scholarly journals Li2O-Based Cathode Additives Enabling Prelithiation of Si Anodes

2021 ◽  
Vol 11 (24) ◽  
pp. 12027
Author(s):  
Yeyoung Ha ◽  
Maxwell C. Schulze ◽  
Sarah Frisco ◽  
Stephen E. Trask ◽  
Glenn Teeter ◽  
...  
Keyword(s):  
Coulombic Efficiency ◽  
High Surface ◽  
Solid Electrolyte Interphase ◽  
Active Material ◽  
High Surface Area ◽  
Lithium Ion ◽  
Particle Morphology ◽  
Lithium Oxide ◽  
Si Anodes ◽  
The Impact

Low first-cycle Coulombic efficiency is especially poor for silicon (Si)-based anodes due to the high surface area of the Si-active material and extensive electrolyte decomposition during the initial cycles forming the solid electrolyte interphase (SEI). Therefore, developing successful prelithiation methods will greatly benefit the development of lithium-ion batteries (LiBs) utilizing Si anodes. In pursuit of this goal, in this study, lithium oxide (Li2O) was added to a LiNi0.6Mn0.2Co0.2O2 (NMC622) cathode using a scalable ball-milling approach to compensate for the initial Li loss at the anode. Different milling conditions were tested to evaluate the impact of particle morphology on the additive performance. In addition, Co3O4, a well-known oxygen evolution reaction catalyst, was introduced to facilitate the activation of Li2O. The Li2O + Co3O4 additives successfully delivered an additional capacity of 1116 mAh/gLi2O when charged up to 4.3 V in half cells and 1035 mAh/gLi2O when charged up to 4.1 V in full cells using Si anodes.

scholarly journals Synthesis of High Surface Area α-KyMnO2 Nanoneedles Using Extract of Broccoli as Bioactive Reducing Agent and Application in Lithium Battery

Materials ◽  
2020 ◽  
Vol 13 (6) ◽  
pp. 1269 ◽  
Author(s):  
Ahmed Hashem ◽  
Hanaa Abuzeid ◽  
Martin Winter ◽  
Jie Li ◽  
Christian Julien
Keyword(s):  
Surface Area ◽  
Coulombic Efficiency ◽  
High Surface ◽  
High Surface Area ◽  
Rate Capability ◽  
Lithium Ion ◽  
Reducing Agent ◽  
Capacity Retention ◽  
Transmission Electron ◽  
Initial Capacity

With the aim to reduce the entire cost of lithium-ion batteries and to diminish the environmental impact, the extract of broccoli is used as a strong benign reducing agent for potassium permanganate to synthesize α-KyMnO2 cathode material with pure nanostructured phase. Material purity is confirmed by X-ray powder diffraction and thermogravimetric analyses. Images of transmission electron microscopy show samples with a spider-net shape consisting of very fine interconnected nanoneedles. The nanostructure is characterized by crystallite of 4.4 nm in diameter and large surface area of 160.7 m2 g−1. The material delivers an initial capacity of 211 mAh g−1 with high Coulombic efficiency of 99% and 82% capacity retention after 100 cycles. Thus, α-KyMnO2 synthesized via a green process exhibits very promising electrochemical performance in terms of initial capacity, cycling stability and rate capability.

Iron Disulfide Cathode Material Incorporated in Highly Ordered Mesoporous Carbon for Rechargeable Lithium Ion Batteries

2020 ◽  
Vol 12 (9) ◽  
pp. 1265-1270
Author(s):  
Ying Liu ◽  
Jungwon Heo ◽  
Xueying Li ◽  
Yuanzheng Sun ◽  
Younki Lee ◽  
...  
Keyword(s):  
Mesoporous Carbon ◽  
High Surface ◽  
Active Material ◽  
High Surface Area ◽  
Lithium Ion ◽  
Mesoporous Structure ◽  
Ordered Mesoporous Carbon ◽  
Iron Disulfide ◽  
Excellent Electrochemical Performance ◽  
Ordered Mesoporous

