Micro-Structural Design of Soft Solid Composite Electrolytes with Enhanced Ionic Conductivity

2022 ◽  
pp. 1-12
Author(s):  
Nastran Khodabandehloo ◽  
Kosar Mozaffari ◽  
Liping Liu ◽  
Pradeep Sharma

Abstract Electrolyte in a rechargeable Li-ion battery plays a critical role in determining its capacity and efficiency. While the typically used electrolytes in Li-ion batteries are liquid, soft solid electrolytes are being increasingly explored as an alternative due to their advantages in terms of increased stability, safety and potential applications in the context of flexible and stretchable electronics. However, ionic conductivity of solid polymer electrolytes is significantly lower compared to liquid electrolytes. In a recent work, we developed a theoretical framework to model the coupled deformation, electrostatics and diffusion in heterogeneous electrolytes and also established a simple homogenization approach for the design of microstructures to enhance ionic conductivity of composite solid electrolytes. Guided by the insights from the theoretical framework, in this paper, we ex- amine specific microstructures that can potentially yield significant improvement in the effective ionic conductivity. We numerically implement our theory in the open source general purpose finite element package FEniCS to solve the governing equations and present numerical solutions and insights on the effect of microstructure on the enhancement of ionic conductivity. Specifically, we investigate the effect of shape by considering ellipsoidal inclusions. We also propose an easily manufacturable microstructure that increases the ionic conductivity of the composite electrolyte by forty times, simply by the addition of dielectric columns parallel to the solid electrolyte phase.

2020 ◽  
Vol 20 (2) ◽  
Author(s):  
Qolby Sabrina ◽  
Titik Lestariningsih ◽  
Christin Rina Ratri ◽  
Achmad Subhan

Solid polymer electrolyte (SPE) appropriate to solve packaging leakage and expansion volume in lithium-ion battery systems. Evaluation of electrochemical performance of SPE consisted of mixture lithium salt, solid plasticizer, and polymer precursor with different ratio. Impedance spectroscopy was used to investigate ionic conduction and dielectric response lithium bis(trifluoromethane)sulfony imide (LiTFSI) salt, and additive succinonitrile (SCN) plasticizer. The result showing enhanced high ionic conductivity. In half-cell configurations, wide electrochemical stability window of the SPE has been tested. Have stability window at room temperature, indicating great potential of SPE for application in lithium ion batteries. Additive SCN contribute to forming pores that make it easier for the li ion to move from the anode to the cathode and vice versa for better perform SPE. Pore of SPE has been charaterization with FE-SEM. Additive 5% w.t SCN shows the best ionic conductivity with 4.2 volt wide stability window and pretty much invisible pores.


2019 ◽  
Vol 12 (06) ◽  
pp. 1930006 ◽  
Author(s):  
Chengjun Yi ◽  
Wenyi Liu ◽  
Linpo Li ◽  
Haoyang Dong ◽  
Jinping Liu

Solid-state polymer lithium-ion batteries with better safety and higher energy density are one of the most promising batteries, which are expected to power future electric vehicles and smart grids. However, the low ionic conductivity at room temperature of solid polymer electrolytes (SPEs) decelerates the entry of such batteries into the market. Creating polymer-in-salt solid electrolytes (PISSEs) where the lithium salt contents exceed 50[Formula: see text]wt.% is a viable technology to enhance ionic conductivity at room temperature of SPEs, which is also suitable for scalable production. In this review, we first clarify the structure and ionic conductivity mechanism of PISSEs by analyzing the interactions between lithium salt and polymer matrix. Then, the recent advances on polyacrylonitrile (PAN)-based PISSEs and polycarbonate derivative-based PISSEs will be reviewed. Finally, we propose possible directions and opportunities to accelerate the commercializing of PISSEs for solid polymer Li-ion batteries.


RSC Advances ◽  
2019 ◽  
Vol 9 (66) ◽  
pp. 38646-38657 ◽  
Author(s):  
Sudeshna Patra ◽  
Pallavi Thakur ◽  
Bhaskar Soman ◽  
Anand B. Puthirath ◽  
Pulickel M. Ajayan ◽  
...  

The studies shown here prove that both the Li salt and ‘inert-polymer’ mixing have paramount importance in the tunability of Li ion conductivity in solid electrolytes for batteries.


