Silicon Carbon Research Articles

Molten salt assisted synthesis of Si/C nanocomposite derived from palygorskite and sodium alginate for electrochemical lithium storage.

Silicon/carbon (Si/C) nanocomposites are considered as one of the most promising anode materials for lithium-ion batteries due to their high capacity and suitable lithiation potential. However, the complex and time-consuming preparation processes of silicon-based nanocomposites and the unexpected silicon carbide generated during high treatment make it difficult to achieve high-performance Si/C nanocomposites for practical applications. Herein, a silicon/carbon nanocomposite is successfully prepared through a facile and eco-friendly molten salt assisted precarbonization-reduction method using palygorskite (PAL) and sodium alginate as raw materials. Based on physical characterizations, it is demonstrated that the sodium alginate plays a key role in the successful preparation of Si/C nanocomposite, which not only boosts uniform embedding of PAL nanoparticles in the carbon matrix but also releases molten sodium salt to suppress the formation of unexpected SiC. When used as an alternative anode material for lithium-ion battery applications, the as-obtained Si/C composite delivers a high reversible specific capacity of 1362.7 mA h g-1 with an initial Coulombic efficiency of 70.3% at a current density of 200 mA g-1 and excellent long-term cycling stability. The findings here provide a facile and eco-friendly molten salt assisted precarbonization-reduction method for high-performance silicon/carbon anode materials.

Progress in the application of silicon-based materials in lithium-ion batteries anodes

From the battery that powers the remote control to the battery that powers electric cars, lithium-ion batteries (LIBs) are a crucial component of contemporary energy storage. The large theoretical capacity of silicon anodes provides significant benefits inside LIBs. However, the main issue with the conventional silicon bulk anode is its considerable volume expansion, which forms an unstable Solid Electrolyte Interface (SEI) layer during the charge and discharge process and severely reduces battery performance and lifespan. Therefore, to solve these issues, researchers have explored multiple improved silicon anodes, three of which are mentioned in this essay. Firstly, the researchers delve into the usage of nanotechnology. When manipulating silicon particles at the nano-scale, the nano-silicon can mitigate the volume expansion, improving the reaction kinetics. Then, a composite of carbon and silicon is proposed, combining silicon's high capacitance and carbon's high conductivity. After that is the silicon-metal composite, which utilizes metals' mechanical strength and conductivity to stabilize Si anodes further and improve thermal stability. Overall, the significance of this study lies in the exploration of the application of silicon anodes in LIBs, highlighting the potential of these composite materials and advanced technology, which may help guide the future exploration of better silicon anodes.

Effect of carbon black and silicon dioxide nanoparticle exposure on corona receptor ACE2 and TMPRSS2 expression in the ocular surface

The Coronavirus disease 2019 (COVID-19) pandemic has led to a global health crisis, including ocular symptoms, primarily targeting the Angiotensin-Converting Enzyme 2 (ACE2) receptor. PM2.5 air pollution may increase infection risk by altering ACE2 expression. Silicon Dioxide (SiO2) and carbon black (CB), major components of PM2.5 from sands and vehicle emissions, were studied for their effects on ACE2 and Transmembrane Protease Serine 2 (TMPRSS2) expression in corneal and conjunctival cells, and ocular tissues. Human corneal epithelial cells (HCECs) and conjunctival epithelial cells (HCjECs) were exposed to nanoparticles (NPs) for 24 hours, assessing viability via WST-8 assay. TNF-α, IL-6, and IL-1β levels in the medium were measured. An in vivo rat study administered NPs via eye drops, with Rose Bengal staining to evaluate damage. ACE2, TMPRSS2, and Angiotensin II (AngII) protein expressions were quantified by Western blot. ACE2 expression in HCjECs increased with NP exposure, while it decreased in HCECs. CB exposure increased TNF-α, IL-6, and IL-1β levels in HCECs. In vivo, corneal exposure to CB decreased ACE2 expression, whereas conjunctival exposure to SiO2 increased ACE2 expression. These changes suggest that SiO2 exposure may increase the risk of COVID-19 through the ocular surface, while CB exposure may decrease it.

