scholarly journals An All-Solid-State Coaxial Structural Battery Using Sodium-Based Electrolyte

Molecules ◽  
2021 ◽  
Vol 26 (17) ◽  
pp. 5226
Author(s):  
Federico Danzi ◽  
Pedro Ponces Camanho ◽  
Maria Helena Braga
Keyword(s):  
Solid State ◽  
Specific Energy ◽  
Alkali Metals ◽  
Mechanical Performance ◽  
Lithium Ion ◽  
Mechanical Tests ◽  
Coaxial Cable ◽  
Safe Alternative ◽  
Structural Cell ◽  
Structural Battery

The transition to a sustainable society is paramount and requires the electrification of vehicles, the grid, industry, data banks, wearables, and IoT. Here, we show an all-solid-state structural battery where a Na+-based ferroelectric glass electrolyte is combined with metallic electrodes/current collectors (no traditional cathode present at fabrication) and thin-ply carbon-fiber laminates to obtain a coaxial multifunctional beam. This new concept aims to optimize the volume of any hollow beam-like structure by integrating an electrochemical system capable of both harvesting thermal and storing electrical energy while improving its mechanical performance. The coaxial cell is a coaxial cable where the dielectric is ferroelectric. The electrochemical results demonstrated the capability of performing three-minute charges to one-day discharges (70 cycles) and long-lasting discharges (>40 days at 1 mA) showing an energy density of 56.2 Wh.L−1 and specific energy of 38.0 Wh.kg−1, including the whole volume and weight of the structural cell. This is the highest specific energy among safe structural cells, while no Na+-based structural cells were found in the literature. The mechanical tests, instead, highlighted the coaxial cell capabilities to withstand severe inelastic deformation without compromising its functionalities, while increasing the flexural strength of the hosting structure. Moreover, the absence of alkali metals and liquid electrolytes together with its enhanced thermal properties makes this coaxial structural battery a valid and safe alternative as an energy reservoir for all the applications where traditional lithium-ion batteries are not suitable.

scholarly journals Shape-morphing carbon fiber composite using electrochemical actuation

2020 ◽  
Vol 117 (14) ◽  
pp. 7658-7664 ◽  
Author(s):  
Wilhelm Johannisson ◽  
Ross Harnden ◽  
Dan Zenkert ◽  
Göran Lindbergh
Keyword(s):  
Solid State ◽  
Carbon Fibers ◽  
Fiber Composite ◽  
Lithium Ion ◽  
Proof Of Concept ◽  
Carbon Fiber Composite ◽  
Shape Morphing ◽  
Commercial Carbon ◽  
Structural Battery ◽  
Shape Changes

Structures that are capable of changing shape can increase efficiency in many applications, but are often heavy and maintenance intensive. To reduce the mass and mechanical complexity solid-state morphing materials are desirable but are typically nonstructural and problematic to control. Here we present an electrically controlled solid-state morphing composite material that is lightweight and has a stiffness higher than aluminum. It is capable of producing large deformations and holding them with no additional power, albeit at low rates. The material is manufactured from commercial carbon fibers and a structural battery electrolyte, and uses lithium-ion insertion to produce shape changes at low voltages. A proof-of-concept material in a cantilever setup is used to show morphing, and analytical modeling shows good correlation with experimental observations. The concept presented shows considerable promise and paves the way for stiff, solid-state morphing materials.

scholarly journals The Role of Areal Capacity in Determining Short Circuiting of Sulfide-Based Solid-State Batteries

2021 ◽  
Author(s):  
John Lewis ◽  
Chanhee Lee ◽  
Yuhgene Liu ◽  
Sang Yun Han ◽  
Dhruv Prakash ◽  
...  
Keyword(s):  
Solid State ◽  
Current Density ◽  
Specific Energy ◽  
Research Effort ◽  
Short Circuit ◽  
Lithium Ion ◽  
Solid State Batteries ◽  
Current Densities ◽  
High Specific Energy ◽  
Areal Capacity

