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Microstructure, pore accessibility, and sodium storage in hard–soft carbon composites: Implications of hard-carbon precursor morphology

Israr Ahmed, Hiroyuki Ueda, Anthony Somers, Maria Forsyth, Nolene Byrne

Electrochimica Acta📚 査読済 / ジャーナル2026-06-08#エネルギー転換Origin: Global経営インパクト: コスト削減対象セクター: automotive
DOI: 10.1016/j.electacta.2026.149308
原典: https://doi.org/10.1016/j.electacta.2026.149308

🤖 gxceed AI 要約

日本語

ハードカーボン(HC)とソフトカーボン(SC)の複合材料における、HC前駆体の形態がナトリウム貯蔵挙動に与える影響を調査。SC添加により細孔へのアクセスが制限され、低電圧プラトー容量が低下するが、適度な添加でレート性能が向上することを示した。

English

This study investigates how the morphology of hard carbon (HC) precursor affects the electrochemical performance of HC-soft carbon (SC) composites for sodium-ion batteries. SC addition restricts access to pore domains, reducing low-voltage plateau capacity but improving rate capability at moderate levels.

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

日本は次世代電池の開発に力を入れており、本研究成果はナトリウムイオン電池の実用化に向けた材料設計に貢献する可能性がある。

In the global GX context

This work advances understanding of sodium-ion battery anodes, which are critical for cost-effective energy storage in global decarbonization efforts. It provides design principles for hard-soft carbon composites that could accelerate grid storage and EV adoption.

👥 読者別の含意

🔬研究者:Materials scientists can use the findings to design better hard-soft carbon composites for sodium-ion batteries, focusing on precursor morphology and pore accessibility.

🏢実務担当者:Battery manufacturers can optimize anode material synthesis by adjusting hard carbon precursor and soft carbon ratio to balance capacity and rate performance.

📄 Abstract(原文)

Hard carbon (HC) is a leading anode material for sodium-ion batteries (SIBs), and combining HC with soft carbon (SC) has been widely explored to tune electrochemical performance. However, it remains unclear how the precursor morphology of HC influences the microstructure ordering and pore accessibility of HC-SC composites and, consequently, their sodium storage behaviour. In this study, HC derived from microcrystalline cellulose (MCC) was co-carbonised with pitch-derived SC to produce composites with varying HC/SC ratios, which were evaluated under identical electrochemical conditions. Structural characterisation shows that SC addition modifies the degree of structural ordering in the carbon matrix, while Raman analysis indicates that the overall defect population remains largely unchanged across the series. Gas adsorption and NMR wetting experiments further reveal that SC addition restricts access to confined pore domains within the HC framework, limiting sodium storage in the low-voltage plateau region. Electrochemically, the sloping capacity and diffusion coefficients remain broadly similar across the composites, whereas the low-voltage plateau capacity and initial Coulombic efficiency (ICE) progressively decrease with increasing SC content. Furthermore, rate capability improves with moderate SC addition, with the MCC HC-SC composite containing 15 wt% SC delivering the highest rate performance (117 mAh g -1 at 500 mA g -1 ). These results show that the electrochemical response of HC–SC composites is not universal but is controlled by the morphology-dependent accessibility and the utilisation of low-voltage sodium storage domains.

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