Osteoblast Growth in Quaternized Silicon Carbon Nitride Coatings for Dental Implants.

The demand for dental implants has increased, establishing them as the standard of care for replacing missing teeth. Several factors contribute to the success or failure of an implant post-placement. Modifications to implant surfaces can enhance the biological interactions between bone cells and the implant, promoting better outcomes. Surface coatings have been developed to electrochemically alter implant surfaces, aiming to reduce healing time, enhance bone growth, and prevent bacterial adhesion. Quaternized silicon carbon nitride (QSiCN) is a novel material with unique electrochemical and biological properties. This study aimed to assess the influence of QSiCN, silicon carbide nitride (SiCN), and silicon carbide (SiC) coatings on the viability of osteoblast cells on nanostructured titanium surfaces. The experiment utilized thirty-two titanium sheets with anodized TiO2 nanotubes featuring nanotube diameters of 50 nm and 150 nm. These sheets were divided into eight groups (n = 4): QSiCN-coated 50 nm, QSiCN-coated 150 nm, SiCN-coated 50 nm, SiCN-coated 150 nm, SiC-coated 50 nm, SiC-coated 150 nm, non-coated 50 nm, and non-coated 150 nm. Preosteoblast MC3T3-E1 Subclone 4 cells (ATCC, USA) were used to evaluate osteoblast viability. After three days of cell growth, samples were assessed using scanning electron microscopy (SEM). The results indicated that QSiCN coatings significantly increased osteoblast proliferation (p < 0.005) compared to other groups. The enhanced cell adhesion observed with QSiCN coatings is likely due to the positive surface charge imparted by N+.

Flexible and lightweight carbon fiber/silicone resin composites with the “soft-rigid” structural interface for thermostable and antistatic applications

To avoid a large difference in modulus between carbon fiber (CF) and silicone resin (SR) and unstable thermal properties, the “soft-rigid” structural interface is constructed by coating polydopamine-polyethyleneimine@octaphenyl-silsesquioxane (PDA-PEI@octaphenyl-POSS) on the fiber surface. The tensile strength of the CF-AE@3P/SR composite was 24.35 % higher than that of the unmodified CF/SR. The mechanism of mechanical enhancement revealed that the rigid layer with nanoparticles effectively deflected the crack and prolonged the path, and the hydrogen bonds and van der Waals forces helped disperse the stress concentration at the interface. The defects in the soft–rigid structural interface were reduced, and the decomposition of the fibers and composites was effectively inhibited, thereby increasing the heat transmission in the composites. After heating for 20 s on the heating plate at 200 °C, the surface temperature of the CF-AE@3P/SR composite was 155.4 °C, which is higher than that of the unmodified CF/SR (131.4 °C). Therefore, the thermal stability of the CF-AE@3P/SR composites was significantly improved compared to that of unmodified CF/SR after holding at 350 °C for 3 h. Surface resistance analysis showed that the soft–rigid modification maintained the antistatic properties of the composites at room and high temperatures. It was also found that the CF-AE@P/SR composites exhibited good flexibility, lightweight, and hardness for application in sealing and electronic components. This work provides ideas for forming a seamless transition and effective bonding between high-modulus carbon fibers and a low-modulus elastomer matrix, increasing the thermal stability and mechanical properties, and maintaining the flexibility, stiffness, lightweight, and antistatic properties of composites at high temperatures