Solid-state batteries (SSBs) with lithium metal anodes offer higher specific energy than conventional lithium-ion batteries, but they must utilize areal capacities >3 mAh cm-2 and cycle at current densities >3 mA cm-2 to achieve commercial viability. Substantial research effort has focused on increasing rate capabilities of SSBs by mitigating detrimental processes such as lithium filament penetration. Less attention has been paid to understanding how areal capacity impacts plating/stripping behavior, despite the importance of areal capacity for achieving high specific energy. Here, we investigate and quantify the relationships among areal capacity, current density, and plating/stripping stability using both symmetric and full-cell configurations with a sulfide solid-state electrolyte (Li6PS5Cl). We show that unstable deposition and short circuiting readily occur at rates much lower than the measured critical current density when a sufficient areal capacity is passed. A systematic study of continuous plating under different electrochemical conditions reveals average “threshold capacity” values at different current densities, beyond which short circuiting occurs. Cycling cells below this threshold capacity significantly enhances cell lifetime, enabling stable symmetric cell cycling at 2.2 mA cm-2 without short circuiting. Finally, we show that full cells also exhibit threshold capacity behavior, but they tend to short circuit at lower current densities and areal capacities. Our results quantify the effects of transferred capacity and demonstrate the importance of using realistic areal capacities in experiments to develop viable solid-state batteries.

Recent advances in the sulfide electrolytes toward high specific energy solid-state lithium batteries

2021 ◽  
Author(s):  
Tao Yu ◽  
Bingyu Ke ◽  
Haoyu Li ◽  
Shaohua Guo ◽  
Haoshen Zhou
Keyword(s):  
Solid State ◽  
Energy Density ◽  
Specific Energy ◽  
Lithium Batteries ◽  
Lithium Ion ◽  
Liquid Lithium ◽  
Specific Energy Density ◽  
Solid State Batteries ◽  
All Solid State Batteries ◽  
High Specific Energy

All solid-state batteries (ASSBs) have gained extensive attention due to the improved safety, and high specific energy density compared with conventional liquid lithium-ion batteries. As the key component of ASSBs,...

Effects of cathode doping on 3D printed continuous carbon fiber structural battery composites by UV-assisted coextrusion deposition

2021 ◽  
pp. 002199832110316
Author(s):  
John M Pappas ◽  
Aditya R Thakur ◽  
Xiangyang Dong
Keyword(s):  
Carbon Fiber ◽  
Mechanical Performance ◽  
Lithium Ion ◽  
Electrical Energy ◽  
System Level ◽  
Solid Polymer ◽  
Complex Geometries ◽  
3D Print ◽  
3D Printed ◽  
Structural Battery

Structural battery composites are capable of significant system level mass and volume reductions not possible with separate battery and structural components by simultaneously carrying mechanical loads and storing electrical energy. The ability to 3D print lithium-ion structural batteries in arbitrary geometries would not only allow a flexible battery design but also facilitate its implementation as a structural component. This study presents a new 3D carbon fiber structural battery composite 3D printed by an ultraviolet (UV)-assisted coextrusion deposition method. With individual carbon fibers coated by solid polymer electrolyte (SPE) and dispersed within cathode doped matrix, energy storage is achieved in micro-battery cells at the fiber level within the 3D printed structural battery composite. The 3D printed structural battery composites with various complex geometries are demonstrated by successfully powering up LEDs. The SPE coating and cathode doping effect on microstructure, printability, mechanical and electrochemical properties are further characterized and investigated. A trade-off between printability and electrochemical performance is observed due to hindered curing by the doped cathode materials. The obtained electrochemical and mechanical performance is comparable to the carbon fiber based structural battery composites fabricated by conventional lay-up processes. These well demonstrate the great potentials of the proposed 3D printing method in rapidly fabricating functional structural battery composite components with complex geometries.

scholarly journals Promotion of Ionic Conductivity of PEO-Based Solid Electrolyte Using Ultrasonic Vibration