A highly ordered mesoporous carbon@iron disulfide (CMK-5@FeS2) composite was prepared via an in-situ impregnation and sulfurization method. The CMK-5 matrix with excellent conductivity and high surface area not only formed a continuous conductive network to improve the performance of the CMK-5@FeS2 composite, but also provided sufficient space to buffer the volume changes during cycling. The CMK-5@FeS2 cell exhibited excellent electrochemical performance. After 80 cycles, the CMK-5@FeS2 cell showed the discharge capacities of 650 and 380 mAh g–1 at 2 C and 5 C, respectively. The excellent results show that CMK-5 with unique mesoporous structure can contribute to accelerating ion transfer in the electrode due to the easy accessibility of the electrolyte, which implies CMK-5@FeS2 composite could be a promising cathode active material for rechargeable lithium ion (Li-ion) batteries.

Reducing Side Reactions Using PF6-based Electrolytes in Multivalent Hybrid Cells

2015 ◽  
Vol 1773 ◽  
pp. 27-32 ◽  
Author(s):  
Danielle L. Proffit ◽  
Albert L. Lipson ◽  
Baofei Pan ◽  
Sang-Don Han ◽  
Timothy T. Fister ◽  
...  
Keyword(s):  
Electrode Materials ◽  
High Surface ◽  
Active Material ◽  
High Surface Area ◽  
Lithium Ion ◽  
Current Collector ◽  
Side Reactions ◽  
Hybrid Cells ◽  
Current Collectors ◽  
Carbon Anodes

ABSTRACTThe need for higher energy density batteries has spawned recent renewed interest in alternatives to lithium ion batteries, including multivalent chemistries that theoretically can provide twice the volumetric capacity if two electrons can be transferred per intercalating ion. Initial investigations of these chemistries have been limited to date by the lack of understanding of the compatibility between intercalation electrode materials, electrolytes, and current collectors. This work describes the utilization of hybrid cells to evaluate multivalent cathodes, consisting of high surface area carbon anodes and multivalent nonaqueous electrolytes that are compatible with oxide intercalation electrodes. In particular, electrolyte and current collector compatibility was investigated, and it was found that the carbon and active material play an important role in determining the compatibility of PF6-based multivalent electrolytes with carbon-based current collectors. Through the exploration of electrolytes that are compatible with the cathode, new cell chemistries and configurations can be developed, including a magnesium-ion battery with two intercalation host electrodes, which may expand the known Mg-based systems beyond the present state of the art sulfide-based cathodes with organohalide-magnesium based electrolytes.

scholarly journals Electrochemical Performance of Thick-Film Li(Ni0.6Mn0.2Co0.2)O2 Cathode with Hierarchic Structures and Laser Ablation

Nanomaterials ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 2962
Author(s):  
Zelai Song ◽  
Penghui Zhu ◽  
Wilhelm Pfleging ◽  
Jiyu Sun
Keyword(s):  
Thin Film ◽  
Particle Size ◽  
Laser Ablation ◽  
Electrochemical Performance ◽  
Thick Film ◽  
Active Material ◽  
Lithium Ion ◽  
Particle Morphology ◽  
Composite Electrodes ◽  
The Impact

The electrochemical performance of lithium-ion batteries is directly influenced by type of active material as well as its morphology. In order to evaluate the impact of particle morphology in thick-film electrodes, Li(Ni0.6Mn0.2Co0.2)O2 (NMC 622) cathodes with bilayer structure consisting of two different particle sizes were manufactured and electrochemically characterized in coin cells design. The hierarchical thick-film electrodes were generated by multiple casting using NMC 622 (TA) with small particle size of 6.7 µm and NMC 622 (BA) with large particle size of 12.8 µm. Besides, reference electrodes with one type of active material as well as with two type of materials established during mixing process (BT) were manufactured. The total film thickness of all hierarchical composite electrodes were kept constant at 150 µm, while the thicknesses of TA and BA were set at 1:2, 1:1, and 2:1. Meanwhile, three kinds of thin-film cathodes with 70 µm were applied to represent the state-of-the-art approach. Subsequently, ultrafast laser ablation was applied to generate groove structures inside the electrodes. The results demonstrate that cells with thin-film or thick-film cathode only containing TA, cells with bilayer electrode containing TBA 1:2, and cells with laser-structured electrodes show higher capacity at C/2 to 5C, respectively.