Synthesis Methods of Si/C Composite Materials for Lithium-Ion Batteries

Silicon anodes present a high theoretical capacity of 4200 mAh/g, positioning them as strong contenders for improving the performance of lithium-ion batteries. Despite their potential, the practical application of Si anodes is constrained by their significant volumetric expansion (up to 400%) during lithiation/delithiation, which leads to mechanical degradation and loss of electrical contact. This issue contributes to poor cycling stability and hinders their commercial viability, and various silicon–carbon composite fabrication methods have been explored to mitigate these challenges. This review covers key techniques, including ball milling, spray drying, pyrolysis, chemical vapor deposition (CVD), and mechanofusion. Each method has unique benefits; ball milling and spray drying are effective for creating homogeneous composites, whereas pyrolysis and CVD offer high-quality coatings that enhance the mechanical stability of silicon anodes. Mechanofusion has been highlighted for its ability to integrate silicon with carbon materials, showing the potential for further optimization. In light of these advancements, future research should focus on refining these techniques to enhance the stability and performance of Si-based anodes. The optimization of the compounding process has the potential to enhance the performance of silicon anodes by addressing the significant volume change and low conductivity, while simultaneously addressing cost-related concerns.

Production and Characterization of Hybrid Al6061 Nanocomposites

Aluminum-based hybrid nanocomposites, namely the Al6061 alloy, have gained prominence in the scientific community due to their unique properties, such as high strength, low density, and good corrosion resistance. The production of these nanocomposites involves incorporating reinforcing nanoparticles into the matrix to improve its mechanical and thermal properties. The Al6061 hybrid nanocomposites were manufactured by conventional powder metallurgy (cold pressing and sintering). Ceramic silicon carbide (SiC) nanoparticles and carbon nanotubes (CNTs) were used as reinforcements. The nanocomposites were produced using different reinforcement amounts (0.50, 0.75, 1.00, and 1.50 wt.%) and sintered from 540 to 620 °C for 120 min. The characterization of the Al6061 hybrid nanocomposites involved the analysis of their mechanical properties, such as hardness and tensile strength, as well as their micro- and nanometric structures. Techniques such as optical microscopy (OM) and scanning electron microscopy (SEM) with electron backscatter diffraction (EBSD) were used to study the distribution of nanoparticles, the grain size of the microstructure, and the presence of defects in the matrix. The microstructural evaluation revealed significant grain refinement and greater homogeneity in the hybrid nanocomposites reinforced with 0.75 wt.% of SiC and CNTs, resulting in better mechanical performance. Tensile tests showed that the Al6061/CNT/SiC hybrid composite had the highest tensile strength of 104 MPa, compared to 63 MPa for the unreinforced Al6061 matrix. The results showed that adding 0.75% SiC nanoparticles and CNTs can significantly improve the properties of Al6061 (65% in the tensile strength). However, some nanoparticle agglomeration remains one of the challenges in manufacturing these nanocomposites; therefore, the expected increase in mechanical properties is not observed.

Efficient and swift heating technique for crafting highly graphitized carbon and crystalline silicon (Si@GC) composite anodes for lithium‐ion batteries

Efficient and swift heating technique for crafting highly graphitized carbon and crystalline silicon (Si@GC) composite anodes for lithium‐ion batteries

Finite Element Simulations and Statistical Analysis for the Tribological Design of Mutually Textured Surfaces and Related Experimental Validation

Abstract In the last few decades, micro-texturing has become a widely studied technique to modify the frictional behavior between surfaces in both dry and lubricated regimes. Among all the available techniques, the laser surface texturing appears to be fast, clean, and flexible, and thus a good candidate in realizing surface micro-patterns, also for the improvement of the tribological performance of automotive components when subjected to dry friction. For this reason, in the present work, the tribological response of four different patterns of micro-holes on two contrasting materials, specifically silicon carbide and carbon black have been investigated with a coupled experimental–numerical approach. The static and the dynamic friction coefficients have been extracted from the 25 different combinations of these surface textures including the flat counterparts. Then, the influence of the holes diameter, their density, and the material has been studied thanks to a multivariate linear regression. Specifically, it emerged that, in a dry regime, the most emerging parameter is the micro-holes diameter, for both static and dynamic frictions. Moreover, for both static and dynamic frictions, the material which more influences the effects of patterns to the overall frictional behavior is here the stiffest one. These insights for the design of micro-patterned surfaces with controlled frictional properties could be useful for those applications in which a dry friction regime is present.

