Nano cellulose fibers and graphene oxide coating on polyolefin separator with uniform Li+ transportation channels for long-life and high-safety Li metal battery

2020 ◽  
pp. 1-25
Author(s):  
Dongmei Dai ◽  
Yixuan Chen ◽  
Boran Chen ◽  
Jinxu Qiu ◽  
Bao Li ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Electrochemical Impedance ◽  
Coating Layer ◽  
Cellulose Fiber ◽  
Oxide Coating ◽  
Thermal Shrinkage ◽  
Retention Capacity ◽  
Nano Cellulose ◽  
Long Life ◽  
Lithium Dendrite

Abstract Lithium anode could greatly increase the energy density of the cell, but inevitable lithium dendrites hinder its application. A powerful coating layer can effectively suppress the growth of dendrite by promoting a fast and uniform Li+ flux. Here a polyolefin separator coated with a layer of nano cellulose fiber (NCF) and graphene oxide (GO) is designed to restrain the growth of Li-dendrite and accommodate thermal shrinkage resistance. The results of electrochemical impedance spectroscopy showed that the NCF/GO coating with a mass ratio of 3:5 showed the highest value of ionic conductivity. The Li/separator/Li symmetrical battery with NCF/GO coated separator can work for 65 hours during continuous charging before the voltage dropping down to zero, which is about 40% longer than the battery with bare polyolefin separator. In addition, the NCF/GO coating layer can also increase the retention capacity ratio of a cell by more than 10% in the 100 charge/discharge cycles. In this paper, the as-prepared NCF/GO coating separator provides a reference for designing a long-life and safety battery with Li-anode by effectively inhibiting the lithium dendrite.

scholarly journals Enhancement of the Electrochemical Performance of LiNi1/3Co1/3Mn1/3O2 Cathode Material by Double-Layer Coating with Graphene Oxide and SnO2 for Lithium-Ion Batteries

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Yuxin Ma ◽  
Ping Cui ◽  
Dan Zhan ◽  
Bing Gan ◽  
Youliang Ma ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Graphene Oxide ◽  
Cathode Material ◽  
Electrochemical Impedance ◽  
Coating Layer ◽  
Rate Capability ◽  
Electrode Polarization ◽  
Transfer Resistance ◽  
X Ray ◽  
Double Coating

The graphene oxide-coated SnO2-Li1/3Co1/3Mn1/3O2 (GO-SnO2-NCM) cathode material was successfully synthesized via a facile wet chemical method. The pristine NCM and GO-SnO2-NCM were characterized by X-ray diffraction, scanning electron microscopy, energy-dispersive spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The results showed that the double-coating layer did not destroy the NCM crystal structure, with multiple nano-SnO2 particles and GO uniformly covering the NCM surface. Electrochemical tests indicated that GO-SnO2-NCM exhibited excellent cycling performance, with 90.7% capacity retention at 1 C after 100 cycles, which was higher than 74.3% for the pristine NCM at the same cycle. The rate capability showed that the double-coating layer enhanced surface electronic–ionic transport. Electrochemical impedance spectroscopy results confirmed that the GO-SnO2-coating layer effectively suppressed the increased electrode polarization and charge transfer resistance during cycling.

scholarly journals Transport of Protons and Capacitive Properties of the Nylon/Porphyrin/Graphene Oxide Coating

2017 ◽  
Author(s):  
César A. García-Pérez ◽  
Carmina Menchaca-Campos ◽  
Miguel A. García-Sánchez ◽  
Ociel Rodríguez-Pérez ◽  
Jorge Uruchurtu
Keyword(s):  
Graphene Oxide ◽  
Electrochemical Impedance ◽  
Composite Films ◽  
Oxide Coating ◽  
Film Coating ◽  
Bipolar Plates ◽  
Transfer Product ◽  
Low Frequencies ◽  
Capacitive Properties ◽  
Acid Environment