2008 ◽  
Vol 73 (12) ◽  
pp. 1777-1798 ◽  
Author(s):  
Olt E. Geiculescu ◽  
Rama V. Rajagopal ◽  
Emilia C. Mladin ◽  
Stephen E. Creager ◽  
Darryl D. Desmarteau

The present work consists of a series of studies with regard to the structure and charge transport in solid polymer electrolytes (SPE) prepared using various new bis(trifluoromethanesulfonyl)imide (TFSI)-based dianionic dilithium salts in crosslinked low-molecular-weight poly(ethylene glycol). Some of the thermal properties (glass transition temperature, differential molar heat capacity) and ionic conductivities were determined for both diluted (EO/Li = 30:1) and concentrated (EO/Li = 10:1) SPEs. Trends in ionic conductivity of the new SPEs with respect to anion structure revealed that while for the dilute electrolytes ionic conductivity is generally rising with increased length of the perfluoroalkylene linking group in the dianions, for the concentrated electrolytes the trend is reversed with respect to dianion length. This behavior could be the result of a combination of two factors: on one hand a decrease in dianion basicity that results in diminished ion pairing and an enhancement in the number of charge carriers with increasing fluorine anion content, thereby increasing ionic conductivity while on the other hand the increasing anion size and concentration produce an increase in the friction/entanglements of the polymeric segments which lowers even more the reduced segmental motion of the crosslinked polymer and decrease the dianion contribution to the overall ionic conductivity. DFT modeling of the same TFSI-based dianionic dilithium salts reveals that the reason for the trend observed is due to the variation in ion dissociation enthalpy, derived from minimum-energy structures, with respect to perfluoroalkylene chain length.


Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3840
Author(s):  
Adrien Méry ◽  
Steeve Rousselot ◽  
David Lepage ◽  
Mickaël Dollé

All-solid-state lithium batteries (ASSLB) are very promising for the future development of next generation lithium battery systems due to their increased energy density and improved safety. ASSLB employing Solid Polymer Electrolytes (SPE) and Solid Composite Electrolytes (SCE) in particular have attracted significant attention. Among the several expected requirements for a battery system (high ionic conductivity, safety, mechanical stability), increasing the energy density and the cycle life relies on the electrochemical stability window of the SPE or SCE. Most published works target the importance of ionic conductivity (undoubtedly a crucial parameter) and often identify the Electrochemical Stability Window (ESW) of the electrolyte as a secondary parameter. In this review, we first present a summary of recent publications on SPE and SCE with a particular focus on the analysis of their electrochemical stability. The goal of the second part is to propose a review of optimized and improved electrochemical methods, leading to a better understanding and a better evaluation of the ESW of the SPE and the SCE which is, once again, a critical parameter for high stability and high performance ASSLB applications.


2020 ◽  
pp. 152808372097062
Author(s):  
Muhammad Yameen Solangi ◽  
Umair Aftab ◽  
Muhammad Ishaque ◽  
Aqeel Bhutto ◽  
Ayman Nafady ◽  
...  

Solid polymer electrolytes (SPEs) are the best choice to replace liquid electrolytes in supercapacitors, fuel cells, solar cells and batteries. The main challenge in this filed is the ionic conductivity and thermal stability of SPEs which is still not up to mark, therefore more investigations are needed to address these issues. In this study, PVA/salt based SPEs was fabricated using both solution cast and electro-spinning methods to probe the effect of different salts such as (NaCl, KCl and KI) and their concentrations on the ionic conductivity. Scanning electron microscopy (SEM) x and Fourier Transform Infra-Red (FTIR) have been employed to study the morphology as well as the different functional groups of SPEs, respectively. It was noted that small addition of NaCl, KCl and KI salts in SPEs dramatically increased the ionic conductivity to 5.95×10−6, 5.31×10−6 and 4.83×10−6 S/cm, respectively. Importantly, the SPEs obtained with NaCl via electro-spinning have higher ionic conductivity (5.95×10−6 S/cm) than their casted SPEs (1.87×10−6 S/cm). Thermal stability was also studied at two different temperatures i.e. 80 °C and 100 °C. The weight loss percentage of electrospun SPEs have zero percent weight loss than the solution based SPEs. The combined results clearly indicated that the nature of salt, concentration and fabrication process play a vital role in the ionic conductivity. Also, the NaCl salt with low molecular weight at low concentrations shows an enhanced ionic conductivity.


Author(s):  
Liying Tian ◽  
Ying Liu ◽  
Zhe Su ◽  
Yu Cao ◽  
Wanyu Zhang ◽  
...  

Solid polymer electrolytes (SPEs) with good flexibility and low cost are very promising for all-solid-state lithium metal batteries, but they suffer from the trad-off between ionic conductivity at room temperature...


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