Image-Based Peridynamic Modeling-Based Micro-CT for Failure Simulation of Composites

By utilizing computed tomography (CT) technology, we can gain a comprehensive understanding of the specific details within the material. When combined with computational mechanics, this approach allows us to predict the structural response through numerical simulation, thereby avoiding the high experimental costs. In this study, the tensile cracking behavior of carbon–silicon carbide (C/SiC) composites is numerically simulated using the bond-based peridynamics model (BB-PD), which is based on geometric models derived from segmented images of three-dimensional (3D) CT data. To obtain results efficiently and accurately, we adopted a deep learning-based image recognition model to identify the kinds of material and then the pixel type that corresponds to the material point, which can be modeled by BB-PD for failure simulation. The numerical simulations of the composites indicate that the proposed image-based peridynamics (IB-PD) model can accurately reconstruct the actual composite microstructure. It can effectively simulate various fracture phenomena such as interfacial debonding, crack propagation affected by defects, and damage to the matrix.

Silicon–carbon superhydrophobic nano-structure for next generation semiconductor industry

Abstract Superhydrophobic surfaces are important in waterproof applications that withstand harsh chemical exposure, ultraviolet radiation, and heat. Surface energy modification of the surface, such as silanization or (fluoro)polymer coatings, increases the hydrophobicity of the nanostructure. The present study follows a bilayer architecture that turns hydrophilic silicon into a superhydrophobic one. The first step creates a unique silicon–graphene hybrid structure on the silicon surface by coating graphene on the P-type silicon substrate. In the second step, low surface energy material (a combination of hexadecyltrimethoxysilane and hexamethyldisilazane) is coated by the dip coating process. This study investigates the durability of superhydrophobicity under severe mechanical, thermal, and chemical conditions. High-temperature tolerance and water jet tests are also performed. The present work also involves the study of coating regeneration. This approach can be applied to all shapes and sizes of silicon–graphene surfaces and is proven to be excellent in the semiconductor industry.

Effect of SiCN thin film interlayer for ZnO-based RRAM.

This study investigates the effect of silicon carbon nitride (SiCN) as an interlayer for ZnO-based resistive random access memory (RRAM). SiCN was deposited using plasma-enhanced chemical vapor deposition (PECVD) with controlled carbon content, achieved by varying the partial pressure of tetramethylsilane (4MS). Our results indicate that increasing the carbon concentration enhances the endurance of RRAM devices but reduces the on/off ratio. Devices with SiCN exhibited lower operating voltages and more uniform resistive switching behavior. Oxygen migration from ZnO to SiCN is examined by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses, promoting the formation of conductive filaments (CFs) and lowering set voltages. Additionally, we examined the impact of top electrode oxidation on RRAM performance. The oxidation of the Ti top electrode was found to reduce endurance and increase low resistive state (LRS) resistance, potentially leading to device failure through the formation of an insulating layer between the electrode and resistive switching material. The oxygen storage capability of SiCN was further confirmed through high-temperature stress tests, demonstrating its potential as an oxygen reservoir. Devices with a 20 nm SiCN interlayer showed significantly improved endurance, with over 500 switching cycles, compared to 62 cycles in those with a 5 nm SiCN layer. However, the thicker SiCN layer resulted in a notably lower on/off ratio due to reduced capacitance. These findings suggest that SiCN interlayers can effectively enhance the performance and endurance of ZnO-based RRAM devices by acting as an oxygen reservoir and mitigating the top electrode oxidation effect.