Electrochemical impedance (EI) measurements were performed to evaluate the nylon 66/-tetra-(para-aminophenyl) porphyrin (H2T(p-NH2)PP)/graphene oxide (GO) film coating on stainless steel and compared to the nylon/H2T(p-NH2)PP and nylon/GO film samples using 1M H2SO4 as electrolyte. The nylon/H2T(p-NH2)PP and nylon/GO composite films showed high electrochemical impedance in the order of 109 ohm-cm2 and a system controlled by mass transfer, product of a diffusion process at low frequencies with a resistance up to 5 orders of magnitude, indicating the diffusion of protons through the coating and a decrease in the metal dissolution. Otherwise, the nylon/H2T(p-NH2)PP/GO film compound evaluated show good ionic conductivity and electrochemical stability in the acid environment, acting porphyrin as a catalyst to the passage of protons through the film, reducing its electrochemical impedance up to 7 orders of magnitude with respect to the compounds nylon/H2T(p-NH2)PP and nylon/GO. Likewise, good capacitance values are also shown by modifying the concentrations of porphyrin and GO reinforcing materials. These properties are important for technological applications, such as anticorrosion coating for bipolar plates or membrane in a fuel cell type PEM, super-capacitors, etc.

scholarly journals Hydrophobic Modification of Graphene Oxide and Its Effect on the Corrosion Resistance of Silicone-Modified Epoxy Resin

Metals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 89
Author(s):  
Wei Yuan ◽  
Qian Hu ◽  
Jiao Zhang ◽  
Feng Huang ◽  
Jing Liu
Keyword(s):  
Contact Angle ◽  
Corrosion Resistance ◽  
Graphene Oxide ◽  
Physical Properties ◽  
Epoxy Resin ◽  
Electrochemical Impedance ◽  
Salt Spray ◽  
X Ray ◽  
Modified Graphene Oxide ◽  
Modified Epoxy

This study modified graphene oxide (GO) with hydrophilic octadecylamine (ODA) via covalent bonding to improve its dispersion in silicone-modified epoxy resin (SMER) coatings. The structural and physical properties of ODA-GO were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and contact angle tests. The ODA-GO composite materials were added to SMER coatings by physical mixing. FE-SEM, water absorption, and contact angle tests were used to evaluate the physical properties of the ODA-GO/SMER coatings, while salt spray, electrochemical impedance spectroscopy (EIS), and scanning Kelvin probe (SKP) methods were used to test the anticorrosive performance of ODA-GO/SMER composite coatings on Q235 steel substrates. It was found that ODA was successfully grafted onto the surfaces of GO. The resulting ODA-GO material exhibited good hydrophobicity and dispersion in SMER coatings. The anticorrosive properties of the ODA-GO/SMER coatings were significantly improved due to the increased interfacial adhesion between the nanosheets and SMER, lengthening of the corrosive solution diffusion path, and increased cathodic peeling resistance. The 1 wt.% ODA-GO/SMER coating provided the best corrosion resistance than SMER coatings with other amounts of ODA-GO (including no addition). After immersion in 3.5 wt.% NaCl solution for 28 days, the low-frequency end impedance value of the 1 wt.% ODA-GO/SMER coating remained high, at 6.2 × 108 Ω·cm2.

scholarly journals Oxygen-Deficient β-MnO2@Graphene Oxide Cathode for High-Rate and Long-Life Aqueous Zinc Ion Batteries

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Shouxiang Ding ◽  
Mingzheng Zhang ◽  
Runzhi Qin ◽  
Jianjun Fang ◽  
Hengyu Ren ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Manganese Oxides ◽  
Rate Capability ◽  
High Energy ◽  
Zinc Ion ◽  
Cycling Stability ◽  
High Rate ◽  
High Energy Density ◽  
Superior Performance ◽  
Long Life

AbstractRecent years have witnessed a booming interest in grid-scale electrochemical energy storage, where much attention has been paid to the aqueous zinc ion batteries (AZIBs). Among various cathode materials for AZIBs, manganese oxides have risen to prominence due to their high energy density and low cost. However, sluggish reaction kinetics and poor cycling stability dictate against their practical application. Herein, we demonstrate the combined use of defect engineering and interfacial optimization that can simultaneously promote rate capability and cycling stability of MnO2 cathodes. β-MnO2 with abundant oxygen vacancies (VO) and graphene oxide (GO) wrapping is synthesized, in which VO in the bulk accelerate the charge/discharge kinetics while GO on the surfaces inhibits the Mn dissolution. This electrode shows a sustained reversible capacity of ~ 129.6 mAh g−1 even after 2000 cycles at a current rate of 4C, outperforming the state-of-the-art MnO2-based cathodes. The superior performance can be rationalized by the direct interaction between surface VO and the GO coating layer, as well as the regulation of structural evolution of β-MnO2 during cycling. The combinatorial design scheme in this work offers a practical pathway for obtaining high-rate and long-life cathodes for AZIBs.

