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비만아 부모의 돌봄 경험: q 방법론

Among the contenders in the new generation energy storage arena, all-solid-state batteries (ASSBs) have emerged as particularly promising, owing to their potential to exhibit high safety, high energy density and long cycle life. The relatively low conductivity of most solid electrolytes and the often sluggish charge transfer kinetics at the interface between solid electrolyte and electrode layers are considered to be amongst the major challenges facing ASSBs. This review presents an overview of the state of the art in solid lithium and sodium ion conductors, with an emphasis on inorganic materials. The correlations between the composition, structure and conductivity of these solid electrolytes are illustrated and strategies to boost ion conductivity are proposed. In particular, the high grain boundary resistance of solid oxide electrolytes is identified as a challenge. Critical issues of solid electrolytes beyond ion conductivity are also discussed with respect to their potential problems for practical applications. The chemical and electrochemical stabilities of solid electrolytes are discussed, as are chemo-mechanical effects which have been overlooked to some extent. Furthermore, strategies to improve the practical performance of ASSBs, including optimizing the interface between solid electrolytes and electrode materials to improve stability and lower charge transfer resistance are also suggested.

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New horizons for inorganic solid state ion conductors

Recent Progress of the Solid-State Electrolytes for High-Energy Metal-Based Batteries

Solid-state batteries have been attracting wide attention for next generation energy storage devices due to the probability to realize higher energy density and superior safety performance compared with the state-of-the-art lithium ion batteries. However, there are still intimidating challenges for developing low cost and industrially scalable solid-state batteries with high energy density and stable cycling life for large-scale energy storage and electric vehicle applications. This review presents an overview on the scientific challenges, fundamental mechanisms, and design strategies for solid-state batteries, specifically focusing on the stability issues of solid-state electrolytes and the associated interfaces with both cathode and anode electrodes. First, we give a brief overview on the history of solid-state battery technologies, followed by introduction and discussion on different types of solid-state electrolytes. Then, the associated stability issues, from phenomena to fundamental understandings, are intensively discussed, including chemical, electrochemical, mechanical, and thermal stability issues; effective optimization strategies are also summarized. State-of-the-art characterization techniques and in situ and operando measurement methods deployed and developed to study the aforementioned issues are summarized as well. Following the obtained insights, perspectives are given in the end on how to design practically accessible solid-state batteries in the future.

Approaching Practically Accessible Solid-State Batteries: Stability Issues Related to Solid Electrolytes and Interfaces

Easy processing and flexibility of polymer electrolytes make them very promising in developing all-solid-state lithium batteries. However, their low room-temperature conductivity and poor mechanical and thermal properties still hinder their applications. Here, we use Li6.75La3Zr1.75Ta0.25O12 (LLZTO) ceramics to trigger structural modification of poly(vinylidene fluoride) (PVDF) polymer electrolyte. By combining experiments and first-principle calculations, we find that La atom of LLZTO could complex with the N atom and C═O group of solvent molecules such as N,N-dimethylformamide along with electrons enriching at the N atom, which behaves like a Lewis base and induces the chemical dehydrofluorination of the PVDF skeleton. Partially modified PVDF chains activate the interactions between the PVDF matrix, lithium salt, and LLZTO fillers, hence leading to significantly improved performance of the flexible electrolyte membrane (e.g., a high ionic conductivity of about 5 × 10–4 S cm–1 at 25 °C, high mechanical s...

Synergistic Coupling between Li6.75La3Zr1.75Ta0.25O12 and Poly(vinylidene fluoride) Induces High Ionic Conductivity, Mechanical Strength, and Thermal Stability of Solid Composite Electrolytes

Polymer nanocomposites are considered as promising dielectric media for electrostatic capacitors which are critical energy storage devices for pulse power applications due to their ultrahigh power density, superior cycle lifetime and reliability. The maximum energy density of percolative nanocomposites filled with conductive fillers is seriously compromised by their intrinsically low breakdown strength despite their very high dielectric permittivity. Here we demonstrate that a trace amount of Ag nanodots (∼0.05 vol%) in situ synthesized in a poly(vinylidene fluoride-hexafluoropropylene) matrix gives rise to concomitant enhancement of dielectric permittivity (∼50%) and breakdown strength (∼15%) and hence ultrahigh discharge energy density (∼27 J cm−3), which is the highest energy density ever achieved for percolative polymer composites. Experimental and first principles calculation results show that the non-intuitive enhancement could be attributed to charge-transfer complexes formed between the nanodots and the polymer chains and enhanced chain mobility in an electric field.

Non-intuitive concomitant enhancement of dielectric permittivity, breakdown strength and energy density in percolative polymer nanocomposites by trace Ag nanodots

Enhanced breakdown strength and suppressed leakage current of polyvinylidene fluoride nanocomposites by two-dimensional ZrO 2 nanosheets

Engineering interfacial adhesion for high-performance lithium metal anode

The manufacturing of both metals and polymer materials strongly relies on melt processing at relatively high temperatures which needs complex shaping-cooling equipment, long molding time, and considerable energy consumption. Reducing the processing temperature to achieve room-temperature malleability is heavily desired for low-carbon demands but continues to be a great challenge. Here, we demonstrate a noncovalent assembly strategy to fabricate room-temperature malleable composites embedded by liquid metals with excellent toughness (105.88 MJ m-3, higher than most traditional plastics and metallic aluminum) and strong mechanical strength (35.49 MPa). The dissociation-reconstruction of supramolecular bonding interactions between assembled nanoparticles and polymer matrix allow the malleable composite with two interchangeable supramolecular states to achieve programming at room temperature stimulated by water vapor and give it self-healing ability (self-healing efficiency of ∼100%; the healed sample can lift about 52,300 times its own weight). Furthermore, the composite also exhibits metallic luster and prospective application in thermal dissipation. This strategy might be an efficient way for the development of a method for strong and tough materials structurally designed to achieve programming at moderate conditions.

Xin Huang

Papers

Synergistic Coupling between Li6.75La3Zr1.75Ta0.25O12 and Poly(vinylidene fluoride) Induces High Ionic Conductivity, Mechanical Strength, and Thermal Stability of Solid Composite Electrolytes

Non-intuitive concomitant enhancement of dielectric permittivity, breakdown strength and energy density in percolative polymer nanocomposites by trace Ag nanodots

Enhanced breakdown strength and suppressed leakage current of polyvinylidene fluoride nanocomposites by two-dimensional ZrO 2 nanosheets

Engineering interfacial adhesion for high-performance lithium metal anode

Noncovalent Assembly Enabled Strong yet Tough Materials with Room-Temperature Malleability and Healability.