A first-principles adsorption study of functionalized carbon, boron nitride, silicon carbon nanotubes with ifosfamide as vehicles for drug delivery: Thermal analysis

We investigated the adsorption of ifosfamide (IFS) on the outer surface of zigzag (10, 0) carbon nanotubes (CNT), boron nitride nanotubes (BNNT), and silicon carbon nanotubes (SiCNT), using density functional theory (DFT) calculations at the PBE-D3 level in a water solvent phase. Based on zero-point corrected binding energies (Ebin), IFS exhibits chemisorption through its O-head and Cl-head on CNT (−1.05 eV) compared to BNNT (−0.93 eV), characterized by covalent interaction. In contrast, IFS undergoes physisorption via its O-head on SiCNT with binding energy of −0.68 eV as the most stable model this interaction is driven by electrostatic forces. The formation of complexes between the drug and nanotubes is influenced by charge transfer dynamics. Our thermodynamic analysis demonstrates the Gibbs free energy (ΔG) and enthalpy energy (ΔH) for all models are exothermic and spontaneous. The observed decrease in binding energy for BNNT and CNT correlates with changes in their energy gap, dipole moment, and charge transfer upon IFS adsorption. Notably, SiCNT exhibits a different response with a significant energy gap change leading to an increase in dipole moment and charge transfer. These findings suggest that these nanotubes demonstrate promising sensitivity to the presence of IFS and could be explored as potential drug delivery systems for this drug.

A Comparative Study of Microwave Welding Using Multiwalled Carbon Nanotubes and Silicon Carbide Nanowhiskers as Microwave Susceptors

Recently, microwave welding has arisen as an advanced joining method due to its versatility and rapid heating capabilities. Among others, microwave susceptors play a crucial role in microwave welding, as different classes of microwave susceptors have distinct microwave heating mechanisms. In this work, polypropylene (PP) was utilized as a thermoplastic substrate and two types of microwaves susceptors, namely multiwalled carbon nanotubes (MWCNTs) and silicon carbide nanowhiskers (SiC NWs), were studied for microwave welding. The susceptor was first dispersed in acetone to form susceptor suspension. Next, the susceptor suspension was deposited onto the targeted area on substrate and paired with another bare PP substrate. The paired sample was then exposed to 800 W microwave radiation in a microwave oven. Afterward, the welded joint was evaluated using a tensile test and scanning electron microscopy to determine its joint strength and cross-section microstructure. The results showed that the joint strength increased as the heating duration increased. The welded joint formed using MWCNTs achieved a maximum strength of 2.26 MPa when 10 s was used, while the SiC NWs-formed welded joint achieved a maximum strength of 2.25 MPa at 15 s. This difference in duration in forming a complete welded joint can be attributed to the higher microwave heating rates and thermal conductivity of MWCNTs. However, increasing the heating duration to 20 s caused severe deformation at the welded joint and resulted in low joint strength. Overall, this study highlights the significance of understanding the microwave heating mechanism of different susceptors and provides essential insight into the selection of a microwave susceptor for microwave welding.

Synergistic Structural Integrity and Remarkable Structural Stability of NC@Si Anodes for Lithium-ion Batteries

The silicon-based anode has attracted wide attention because of its high theoretical specific capacity, which is expected to greatly improve the batteries’ energy density. However, during the charge-discharge cycles, the great volume expansion of the anode active silicon seriously restricts its electrochemical stability. Herein, N-doping carbon-coated silicon microsphere was prepared for lithium-ion batteries. Benefit from the core-shell structure formed from silicon carbon, the volume change of silicon anode during the cycle is well coordinated. What's more, N-doping carbon reduces the reaction energy barrier between silicon and lithium and accelerates the electrochemical reaction, which improves the cycling performance of the battery. The specific capacity of the prepared button battery is as high as 2913.13 mAh g−1 at the current density of 0.21 mA g−1, and the average coulomb efficiency is higher than 99.84% during the cycling. And the capacity of NC@SiO2 anode gradually stabilizes after 500 cycles.