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1889 ◽  
Author(s):  
Hui Wang ◽  
Xiaodong Cui ◽  
Cong Zhang ◽  
Huang Gao ◽  
Wei Du ◽  
...  
Keyword(s):  
Solid State ◽  
Ionic Conductivity ◽  
Solid Electrolyte ◽  
Ultrasonic Vibration ◽  
Ultrasonic Treatment ◽  
Mechanical Performance ◽  
Lithium Ion ◽  
High Energy ◽  
Frictional Heat ◽  
Power Ultrasound

All solid-state lithium-ion batteries based on polymer electrolytes have higher safety and energy density, but the low conductivity of lithium ion restricts its application. This study proposes a new method to promote the ionic conductivity of polyethylene oxide (PEO)-based solid electrolytes. In this method, the PEO-based solid electrolyte was first prepared by casting, and then power ultrasound was exerted on the electrolyte by a sandwich structure to modify the electrolyte structure. Through analysis of the performance and microstructure of the electrolyte, it was found that the ultrasonic treatment increased the ionic conductivity by 78%, improved tensile strength and plastic deformation ability, but did not affect the thermal stability and the chemical composition. The ultrasonic vibration, exerting high energy to the solid electrolyte through high-frequency vibration, broke PEO grains and melted them with the frictional heat at boundary. Due to the slight melting and fast solidifying produced by the pulsed ultrasonic treatment, the crystallization was suppressed. The crystallinity was thus reduced by 6.2%, which increased the migration channels of lithium ions and reduced the tortuosity effect. Furthermore, the ultrasonic vibration compressed the electrolyte to produce plastic flow of the material, which made the electrolyte structure more compact. The density of ethylene oxide (EO) units thus increased in the amorphous phase, providing multiple electron-donor coordination sites for the Li+. The hopping distance of the ion between donors decreased, which also facilitated the migration. In addition, the mechanical performance of the electrolyte membrane improved. This study provides a reference for the improvement of polymer based all-solid-state batteries.

Experimental Assessment of the Practical Oxidative Stability of Lithium Thiophosphate Solid Electrolytes

2019 ◽  
Author(s):  
Georg Dewald ◽  
Saneyuki Ohno ◽  
Marvin Kraft ◽  
Raimund Koerver ◽  
Paul Till ◽  
...  
Keyword(s):  
Cyclic Voltammetry ◽  
Solid State ◽  
Oxidative Stability ◽  
Photoelectron Spectroscopy ◽  
Solid Electrolytes ◽  
Stability Limit ◽  
Lithium Ion ◽  
High Energy ◽  
Redox Activity ◽  
Solid State Batteries

<p>All-solid-state batteries are often expected to replace conventional lithium-ion batteries in the future. However, the practical electrochemical and cycling stability of the best-conducting solid electrolytes, i.e. lithium thiophosphates, are still critical issues that prevent long-term stable high-energy cells. In this study, we use <i>stepwise</i><i>cyclic voltammetry </i>to obtain information on the practical oxidative stability limit of Li<sub>10</sub>GeP<sub>2</sub>S<sub>12</sub>, a Li<sub>2</sub>S‑P<sub>2</sub>S<sub>5</sub>glass, as well as the argyrodite Li<sub>6</sub>PS<sub>5</sub>Cl solid electrolytes. We employ indium metal and carbon black as the counter and working electrode, respectively, the latter to increase the interfacial contact area to the electrolyte as compared to the commonly used planar steel electrodes. Using a stepwise increase in the reversal potentials, the onset potential at 25 °C of oxidative decomposition at the electrode-electrolyte interface is identified. X‑ray photoelectron spectroscopy is used to investigate the oxidation of sulfur(-II) in the thiophosphate polyanions to sulfur(0) as the dominant redox process in all electrolytes tested. Our results suggest that after the formation of these decomposition products, significant redox behavior is observed. This explains previously reported redox activity of thiophosphate solid electrolytes, which contributes to the overall cell performance in solid-state batteries. The <i>stepwise cyclic voltammetry</i>approach presented here shows that the practical oxidative stability at 25 °C of thiophosphate solid electrolytes against carbon is kinetically higher than predicted by thermodynamic calculations. The method serves as an efficient guideline for the determination of practical, kinetic stability limits of solid electrolytes. </p>

