

Abstract Currently, there is considerable interest in developing advanced rechargeable batteries that boast efficient distribution of electricity and economic feasibility for use in large-scale energy storage systems. Rechargeable aqueous zinc batteries are promising alternatives to lithium-ion batteries in terms of rate performance, cost, and safety. In this investigation, we employ Cu3(HHTP)2, a two-dimensional (2D) conductive metal-organic framework (MOF) with large one-dimensional channels, as a zinc battery cathode. Owing to its unique structure, hydrated Zn2+ ions which are inserted directly into the host structure, Cu3(HHTP)2, allow high diffusion rate and low interfacial resistance which enable the Cu3(HHTP)2 cathode to follow the intercalation pseudocapacitance mechanism. Cu3(HHTP)2 exhibits a high reversible capacity of 228 mAh g−1 at 50 mA g−1. At a high current density of 4000 mA g−1 (~18 C), 75.0% of the initial capacity is maintained after 500 cycles. These results provide key insights into high-performance, 2D conductive MOF designs for battery electrodes.

scholarly journals N-Doped Carbon Boosted the Formation of Few-Layered MoS2 for High-Performance Lithium and Sodium Storage

2021 ◽  
Vol 8 ◽  
Author(s):  
Junfeng Li ◽  
Xianzi Zhou ◽  
Kai Lu ◽  
Chao Ma ◽  
Liang Li ◽  
...  
Keyword(s):  
Current Density ◽  
High Performance ◽  
High Current Density ◽  
Low Cost ◽  
Lithium Ion ◽  
Reversible Capacity ◽  
Molybdenum Sulfide ◽  
High Current ◽  
High Theoretical Capacity ◽  
Sodium Storage

Molybdenum sulfide (MoS2) has become a potential anode of lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) due to its high theoretical capacity and low cost. However, the volume expansion, poor electrical conductivity and dissolution of polysulfides in the electrolyte during the cycling process severely limited its applications. Herein, few-layered MoS2@N-doped carbon (F-MoS2@NC) was synthesized through a facile solvothermal and annealing process. It was found that the addition of N-doped carbon precursor could significantly promote the formation of few-layered MoS2 and improve the performances of lithium and sodium storage. A high reversible capacity of 482.6 mA h g−1 at a high current density of 2000 mA g−1 could be obtained for LIBs. When used as anode material for SIBs, F-MoS2@NC hybrids could maintain a reversible capacity of 171 mA h g−1 at a high current density of 1,000 mA g−1 after 600 cycles. This work should provide new insights into carbon hybrid anode materials for both LIBs and SIBs.

scholarly journals Hierarchical Porous Carbon Derived from Sichuan Pepper for High-Performance Symmetric Supercapacitor with Decent Rate Capability and Cycling Stability

Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 553 ◽  
Author(s):  
Hengshuo Zhang ◽  
Wei Xiao ◽  
Wenjie Zhou ◽  
Shanyong Chen ◽  
Yanhua Zhang
Keyword(s):  
Specific Capacitance ◽  
Current Density ◽  
High Performance ◽  
High Current Density ◽  
Rate Capability ◽  
Cycling Stability ◽  
Koh Activation ◽  
High Current ◽  
Symmetric Supercapacitor ◽  
Hierarchical Porous

Hierarchical micro-mesoporous carbon (denoted as HPC-2 in this study) was synthesized by pre-carbonization of biomass Sichuan pepper followed by KOH activation. It possessed well-developed porosity with the specific surface area of 1823.1 m2 g−1 and pore volume of 0.906 cm3 g−1, and exhibited impressive supercapacitive behaviors. For example, the largest specific capacitance of HPC-2 was tested to be ca. 171 F g−1 in a three-electrode setup with outstanding rate capability and stable electrochemical property, whose capacitance retention was near 100% after cycling at rather a high current density of 40 A g−1 for up to 10,000 cycles. Furthermore, a two-electrode symmetric supercapacitor cell of HPC-2//HPC-2 was constructed, which delivered the maximum specific capacitance and energy density of ca. 30 F g−1 and 4.2 Wh kg−1, respectively, had prominent rate performance and cycling stability with negligible capacitance decay after repetitive charge/discharge at a high current density of 10 A g−1 for over 10,000 cycles. Such electrochemical properties of HPC-2 in both three- and two-electrode systems are superior or comparable to those of a great number of porous biomass carbon reported previously, hence making it a promising candidate for the development of high-performance energy storage devices.

