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Organic molecular design for high-power density sodium-ion batteries.

Chem Commun (Camb)

January 2025

Fachgebiet Angewandte Nanophysik, Institut für Physik & IMN MacroNano, Technische Universität Ilmenau, Ilmenau 98693, Germany.

Organic materials, with abundant resources, low cost, high flexibility, tunable structures, lightweight nature, and wide operating temperature range, are regarded as promising candidates for sodium-ion batteries (SIBs). Unfortunately, their poor electronic and ionic conductivity remain significant challenges, hindering the achievement of high power density for sodium storage. Power density, a critical factor in battery performance evaluation, is essential for assessing fast charging capabilities.

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With the rapid advancement of information technology, the need to achieve ultra-high-density data storage has become a pressing necessity. This study synthesized three hyperbranched polyimides (HBPI-TAPP, HBPI-(Zn)TAPP, and HBPI-(Cu)TAPP) by polymerizing 5,10,15,20-tetrakis(4-aminophenyl)porphyrin (TAPP), which features a cavity for metal ion coordination, with 4,4'-(hexafluoroisopropylidene)diphthalic anhydride (6FDA), to systematically investigate the effect of metal ion species on storage performance. According to the results, memory devices based on HBPI-(Zn)TAPP exhibit volatile SRAM (static random-access memory) characteristics, whereas devices employing HBPI-TAPP and HBPI-(Cu)TAPP demonstrate non-volatile WORM (write-once, read-many) characteristics.

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Amorphization Stabilizes Te-based Aqueous Batteries via Confining Free Water.

Angew Chem Int Ed Engl

January 2025

Fudan University, Laboratory of Advanced Materials, Shanghai, 200433, Shanghai, CHINA.

Tellurium (Te), with its rich valence states (-2 to +6), could endow aqueous batteries with potentially high specific capacity. However, achieving complete and stable hypervalent Te0/Te4+ electrochemistry in an aqueous environment poses significant challenges, owing to the sluggish reduction kinetics, the easy dissolution of Te4+ species, and a controversial energy storage mechanism. Herein, for the first time, we demonstrate an amorphous strategy for robust aqueous TeO2/Te electrochemistry.

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Recent Advances on Characterization Techniques for the Composition-Structure-Property Relationships of Solid Electrolyte Interphase.

Small Methods

January 2025

College of Physics and Energy, Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, Fujian Normal University, Fuzhou, 350117, China.

The Solid Electrolyte Interphase (SEI) is a nanoscale thickness passivation layer that forms as a product of electrolyte decomposition through a combination of chemical and electrochemical reactions in the cell and evolves over time with charge/discharge cycling. The formation and stability of SEI directly determine the fundamental properties of the battery such as first coulombic efficiency (FCE), energy/power density, storage life, cycle life, and safety. The dynamic nature of SEI along with the presence of spatially inhomogeneous organic and inorganic components in SEI encompassing crystalline, amorphous, and polymeric nature distributed across the electrolyte to the electrolyte-electrode interface, highlights the need for advanced in situ/operando techniques to understand the formation and structure of these materials in creating a stable interface in real-world operating conditions.

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2D materials feature large specific surface areas and abundant active sites, showing great potential in energy storage and conversion. However, the dense, stacked structure severely restricts its practical application. Inspired by the structure of bamboo in nature, hollow interior and porous exterior wall, hollow MXene aerogel fiber (HA-TiCT fiber) is proposed.

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