Tailored Mesoporous Silicas: From Confinement Effects to Catalysis

2009 ◽  
Vol 1217 ◽  
Author(s):  
A. C. Buchanan, III ◽  
Michelle K. Kidder
Keyword(s):  
Chemical Reactivity ◽  
High Surface ◽  
High Surface Area ◽  
Mesoporous Silicas ◽  
Surface Immobilization ◽  
Product Selectivity ◽  
Aryl Ether ◽  
Ether Linkage ◽  
Synthetic Methodologies ◽  
The Impact

AbstractOrdered mesoporous silicas continue to find widespread use as supports for diverse applications such as catalysis, separations, and sensors. They provide a versatile platform for these studies because of their high surface area and the ability to control pore size, topology, and surface properties over wide ranges. Furthermore, there is a diverse array of synthetic methodologies for tailoring the pore surface with organic, organometallic, and inorganic functional groups. In this paper, we will discuss two examples of tailored mesoporous silicas and the resultant impact on chemical reactivity. First, we explore the impact of pore confinement on the thermochemical reactivity of phenethyl phenyl ether (PhCH2CH2OPh, PPE), which is a model of the dominant β-aryl ether linkage present in lignin derived from woody biomass. The influence of PPE surface immobilization, grafting density, silica pore diameter, and presence of a second surface-grafted inert “spacer” molecule on the product selectivity has been examined. We will show that the product selectivity can be substantially altered compared with the inherent gas-phase selectivity. Second, we have recently initiated an investigation of mesoporous silica supported, heterobimetallic oxide materials for photocatalytic conversion of carbon dioxide. Through surface organometallic chemistry, isolated M-O-M’ species can be generated on mesoporous silicas that, upon irradiation, form metal to metal charge transfer bands capable of converting CO2 into CO. Initial results from studies of Ti(IV)-O-Sn(II) on SBA-15 will be presented.

scholarly journals Probing the Influence of Multiscale Heterogeneity on Effective Properties of Graphite Electrodes

2021 ◽  
Author(s):  
Chance A. Norris ◽  
Mukul Parmananda ◽  
Scott Alan Roberts ◽  
Partha P. Mukherjee
Keyword(s):  
Spatial Heterogeneity ◽  
Transport Properties ◽  
Effective Properties ◽  
Lithium Ion ◽  
Particle Morphology ◽  
Electrochemical Characteristics ◽  
Pore Scale ◽  
Structural Anisotropy ◽  
Graphite Electrodes ◽  
The Impact

Graphite electrodes in the lithium-ion battery exhibit various particle shapes, including spherical and platelet morphologies, which influence structural and electrochemical characteristics. It is well established that porous structures exhibit spatial heterogeneity, and particle morphology can influence transport properties. The impact of particle morphology on the heterogeneity and anisotropy of geometric and transport properties has not been previously studied. This study characterizes the spatial heterogeneities of eighteen graphite electrodes at multiple length scales by calculating and comparing structural anisotropy, geometric quantities, and transport properties (pore-scale tortuosity and electrical conductivity). We found that particle morphology and structural anisotropy play an integral role in determining the spatial heterogeneity of directional tortuosity and its dependency on pore-scale heterogeneity. Our analysis reveals that the magnitude of in-plane and through-plane tortuosity difference influences the multiscale heterogeneity in graphite electrodes.

Probing the morphological influence on solid electrolyte interphase and impedance response in intercalation electrodes

2015 ◽  
Vol 17 (15) ◽  
pp. 9812-9827 ◽  
Author(s):  
Chien-Fan Chen ◽  
Partha P. Mukherjee
Keyword(s):  
Solid Electrolyte ◽  
Solid Electrolyte Interphase ◽  
Active Material ◽  
Impedance Model ◽  
Impedance Response ◽  
Intercalation Electrodes ◽  
The Impact

The microstructure-aware impedance model allows for the impact of active material morphology on the SEI formation and corresponding impedance response.