Experimental Assessment of the Practical Oxidative Stability of Lithium Thiophosphate Solid Electrolytes

2019 ◽  
Author(s):  
Georg Dewald ◽  
Saneyuki Ohno ◽  
Marvin Kraft ◽  
Raimund Koerver ◽  
Paul Till ◽  
...  
Keyword(s):  
Cyclic Voltammetry ◽  
Solid State ◽  
Oxidative Stability ◽  
Photoelectron Spectroscopy ◽  
Solid Electrolytes ◽  
Stability Limit ◽  
Lithium Ion ◽  
High Energy ◽  
Redox Activity ◽  
Solid State Batteries

<p>All-solid-state batteries are often expected to replace conventional lithium-ion batteries in the future. However, the practical electrochemical and cycling stability of the best-conducting solid electrolytes, i.e. lithium thiophosphates, are still critical issues that prevent long-term stable high-energy cells. In this study, we use <i>stepwise</i><i>cyclic voltammetry </i>to obtain information on the practical oxidative stability limit of Li<sub>10</sub>GeP<sub>2</sub>S<sub>12</sub>, a Li<sub>2</sub>S‑P<sub>2</sub>S<sub>5</sub>glass, as well as the argyrodite Li<sub>6</sub>PS<sub>5</sub>Cl solid electrolytes. We employ indium metal and carbon black as the counter and working electrode, respectively, the latter to increase the interfacial contact area to the electrolyte as compared to the commonly used planar steel electrodes. Using a stepwise increase in the reversal potentials, the onset potential at 25 °C of oxidative decomposition at the electrode-electrolyte interface is identified. X‑ray photoelectron spectroscopy is used to investigate the oxidation of sulfur(-II) in the thiophosphate polyanions to sulfur(0) as the dominant redox process in all electrolytes tested. Our results suggest that after the formation of these decomposition products, significant redox behavior is observed. This explains previously reported redox activity of thiophosphate solid electrolytes, which contributes to the overall cell performance in solid-state batteries. The <i>stepwise cyclic voltammetry</i>approach presented here shows that the practical oxidative stability at 25 °C of thiophosphate solid electrolytes against carbon is kinetically higher than predicted by thermodynamic calculations. The method serves as an efficient guideline for the determination of practical, kinetic stability limits of solid electrolytes. </p>

Electrolytes for advanced lithium ion batteries using silicon-based anodes

2019 ◽  
Vol 7 (16) ◽  
pp. 9432-9446 ◽  
Author(s):  
Zhixin Xu ◽  
Jun Yang ◽  
Hongping Li ◽  
Yanna Nuli ◽  
Jiulin Wang
Keyword(s):  
Solid State ◽  
Lithium Ion Batteries ◽  
Recent Progress ◽  
Lithium Ion ◽  
Review Article ◽  
Silicon Based

Recent progress in electrolytes from the liquid to the solid state for Si-based anodes is comprehensively summarized in this review article.

Experimental and numerical analysis to identify the performance limiting mechanisms in solid-state lithium cells under pulse operating conditions

2019 ◽  
Vol 21 (41) ◽  
pp. 22740-22755 ◽  
Author(s):  
Mei-Chin Pang ◽  
Yucang Hao ◽  
Monica Marinescu ◽  
Huizhi Wang ◽  
Mu Chen ◽  
...  
Keyword(s):  
Solid State ◽  
Numerical Analysis ◽  
Energy Density ◽  
Lithium Ion Batteries ◽  
Lithium Batteries ◽  
Safety Concern ◽  
Lithium Ion ◽  
Thermal Runaway ◽  
Operating Conditions ◽  
Lithium Cells

Solid-state lithium batteries could reduce the safety concern due to thermal runaway while improving the gravimetric and volumetric energy density beyond the existing practical limits of lithium-ion batteries.

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