scholarly journals Graphene oxide-based rechargeable respiratory masks

2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Stelbin Peter Figerez ◽  
Sudeshna Patra ◽  
G Rajalakshmi ◽  
Tharangattu N Narayanan
Keyword(s):  
Graphene Oxide ◽  
Polyvinylidene Fluoride ◽  
Occupational Safety ◽  
Low Cost ◽  
Triboelectric Nanogenerator ◽  
Layer System ◽  
Retention Capacity ◽  
Simple Modification ◽  
Nonwoven Fabrics ◽  
Mask Design

Abstract Respiratory masks having similar standards of ‘N95’, defined by the US National Institute for Occupational Safety and Health, will be highly sought after, post the current COVID-19 pandemic. Here, such a low-cost (∼$1/mask) mask design having electrostatic rechargeability and filtration efficiency of >95% with a quality factor of ∼20 kPa−1 is demonstrated. This filtration efficacy is for particles of size 300 nm. The tri-layer mask, named PPDFGO tri, contains nylon, modified polypropylene (PPY), and cotton nonwoven fabrics as three layers. The melt-spun PPY, available in a conventional N95 mask, modified with graphene oxide and polyvinylidene fluoride mixture containing paste using a simple solution casting method acts as active filtration layer. The efficacy of this tri-layer system toward triboelectric rechargeability using small mechanical agitations is demonstrated here. These triboelectric nanogenerator (TENG)-assisted membranes have high electrostatic charge retention capacity (∼1 nC/cm2 after 5 days in ambient condition) and high rechargeability even in very humid conditions (>80% RH). A simple but robust permeability measurement set up is also constructed to test these TENG-based membranes, where a flow rate of 30–35 L/min is maintained during the testing. Such a simple modification to the existing mask designs enabling their rechargeability via external mechanical disturbances, with enhanced usability for single use as well as for reuse with decontantamination, will be highly beneficial in the realm of indispensable personal protective equipment.

scholarly journals A Facile and Green Synthesis of a MoO2-Reduced Graphene Oxide Aerogel for Energy Storage Devices

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 594 ◽  
Author(s):  
Mara Serrapede ◽  
Marco Fontana ◽  
Arnaud Gigot ◽  
Marco Armandi ◽  
Glenda Biasotto ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Chemical Reduction ◽  
Low Cost ◽  
Xps Analysis ◽  
3D Scaffold ◽  
Energy Storage Devices ◽  
Reduced Graphene

A simple, low cost, and “green” method of hydrothermal synthesis, based on the addition of l-ascorbic acid (l-AA) as a reducing agent, is presented in order to obtain reduced graphene oxide (rGO) and hybrid rGO-MoO2 aerogels for the fabrication of supercapacitors. The resulting high degree of chemical reduction of graphene oxide (GO), confirmed by X-Ray Photoelectron Spectroscopy (XPS) analysis, is shown to produce a better electrical double layer (EDL) capacitance, as shown by cyclic voltammetric (CV) measurements. Moreover, a good reduction yield of the carbonaceous 3D-scaffold seems to be achievable even when the precursor of molybdenum oxide is added to the pristine slurry in order to get the hybrid rGO-MoO2 compound. The pseudocapacitance contribution from the resulting embedded MoO2 microstructures, was then studied by means of CV and electrochemical impedance spectroscopy (EIS). The oxidation state of the molybdenum in the MoO2 particles embedded in the rGO aerogel was deeply studied by means of XPS analysis and valuable information on the electrochemical behavior, according to the involved redox reactions, was obtained. Finally, the increased stability of the aerogels prepared with l-AA, after charge-discharge cycling, was demonstrated and confirmed by means of Field Emission Scanning Electron Microscopy (FESEM) characterization.

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