Influence of nanoparticles on the polymer-conditioned dewatering of wastewater sludges

2013 ◽  
Vol 67 (9) ◽  
pp. 2117-2123
Author(s):  
N. J. Boyle ◽  
G. M. Evans
Keyword(s):  
Activated Sludge ◽  
Titanium Dioxide Nanoparticles ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Wastewater Sludge ◽  
Small Scale ◽  
Sludge Dewatering ◽  
Solids Content ◽  
The Impact

The effect of using small-scale, high surface area, nanoparticles to supplement polymer-conditioned wastewater sludge dewatering was investigated. Aerobically digested sludge and waste activated sludge sourced from the Hunter Valley, NSW, Australia, were tested with titanium dioxide nanoparticles. The sludge samples were dosed with the nanoparticles in an attempt to adsorb a component of the charged biopolymer surfactants present naturally in sludge. The sludge was conditioned with a cationic polymer. The dewatering characteristics were assessed by measuring the specific resistance to filtration through a modified time-to-filter testing apparatus. The solids content of the dosed samples was determined by a mass balance and compared to the original solids content in the activated sludge. Test results indicated that nanoparticle addition modified the structure of the sludge and provided benefits in terms of the dewatering rate. The samples dosed with nanoparticles exhibited faster water removal, indicating a more permeable filter cake and hence more permeable sludge. A concentration of 2–4% nanoparticles was required to achieve a noticeable benefit. As a comparison, the sludge samples were also tested with a larger particle size, powdered activated carbon (PAC). It was found that the PAC did provide some minor benefits to sludge dewatering but was outperformed by the nanoparticles. The solids content of the final sludge was increased by a maximum of up to 0.6%. The impact of the order sequence of particles and polymer was also investigated. It was found that nanoparticles added before polymer addition provided the best dewatering performance. This outcome was consistent with current theories and previous research through the literature. An economic analysis was undertaken to confirm the viability of the technology for implementation at a full-scale plant. It was found that, currently, this technology is unlikely to be favourable unless the nanoparticles can be sourced for a low cost.

scholarly journals Fluorine-donating electrolytes enable highly reversible 5-V-class Li metal batteries

2018 ◽  
Vol 115 (6) ◽  
pp. 1156-1161 ◽  
Author(s):  
Liumin Suo ◽  
Weijiang Xue ◽  
Mallory Gobet ◽  
Steve G. Greenbaum ◽  
Chao Wang ◽  
...  
Keyword(s):  
Coulombic Efficiency ◽  
High Surface ◽  
Solid Electrolyte Interphase ◽  
Current Collector ◽  
Wide Bandgap ◽  
Fluorine Concentration ◽  
Metal Anode ◽  
Key Factor ◽  
Significant Loading ◽  
Fluoroethylene Carbonate

Lithium metal has gravimetric capacity ∼10× that of graphite which incentivizes rechargeable Li metal batteries (RLMB) development. A key factor that limits practical use of RLMB is morphological instability of Li metal anode upon electrodeposition, reflected by the uncontrolled area growth of solid–electrolyte interphase that traps cyclable Li, quantified by the Coulombic inefficiency (CI). Here we show that CI decreases approximately exponentially with increasing donatable fluorine concentration of the electrolyte. By using up to 7 m of Li bis(fluorosulfonyl)imide in fluoroethylene carbonate, where both the solvent and the salt donate F, we can significantly suppress anode porosity and improve the Coulombic efficiency to 99.64%. The electrolyte demonstrates excellent compatibility with 5-V LiNi0.5Mn1.5O4 cathode and Al current collector beyond 5 V. As a result, an RLMB full cell with only 1.4× excess lithium as the anode was demonstrated to cycle above 130 times, at industrially significant loading of 1.83 mAh/cm2 and 0.36 C. This is attributed to the formation of a protective LiF nanolayer, which has a wide bandgap, high surface energy, and small Burgers vector, making it ductile at room temperature and less likely to rupture in electrodeposition.

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