Facile Synthesis of Polypyrrole Nanofibers/Co-MOF Composite and Its Lithium Storage Properties

2020 ◽  
Vol 12 (4) ◽  
pp. 486-491
Author(s):  
Jinlei Wang ◽  
Na Cao ◽  
Huiling Du ◽  
Xian Du ◽  
Hai Lu ◽  
...  
Keyword(s):  
Electrode Materials ◽  
Rate Capability ◽  
Lithium Ion ◽  
Reversible Capacity ◽  
Cycling Performance ◽  
Charge Transfer Resistance ◽  
Growth Strategy ◽  
Composite Electrodes ◽  
Lithium Storage ◽  
Transfer Resistance

Metal-organic frameworks (MOFs) have recently emerged as promising electrode materials for lithium-ion batteries (LIBs). However, poor electrical conductivity in most MOFs limits their electrochemical performance. In this work, the integration of flaky cobalt 1,4-benzenedicarboxylate (Co-BDC) MOF with conductive polypyrrole (PPy) nanofibers via in-situ growth strategy was explored for developing novel anode materials for LIBs. Electrochemical studies showed that PPy/Co-BDC composites exhibited enhanced cycling performance (a reversible capacity of ca. 364 mA h g–1 at a current density of 50 mA g–1 after 100 cycles) and rate capability, com- pared with the pristine Co-BDC. The well dispersion of Co-BDC on polypyrrole nanofibers and the decrease in charge-transfer resistance of the composite electrodes accounted for the improvement of electrochemical properties.

scholarly journals Aggregation-Morphology-Dependent Electrochemical Performance of Co3O4 Anode Materials for Lithium-Ion Batteries

Molecules ◽  
2019 ◽  
Vol 24 (17) ◽  
pp. 3149 ◽  
Author(s):  
Linglong Kong ◽  
Lu Wang ◽  
Deye Sun ◽  
Su Meng ◽  
Dandan Xu ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Lithium Ion Batteries ◽  
Anode Materials ◽  
High Performance ◽  
Retention Rate ◽  
Lithium Ion ◽  
Charge Transfer Resistance ◽  
Superior Performance ◽  
Electrode Structure ◽  
Transfer Resistance

The aggregation morphology of anode materials plays a vital role in achieving high performance lithium-ion batteries. Herein, Co3O4 anode materials with different aggregation morphologies were successfully prepared by modulating the morphology of precursors with different cobalt sources by the mild coprecipitation method. The fabricated Co3O4 can be flower-like, spherical, irregular, and urchin-like. Detailed investigation on the electrochemical performance demonstrated that flower-like Co3O4 consisting of nanorods exhibited superior performance. The reversible capacity maintained 910.7 mAh·g−1 at 500 mA·g−1 and 717 mAh·g−1 at 1000 mA·g−1 after 500 cycles. The cyclic stability was greatly enhanced, with a capacity retention rate of 92.7% at 500 mA·g−1 and 78.27% at 1000 mA·g−1 after 500 cycles. Electrochemical performance in long-term storage and high temperature conditions was still excellent. The unique aggregation morphology of flower-like Co3O4 yielded a reduction of charge-transfer resistance and stabilization of electrode structure compared with other aggregation morphologies.

Porous CuCo2O4 nanocubes wrapped by reduced graphene oxide as high-performance lithium-ion battery anodes

Nanoscale ◽  
2014 ◽  
Vol 6 (12) ◽  
pp. 6551-6556 ◽  
Author(s):  
Wenpei Kang ◽  
Yongbing Tang ◽  
Wenyue Li ◽  
Zhangpeng Li ◽  
Xia Yang ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Lithium Ion Battery ◽  
Reduced Graphene Oxide ◽  
Current Density ◽  
High Performance ◽  
High Current Density ◽  
Lithium Ion ◽  
High Current ◽  
Reduced Graphene ◽  
Graphene Oxide Sheets

Porous CuCo2O4 nanocubes well wrapped by reduced graphene oxide sheets were facilely prepared and they showed impressive performance at high current density as the anode material of a lithium ion battery.

scholarly journals Improved Electrochemical Performance of 0.5Li2MnO3·0.5LiNi0.5Mn0.5O2 Cathode Materials for Lithium Ion Batteries Synthesized by Ionic-Liquid-Assisted Hydrothermal Method

2020 ◽  
Vol 8 ◽  
Author(s):  
Yanhong Xiang ◽  
Youliang Jiang ◽  
Saiqiu Liu ◽  
Jianhua Wu ◽  
Zhixiong Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Electrochemical Performance ◽  
Hydrothermal Method ◽  
Cathode Materials ◽  
Electrochemical Impedance ◽  
Rate Capability ◽  
Lithium Ion ◽  
Charge Transfer Resistance ◽  
Transfer Resistance

