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The stabilization of sulfur species in coal-derived hard carbon by micropore confinement and chemical bonding to improve sodium storage

石炭由来ハードカーボンにおける硫黄種の細孔閉じ込めと化学結合による安定化とナトリウム貯蔵の向上 (AI 翻訳)

zhu hong, Guo Chunli, Shenyan Peak

Science Data Bankデータセット2026-07-27#エネルギー転換
DOI: 10.57760/sciencedb.j00125.00240
原典: https://doi.org/10.57760/sciencedb.j00125.00240

🤖 gxceed AI 要約

日本語

石炭由来のハードカーボンアノードに硫黄種を微細孔閉じ込めと化学結合で安定化する戦略を提案。800サイクル後も450 mAh/gの高い可逆容量を示し、ナトリウムイオン電池の性能向上に寄与する。

English

A stabilization strategy for sulfur species in coal-derived hard carbon anodes using micropore confinement and chemical bonding is proposed. It achieves high reversible capacity of 450 mAh/g after 800 cycles, improving sodium-ion battery performance for energy storage.

Unofficial AI-generated summary based on the public title and abstract. Not an official translation.

📝 gxceed 編集解説 — Why this matters

日本のGX文脈において

日本では再生可能エネルギーの導入拡大に伴い、大規模蓄電池の需要が高まっている。本研究成果は低コストで高性能なナトリウムイオン電池の実現に寄与し、日本のエネルギー転換に間接的に貢献する可能性がある。

In the global GX context

The paper advances sodium-ion battery technology using coal-derived hard carbon, which is relevant for low-cost grid storage and electric vehicle batteries. This supports global decarbonization by enabling greater renewable energy integration.

👥 読者別の含意

🔬研究者:Materials scientists and battery researchers can leverage the dual stabilization mechanism to design better carbon anodes for sodium-ion batteries.

📄 Abstract(原文)

To solve the problems of limited capacity, low initial coulombic efficiency, and poor long-term cycling stability in hard carbon anodes for sodium-ion batteries, a stabilization strategy is proposed that uses both microporous confinement and chemical bonding to control the sulfur species. Hard carbon is derived from bituminous coal, taking advantage of its naturally condensed aromatic framework. Using a two-step thermal process, a microporous carbon framework was constructed, followed by gas-phase sulfidation to introduce sulfur species. The sulfur is confined in the micropores while forming stable covalent C-S bonds with the carbon matrix, which stabilizes the sulfur by both physical and chemical means and thus suppresses sulfur migration, which prevents interfacial side reactions and introduces additional redox-active sites. As a result, the sample delivers a high reversible capacity of 450 mAh/g after 800 cycles at a current density of 1 A/g, with excellent rate capability and cycling stability. Analysis of the storage mechanism shows that the stabilized sulfur species can reversibly participate in the sodium-ion storage and improve interfacial kinetics .

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