Synergistic catalysis of dual-sites promoted cycloaddition of CO2 with epoxides

This study explores the catalytic efficacy of fluorine-modified 1 wt% copper oxide on MCM-41 (F-1Cu/MCM-41) in carbon dioxide cycloaddition reactions. It delves into reaction mechanisms, active sites, and the practical applicability of the catalyst. Comprehensive examination through in situ diffuse reflectance infrared Fourier transform spectroscopy and other analytical methods substantiated the role of halogen-modified mono-dispersed copper species in carbon dioxide activation and silicon hydroxide sites in epoxide activation, while underscoring the role of Lewis bases and Brønsted acids. Kinetic studies and density functional theory calculations pinpointed carbon dioxide activation as the pivotal step. Furthermore, the catalyst exhibited robust stability and efficiency in continuous flow experiments, sustaining a 99% selectivity towards cyclic carbonate over 150 h. An eco-friendly evaluation confirmed the sustainability of the process, emphasizing its minimal environmental footprint and high efficiency. These results establish fluorine-modified 1 wt% copper oxide on MCM-41 as a formidable candidate for industrial-scale cyclic carbonate production, due to its promising performance and sustainability.

Three-dimensional CNTs boosting the conductive confinement structure of silicon/carbon anodes in lithium-ion batteries

In this study, a surface functionalization strategy was proposed to involve carbon nanotubes and silicon nanoparticles encapsulated within carbon derived from a zeolite imidazole framework (ZIF-67). Multidimensional interconnected carbon nanotubes bolster the structural stability and facilitate ion/electron transfer within silicon/carbon composites. Silicon nanoparticles were successfully encapsulated in ZIF-67-derived carbon shells, with carbon nanotubes effectively transferring interfacial stress between silicon and carbon shell during lithiation, where ZIF-67-derived carbon reduces the volume expansion in silicon anodes. As a consequence, the outstanding cycle life and rate performance were demonstrated in the silicon/carbon composites. The specific capacity was maintained at 660 mAh g-1 over 200 cycles at 1 A g-1. The in-situ construction of this conductive confinement structure based on three-dimensional carbon nanotubes offers a promising design approach for advancing silicon/carbon anode technologies.

Electronic Skin as Human–Robot Interface for Human Grasp Recognition in Home-Care Robots: Introducing a Complete Set of Resources

Population aging has highlighted the significance of developing home-care robots to assist human life. However, traditional home-care robots work according to fixed procedures, which lack human–robot interaction to mimic human hand action. Human–robot interfaces provide an opportunity for interactions between robots and users, which play an important role in home-care robots. Traditional human–robot interfaces are based on rigid, cumbersome, and high-priced machines, which prevent their wide application in performing home-care tasks. An e-skin sensor with 11 stretchable resistors evenly distributed on the back of the human hand, which could be applied to monitor human finger motion and control robotic fingers to dexterously grasp diverse objects, is presented in this article. A 3D printer is employed to pattern high-performance wires into structurally soft and stretchable filamentary serpentines. The stretchable resistors are fabricated by a thin sensing film of mixed multiwalled carbon nanotubes (MWCNTs) and silicone elastomer. The e-skin sensor is applied in a hand-in-the-loop system for controlling a robotic hand to help grasp an object synchronously. A robot system is developed to connect the e-skin with the robotic hand to perform grasp actions with a success rate of more than 80%. By analyzing the experimental results of the e-skin sensor and robotic hand grasp, this work obtains insights showing that the skin sensor can help engineers design a home-care assistant plan for patients according to monitoring value or a human–robot interaction mode by robotic fingers mimicking human finger actions.