Well-dispersed Li-rich Mn-based 0.5Li2MnO3·0.5LiNi0.5Mn0.5O2 nanoparticles with diameter ranging from 50 to 100 nm are synthesized by a hydrothermal method in the presence of N-hexyl pyridinium tetrafluoroborate ionic liquid ([HPy][BF4]). The microstructures and electrochemical performance of the prepared cathode materials are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical measurements. The XRD results show that the sample prepared by ionic-liquid-assisted hydrothermal method exhibits a typical Li-rich Mn-based pure phase and lower cation mixing. SEM and TEM images indicate that the extent of particle agglomeration of the ionic-liquid-assisted sample is lower compared to the traditional hydrothermal sample. Electrochemical test results indicate that the materials synthesized by ionic-liquid-assisted hydrothermal method exhibit better rate capability and cyclability. Besides, electrochemical impedance spectroscopy (EIS) results suggest that the charge transfer resistance of 0.5Li2MnO3· 0.5LiNi0.5Mn0.5O2 synthesized by ionic-liquid-assisted hydrothermal method is much lower, which enhances the reaction kinetics.

scholarly journals Macromolecular Engineering of Poly(catechol) Cathodes towards High-Performance Aqueous Zinc-Polymer Batteries

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1673
Author(s):  
Nagaraj Patil ◽  
Jesus Palma ◽  
Rebeca Marcilla
Keyword(s):  
High Performance ◽  
Rate Capability ◽  
Charge Transfer Resistance ◽  
Transfer Resistance ◽  
Metal Anode ◽  
Redox Active ◽  
Diffusion Controlled ◽  
Metal Organic ◽  
Improved Performance ◽  
Organic Batteries

Aqueous zinc-polymer batteries (AZPBs) comprising abundant Zn metal anode and redox-active polymer (RAP) cathodes can be a promising solution for accomplishing viable, safe and sustainable energy storage systems. Though a limited number of RAPs have been successfully applied as organic cathodes in AZPBs, their macromolecular engineering towards improving electrochemical performance is rarely considered. In this study, we systematically compare performance of AZPB comprising Zn metal anode and either poly(catechol) homopolymer (named P(4VC)) or poly(catechol) copolymer (named P(4VC86-stat-SS14)) as polymer cathodes. Sulfonate anionic pendants in copolymer not only rendered lower activation energy and higher rate constant, but also conferred lower charge-transfer resistance, as well as facilitated Zn2+ mobility and less diffusion-controlled current responses compared to its homopolymer analogue. Consequently, the Zn||P(4VC86-stat-SS14) full-cell exhibits enhanced gravimetric (180 versus 120 mAh g−1 at 30 mg cm−2) and areal capacity (5.4 versus 3.6 mAh cm−2 at 30 mg cm−2) values, as well as superior rate capability both at room temperature (149 versus 105 mAh g−1 at 150 C) and at −35 °C (101 versus 35 mAh g−1 at 30 C) compared to Zn||P(4VC)100. This overall improved performance for Zn||P(4VC86-stat-SS14) is highly encouraging from the perspective applying macromolecular engineering strategies and paves the way for the design of advanced high-performance metal-organic batteries.

scholarly journals Effect of Structural and Electrochemical Properties of Yttrium-doped LiNi0.90Co0.05Al0.05O2 Electrode by Co-precipitation for Lithium Ion-batteries

2015 ◽  
Vol 18 (1) ◽  
pp. 009-016 ◽  
Author(s):  
Gi-Won Yoo ◽  
Tae-Jun Tae-Jun Park ◽  
Jong-Tae Son
Keyword(s):  
Electrochemical Properties ◽  
Rate Capability ◽  
Lithium Ion ◽  
Solid State Reaction Method ◽  
Charge Transfer Resistance ◽  
Hexagonal Structure ◽  
High Rate ◽  
Transfer Resistance ◽  
Cation Mixing ◽  
Co Precipitation

In this study, the LiNi0.90−xCo0.05Al0.05YxO2 (x = 0, 0.025, 0.075) have been synthesized by a co-precipitation and solid-state reaction method. The effect of the Y3+-doping on the structural and electrochemical properties were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), and by electrochemical and impedance spectroscopy (EIS). From the results of the XRD pattern changes between before and after the doping, less cation mixing and more ordered hexagonal structure were observed for the LiNi0.875Co0.05Al0.05Y0.025O2 cathode and the cell delivered an initial discharge capacity of 195.8 mAhg-1 and was 10.2 mAhg-1 higher than the pristine cell by yttrium doping effect. High rate capability studies were also performed and showed the capacity retention of 95, 81.7 and 63.8 % at 0.2, 1.0 and 5.0 C-rate, respectively during the cycling. The impedance spectra showed that the charge transfer resistance for the pristine cathode grew significantly, while that for the Y3+-doped cathode decreased during cycling. It was concluded that the capacity fading for LiNi0.90Co0.05Al0.05O2 mainly due to the cation mixing, partially contributed by the impedance growth and by doping the pristine material with Y3+, cation mixing can be efficiently suppressed, which results in the improved rate capability.

Sign in / Sign up

Export Citation Format

Share Document