(Invited) A Study of the SEI Layer Cross-Talk in Si/C Composite Li-Ion Anodes

Composite electrodes, especially silicon/carbon (Si/C) anodes, present significant opportunities for advancing the energy density of lithium-ion batteries (LIBs). However, challenges emerge, particularly in performance metrics when a high weight percentage of Si beyond 8-10 wt.% is employed 1. A nuanced understanding of the solid electrolyte interphase (SEI) in Si/C composites is imperative to overcome these limitations and enhance energy density. Conventional techniques such as ex-situ X-ray photoelectron spectroscopy and cryogenic electron microscopy face inherent drawbacks, including exposure to ultrahigh vacuum and the need for solvent washing, potentially altering the SEI layer 2. In contrast, nano-FTIR, utilizing Fourier transform infrared near-field spectroscopy, overcomes these challenges, enabling non-destructive probing of the SEI layer's chemistry and structure at room temperature within an inert atmosphere 3–5.In this study, we engineer custom-patterned electrodes featuring amorphous Si on atomically flat highly ordered pyrolytic graphite (HOPG) to emulate model composite electrodes. Leveraging nano-FTIR spectroscopy, near-field nanoscale white-light imaging, and atomic force microscopy measurements, our investigation reveals that the SEI on HOPG is enriched in organic lithium ethylene decarbonate (LiEDC), while the SEI on lithiated silicon unveils the presence of inorganic Li2CO3. Notably, we unveil a unique "mixed" SEI layer zone at the Si/HOPG interface, comprising a mixture of dominant SEI species from the surfaces of both the lithiated Si and the HOPG. The coexistence of these species suggests the formation of an SEI layer with presumably unique physicochemical properties, forming along Si-C interfaces in Si/C composite electrodes. These findings provide a comprehensive approach to studying model composite electrodes and offer valuable insights into optimizing the surface passivation of Si/C composite electrodes for high-performance LIBs. Acknowledgments This research was supported by the US Department of Energy (DOE)’s Vehicle Technologies Office under the Silicon Consortium Project directed by Brian Cunningham and managed by Anthony Burrell. References V. G. Khomenko and V. Z. Barsukov, Electrochim Acta, 52, 2829–2840 (2007).J. Wu, M. Ihsan-Ul-Haq, Y. Chen, and J. K. Kim, Nano Energy, 89, 106489 (2021).X. He, J. M. Larson, H. A. Bechtel, and R. Kostecki, Nat Commun, 13, 1398 (2022).I. Yoon, J. M. Larson, and R. Kostecki, ACS Nano, 17, 6943–6954 (2023).A. Dopilka, Y. Gu, J. M. Larson, V. Zorba, and R. Kostecki, ACS Appl Mater Interfaces, 15, 6755–6767 (2023).

Gel Polymer Electrolyte Enables Low-Temperature and High-Rate Lithium-Ion Batteries via Bionic Interface Design.

Traditional ethylene carbonate (EC)-based electrolytes constrain the applications of silicon carbon (Si-C) anodes under fast-charging and low-temperature conditions due to sluggish Li+ migration kinetics and unstable solid electrolyte interphase (SEI). Herein, inspired by the efficient water purification and soil stabilization of aquatic plants, a stable SEI with a 3D desolvation interface is designed with gel polymer electrolyte (GPE), accelerating Li+ desolvation and migration at the interface and within stable SEI. As demonstrated by theoretical simulations and experiment results, the resulting poly(1,3-dioxolane) (PDOL), prepared by in situ ring-opening polymerization of 1,3-dioxolane (DOL), creates a 3D desolvation area, improving the Li+ desolvation at the interface and yielding an amorphous GPE with a high Li+ ionic conductivity (5.73 mS cm-1). Furthermore, more anions participate in the solvated structure, forming an anion-derived stable SEI and improving Li+ transport through SEI. Consequently, the Si-C anode achieves excellent rate performance with GPE at room temperature (RT) and low temperature (-40°C). The pouch full cell coupled with LiFePO4 cathode obtains 97.42 mAh g-1 after 500 cycles at 5 C/5 C. This innovatively designed 3D desolvation interface and SEI represent significant breakthroughs for developing fast-charging and low-temperature batteries.